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Graeme I. Bell - Publications

Affiliations: 
University of Chicago, Chicago, IL 
Area:
Molecular Biology, Biochemistry, Physiology Biology
Website:
https://biomedsciences.uchicago.edu/page/graeme-bell-phd
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320 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Støy J, De Franco E, Ye H, Park SY, Bell GI, Hattersley AT. In celebration of a century with insulin - Update of insulin gene mutations in diabetes. Molecular Metabolism. 101280. PMID 34174481 DOI: 10.1016/j.molmet.2021.101280  0.312
2019 Petty LE, Highland HM, Gamazon ER, Hu H, Karhade M, Chen HH, de Vries PS, Grove ML, Aguilar D, Bell GI, Huff CD, Hanis CL, Doddapaneni H, Munzy DM, Gibbs RA, et al. Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample. Human Molecular Genetics. PMID 30624610 DOI: 10.1093/Hmg/Ddy435  0.335
2017 Jun G, Manning A, Almeida M, Zawistowski M, Wood AR, Teslovich TM, Fuchsberger C, Feng S, Cingolani P, Gaulton KJ, Dyer T, Blackwell TW, Chen H, Chines PS, Choi S, ... ... Bell GI, et al. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proceedings of the National Academy of Sciences of the United States of America. PMID 29279374 DOI: 10.1073/Pnas.1705859115  0.347
2017 Jason F, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Bell GI, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179. PMID 29257133 DOI: 10.1038/Sdata.2017.179  0.319
2017 Mercader JM, Liao RG, Davis A, Dymek Z, Estrada K, Tukiainen T, Huerta-Chagoya A, Moreno-Macías H, Jablonski KA, Hanson RL, Walford GA, Moran I, Chen L, Agarwala V, Ordoñez-Sánchez ML, ... ... Bell GI, et al. A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes. Diabetes. PMID 28838971 DOI: 10.2337/Db17-0187  0.359
2017 Støy J, Olsen J, Park SY, Gregersen S, Hjørringgaard CU, Bell GI. In vivo measurement and biological characterisation of the diabetes-associated mutant insulin p.R46Q (GlnB22-insulin). Diabetologia. PMID 28478482 DOI: 10.1007/S00125-017-4295-2  0.409
2017 Manning A, Highland HM, Gasser J, Sim X, Tukiainen T, Fontanillas P, Grarup N, Rivas MA, Mahajan A, Locke AE, Cingolani P, Pers TH, Viñuela A, Brown AA, Wu Y, ... ... Bell GI, et al. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. PMID 28341696 DOI: 10.2337/Db16-1329  0.402
2017 Im HK, Barbeira A, Zheng J, Torres J, Dickinson S, Wheeler H, Bell G, Nicolae D, Cox N. Generating A Database of Phenotypic Consequences of Gene Regulation Across 40 Human Tissues European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.466  0.323
2016 Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ, Rivas MA, Perry JR, Sim X, Blackwell TW, Robertson NR, ... ... Bell GI, et al. The genetic architecture of type 2 diabetes. Nature. PMID 27398621 DOI: 10.1038/Nature18642  0.345
2016 Horikoshi M, Pasquali L, Wiltshire S, Huyghe JR, Mahajan A, Asimit JL, Ferreira T, Locke AE, Robertson NR, Wang X, Sim X, Fujita H, Hara K, Young R, Zhang W, ... ... Bell GI, et al. Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. Human Molecular Genetics. PMID 26911676 DOI: 10.1093/Hmg/Ddw048  0.32
2015 Carmody D, Park SY, Ye H, Perrone ME, Alkorta-Aranburu G, Highland HM, Hanis CL, Philipson LH, Bell GI, Greeley SA. Continued lessons from the INS gene: an intronic mutation causing diabetes through a novel mechanism. Journal of Medical Genetics. PMID 26101329 DOI: 10.1136/Jmedgenet-2015-103220  0.368
2015 Mahajan A, Sim X, Ng HJ, Manning A, Rivas MA, Highland HM, Locke AE, Grarup N, Im HK, Cingolani P, Flannick J, Fontanillas P, Fuchsberger C, Gaulton KJ, Teslovich TM, ... ... Bell GI, et al. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. Plos Genetics. 11: e1004876. PMID 25625282 DOI: 10.1371/Journal.Pgen.1004876  0.347
2015 Bailey KA, Savic D, Zielinski M, Park SY, Wang LJ, Witkowski P, Brady M, Hara M, Bell GI, Nobrega MA. Evidence of non-pancreatic beta cell-dependent roles of Tcf7l2 in the regulation of glucose metabolism in mice. Human Molecular Genetics. 24: 1646-54. PMID 25398947 DOI: 10.1093/Hmg/Ddu577  0.367
2015 Hara M, Fowler JL, Bell GI, Philipson LH. Resting beta-cells - A functional reserve? Diabetes and Metabolism. DOI: 10.1016/J.Diabet.2016.01.001  0.322
2014 Estrada K, Aukrust I, Bjørkhaug L, Burtt NP, Mercader JM, García-Ortiz H, Huerta-Chagoya A, Moreno-Macías H, Walford G, Flannick J, Williams AL, Gómez-Vázquez MJ, Fernandez-Lopez JC, Martínez-Hernández A, ... ... Bell GI, et al. Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population. Jama. 311: 2305-14. PMID 24915262 DOI: 10.1001/Jama.2014.6511  0.302
2014 Ren D, Sun J, Wang C, Ye H, Mao L, Cheng EH, Bell GI, Polonsky KS. Role of BH3-only molecules Bim and Puma in β-cell death in Pdx1 deficiency. Diabetes. 63: 2744-50. PMID 24658302 DOI: 10.2337/Db13-1513  0.34
2014 Mahajan A, Go MJ, Zhang W, Below JE, Gaulton KJ, Ferreira T, Horikoshi M, Johnson AD, Ng MC, Prokopenko I, ... ... Bell GI, et al. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics. 46: 234-44. PMID 24509480 DOI: 10.1038/Ng.2897  0.314
2014 He BZ, Ludwig MZ, Dickerson DA, Barse L, Arun B, Vilhjálmsson BJ, Jiang P, Park SY, Tamarina NA, Selleck SB, Wittkopp PJ, Bell GI, Kreitman M. Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin. Genetics. 196: 557-67. PMID 24281155 DOI: 10.1534/Genetics.113.157800  0.374
2014 Park SY, Ludwig MZ, Tamarina NA, He BZ, Carl SH, Dickerson DA, Barse L, Arun B, Williams CL, Miles CM, Philipson LH, Steiner DF, Bell GI, Kreitman M. Genetic complexity in a Drosophila model of diabetes-associated misfolded human proinsulin. Genetics. 196: 539-55. PMID 24281154 DOI: 10.1534/Genetics.113.157602  0.305
2014 Shalev SA, Tenenbaum-Rakover Y, Horovitz Y, Paz VP, Ye H, Carmody D, Highland HM, Boerwinkle E, Hanis CL, Muzny DM, Gibbs RA, Bell GI, Philipson LH, Greeley SA. Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder. Pediatric Diabetes. 15: 252-6. PMID 24138066 DOI: 10.1111/Pedi.12086  0.36
2013 Savic D, Park SY, Bailey KA, Bell GI, Nobrega MA. In vitro scan for enhancers at the TCF7L2 locus. Diabetologia. 56: 121-5. PMID 23011354 DOI: 10.1007/S00125-012-2730-Y  0.339
2012 Ogata M, Awaji T, Iwasaki N, Fujimaki R, Takizawa M, Maruyama K, Bell GI, Iwamoto Y, Uchigata Y. Localization of hepatocyte nuclear factor-4α in the nucleolus and nucleus is regulated by its C-terminus. Journal of Diabetes Investigation. 3: 449-56. PMID 24843605 DOI: 10.1111/J.2040-1124.2012.00210.X  0.355
2012 Johansson S, Irgens H, Chudasama KK, Molnes J, Aerts J, Roque FS, Jonassen I, Levy S, Lima K, Knappskog PM, Bell GI, Molven A, Njølstad PR. Exome sequencing and genetic testing for MODY. Plos One. 7: e38050. PMID 22662265 DOI: 10.1371/Journal.Pone.0038050  0.358
2012 Savic D, Bell GI, Nobrega MA. An in vivo cis-regulatory screen at the type 2 diabetes associated TCF7L2 locus identifies multiple tissue-specific enhancers. Plos One. 7: e36501. PMID 22590553 DOI: 10.1371/Journal.Pone.0036501  0.368
2012 Chong AS, Bell GI. Three Strikes and You're Cured. Science Translational Medicine. 4: 133fs12. PMID 22572878 DOI: 10.1126/Scitranslmed.3004020  0.343
2011 Naylor RN, Greeley SA, Bell GI, Philipson LH. Genetics and pathophysiology of neonatal diabetes mellitus. Journal of Diabetes Investigation. 2: 158-69. PMID 24843477 DOI: 10.1111/J.2040-1124.2011.00106.X  0.413
2011 Greeley SA, Naylor RN, Philipson LH, Bell GI. Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment. Current Diabetes Reports. 11: 519-32. PMID 21993633 DOI: 10.1007/S11892-011-0234-7  0.44
2011 Fajans SS, Bell GI. MODY: history, genetics, pathophysiology, and clinical decision making. Diabetes Care. 34: 1878-84. PMID 21788644 DOI: 10.2337/Dc11-0035  0.351
2011 Savic D, Ye H, Aneas I, Park SY, Bell GI, Nobrega MA. Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism. Genome Research. 21: 1417-25. PMID 21673050 DOI: 10.1101/Gr.123745.111  0.387
2011 Below JE, Gamazon ER, Morrison JV, Konkashbaev A, Pluzhnikov A, McKeigue PM, Parra EJ, Elbein SC, Hallman DM, Nicolae DL, Bell GI, Cruz M, Cox NJ, Hanis CL. Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. Diabetologia. 54: 2047-55. PMID 21647700 DOI: 10.1007/S00125-011-2188-3  0.315
2011 Lipton RB, Drum M, Greeley SA, Danielson KK, Bell GI, Hagopian WA. HLA-DQ haplotypes differ by ethnicity in patients with childhood-onset diabetes. Pediatric Diabetes. 12: 388-95. PMID 21418452 DOI: 10.1111/J.1399-5448.2010.00712.X  0.322
2011 Greeley SA, John PM, Winn AN, Ornelas J, Lipton RB, Philipson LH, Bell GI, Huang ES. The cost-effectiveness of personalized genetic medicine: the case of genetic testing in neonatal diabetes. Diabetes Care. 34: 622-7. PMID 21273495 DOI: 10.2337/Dc10-1616  0.356
2011 Støy J, Steiner DF, Park S, Ye H, Philipson LH, Bell GI. Erratum to: Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene Reviews in Endocrine and Metabolic Disorders. 13: 79-81. DOI: 10.1007/S11154-011-9158-4  0.394
2010 Støy J, Steiner DF, Park SY, Ye H, Philipson LH, Bell GI. Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene. Reviews in Endocrine & Metabolic Disorders. 11: 205-15. PMID 20938745 DOI: 10.1007/S11154-010-9151-3  0.404
2010 Fu YP, Hallman DM, Gonzalez VH, Klein BE, Klein R, Hayes MG, Cox NJ, Bell GI, Hanis CL. Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas. Journal of Ophthalmology. 2010. PMID 20871662 DOI: 10.1155/2010/861291  0.39
2010 Fajans SS, Bell GI, Paz VP, Below JE, Cox NJ, Martin C, Thomas IH, Chen M. Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60. Translational Research : the Journal of Laboratory and Clinical Medicine. 156: 7-14. PMID 20621032 DOI: 10.1016/J.Trsl.2010.03.003  0.334
2010 Greeley SA, Tucker SE, Naylor RN, Bell GI, Philipson LH. Neonatal diabetes mellitus: a model for personalized medicine. Trends in Endocrinology and Metabolism: Tem. 21: 464-72. PMID 20434356 DOI: 10.1016/J.Tem.2010.03.004  0.369
2010 Cheverud JM, Fawcett GL, Jarvis JP, Norgard EA, Pavlicev M, Pletscher LS, Polonsky KS, Ye H, Bell GI, Semenkovich CF. Calpain-10 is a component of the obesity-related quantitative trait locus Adip1. Journal of Lipid Research. 51: 907-13. PMID 20388922 DOI: 10.1194/Jlr.M900128  0.331
2010 Grossman EJ, Lee DD, Tao J, Wilson RA, Park SY, Bell GI, Chong AS. Glycemic control promotes pancreatic beta-cell regeneration in streptozotocin-induced diabetic mice. Plos One. 5: e8749. PMID 20090914 DOI: 10.1371/Journal.Pone.0008749  0.326
2010 Park SY, Ye H, Steiner DF, Bell GI. Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted. Biochemical and Biophysical Research Communications. 391: 1449-54. PMID 20034470 DOI: 10.1016/J.Bbrc.2009.12.090  0.353
2010 Greeley SA, Tucker SE, Worrell HI, Skowron KB, Bell GI, Philipson LH. Update in neonatal diabetes. Current Opinion in Endocrinology, Diabetes, and Obesity. 17: 13-9. PMID 19952737 DOI: 10.1097/Med.0B013E328334F158  0.369
2010 Rajan S, Eames SC, Park SY, Labno C, Bell GI, Prince VE, Philipson LH. In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes. American Journal of Physiology. Endocrinology and Metabolism. 298: E403-10. PMID 19952343 DOI: 10.1152/Ajpendo.00592.2009  0.411
2010 Villareal DT, Robertson H, Bell GI, Patterson BW, Tran H, Wice B, Polonsky KS. TCF7L2 variant rs7903146 affects the risk of type 2 diabetes by modulating incretin action. Diabetes. 59: 479-85. PMID 19934000 DOI: 10.2337/Db09-1169  0.347
2009 Johnson JD, Otani K, Bell GI, Polonsky KS. Impaired insulin secretion in transgenic mice over-expressing calpastatin in pancreatic β-cells. Islets. 1: 242-8. PMID 21099278 DOI: 10.4161/Isl.1.3.9780  0.383
2009 Steiner DF, Park SY, Støy J, Philipson LH, Bell GI. A brief perspective on insulin production. Diabetes, Obesity & Metabolism. 11: 189-96. PMID 19817801 DOI: 10.1111/J.1463-1326.2009.01106.X  0.399
2009 Kawai T, Ng MC, Hayes MG, Yoshiuchi I, Tsuchiya T, Robertson H, Cox NJ, Polonsky KS, Bell GI, Ehrmann DA. Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome. Diabetes Research and Clinical Practice. 86: 186-92. PMID 19782423 DOI: 10.1016/J.Diabres.2009.09.002  0.327
2009 Villareal DT, Koster JC, Robertson H, Akrouh A, Miyake K, Bell GI, Patterson BW, Nichols CG, Polonsky KS. Kir6.2 variant E23K increases ATP-sensitive K+ channel activity and is associated with impaired insulin release and enhanced insulin sensitivity in adults with normal glucose tolerance. Diabetes. 58: 1869-78. PMID 19491206 DOI: 10.2337/Db09-0025  0.367
2008 Støy J, Greeley SA, Paz VP, Ye H, Pastore AN, Skowron KB, Lipton RB, Cogen FR, Bell GI, Philipson LH. Diagnosis and treatment of neonatal diabetes: a United States experience. Pediatric Diabetes. 9: 450-9. PMID 18662362 DOI: 10.1111/J.1399-5448.2008.00433.X  0.322
2008 Molven A, Ringdal M, Nordbø AM, Raeder H, Støy J, Lipkind GM, Steiner DF, Philipson LH, Bergmann I, Aarskog D, Undlien DE, Joner G, Søvik O, Bell GI, et al. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes. 57: 1131-5. PMID 18192540 DOI: 10.2337/Db07-1467  0.402
2008 Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI, et al. Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood. Diabetes. 57: 1034-42. PMID 18162506 DOI: 10.2337/Db07-1405  0.386
2008 Norton L, Parr T, Chokkalingam K, Bardsley RG, Ye H, Bell GI, Pelsers MM, van Loon LJ, Tsintzas K. Calpain-10 gene and protein expression in human skeletal muscle: effect of acute lipid-induced insulin resistance and type 2 diabetes. The Journal of Clinical Endocrinology and Metabolism. 93: 992-8. PMID 18089694 DOI: 10.1210/Jc.2007-1981  0.351
2008 Hara M, Shen J, Pugh W, Polonsky KS, Le Beau MM, Bell GI. Sustained expression of hepatocyte nuclear factor-6 leads to loss of pancreatic beta-cells by apoptosis. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. 115: 654-61. PMID 18058600 DOI: 10.1055/S-2007-982514  0.349
2007 Fajans SS, Bell GI. Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4α (HNF4A) Diabetologia. 50: 2600-2601. PMID 17891372 DOI: 10.1007/S00125-007-0833-7  0.31
2007 Støy J, Edghill EL, Flanagan SE, Ye H, Paz VP, Pluzhnikov A, Below JE, Hayes MG, Cox NJ, Lipkind GM, Lipton RB, Greeley SA, Patch AM, Ellard S, Steiner DF, ... ... Bell GI, et al. Insulin gene mutations as a cause of permanent neonatal diabetes. Proceedings of the National Academy of Sciences of the United States of America. 104: 15040-4. PMID 17855560 DOI: 10.1073/Pnas.0707291104  0.426
2007 Hayes MG, Pluzhnikov A, Miyake K, Sun Y, Ng MC, Roe CA, Below JE, Nicolae RI, Konkashbaev A, Bell GI, Cox NJ, Hanis CL. Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies. Diabetes. 56: 3033-44. PMID 17846124 DOI: 10.2337/Db07-0482  0.348
2007 Njølstad P, Cockburn B, Bell G, Søvik O. A missense mutation, Val62Ala, in the glucokinase gene in a Norwegian family with maturity-onset diabetes of the young. Acta Paediatrica. 87: 853-856. DOI: 10.1111/J.1651-2227.1998.Tb01550.X  0.413
2006 Pihlajamäki J, Salmenniemi U, Vänttinen M, Ruotsalainen E, Kuusisto J, Vauhkonen I, Kainulainen S, Ng MCY, Cox NJ, Bell GI, Laakso M. Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes. Diabetologia. 49: 1560-1566. PMID 16752174 DOI: 10.1007/S00125-006-0270-Z  0.379
2006 Hathout E, Mace J, Bell GI, Njølstad PR. Treatment of hyperglycemia in a 7-year-old child diagnosed with neonatal diabetes. Diabetes Care. 29: 1458. PMID 16732049 DOI: 10.2337/Dc06-0487  0.382
2006 Sagen JV, Odili S, Bjørkhaug L, Zelent D, Buettger C, Kwagh J, Stanley C, Dahl-Jørgensen K, de Beaufort C, Bell GI, Han Y, Grimsby J, Taub R, Molven A, Søvik O, et al. From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation. Diabetes. 55: 1713-22. PMID 16731834 DOI: 10.2337/Db05-1513  0.348
2005 Hayes MG, del Bosque-Plata L, Tsuchiya T, Hanis CL, Bell GI, Cox NJ. Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10. Diabetes. 54: 3573-6. PMID 16306378 DOI: 10.2337/Diabetes.54.12.3573  0.371
2005 Ng MCY, Miyake K, So WY, Poon EWM, Lam VKL, Li JKY, Cox NJ, Bell GI, Chan JCN. The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population Diabetologia. 48: 2018-2024. PMID 16132950 DOI: 10.1007/S00125-005-1914-0  0.373
2005 Park SY, Wang X, Chen Z, Powers AC, Magnuson MA, Head WS, Piston DW, Bell GI. Optical imaging of pancreatic beta cells in living mice expressing a mouse insulin I promoter-firefly luciferase transgene. Genesis (New York, N.Y. : 2000). 43: 80-6. PMID 16108006 DOI: 10.1002/Gene.20157  0.309
2005 Xie JT, Mehendale SR, Li X, Quigg R, Wang X, Wang CZ, Wu JA, Aung HH, A Rue P, Bell GI, Yuan CS. Anti-diabetic effect of ginsenoside Re in ob/ob mice. Biochimica Et Biophysica Acta. 1740: 319-25. PMID 15949698 DOI: 10.1016/J.Bbadis.2004.10.010  0.323
2005 Grasberger H, Bell GI. Subcellular recruitment by TSG118 and TSPYL implicates a role for zinc finger protein 106 in a novel developmental pathway. The International Journal of Biochemistry & Cell Biology. 37: 1421-37. PMID 15833274 DOI: 10.1016/J.Biocel.2005.01.013  0.31
2005 Wang CZ, Wang Y, Di A, Magnuson MA, Ye H, Roe MW, Nelson DJ, Bell GI, Philipson LH. 5-amino-imidazole carboxamide riboside acutely potentiates glucose-stimulated insulin secretion from mouse pancreatic islets by KATP channel-dependent and -independent pathways. Biochemical and Biophysical Research Communications. 330: 1073-9. PMID 15823553 DOI: 10.1016/J.Bbrc.2005.03.093  0.339
2005 Iwasaki N, Horikawa Y, Tsuchiya T, Kitamura Y, Nakamura T, Tanizawa Y, Oka Y, Hara K, Kadowaki T, Awata T, Honda M, Yamashita K, Oda N, Yu L, Yamada N, ... ... Bell GI, et al. Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population Journal of Human Genetics. 50: 92-98. PMID 15696376 DOI: 10.1007/S10038-004-0225-5  0.357
2005 Grasberger H, Ye H, Mashima H, Bell GI. Dual promoter structure of ZFP106: regulation by myogenin and nuclear respiratory factor-1. Gene. 344: 143-59. PMID 15656981 DOI: 10.1016/J.Gene.2004.09.035  0.32
2004 Sagen JV, Raeder H, Hathout E, Shehadeh N, Gudmundsson K, Baevre H, Abuelo D, Phornphutkul C, Molnes J, Bell GI, Gloyn AL, Hattersley AT, Molven A, Søvik O, Njølstad PR. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy. Diabetes. 53: 2713-8. PMID 15448106 DOI: 10.2337/Diabetes.53.10.2713  0.415
2004 Ng MC, So WY, Lam VK, Cockram CS, Bell GI, Cox NJ, Chan JC. Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25. Diabetes. 53: 2676-83. PMID 15448100 DOI: 10.2337/Diabetes.53.10.2676  0.352
2004 Alcoser SY, Hara M, Bell GI, Ehrmann DA. Association of the (AU)AT-rich element polymorphism in PPP1R3 with hormonal and metabolic features of polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 89: 2973-6. PMID 15181086 DOI: 10.1210/Jc.2003-031189  0.79
2004 Ng MC, So WY, Cox NJ, Lam VK, Cockram CS, Critchley JA, Bell GI, Chan JC. Genome-wide scan for type 2 diabetes loci in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25. Diabetes. 53: 1609-13. PMID 15161769 DOI: 10.2337/Diabetes.53.6.1609  0.348
2004 Johnson JD, Han Z, Otani K, Ye H, Zhang Y, Wu H, Horikawa Y, Misler S, Bell GI, Polonsky KS. RyR2 and calpain-10 delineate a novel apoptosis pathway in pancreatic islets. The Journal of Biological Chemistry. 279: 24794-802. PMID 15044459 DOI: 10.1074/Jbc.M401216200  0.322
2004 Odom DT, Zizlsperger N, Gordon DB, Bell GW, Rinaldi NJ, Murray HL, Volkert TL, Schreiber J, Rolfe PA, Gifford DK, Fraenkel E, Bell GI, Young RA. Control of pancreas and liver gene expression by HNF transcription factors. Science (New York, N.Y.). 303: 1378-81. PMID 14988562 DOI: 10.1126/Science.1089769  0.334
2004 Cockburn BN, Bermano G, Boodram LL, Teelucksingh S, Tsuchiya T, Mahabir D, Allan AB, Stein R, Docherty K, Bell GI. Insulin promoter factor-1 mutations and diabetes in Trinidad: identification of a novel diabetes-associated mutation (E224K) in an Indo-Trinidadian family. The Journal of Clinical Endocrinology and Metabolism. 89: 971-8. PMID 14764823 DOI: 10.1210/Jc.2003-031282  0.375
2004 Cox NJ, Hayes MG, Roe CA, Tsuchiya T, Bell GI. Linkage of calpain 10 to type 2 diabetes: the biological rationale. Diabetes. 53: S19-25. PMID 14749261 DOI: 10.2337/Diabetes.53.2007.S19  0.352
2004 del Bosque-Plata L, Aguilar-Salinas CA, Tusié-Luna MT, Ramírez-Jiménez S, Rodríguez-Torres M, Aurón-Gómez M, Ramírez E, Velasco-Pérez ML, Ramírez-Silva A, Gómez-Pérez F, Hanis CL, Tsuchiya T, Yoshiuchi I, Cox NJ, Bell GI. Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population. Molecular Genetics and Metabolism. 81: 122-6. PMID 14741193 DOI: 10.1016/J.Ymgme.2003.10.005  0.352
2003 So WY, Ng MC, Horikawa Y, Njølstad PR, Li JK, Ma RC, Bell GI, Chan JC. Genetic variants of hepatocyte nuclear factor-1beta in Chinese young-onset diabetic patients with nephropathy. Journal of Diabetes and Its Complications. 17: 369-73. PMID 14583183 DOI: 10.1016/S1056-8727(02)00221-0  0.404
2003 Zhou YP, Sreenan S, Pan CY, Currie KP, Bindokas VP, Horikawa Y, Lee JP, Ostrega D, Ahmed N, Baldwin AC, Cox NJ, Fox AP, Miller RJ, Bell GI, Polonsky KS. A 48-hour exposure of pancreatic islets to calpain inhibitors impairs mitochondrial fuel metabolism and the exocytosis of insulin. Metabolism: Clinical and Experimental. 52: 528-34. PMID 12759879 DOI: 10.1053/Meta.2003.50091  0.413
2003 Polonsky KS, Bell GI. Organ alchemy: producing insulin in the liver. Nature Medicine. 9: 504-5. PMID 12724755 DOI: 10.1038/Nm0503-504  0.38
2003 Iwasaki N, Cox NJ, Wang YQ, Schwarz PEH, Bell GI, Honda M, Imura M, Ogata M, Saito M, Kamatani N, Iwamoto Y. Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects Diabetes. 52: 209-213. PMID 12502515 DOI: 10.2337/Diabetes.52.1.209  0.346
2003 Hara M, Wang X, Kawamura T, Bindokas VP, Dizon RF, Alcoser SY, Magnuson MA, Bell GI. Transgenic mice with green fluorescent protein-labeled pancreatic beta -cells. American Journal of Physiology. Endocrinology and Metabolism. 284: E177-83. PMID 12388130 DOI: 10.1152/Ajpendo.00321.2002  0.774
2002 Rasmussen SK, Urhammer SA, Berglund L, Jensen JN, Hansen L, Echwald SM, Borch-Johnsen K, Horikawa Y, Mashima H, Lithell H, Cox NJ, Hansen T, Bell GI, Pedersen O. Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians. Diabetes. 51: 3561-7. PMID 12453914 DOI: 10.2337/Diabetes.51.12.3561  0.424
2002 Ehrmann DA, Tang X, Yoshiuchi I, Cox NJ, Bell GI. Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 87: 4297-300. PMID 12213887 DOI: 10.1210/Jc.2002-020216  0.38
2002 Haddad L, Evans JC, Gharani N, Robertson C, Rush K, Wiltshire S, Frayling TM, Wilkin TJ, Demaine A, Millward A, Hattersley AT, Conway G, Cox NJ, Bell GI, Franks S, et al. Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 87: 2606-10. PMID 12050223 DOI: 10.1210/Jcem.87.6.8608  0.369
2002 Ehrmann DA, Schwarz PE, Hara M, Tang X, Horikawa Y, Imperial J, Bell GI, Cox NJ. Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 87: 1669-73. PMID 11932299 DOI: 10.1210/Jcem.87.4.8385  0.394
2002 Fullerton SM, Bartoszewicz A, Ybazeta G, Horikawa Y, Bell GI, Kidd KK, Cox NJ, Hudson RR, Di Rienzo A. Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus. American Journal of Human Genetics. 70: 1096-106. PMID 11891618 DOI: 10.1086/339930  0.352
2002 Ogata M, Awaji T, Iwasaki N, Miyazaki S, Bell GI, Iwamoto Y. Nuclear translocation of SHP and visualization of interaction with HNF-4α in living cells Biochemical and Biophysical Research Communications. 292: 8-12. PMID 11890664 DOI: 10.1006/Bbrc.2002.6593  0.301
2002 Forsythe SM, Kogut PC, McConville JF, Fu Y, McCauley JA, Halayko AJ, Liu HW, Kao A, Fernandes DJ, Bellam S, Fuchs E, Sinha S, Bell GI, Camoretti-Mercado B, Solway J. Structure and transcription of the human m3 muscarinic receptor gene. American Journal of Respiratory Cell and Molecular Biology. 26: 298-305. PMID 11867338 DOI: 10.1165/Ajrcmb.26.3.4564  0.354
2002 Lynn S, Evans JC, White C, Frayling TM, Hattersley AT, Turnbull DM, Horikawa Y, Cox NJ, Bell GI, Walker M. Variation in the calpain-10 gene affects blood glucose levels in the British population. Diabetes. 51: 247-50. PMID 11756349 DOI: 10.2337/Diabetes.51.1.247  0.385
2001 Bell GI, Polonsky KS. Diabetes mellitus and genetically programmed defects in β-cell function Nature. 414: 788-791. PMID 11742410 DOI: 10.1038/414788A  0.398
2001 Fajans SS, Bell GI, Polonsky KS. Molecular Mechanisms and Clinical Pathophysiology of Maturity-Onset Diabetes of the Young The New England Journal of Medicine. 345: 971-980. PMID 11575290 DOI: 10.1056/Nejmra002168  0.382
2001 Sreenan SK, Zhou YP, Otani K, Hansen PA, Currie KP, Pan CY, Lee JP, Ostrega DM, Pugh W, Horikawa Y, Cox NJ, Hanis CL, Burant CF, Fox AP, Bell GI, et al. Calpains play a role in insulin secretion and action. Diabetes. 50: 2013-20. PMID 11522666 DOI: 10.2337/Diabetes.50.9.2013  0.373
2001 Evans JC, Frayling TM, Cassell PG, Saker PJ, Hitman GA, Walker M, Levy JC, O'Rahilly S, Rao PV, Bennett AJ, Jones EC, Menzel S, Prestwich P, Simecek N, Wishart M, ... ... Bell GI, et al. Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom. American Journal of Human Genetics. 69: 544-52. PMID 11481585 DOI: 10.1086/323315  0.375
2001 Njølstad PR, Søvik O, Cuesta-Muñoz A, Bjørkhaug L, Massa O, Barbetti F, Undlien DE, Shiota C, Magnuson MA, Molven A, Matschinsky FM, Bell GI. Neonatal diabetes mellitus due to complete glucokinase deficiency. The New England Journal of Medicine. 344: 1588-92. PMID 11372010 DOI: 10.1056/Nejm200105243442104  0.39
2001 Hara M, Wang X, Paz VP, Iwasaki N, Honda M, Iwamoto Y, Bell GI. Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young. Journal of Human Genetics. 46: 285-8. PMID 11355020 DOI: 10.1007/S100380170080  0.359
2001 Del Bosque-Plata L, Lin J, Horikawa Y, Schwarz PEH, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, German MS, Bell GI. Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects Diabetes. 50: 694-696. PMID 11246894 DOI: 10.2337/Diabetes.50.3.694  0.417
2001 Fajans SS, Bell GI, Herman WH, Polonsky KS, Halter JB. Beta-cell dysfunction in prediabetic and diabetic MODY subjects Journal of Diabetes and Its Complications. 15: 15. DOI: 10.1016/S1056-8727(00)00102-1  0.32
2000 Horikawa Y, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, Schwitzgebel V, German MS, Bell GI. β-Cell transcription factors and diabetes: No evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY Diabetes. 49: 1955-1957. PMID 11078465 DOI: 10.2337/Diabetes.49.11.1955  0.409
2000 Baier LJ, Permana PA, Yang X, Pratley RE, Hanson RL, Shen GQ, Mott D, Knowler WC, Cox NJ, Horikawa Y, Oda N, Bell GI, Bogardus C. A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance. The Journal of Clinical Investigation. 106: R69-73. PMID 11018080 DOI: 10.1172/Jci10665  0.41
2000 Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, Hinokio Y, Lindner TH, Mashima H, Schwarz PEH, Del Bosque-Plata L, Oda Y, Yoshiuchi I, Colilla S, Polonsky KS, ... ... Bell GI, et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus Nature Genetics. 26: 163-175. PMID 11017071 DOI: 10.1038/79876  0.412
2000 Laine B, Eeckhoute J, Suaud L, Briche I, Furuta H, Bell GI, Formstecher P. Functional properties of the R154X HNF-4alpha protein generated by a mutation associated with maturity-onset diabetes of the young, type 1. Febs Letters. 479: 41-5. PMID 10940385 DOI: 10.1016/S0014-5793(00)01864-0  0.334
2000 Abderrahmani A, Chèvre JC, Otabe S, Chikri M, Hani EH, Vaxillaire M, Hinokio Y, Horikawa Y, Bell GI, Froguel P. Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians. Diabetes. 49: 306-8. PMID 10868949 DOI: 10.2337/Diabetes.49.2.306  0.389
2000 Hinokio Y, Horikawa Y, Furuta H, Cox NJ, Iwasaki N, Honda M, Ogata M, Iwamoto Y, Bell GI. β-cell transcription factors and diabetes: No evidence for diabetes- associated mutations in the hepatocyte nuclear factor-3β gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young Diabetes. 49: 302-305. PMID 10868948 DOI: 10.2337/Diabetes.49.2.302  0.374
2000 Ilag LL, Tabaei BP, Herman WH, Zawacki CM, D'Souza E, Bell GI, Fajans SS. Reduced pancreatic polypeptide response to hypoglycemia and amylin response to arginine in subjects with a mutation in the HNF-4alpha/MODY1 gene. Diabetes. 49: 961-968. PMID 10866048 DOI: 10.2337/Diabetes.49.6.961  0.391
1999 Lindner TH, Njølstad PR, Horikawa Y, Bostad L, Bell GI, Søvik O. A Novel Syndrome of Diabetes Mellitus, Renal Dysfunction and Genital Malformation Associated with a Partial Deletion of the Pseudo-POU Domain of Hepatocyte Nuclear Factor-1β Human Molecular Genetics. 8: 2001-2008. PMID 10484768 DOI: 10.1093/Hmg/8.11.2001  0.383
1999 Miller SP, Anand GR, Karschnia EJ, Bell GI, LaPorte DC, Lange AJ. Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY-2): different glucokinase defects lead to a common phenotype. Diabetes. 48: 1645-51. PMID 10426385 DOI: 10.2337/Diabetes.48.8.1645  0.327
1999 Rouard M, Bass J, Grigorescu F, Garrett TP, Ward CW, Lipkind G, Jaffiole C, Steiner DF, Bell GI. Congenital insulin resistance associated with a conformational alteration in a conserved beta-sheet in the insulin receptor L1 domain. The Journal of Biological Chemistry. 274: 18487-91. PMID 10373457 DOI: 10.1074/Jbc.274.26.18487  0.316
1999 Hathout EH, Cockburn BN, Mace JW, Sharkey J, Chen-Daniel J, Bell GI. A case of hepatocyte nuclear factor-1 alpha diabetes/MODY3 masquerading as type 1 diabetes in a Mexican-American adolescent and responsive to a low dose of sulfonylurea. Diabetes Care. 22: 867-8. PMID 10332709 DOI: 10.2337/Diacare.22.5.867  0.303
1999 Cox NJ, Frigge M, Nicolae DL, Concannon P, Hanis CL, Bell GI, Kong A. Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans Nature Genetics. 21: 213-215. PMID 9988276 DOI: 10.1038/6002  0.352
1998 Sreenan SK, Cockburn BN, Baldwin AC, Ostrega DM, Levisetti M, Grupe A, Bell GI, Stewart TA, Roe MW, Polonsky KS. Adaptation to hyperglycemia enhances insulin secretion in glucokinase mutant mice. Diabetes. 47: 1881-8. PMID 9836519 DOI: 10.2337/Diabetes.47.12.1881  0.358
1998 Dukes ID, Sreenan S, Roe MW, Levisetti M, Zhou Y, Ostrega D, Bell GI, Pontoglio M, Yaniv M, Philipson L, Polonsky KS. Defective Pancreatic β-Cell Glycolytic Signaling in Hepatocyte Nuclear Factor-1α-deficient Mice Journal of Biological Chemistry. 273: 24457-24464. PMID 9733737 DOI: 10.1074/Jbc.273.38.24457  0.373
1998 Nishigori H, Yamada S, Kohama T, Tomura H, Sho K, Horikawa Y, Bell GI, Takeuchi T, Takeda J. Frameshift mutation, A263fsinsGG, in the hepatocyte nuclear factor-1beta gene associated with diabetes and renal dysfunction. Diabetes. 47: 1354-1355. PMID 9703339 DOI: 10.2337/Diab.47.8.1354  0.34
1998 Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, Mitra M, Farmer J, Williams SR, Cox NJ, Bell GI, Risch N, Spielman RS. A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nature Genetics. 19: 292-6. PMID 9662408 DOI: 10.1038/985  0.413
1998 Pontoglio M, Sreenan S, Roe M, Pugh W, Ostrega D, Doyen A, Pick AJ, Baldwin A, Velho G, Froguel P, Levisetti M, Bonner-Weir S, Bell GI, Yaniv M, Polonsky KS. Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice. The Journal of Clinical Investigation. 101: 2215-22. PMID 9593777 DOI: 10.1172/Jci2548  0.374
1998 Hara M, Lindner TH, Paz VP, Wang X, Iwasaki N, Ogata M, Iwamoto Y, Bell GI. Mutations in the coding region of the insulin promoter factor 1 gene are not a common cause of maturity-onset diabetes of the young in Japanese subjects Diabetes. 47: 845-846. PMID 9588461 DOI: 10.2337/Diabetes.47.5.845  0.444
1998 Hani EH, Suaud L, Boutin P, Chèvre JC, Durand E, Philippi A, Demenais F, Vionnet N, Furuta H, Velho G, Bell GI, Laine B, Froguel P. A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus. The Journal of Clinical Investigation. 101: 521-6. PMID 9449683 DOI: 10.1172/Jci1403  0.424
1997 Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI. Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY. Nature Genetics. 17: 384-5. PMID 9398836 DOI: 10.1038/Ng1297-384  0.312
1997 Herman WH, Fajans SS, Smith MJ, Polonsky KS, Bell GI, Halter JB. Diminished Insulin and Glucagon Secretory Responses to Arginine in Nondiabetic Subjects With a Mutation in the Hepatocyte Nuclear Factor–4α/MODY1 Gene Diabetes. 46: 1749-1754. PMID 9356021 DOI: 10.2337/Diab.46.11.1749  0.379
1997 Kong A, Frigge M, Bell GI, Lander ES, Daly MJ, Cox NJ. Diabetes, dependence, asymptotics, selection and significance. Nature Genetics. 17: 148. PMID 9326932 DOI: 10.1038/Ng1097-148  0.304
1997 Furuta H, Iwasaki N, Oda N, Hinokio Y, Horikawa Y, Yamagata K, Yano N, Sugahiro J, Ogata M, Ohgawara H, Omori Y, Iwamoto Y, Bell GI. Organization and partial sequence of the hepatocyte nuclear factor- 4αMODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY Diabetes. 46: 1652-1657. PMID 9313765 DOI: 10.2337/Diacare.46.10.1652  0.383
1997 Gragnoli C, Lindner T, Cockburn BN, Kaisaki PJ, Gragnoli F, Marozzi G, Bell GI. Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene. Diabetes. 46: 1648-51. PMID 9313764 DOI: 10.2337/Diacare.46.10.1648  0.355
1997 Lindner T, Gragnoli C, Furuta H, Cockburn BN, Petzold C, Rietzsch H, Weiss U, Schulze J, Bell GI. Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene. The Journal of Clinical Investigation. 100: 1400-5. PMID 9294105 DOI: 10.1172/Jci119660  0.379
1997 Iwasaki N, Oda N, Ogata M, Hara M, Hinokio Y, Oda Y, Yamagata K, Kanematsu S, Ohgawara H, Omori Y, Bell GI. Mutations in the hepatocyte nuclear factor-1α/MODY3 gene in japanese subjects early- and late-onset NIDDM Diabetes. 46: 1504-1508. PMID 9287053 DOI: 10.2337/Diab.46.9.1504  0.323
1997 Cockburn BN, Ostrega DM, Sturis J, Kubstrup C, Polonsky KS, Bell GI. Changes in pancreatic islet glucokinase and hexokinase activities with increasing age, obesity, and the onset of diabetes. Diabetes. 46: 1434-9. PMID 9287043 DOI: 10.2337/Diab.46.9.1434  0.348
1997 Lindner T, Gragnoli C, Schulze J, Rietzsch H, Petzold C, Schröder H, Cox NJ, Bell GI. The 31-cM Region of Chromosome 11 Including the Obesity Gene Tubby and ATP-Sensitive Potassium Channel Genes, SUR1 and Kir6.2, Does Not Contain a Major Susceptibility Locus for NIDDM in 127 Non-Hispanic White Affected Sibships Diabetes. 46: 1227-1229. PMID 9200660 DOI: 10.2337/Diab.46.7.1227  0.331
1997 Vaxillaire M, Rouard M, Yamagata K, Oda N, Kaisaki PJ, Boriraj VV, Chevre JC, Boccio V, Cox RD, Lathrop GM, Dussoix P, Philippe J, Timsit J, Charpentier G, Velho G, ... Bell GI, et al. Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3) Human Molecular Genetics. 6: 583-586. PMID 9097962 DOI: 10.1093/Hmg/6.4.583  0.415
1997 Hansen T, Eiberg H, Rouard M, Vaxillaire M, Møller AM, Rasmussen SK, Fridberg M, Urhammer SA, Holst JJ, Almind K, Echwald SM, Hansen L, Bell GI, Pedersen O. Novel MODY3 mutations in the hepatocyte nuclear factor-1α gene: Evidence for a hyperexcitability of pancreatic β-cells to intravenous secretagogues in a glucose-tolerant carrier of a P447L mutation Diabetes. 46: 726-730. PMID 9075819 DOI: 10.2337/Diab.46.4.726  0.378
1997 Frayling TM, Bulamn MP, Ellard S, Appleton M, Dronsfield MJ, Mackie AD, Baird JD, Kaisaki PJ, Yamagata K, Bell GI, Bain SC, Hattersley AT. Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K. Diabetes. 46: 720-5. PMID 9075818 DOI: 10.2337/Diab.46.4.720  0.319
1997 Velho G, Blanché H, Vaxillaire M, Bellanné-Chantelot C, Pardini VC, Timsit J, Passa P, Deschamps I, Robert JJ, Weber IT, Marotta D, Pilkis SJ, Lipkind GM, Bell GI, Froguel P. Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families. Diabetologia. 40: 217-24. PMID 9049484 DOI: 10.1007/S001250050666  0.386
1997 Kaisaki PJ, Menzel S, Lindner T, Oda N, Rjasanowski I, Sahm J, Meincke G, Schulze J, Schmechel H, Petzold C, Ledermann HM, Sachse G, Boriraj VV, Menzel R, Kerner W, ... ... Bell GI, et al. Mutations in the hepatocyte nuclear factor-1alpha gene in MODY and early-onset NIDDM: evidence for a mutational hotspot in exon 4. Diabetes. 46: 528-35. PMID 9032114 DOI: 10.2337/Diab.46.3.528  0.369
1997 Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ, Fajans SS, Signorini S, Stoffel M, Bell GI. Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1) Nature. 384: 458-60. PMID 8945471 DOI: 10.1038/384458a0  0.59
1996 Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, ... ... Bell GI, et al. Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) Nature. 384: 455-458. PMID 8945470 DOI: 10.1038/384455A0  0.473
1996 Wasserman D, Hoekstra JH, Tolia V, Taylor CJ, Kirschner BS, Takeda J, Bell GI, Taub R, Rand EB. Molecular analysis of the fructose transporter gene (GLUT5) in isolated fructose malabsorption. Journal of Clinical Investigation. 98: 2398-2402. PMID 8941659 DOI: 10.1172/Jci119053  0.349
1996 Pontiroli AE, Capra F, Veglia F, Ferrari M, Xiang KS, Bell GI, Baroni MG, Galton DJ, Weaver JU, Hitman GA, Kopelman PG, Mohan V, Viswanathan M. Genetic contribution of polymorphism of the GLUT1 and GLUT4 genes to the susceptibility to type 2 (non-insulin-dependent) diabetes mellitus in different populations Acta Diabetologica. 33: 193-197. PMID 8904924 DOI: 10.1007/Bf02048542  0.393
1996 Fajans SS, Bell GI, Bowden DW, Halter JB, Polonsky KS. Maturity onset diabetes of the young (MODY) Diabetic Medicine. 13. PMID 8894490  0.356
1996 Byrne MM, Sturis J, Menzel S, Yamagata K, Fajans SS, Dronsfield MJ, Bain SC, Hattersley AT, Velho G, Froguel P, Bell GI, Polonsky KS. Altered Insulin Secretory Responses to Glucose in Diabetic and Nondiabetic Subjects With Mutations in the Diabetes Susceptibility Gene MODY3 on Chromosome 12 Diabetes. 45: 1503-1510. PMID 8866553 DOI: 10.2337/Diab.45.11.1503  0.4
1996 Bell GI, Pilkis SJ, Weber IT, Polonsky KS. Glucokinase mutations, insulin secretion, and diabetes mellitus. Annual Review of Physiology. 58: 171-86. PMID 8815790 DOI: 10.1146/Annurev.Ph.58.030196.001131  0.41
1996 Furuta H, Nishi S, Le Beau MM, Fernald AA, Yano H, Bell GI. Sequence of human hexokinase III cDNA and assignment of the human hexokinase III gene (HK3) to chromosome band 5q35.2 by fluorescence in situ hybridization. Genomics. 36: 206-9. PMID 8812439 DOI: 10.1006/Geno.1996.0448  0.37
1996 Yamagata K, Takeda J, Menzel S, Chen X, Eng S, Lim LR, Concannon P, Hanis CL, Spielman RS, Cox NJ, Bell GI. Searching for NIDDM susceptibility genes: Studies of genes with triplet repeats expressed in skeletal muscle Diabetologia. 39: 725-730. PMID 8781769 DOI: 10.1007/Bf00418545  0.429
1996 Roe MW, Worley JF, Tokuyama Y, Philipson LH, Sturis J, Tang J, Dukes ID, Bell GI, Polonsky KS. NIDDM is associated with loss of pancreatic beta-cell L-type Ca2+ channel activity. The American Journal of Physiology. 270: E133-40. PMID 8772485 DOI: 10.1152/Ajpendo.1996.270.1.E133  0.396
1996 Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus. Autoimmunity. 21: 127-30. PMID 8679901 DOI: 10.3109/08916939508993360  0.431
1996 Hanis CL, Boerwinkle E, Chakraborty R, Ellsworth DL, Concannon P, Stirling B, Morrison VA, Wapelhorst B, Spielman RS, Gogolin-Ewens KJ, Shephard JM, Williams SR, Risch N, Hinds D, Iwasaki N, ... ... Bell GI, et al. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 Nature Genetics. 13: 161-166. PMID 8640221 DOI: 10.1038/Ng0696-161  0.451
1996 Stoffel M, Le Beau MM, Espinosa R, Bohlander SF, Le Paslier D, Cohen D, Xiang KS, Cox NJ, Fajans SS, Bell GI. A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene. Proceedings of the National Academy of Sciences of the United States of America. 93: 3937-41. PMID 8632993 DOI: 10.1073/Pnas.93.9.3937  0.56
1996 Tokuyama Y, Fan Z, Furuta H, Makielski JC, Polonsky KS, Bell GI, Yano H. Rat inwardly rectifying potassium channel Kir6.2: cloning electrophysiological characterization, and decreased expression in pancreatic islets of male Zucker diabetic fatty rats. Biochemical and Biophysical Research Communications. 220: 532-8. PMID 8607800 DOI: 10.1006/Bbrc.1996.0439  0.345
1996 Gambino V, Menzel S, Trabb JB, Xiang KS, Lindner T, Louït A, Chen E, Mereu LE, Furuta H, Iwasaki N, Kawamura M, Omori Y, Rietzsch H, Schulze J, Schröder HE, ... ... Bell GI, et al. An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes: Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM Diabetes. 45: 291-294. PMID 8593932 DOI: 10.2337/Diab.45.3.291  0.424
1996 Polonsky KS, Sturis J, Bell GI. Seminars in Medicine of the Beth Israel Hospital, Boston. Non-insulin-dependent diabetes mellitus - a genetically programmed failure of the beta cell to compensate for insulin resistance. The New England Journal of Medicine. 334: 777-783. PMID 8592553 DOI: 10.1056/Nejm199603213341207  0.388
1996 Becker TC, Noel RJ, Johnson JH, Lynch RM, Hirose H, Tokuyama Y, Bell GI, Newgard CB. Differential effects of overexpressed glucokinase and hexokinase I in isolated islets. Evidence for functional segregation of the high and low Km enzymes. The Journal of Biological Chemistry. 271: 390-4. PMID 8550593 DOI: 10.1074/Jbc.271.1.390  0.357
1996 Iwasaki N, Kawamura M, Yamagata K, Cox NJ, Karibe S, Ohgawara H, Inagaki N, Seino S, Bell GI, Omori Y. Identification of microsatellite markers near the human genes encoding the β-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese Diabetes. 45: 267-269. PMID 8549873 DOI: 10.2337/Diab.45.2.267  0.401
1996 Takeda J, Espinosa R, Eng S, Le Beau MM, Bell GI. Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library. Genomics. 29: 276-81. PMID 8530086 DOI: 10.1006/Geno.1995.1245  0.361
1995 Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P. Linkage studies in NIDDM with markers near the sulphonylurea receptor gene Diabetologia. 38: 1479-1481. PMID 8786023 DOI: 10.1007/Bf00400610  0.441
1995 Lehto M, Huang X, Davis EM, Beau MML, Laurila E, Eriksson KF, Bell GI, Groop L. Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activity. Diabetologia. 38: 1466-1474. PMID 8786021 DOI: 10.1007/Bf00400608  0.429
1995 Zhang Y, Warren-Perry M, Saker PJ, Hattersley AT, Mackie AD, Baird JD, Greenwood RH, Stoffel M, Bell GI, Turner RC. Candidate gene studies in pedigrees with maturity-onset diabetes of the young not linked with glucokinase. Diabetologia. 38: 1055-60. PMID 8591819 DOI: 10.1007/Bf00402175  0.625
1995 Stoffel M, Espinosa R, Trabb JB, Le Beau MM, Bell GI. Human type I pituitary adenylate cyclase activating polypeptide receptor (ADCYAP1R): localization to chromosome band 7p14 and integration into the cytogenetic, physical, and genetic map of chromosome 7. Genomics. 23: 697-9. PMID 7851900 DOI: 10.1006/Geno.1994.1560  0.581
1995 Byrne MM, Sturis J, Fajans SS, Ortiz FJ, Stoltz A, Stoffel M, Smith MJ, Bell GI, Halter JB, Polonsky KS. Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20. Diabetes. 44: 699-704. PMID 7789636 DOI: 10.2337/Diab.44.6.699  0.596
1995 Page RCL, Hattersley AT, Levy JC, Barrow B, Patel P, Lo D, Wainscoat JS, Permutt MA, Bell GI, Turner RC. Clinical Characteristics of Subjects with a Missense Mutation in Glucokinase Diabetic Medicine. 12: 209-217. PMID 7758256 DOI: 10.1111/J.1464-5491.1995.Tb00460.X  0.363
1995 Wilson BD, Ollmann MM, Kang L, Stoffel M, Bell GI, Barsh GS. Structure and function of ASP, the human homolog of the mouse agouti gene. Human Molecular Genetics. 4: 223-30. PMID 7757071 DOI: 10.1093/Hmg/4.2.223  0.62
1995 Zhang Y, Warren-Perry M, Sakura H, Adelman J, Stoffel M, Bell GI, Ashcroft FM, Turner RC. No evidence for mutations in a putative beta-cell ATP-sensitive K+ channel subunit in MODY, NIDDM, or GDM. Diabetes. 44: 597-600. PMID 7729622 DOI: 10.2337/Diab.44.5.597  0.59
1995 Shimada F, Makino H, Iwaoka H, Miyamoto S, Hashimoto N, Kanatsuka A, Bell GI, Yoshida S. Identification of two novel amino acid polymorphisms in beta-cell/liver (GLUT2) glucose transporter in Japanese subjects Diabetologia. 38: 211-215. PMID 7713316 DOI: 10.1007/Bf00400096  0.423
1995 DePaoli AM, Bell GI, Stoffel M. G protein-activated inwardly rectifying potassium channel (GIRK1/KGA) mRNA in adult rat heart and brain by in situ hybridization histochemistry. Molecular and Cellular Neurosciences. 5: 515-22. PMID 7704424 DOI: 10.1006/Mcne.1994.1063  0.499
1995 Rowe RE, Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7. Nature Genetics. 10: 240-2. PMID 7663523 DOI: 10.1038/Ng0695-240  0.454
1995 Stoffel M, Tokuyama Y, Trabb JB, German MS, Tsaar ML, Jan LY, Polonsky KS, Bell GI. Cloning of rat KATP-2 channel and decreased expression in pancreatic islets of male Zucker diabetic fatty rats. Biochemical and Biophysical Research Communications. 212: 894-9. PMID 7626127 DOI: 10.1006/Bbrc.1995.2053  0.582
1995 Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P. Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs Diabetes. 44: 999-1001. PMID 7622007 DOI: 10.2337/Diab.44.8.999  0.427
1995 Takeda J, Fernald AA, Yamagata K, Le Beau MM, Bell GI. Localization of human somatostatin receptor 5 gene (SSTR5) to chromosome band 16p13.3 by fluorescence in situ hybridization. Genomics. 26: 638-9. PMID 7607700 DOI: 10.1016/0888-7543(95)80195-R  0.309
1995 Stoffel M, Stein R, Wright CV, Espinosa R, Le Beau MM, Bell GI. Localization of human homeodomain transcription factor insulin promoter factor 1 (IPF1) to chromosome band 13q12.1. Genomics. 28: 125-6. PMID 7590740 DOI: 10.1006/Geno.1995.1120  0.565
1995 Tokuyama Y, Sturis J, DePaoli AM, Takeda J, Stoffel M, Tang J, Sun X, Polonsky KS, Bell GI. Evolution of beta-cell dysfunction in the male Zucker diabetic fatty rat. Diabetes. 44: 1447-57. PMID 7589853 DOI: 10.2337/Diab.44.12.1447  0.618
1995 Jones EM, Fernald A, Bell GI, Le Beau MM. Assignment of SLC6A9 to human chromosome band 1p33 by in situ hybridization. Cytogenetics and Cell Genetics. 71: 211. PMID 7587377 DOI: 10.1159/000134110  0.306
1995 el-Maghrabi MR, Lange AJ, Jiang W, Yamagata K, Stoffel M, Takeda J, Fernald AA, Le Beau MM, Bell GI, Baker L. Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency. Genomics. 27: 520-5. PMID 7558035 DOI: 10.1006/Geno.1995.1085  0.583
1995 Iwasaki N, Ohgawara H, Nagahara H, Kawamura M, Bell GI, Omori Y. Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNALeu(UUR) genes Acta Diabetologica. 32: 17-22. PMID 7542040 DOI: 10.1007/Bf00581039  0.386
1995 Stoffel M, Fernald AA, Le Beau MM, Bell GI. Assignment of the gastric inhibitory polypeptide receptor gene (GIPR) to chromosome bands 19q13.2-q13.3 by fluorescence in situ hybridization. Genomics. 28: 607-9. PMID 7490109 DOI: 10.1006/Geno.1995.1203  0.595
1995 Tokuyama Y, Sturis J, DePaoli AM, Takeda J, Stoffel M, Tang J, Sun X, Polonsky KS, Bell GI. Evolution of beta-cell dysfunction in the male Zucker diabetic fatty rat Diabetes. 44: 1447-1457. DOI: 10.2337/diabetes.44.12.1447  0.478
1994 Lehto M, Xiang K, Stoffel M, Espinosa R, Groop LC, Le Beau MM, Bell GI. Human hexokinase II: localization of the polymorphic gene to chromosome 2. Diabetologia. 36: 1299-302. PMID 8307259 DOI: 10.1007/Bf00400809  0.63
1994 Herman WH, Fajans SS, Ortiz FJ, Smith MJ, Sturis J, Bell GI, Polonsky KS, Halter JB. Abnormal Insulin Secretion, Not Insulin Resistance, Is the Genetic or Primary Defect of MODY in the RW Pedigree Diabetes. 43: 40-46. PMID 8262315 DOI: 10.2337/Diab.43.1.40  0.413
1994 Nishi S, Hinata S, Matsukage T, Takeda J, Ichiyama A, Bell GI, Yoshimi T. Mutations in the Glucokinase Gene are not a Major Cause of Late-onset Type 2 (Non-insulin-dependent) Diabetes Mellitus in Japanese subjects Diabetic Medicine. 11: 193-197. PMID 8200206 DOI: 10.1111/J.1464-5491.1994.Tb02019.X  0.395
1994 St Charles R, Harrison RW, Bell GI, Pilkis SJ, Weber IT. Molecular model of human beta-cell glucokinase built by analogy to the crystal structure of yeast hexokinase B. Diabetes. 43: 784-91. PMID 8194664 DOI: 10.2337/Diab.43.6.784  0.355
1994 Yasuda K, Espinosa R, Takeda J, Le Beau MM, Bell GI. Localization of the kappa opioid receptor gene to human chromosome band 8q11.2. Genomics. 19: 596-7. PMID 8188308 DOI: 10.1006/Geno.1994.1117  0.358
1994 Sturis J, Kurland IJ, Byrne MM, Mosekilde E, Froguel P, Pilkis SJ, Bell GI, Polonsky KS. Compensation in pancreatic β-cell function in subjects with glucokinase mutations Diabetes. 43: 718-723. PMID 8168650 DOI: 10.2337/Diab.43.5.718  0.363
1994 Byrne MM, Sturis J, Clément K, Vionnet N, Pueyo ME, Stoffel M, Takeda J, Passa P, Cohen D, Bell GI. Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations. The Journal of Clinical Investigation. 93: 1120-30. PMID 8132752 DOI: 10.1172/Jci117064  0.565
1994 Stoffel M, Espinosa R, Powell KL, Philipson LH, Le Beau MM, Bell GI. Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): Localization to chromosome 2 and identification of a simple tandem repeat polymorphism Genomics. 21: 254-256. PMID 8088798 DOI: 10.1006/Geno.1994.1253  0.579
1994 Mahraoui L, Takeda J, Mesonero J, Chantret I, Dussaulx E, Bell GI, Brot-Laroche E. Regulation of expression of the human fructose transporter (GLUT5) by cyclic AMP Biochemical Journal. 301: 169-175. PMID 8037665 DOI: 10.1042/Bj3010169  0.32
1994 Fajans SS, Bell GI, Bowden DW, Halter JB, Polonsky KS. Maturity-onset diabetes of the young Life Sciences. 55: 413-422. PMID 8035658 DOI: 10.1016/0024-3205(94)90052-3  0.456
1994 Menzel S, Stoffel M, Espinosa R, Fernald AA, Le Beau MM, Bell GI. Localization of the glucagon receptor gene to human chromosome band 17q25. Genomics. 20: 327-8. PMID 8020989 DOI: 10.1006/Geno.1994.1179  0.582
1994 Blondel O, Moody MM, Depaoli AM, Sharp AH, Ross CA, Swift H, Bell GI. Localization of inositol trisphosphate receptor subtype 3 to insulin and somatostatin secretory granules and regulation of expression in islets and insulinoma cells. Proceedings of the National Academy of Sciences of the United States of America. 91: 7777-81. PMID 7914371 DOI: 10.1073/Pnas.91.16.7777  0.357
1994 Jones EM, Menzel S, Espinosa R, Le Beau MM, Bell GI, Takeda J. Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism. Genomics. 23: 490-1. PMID 7835902 DOI: 10.1006/Geno.1994.1529  0.388
1994 German MS, Wang J, Fernald AA, Espinosa R, Le Beau MM, Bell GI. Localization of the genes encoding two transcription factors, LMX1 and CDX3, regulating insulin gene expression to human chromosomes 1 and 13. Genomics. 24: 403-4. PMID 7698771 DOI: 10.1006/geno.1994.1639  0.303
1993 Bell GI, Froguel P, Nishi S, Pilkis SJ, Stoffel M, Takeda J, Vionnet N, Yasuda K. Mutations of the human glucokinase gene and diabetes mellitus Trends in Endocrinology and Metabolism. 4: 86-90. PMID 18407139 DOI: 10.1016/1043-2760(93)90084-R  0.622
1993 Stoffel M, Xiang KS, Espinosa R, Cox NJ, Le Beau MM, Bell GI. cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young. Human Molecular Genetics. 2: 1-4. PMID 8490617 DOI: 10.1093/Hmg/2.1.1  0.639
1993 Takeda J, Kayano T, Fukomoto H, Bell GI. Organization of the human GLUT2 (pancreatic beta-cell and hepatocyte) glucose transporter gene. Diabetes. 42: 773-7. PMID 8482435 DOI: 10.2337/Diab.42.5.773  0.444
1993 Stoffel M, Espinosa R, Keller SR, Lienhard GE, Le Beau MM, Bell GI. Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism. Diabetologia. 36: 335-7. PMID 8477879 DOI: 10.1007/Bf00400237  0.639
1993 Stoffel M, Bell GI. Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene. Diabetologia. 36: 170-1. PMID 8458532 DOI: 10.1007/Bf00400700  0.618
1993 Philipson LH, Eddy RL, Shows TB, Bell GI. Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1. Genomics. 15: 463-4. PMID 8449523 DOI: 10.1006/Geno.1993.1094  0.336
1993 Lehto M, Stoffel M, Groop L, Espinosa R, Le Beau MM, Bell GI. Assignment of the gene encoding glycogen synthase (GYS) to human chromosome 19, band q13.3. Genomics. 15: 460-1. PMID 8449521 DOI: 10.1006/Geno.1993.1092  0.63
1993 Yamada Y, Stoffel M, Espinosa R, Xiang KS, Seino M, Seino S, Le Beau MM, Bell GI. Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms. Genomics. 15: 449-52. PMID 8449518 DOI: 10.1006/Geno.1993.1088  0.588
1993 Stoffel M, Espinosa R, Le Beau MM, Bell GI. Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6. Diabetes. 42: 1215-8. PMID 8392011 DOI: 10.2337/Diab.42.8.1215  0.611
1993 Rand EB, Depaoli AM, Davidson NO, Bell GI, Burant CF. Sequence, tissue distribution, and functional characterization of the rat fructose transporter GLUT5. The American Journal of Physiology. 264: G1169-76. PMID 8333543 DOI: 10.1152/Ajpgi.1993.264.6.G1169  0.311
1993 Shimada F, Makino H, Hashimoto N, Taira M, Seino S, Bell GI, Kanatsuka A, Yoshida S. Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family. Diabetologia. 36: 433-437. PMID 8314448 DOI: 10.1007/Bf00402280  0.419
1993 Seo T, Hanabusa T, Ohagi S, Steiner DF, Bell GI. Dinucleotide repeat polymorphism in the NEC2 gene Human Molecular Genetics. 2: 1983. PMID 8281173 DOI: 10.1093/Hmg/2.11.1983  0.329
1993 Yasuda K, Espinosa R, Davis EM, Le Beau MM, Bell GI. Human somatostatin receptor genes: Localization of SSTR5 to human chromosome 20p11.2 Genomics. 17: 785-786. PMID 8244401 DOI: 10.1006/Geno.1993.1410  0.357
1993 Hayashi Y, Mori Y, Janssen OE, Sunthornthepvarakul T, Weiss RE, Takeda K, Weinberg M, Seo H, Bell GI, Refetoff S. Human thyroxine-binding globulin gene: complete sequence and transcriptional regulation. Molecular Endocrinology (Baltimore, Md.). 7: 1049-60. PMID 8232304 DOI: 10.1210/Mend.7.8.8232304  0.35
1993 Iwashima Y, Pugh W, Depaoli AM, Takeda J, Seino S, Bell GI, Polonsky KS. Expression of Calcium Channel mRNAs in Rat Pancreatic Islets and Downregulation After Glucose Infusion Diabetes. 42: 948-955. PMID 7685720 DOI: 10.2337/Diab.42.7.948  0.319
1993 Takeda J, Yano H, Eng S, Zeng Y, Bell GI. A molecular inventory of human pancreatic islets: sequence analysis of 1000 cDNA clones Human Molecular Genetics. 2: 1793-1798. PMID 7506601 DOI: 10.1093/Hmg/2.11.1793  0.45
1993 Stoffel M, Patel P, Lo YM, Hattersley AT, Lucassen AM, Page R, Bell JI, Bell GI, Turner RC, Wainscoat JS. Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes. Nature Genetics. 2: 153-6. PMID 1303265 DOI: 10.1038/Ng1092-153  0.556
1993 Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nature Genetics. 2: 46-9. PMID 1303248 DOI: 10.1038/Ng0992-46  0.357
1993 Stoffel M, Xiang K, Bell GI. Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q. Human Molecular Genetics. 1: 656. PMID 1301181 DOI: 10.1093/Hmg/1.8.656  0.547
1993 Roulston D, Espinosa Rd, Stoffel M, Bell G, Beau ML. Molecular genetics of myeloid leukemia : identification of the commonly deleted segment of chromosome 20 Blood. 82: 3424-3429. DOI: 10.1182/Blood.V82.11.3424.3424  0.543
1992 Patel P, Bell GI, Cook JT, Turner RC, Wainscoat JS. Multiple restriction fragment length polymorphisms at the GLUT2 locus: GLUT2 haplotypes for genetic analysis of type 2 (non-insulin-dependent) diabetes mellitus. Diabetologia. 34: 817-21. PMID 1685129 DOI: 10.1007/BF00408357  0.318
1992 Patel P, Lo YMD, Hattersley A, Bell GI, Tybjaerg-Hansen A, Nerup J, Turner RC, Wainscoat JS. Linkage Analysis of Maturity-Onset Diabetes of the Young With Microsatellite Polymorphisms: No Linkage to ADA or GLUT2 Genes in Two Families Diabetes. 41: 962-967. PMID 1628771 DOI: 10.2337/Diab.41.8.962  0.363
1992 Cox NJ, Xiang K, Fajans SS, Bell GI. Mapping Diabetes-Susceptibility Genes: Lessons Learned From Search for DNA Marker for Maturity-Onset Diabetes of the Young Diabetes. 41: 401-407. PMID 1607066 DOI: 10.2337/Diab.41.4.401  0.384
1992 Vionnet N, Stoffel M, Takeda J, Yasuda K, Bell GI, Zouali H, Lesage S, Velho G, Iris F, Passa P. Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus. Nature. 356: 721-2. PMID 1570017 DOI: 10.1038/356721A0  0.63
1992 Pessin JE, Bell GI. Mammalian facilitative glucose transporter family: structure and molecular regulation. Annual Review of Physiology. 54: 911-30. PMID 1562197 DOI: 10.1146/Annurev.Ph.54.030192.004403  0.32
1992 Davidson NO, Hausman AM, Ifkovits CA, Buse JB, Gould GW, Burant CF, Bell GI. Human intestinal glucose transporter expression and localization of GLUT5. The American Journal of Physiology. 262: C795-800. PMID 1550217 DOI: 10.1152/Ajpcell.1992.262.3.C795  0.301
1992 Nishi S, Stoffel M, Xiang K, Shows TB, Bell GI, Takeda J. Human pancreatic beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13. Diabetologia. 35: 743-7. PMID 1511800 DOI: 10.1007/Bf00429094  0.628
1992 Bowcock AM, Azuma T, Barnes RI, Wu SH, Bell GI, Taggart RT. Detection of a polymorphism within the pepsinogen C gene with PCR: Construction of a linkage map around PGC from 6p11-6p21.3 Genomics. 14: 398-402. PMID 1427855 DOI: 10.1016/S0888-7543(05)80232-0  0.337
1992 Takeda J, Seino S, Bell GI. Human Oct3 gene family: cDNA sequences, alternative splicing, gene organization, chromosomal location, and expression at low levels in adult tissues Nucleic Acids Research. 20: 4613-4620. PMID 1408763 DOI: 10.1093/Nar/20.17.4613  0.404
1992 Buse JB, Yasuda K, Lay TP, Seo TS, Olson AL, Pessin JE, Karam JH, Seino S, Bell GI. Human GLUT4/muscle-fat glucose-transporter gene: Characterization and genetic variation Diabetes. 41: 1436-1445. PMID 1397719 DOI: 10.2337/Diab.41.11.1436  0.47
1992 Nishi M, Sanke T, Ohagi S, Ekawa K, Wakasaki H, Nanjo K, Bell GI, Steiner dF. Molecular biology of islet amyloid polypeptide Diabetes Research and Clinical Practice. 15: 37-44. PMID 1371737 DOI: 10.1016/0168-8227(92)90065-Y  0.397
1992 Yamada Y, Post SR, Wang K, Tager HS, Bell GI, Seino S. Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney. Proceedings of the National Academy of Sciences of the United States of America. 89: 251-5. PMID 1346068 DOI: 10.1073/Pnas.89.1.251  0.32
1992 Yamada Y, Reisine T, Law SF, Ihara Y, Kubota A, Kagimoto S, Seino M, Seino Y, Bell GI, Seino S. Somatostatin receptors, an expanding gene family: cloning and functional characterization of human SSTR3, a protein coupled to adenylyl cyclase. Molecular Endocrinology. 6: 2136-2142. PMID 1337145 DOI: 10.1210/Mend.6.12.1337145  0.35
1992 Seino S, Yamada Y, Espinosa R, Le Beau MM, Bell GI. Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3. Genomics. 13: 1375-7. PMID 1324226 DOI: 10.1016/0888-7543(92)90078-7  0.313
1992 Drummond IA, Madden SL, Rohwer-Nutter P, Bell GI, Sukhatme VP, Rauscher FJ. Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1 Science. 257: 674-678. PMID 1323141 DOI: 10.1126/Science.1323141  0.308
1992 Seino S, Chen L, Seino M, Blondel O, Takeda J, Johnson JH, Bell GI. Cloning of the alpha 1 subunit of a voltage-dependent calcium channel expressed in pancreatic beta cells Proceedings of the National Academy of Sciences of the United States of America. 89: 584-588. PMID 1309948 DOI: 10.1073/Pnas.89.2.584  0.337
1992 Sakurai A, Bell GI, DeGroot LJ. Dinucleotide repeat polymorphism in the human thyroid hormone receptor α gene (THRA1) on chromosome 17 Human Molecular Genetics. 1: 553. PMID 1307263 DOI: 10.1093/Hmg/1.7.553-A  0.345
1991 Bell GI. Molecular defects in diabetes mellitus Diabetes. 40: 413-422. PMID 2010042 DOI: 10.2337/Diab.40.4.413  0.406
1991 Steiner DF, Ohagi S, Nagamatsu S, Bell GI, Nishi M. Is islet amyloid polypeptide a significant factor in pathogenesis or pathophysiology of diabetes? Diabetes. 40: 305-309. PMID 1999269 DOI: 10.2337/Diab.40.3.305  0.412
1991 Philipson LH, Hice RE, Schaefer K, Lamendola J, Bell GI, Nelson DJ, Steiner DF. Sequence and functional expression in Xenopus oocytes of a human insulinoma and islet potassium channel Proceedings of the National Academy of Sciences of the United States of America. 88: 53-57. PMID 1986382 DOI: 10.1073/Pnas.88.1.53  0.301
1991 Xiang K, Granqvist M, Seino M, Seino S, Bell GI. Microsatellite polymorphism in human insulin receptor gene (INSR) on chromosome 19. Nucleic Acids Research. 19: 5094. PMID 1923792 DOI: 10.1093/NAR/19.18.5094-A  0.319
1991 Bell GI, Xiang KS, Newman MV, Wu SH, Wright LG, Fajans SS, Spielman RS, Cox NJ. Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q. Proceedings of the National Academy of Sciences of the United States of America. 88: 1484-8. PMID 1899928 DOI: 10.1073/PNAS.88.4.1484  0.348
1991 Patel P, Lo YD, Bell GI, Turner RC, Wainscoat JS. Dinucleotide repeat polymorphism at the human GLUT2 locus Nucleic Acids Research. 19: 4017-4017. PMID 1862003 DOI: 10.1093/Nar/19.14.4017  0.322
1991 Taggart RT, Azuma T, Wu S, Bell GI, Bowcock AM. A highly informative polymorphism of the pepsinogen C gene detected by polymerase chain reaction Advances in Experimental Medicine and Biology. 306: 95-99. PMID 1812765 DOI: 10.1007/978-1-4684-6012-4_10  0.4
1991 Burant CF, Sivitz WI, Fukumoto H, Kayano T, Nagamatsu S, Seino S, Pessin JE, Bell GI. Mammalian glucose transporters: structure and molecular regulation. Recent Progress in Hormone Research. 47: 349-87; discussion 3. PMID 1745825 DOI: 10.1016/B978-0-12-571147-0.50015-9  0.313
1991 Ohagi S, Nishi M, Bell GI, Ensinck JW, Steiner DF. Sequences of islet amyloid polypeptide precursors of an old world monkey, the pig-tailed macaque (Macaca nemestrina), and the dog (Canis familiaris) Diabetologia. 34: 555-558. PMID 1718805 DOI: 10.1007/Bf00400272  0.34
1991 Yamada Y, Xiang K, Bell GI, Seino S, Nishi M. Dinucleotide repeat polymorphism in a gene on chromosome 20 encoding a G-protein coupled receptor (D20S32e) Nucleic Acids Research. 19: 2519-2519. PMID 1645874 DOI: 10.1093/Nar/19.9.2519  0.345
1990 Nishi M, Sanke T, Seino S, Eddy RL, Fan YS, Byers MG, Shows TB, Bell GI, Steiner DF. Human islet amyloid polypeptide gene: complete nucleotide sequence, chromosomal localization, and evolutionary history. Molecular Endocrinology (Baltimore, Md.). 3: 1775-81. PMID 2608057 DOI: 10.1210/Mend-3-11-1775  0.399
1990 Bell GI, Kayano T, Buse JB, Burant CF, Takeda J, Lin D, Fukumoto H, Seino S. Molecular biology of mammalian glucose transporters. Diabetes Care. 13: 198-208. PMID 2407475 DOI: 10.2337/Diacare.13.3.198  0.327
1990 Nishi M, Bell GI, Steiner DF. Islet amyloid polypeptide (amylin): no evidence of an abnormal precursor sequence in 25 Type 2 (non-insulin-dependent) diabetic patients Diabetologia. 33: 628-630. PMID 2258001 DOI: 10.1007/Bf00400208  0.398
1990 Seino S, Seino M, Bell GI. Human Insulin-Receptor Gene Diabetes. 39: 129-133. PMID 2227119 DOI: 10.2337/Diab.39.2.129  0.448
1990 Seino S, Seino M, Bell GI. Human insulin-receptor gene. Partial sequence and amplification of exons by polymerase chain reaction Diabetes Care. 39: 123-128. PMID 2210055 DOI: 10.2337/Diacare.39.1.123  0.422
1990 De Meyts P, Gu JL, Shymko RM, Kaplan BE, Bell GI, Whittaker J. Identification of a ligand-binding region of the human insulin receptor encoded by the second exon of the gene. Molecular Endocrinology (Baltimore, Md.). 4: 409-16. PMID 2188117 DOI: 10.1210/Mend-4-3-409  0.381
1990 Sivitz WI, DeSautel SL, Kayano T, Bell GI, Pessin JE. Regulation of glucose transporter messenger RNA levels in rat adipose tissue by insulin. Molecular Endocrinology (Baltimore, Md.). 4: 583-8. PMID 2149165 DOI: 10.1210/Mend-4-4-583  0.365
1990 Becker MA, Heidler SA, Bell GI, Seino S, Le Beau MM, Westbrook CA, Neuman W, Shapiro LJ, Mohandas TK, Roessler BJ. Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes. Genomics. 8: 555-61. PMID 1962753 DOI: 10.1016/0888-7543(90)90043-T  0.383
1989 Seino S, Seino M, Nishi S, Bell GI. Structure of the human insulin receptor gene and characterization of its promoter Proceedings of the National Academy of Sciences of the United States of America. 86: 114-118. PMID 2911561 DOI: 10.1073/Pnas.86.1.114  0.387
1989 Getzoff ED, Tainer JA, Stempien MM, Bell GI, Hallewell RA. Evolution of CuZn superoxide dismutase and the Greek key β-barrel structural motif Proteins: Structure, Function and Genetics. 5: 322-336. PMID 2798409 DOI: 10.1002/Prot.340050408  0.312
1989 Inagaki N, Seino Y, Takeda J, Yano H, Yamada Y, Bell GI, Eddy RL, Fukushima Y, Byers MG, Shows TB, Imura H. Gastric inhibitory polypeptide: structure and chromosomal localization of the human gene Molecular Endocrinology. 3: 1014-1021. PMID 2739653 DOI: 10.1210/Mend-3-6-1014  0.416
1989 Yano H, Seino Y, Fujita J, Yamada Y, Inagaki N, Takeda J, Bell GI, Eddy RL, Fan Y-, Byers MG, Shows TB, Imura H. Exon-intron organization, expression, and chromosomal localization of the human motilin gene. Febs Letters. 249: 248-252. PMID 2737284 DOI: 10.1016/0014-5793(89)80633-7  0.401
1989 Nishi M, Chan SJ, Nagamatsu S, Bell GI, Steiner DF. Conservation of the sequence of islet amyloid polypeptide in five mammals is consistent with its putative role as an islet hormone. Proceedings of the National Academy of Sciences of the United States of America. 86: 5738-42. PMID 2668946 DOI: 10.1073/Pnas.86.15.5738  0.345
1989 Sivitz WI, DeSautel SL, Kayano T, Bell GI, Pessin JE. Regulation of glucose transporter messenger RNA in insulin-deficient states. Nature. 340: 72-4. PMID 2662016 DOI: 10.1038/340072A0  0.361
1989 Cox NJ, Bell GI. Disease associations. Chance, artifact, or susceptibility genes? Diabetes. 38: 947-950. PMID 2568956 DOI: 10.2337/Diab.38.8.947  0.391
1989 Bell GI, Murray JC, Nakamura Y, Kayano T, Eddy RL, Fan YS, Byers MG, Shows TB. Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13. Diabetes. 38: 1072-5. PMID 2568955 DOI: 10.2337/Diab.38.8.1072  0.427
1989 Pals G, Azuma T, Mohandas TK, Bell GI, Bacon J, Samloff IM, Walz DA, Barr PJ, Taggart RT. Human pepsinogen C (progastricsin) polymorphism: evidence for a single locus located at 6p21.1-pter. Genomics. 4: 137-48. PMID 2567697 DOI: 10.1016/0888-7543(89)90292-9  0.39
1989 Xiang K, Cox NJ, Sanz N, Huang P, Karam JH, Bell GI. Insulin-receptor and apolipoprotein genes contribute to development of NIDDM in Chinese Americans. Diabetes. 38: 17-23. PMID 2562831 DOI: 10.2337/Diab.38.1.17  0.397
1989 Seino S, Bell GI. Alternative splicing of human insulin receptor messenger RNA Biochemical and Biophysical Research Communications. 159: 312-316. PMID 2538124 DOI: 10.1016/0006-291X(89)92439-X  0.383
1989 Takeda K, Mori Y, Sobieszczyk S, Seo H, Dick M, Watson F, Flink IL, Seino S, Bell GI, Refetoff S. Sequence of the variant thyroxine-binding globulin of Australian aborigines. Only one of two amino acid replacements is responsible for its altered properties. The Journal of Clinical Investigation. 83: 1344-8. PMID 2495303 DOI: 10.1172/Jci114021  0.321
1988 McCreary V, Kartha S, Bell GI, Toback FG. Sequence of a human kidney cDNA clone encoding thymosin β10 Biochemical and Biophysical Research Communications. 152: 862-866. PMID 3365256 DOI: 10.1016/S0006-291X(88)80118-9  0.332
1988 Nakai A, Seino S, Sakurai A, Szilak I, Bell GI, DeGroot LJ. Characterization of a thyroid hormone receptor expressed in human kidney and other tissues Proceedings of the National Academy of Sciences of the United States of America. 85: 2781-2785. PMID 3357890 DOI: 10.1073/Pnas.85.8.2781  0.303
1988 Yoshimasa Y, Seino S, Whittaker J, Kakehi T, Kosaki A, Kuzuya H, Imura H, Bell GI, Steiner DF. Insulin-resistant diabetes due to a point mutation that prevents insulin proreceptor processing. Science (New York, N.Y.). 240: 784-7. PMID 3283938 DOI: 10.1126/Science.3283938  0.4
1988 Vinik AJ, Cox NJ, Xiang K, Fajans SS, Bell GI. Linkage studies of maturity onset diabetes of the young--R.W. pedigree. Diabetologia. 31: 778-778. PMID 3240841 DOI: 10.1007/Bf00274785  0.304
1988 Nishi S, Seino S, Bell GI. Human hexokinase: sequences of amino- and carboxyl-terminal halves are homologous. Biochemical and Biophysical Research Communications. 157: 937-943. PMID 3207429 DOI: 10.1016/S0006-291X(88)80964-1  0.341
1988 Wang LM, Killary AM, Fang XE, Parriott SK, Lalley PA, Bell GI, Sakaguchi AY. Chromosome assignment of mouse insulin, colony stimulating factor 1, and low-density lipoprotein receptors. Genomics. 3: 172-6. PMID 3066742 DOI: 10.1016/0888-7543(88)90150-4  0.406
1988 Ardinger HH, Ardinger RH, Bell GI, Murray JC. RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19. Nucleic Acids Research. 16: 8202-8202. PMID 2901721 DOI: 10.1093/Nar/16.16.8202  0.384
1988 Cox N, Xiang K, Bell G, Karam J. Glucose transporter gene and non-insulin-dependent diabetes. The Lancet. 332: 793-794. PMID 2901632 DOI: 10.1016/S0140-6736(88)92440-3  0.413
1988 Figueroa F, Vincek V, Kasahara M, Bell GI, Klein J. Mapping of the Sod-2 locus into the t complex on mouse chromosome 17. Immunogenetics. 28: 260-264. PMID 2901401 DOI: 10.1007/Bf00345503  0.358
1988 Bell GI, Xiang K, Horita S, Sanz N, Karam JH. The molecular genetics of diabetes mellitus. Ciba Foundation Symposium. 130: 167-83. PMID 2894928 DOI: 10.1002/9780470513507.CH10  0.358
1988 Fukumoto H, Seino S, Imura H, Seino Y, Bell GI. Characterization and expression of human HepG2/erythrocyte glucose-transporter gene. Diabetes. 37: 657-661. PMID 2834252 DOI: 10.2337/Diab.37.5.657  0.366
1988 Nakai A, Sakurai A, Bell GI, DeGroot LJ. Characterization of a third human thyroid hormone receptor coexpressed with other thyroid hormone receptors in several tissues Molecular Endocrinology. 2: 1087-1092. PMID 2464749 DOI: 10.1210/Mend-2-11-1087  0.301
1988 Fukushima Y, Bell GI, Shows TB. The polymorphic human α2-macroglobulin gene (A2M) is located in chromosome region 12p12.3→p13.3 Cytogenetic and Genome Research. 48: 58-59. PMID 2460294 DOI: 10.1159/000132587  0.356
1988 Seino S, Blackstone CD, Chan SJ, Whittaker J, Bell GI, Steiner DF. Appalachian spring: variations on ancient gastro-entero-pancreatic themes in New World mammals. Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme. 20: 430-5. PMID 2459041 DOI: 10.1055/S-2007-1010853  0.374
1987 Whittaker J, Okamoto AK, Thys R, Bell GI, Steiner DF, Hofmann CA. High-level expression of human insulin receptor cDNA in mouse NIH 3T3 cells. Proceedings of the National Academy of Sciences of the United States of America. 84: 5237-41. PMID 3299382 DOI: 10.1073/Pnas.84.15.5237  0.366
1987 Seino S, Steiner DF, Bell GI. Sequence of a New World primate insulin having low biological potency and immunoreactivity. Proceedings of the National Academy of Sciences of the United States of America. 84: 7423-7. PMID 3118367 DOI: 10.1073/Pnas.84.21.7423  0.4
1987 Taggart RT, Mohandas TK, Bell GI. Parasexual analysis of human pepsinogen molecular heterogeneity Somatic Cell and Molecular Genetics. 13: 167-172. PMID 3031827 DOI: 10.1007/BF01534696  0.312
1987 Betsholtz C, Bergh J, Bywater M, Pettersson M, Johnsson A, Heldin CH, Ohlsson R, Knott TJ, Scott J, Bell GI. Expression of multiple growth factors in a human lung cancer cell line. International Journal of Cancer. 39: 502-7. PMID 3030941 DOI: 10.1002/Ijc.2910390417  0.312
1987 Shows TB, Eddy RL, Byers MG, Fukushima Y, Dehaven CR, Murray JC, Bell GI. Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35. Diabetes. 36: 546-549. PMID 3028891 DOI: 10.2337/Diab.36.4.546  0.429
1987 Xiang K, Karam JH, Bell GI. BamHI RFLP at the insulin-like growth factor II (IGF2) locus on chromosome 11. Nucleic Acids Research. 17: 466-466. PMID 2889194 DOI: 10.1093/Nar/15.18.7655  0.352
1987 Lalley PA, Sakaguchi AY, Eddy RL, Honey NH, Bell GI, Shen LP, Rutter WJ, Jacobs JW, Heinrich G, Chin WW. Mapping polypeptide hormone genes in the mouse: somatostatin, glucagon, calcitonin, and parathyroid hormone. Cytogenetics and Cell Genetics. 44: 92-7. PMID 2882956 DOI: 10.1159/000132350  0.573
1986 Bell GI, Stempien MM, Fong NM, Rall LB. Sequences of liver cDNAs encoding two different mouse insulin-like growth factor I precursors Nucleic Acids Research. 14: 7873-7882. PMID 3774549 DOI: 10.1093/Nar/14.20.7873  0.335
1986 Seino S, Welsh M, Bell GI, Chan SJ, Steiner DF. Mutations in the guinea pig preproglucagon gene are restricted to a specific portion of the prohormone sequence. Febs Letters. 203: 25-30. PMID 3755107 DOI: 10.1016/0014-5793(86)81429-6  0.36
1986 Le Beau MM, McKeithan TW, Shima EA, Goldman-Leikin RE, Chan SJ, Bell GI, Rowley JD, Diaz MO. T-cell receptor α-chain gene is split in a human T-cell leukemia cell line with a t(11;14)(p15;q11) Proceedings of the National Academy of Sciences of the United States of America. 83: 9744-9748. PMID 3540949 DOI: 10.1073/Pnas.83.24.9744  0.362
1986 Sanz N, Karam JH, Horita S, Bell GI. Prevalence of insulin-gene mutations in non-insulin-dependent diabetes mellitus. The New England Journal of Medicine. 314: 1322-3. PMID 3517647 DOI: 10.1056/NEJM198605153142017  0.307
1986 Bell GI, Fong NM, Stempien MM, Wormsted MA, Caput D, Ku L, Urdea MS, Rall LB, Sanchez-Pescador R. Human epidermal growth factor precursor: cDNA sequence, expression in vitro and gene organization Nucleic Acids Research. 14: 8427-8446. PMID 3491360 DOI: 10.1093/Nar/14.21.8427  0.348
1986 Morton CC, Byers MG, Nakai H, Bell GI, Shows TB. Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22----q24.1, 11p15, and 4q25----q27, respectively. Cytogenetic and Genome Research. 41: 245-249. PMID 3486749 DOI: 10.1159/000132237  0.358
1986 Takeda J, Seino Y, Fukumoto H, Koh G, Imura H, Bell GI. PvuII polymorphic sites in the human insulin receptor gene INSR Nucleic Acids Research. 14: 6777-6777. PMID 3018679 DOI: 10.1093/Nar/14.16.6777  0.393
1986 Sanna MA, Bell GI, Cao A, Pirastu M. Three RFLPs for the insulin receptor gene INSR: EcoRI, Pst I, Hind III Nucleic Acids Research. 14: 6776. PMID 3018678 DOI: 10.1093/Nar/14.16.6776  0.383
1986 Shaw DJ, Meredith AL, Brook JD, Sarfarzi M, Harley HG, Huson SM, Bell GI, Harper PS. Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19. Human Genetics. 74: 267-9. PMID 2877934 DOI: 10.1007/Bf00282546  0.429
1985 Bell GI, Gerhard DS, Fong NM, Sanchez-Pescador R, Rall LB. Isolation of the human insulin-like growth factor genes: insulin-like growth factor II and insulin genes are contiguous. Proceedings of the National Academy of Sciences of the United States of America. 82: 6450-6454. PMID 3901002 DOI: 10.1073/Pnas.82.19.6450  0.401
1985 Zabel BU, Kronenberg HM, Bell GI, Shows TB. Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-ras 1, and beta-hemoglobin. Cytogenetic and Genome Research. 39: 200-205. PMID 3899525 DOI: 10.1159/000132135  0.409
1985 Elbein S, Rotwein P, Permutt MA, Bell GI, Sanz N, Karam JH. Lack of Association of the Polymorphic Locus in the 5'-Flanking Region of the Human Insulin Gene and Diabetes in American Blacks Diabetes. 34: 433-439. PMID 3886460 DOI: 10.2337/Diab.34.5.433  0.4
1985 Zabel BU, Eddy RL, Lalley PA, Scott J, Bell GI, Shows TB. Chromosomal locations of the human and mouse genes for precursors of epidermal growth factor and the beta subunit of nerve growth factor. Proceedings of the National Academy of Sciences of the United States of America. 82: 469-473. PMID 3871525 DOI: 10.1073/Pnas.82.2.469  0.382
1985 Shaw DJ, Bell GI. Rsal polymorphism at the insulin receptor locus (INSR) on chromosome 19 Nucleic Acids Research. 13: 8661-8661. PMID 3001646 DOI: 10.1093/Nar/13.23.8661  0.392
1985 Scott J, Cowell JK, Robertson ME, Priestley LM, Wadey R, Hopkins B, Pritchard J, Bell GI, Rall LB, Graham CF, Knott TJ. Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues Nature. 317: 260-262. PMID 2995818 DOI: 10.1038/317260A0  0.367
1985 Reeve AE, Eccles MR, Wilkins RJ, Bell GI, Millow LJ. Expression of insulin-like growth factor-II transcripts in Wilms' tumour. Nature. 317: 258-60. PMID 2995817 DOI: 10.1038/317258A0  0.401
1985 Bell GI, Rall LB, Sanchez-Pescador R, Merryweather JP, Scott J, Eddy RL, Shows TB. Human alpha 2-macroglobulin gene is located on chromosome 12. Somatic Cell and Molecular Genetics. 11: 285-289. PMID 2408344 DOI: 10.1007/Bf01534685  0.376
1985 Raffel LJ, Hitman GA, Bell GI, Karam JH, Yen PH, Galton DJ, Bottazzo GF, Rotter H. 849 The Insulin Gene Polymorphism In Type I Diabetes (Iddm) Families Pediatric Research. 19. DOI: 10.1203/00006450-198504000-00879  0.414
1985 Rall LB, Bell GI, Caput D, Truett MA, Masiarz FR, Najarian RC, Valenzuela P, Anderson HD, Din N, Hansen B. FACTOR VIII:C SYNTHESIS IN THE KIDNEY The Lancet. 325: 44. DOI: 10.1016/S0140-6736(85)90987-0  0.471
1984 Tricoli JV, Bell GI, Shows TB. The Human Glucagon Gene Is Located on Chromosome 2 Diabetes. 33: 200-202. PMID 6692997 DOI: 10.2337/Diab.33.2.200  0.378
1984 Honey NK, Sakaguchi AY, Lalley PA, Quinto C, MacDonald RJ, Craik C, Bell GI, Rutter WJ, Naylor SL. Chromosomal assignments of genes for trypsin, chymotrypsin B, and elastase in mouse Somatic Cell and Molecular Genetics. 10: 377-383. PMID 6589791 DOI: 10.1007/Bf01535633  0.652
1984 Honey NK, Sakaguchi AY, Quinto C, MacDonald RJ, Bell GI, Craik C, Rutter WJ, Naylor SL. Chromosomal assignments of human genes for serine proteases trypsin, chymotrypsin B, and elastase Somatic Cell and Molecular Genetics. 10: 369-376. PMID 6589790 DOI: 10.1007/Bf01535632  0.658
1984 Tricoli JV, Rall LB, Scott J, Bell GI, Shows TB. Localization of insulin-like growth factor genes to human chromosomes 11 and 12. Nature. 310: 784-786. PMID 6382024 DOI: 10.1038/310784A0  0.393
1984 Bell GI, Merryweather JP, Sanchez-Pescador R, Stempien MM, Priestley L, Scott J, Rall LB. Sequence of a cDNA clone encoding human preproinsulin-like growth factor II Nature. 310: 775-777. PMID 6382021 DOI: 10.1038/310775A0  0.31
1984 Bell GI, Sanchez-Pescador R. Sequence of a cDNA Encoding Syrian Hamster Preproinsulin Diabetes. 33: 297-300. PMID 6365663 DOI: 10.2337/Diab.33.3.297  0.37
1984 Bell GI, Horita S, Karam JH. A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus. Diabetes. 33: 176-183. PMID 6363172 DOI: 10.2337/Diab.33.2.176  0.389
1984 Bell GI, Quinto C, Quiroga M, Valenzuela P, Craik CS, Rutter WJ. Isolation and sequence of a rat chymotrypsin B gene. Journal of Biological Chemistry. 259: 14265-14270. DOI: 10.1016/s0021-9258(18)89887-8  0.423
1983 Bell GI, Sanchez-Pescador R, Laybourn PJ, Najarian RC. Exon duplication and divergence in the human preproglucagon gene Nature. 304: 368-371. PMID 6877358 DOI: 10.1038/304368A0  0.352
1983 Bell GI, Santerre RF, Mullenbach GT. Hamster preproglucagon contains the sequence of glucagon and two related peptides Nature. 302: 716-718. PMID 6835407 DOI: 10.1038/302716A0  0.316
1983 Scott J, Urdea M, Quiroga M, Sanchez-Pescador R, Fong N, Selby M, Rutter WJ, Bell GI. Structure of a mouse submaxillary messenger RNA encoding epidermal growth factor and seven related proteins Science. 221: 236-240. PMID 6602382 DOI: 10.1126/Science.6602382  0.513
1983 Scott J, Selby M, Urdea M, Quiroga M, Bell GI, Rutter WJ. Isolation and nucleotide sequence of a cDNA encoding the precursor of mouse nerve growth factor Nature. 302: 538-540. PMID 6336309 DOI: 10.1038/302538A0  0.478
1983 Zabel BU, Naylor SL, Sakaguchi AY, Bell GI, Shows TB. High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization Proceedings of the National Academy of Sciences of the United States of America. 80: 6932-6936. PMID 6196780 DOI: 10.1073/Pnas.80.22.6932  0.371
1983 Naylor SL, Sakaguchi AY, Lu Ping Shen, Bell GI, Rutter WJ, Shows TB. Polymorphic human somatostatin gene is located on chromosome 3 Proceedings of the National Academy of Sciences of the United States of America. 80: 2686-2689. PMID 6133281 DOI: 10.1073/Pnas.80.9.2686  0.542
1982 Bell GI, Selby MJ, Rutter WJ. The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences. Nature. 295: 31-5. PMID 7035959 DOI: 10.1038/295031A0  0.591
1982 Bell GI, Karam JH, Rutter WJ. Polymorphic DNA region adjacent to the 5' end of the human insulin gene. Proceedings of the National Academy of Sciences of the United States of America. 78: 5759-63. PMID 6272317 DOI: 10.1073/Pnas.78.9.5759  0.588
1981 Bull P, Campino C, Bell GI, Venegas A, Valenzuela P. The effect of pH on the structure and activity of yeast RNA polymerase I Archives of Biochemistry and Biophysics. 209: 637-642. PMID 7027960 DOI: 10.1016/0003-9861(81)90323-4  0.49
1981 Owerbach D, Bell GI, Rutter WJ, Brown JA, Shows TB. The insulin gene is located on the short arm of chromosome 11 in humans. Diabetes. 30: 267-70. PMID 7009275 DOI: 10.2337/Diab.30.3.267  0.604
1980 Bell GI, Pictet R, Rutter WJ. Analysis of the regions flanking the human insulin gene and sequence of an Alu family member. Nucleic Acids Research. 8: 4091-109. PMID 6253909 DOI: 10.1093/Nar/8.18.4091  0.588
1980 Owerbach D, Bell GI, Rutter WJ, Shows TB. The insulin gene is located on chromosome 11 in humans. Nature. 286: 82-4. PMID 6248796 DOI: 10.1038/286082A0  0.623
1980 Bell GI, Pictet RL, Rutter WJ, Cordell B, Tischer E, Goodman HM. Sequence of the human insulin gene. Nature. 284: 26-32. PMID 6243748 DOI: 10.1038/284026A0  0.605
1979 Bell GI, Swain WF, Pictet R, Cordell B, Goodman HM, Rutter WJ. Nucleotide sequence of a cDNA clone encoding human preproinsulin. Nature. 282: 525-7. PMID 503234 DOI: 10.1038/282525A0  0.566
1979 Cordell B, Bell G, Tischer E, DeNoto FM, Ullrich A, Pictet R, Rutter WJ, Goodman HM. Isolation and characterization of a cloned rat insulin gene. Cell. 18: 533-43. PMID 498283 DOI: 10.1016/0092-8674(79)90070-9  0.583
1978 Valenzuela P, Bell GI, Weinberg F, Rutter WJ. Isolation and assay of eukaryotic DNA-dependent RNA polymerases Methods in Cell Biology. 19: 1-26. PMID 357912 DOI: 10.1016/S0091-679X(08)60006-0  0.624
1977 Valenzuela P, Bell GI, Masiarz FR, Degennaro LJ, Rutter WJ. Nucleotide sequence of the yeast 5S ribosomal RNA gene and adjacent putative control regions [28] Nature. 267: 641-643. PMID 327335 DOI: 10.1038/267641A0  0.65
1977 Gordon JS, Bell GI, Martinson HC, Rutter WJ. Selective interaction of 5'-bromodeoxyuridine substituted DNA with different chromosomal proteins. Biochemistry. 15: 4778-85. PMID 186094 DOI: 10.1021/Bi00667A005  0.492
1976 Valenzuela P, Bell GI, Weinberg F, Rutter WJ. Yeast DNA dependent RNA polymerases I, II and III. The existence of subunits common to the three enzymes Biochemical and Biophysical Research Communications. 71: 1319-1325. PMID 823944 DOI: 10.1016/0006-291X(76)90799-3  0.62
1976 Valenzuela P, Bell GI, Rutter WJ. The 24,000 dalton subunit and the activity of yeast RNA polymerases Biochemical and Biophysical Research Communications. 71: 26-31. PMID 786283 DOI: 10.1016/0006-291X(76)90244-8  0.617
1976 Bell GI, Valenzuela P, Rutter WJ. Phosphorylation of yeast RNA polymerases Nature. 261: 429-431. PMID 778627 DOI: 10.1038/261429A0  0.619
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