cached image

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

172 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
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2014 Naylor RN, John PM, Winn AN, Carmody D, Greeley SA, Philipson LH, Bell GI, Huang ES. Cost-effectiveness of MODY genetic testing: translating genomic advances into practical health applications. Diabetes Care. 37: 202-9. PMID 24026547 DOI: 10.2337/Dc13-0410  1
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  1
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  1
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  1
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  1
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  1
2011 Lipton RB, Drum ML, Danielson KK, Greeley SA, Bell GI, Hagopian WA. Onset features and subsequent clinical evolution of childhood diabetes over several years. Pediatric Diabetes. 12: 326-34. PMID 21426455 DOI: 10.1111/J.1399-5448.2010.00706.X  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2009 Park SY, Bell GI. Noninvasive monitoring of changes in pancreatic beta-cell mass by bioluminescent imaging in MIP-luc transgenic mice Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et MéTabolisme. 41: 1-4. PMID 18949679 DOI: 10.1055/S-0028-1087209  1
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  1
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  1
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  1
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  1
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  1
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  1
2006 Tsuchiya T, Schwarz PE, Bosque-Plata LD, Geoffrey Hayes M, Dina C, Froguel P, Wayne Towers G, Fischer S, Temelkova-Kurktschiev T, Rietzsch H, Graessler J, Vcelák J, Palyzová D, Selisko T, Bendlová B, ... ... Bell GI, et al. Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses. Molecular Genetics and Metabolism. 89: 174-84. PMID 16837224 DOI: 10.1016/J.Ymgme.2006.05.013  1
2006 Odom DT, Dowell RD, Jacobsen ES, Nekludova L, Rolfe PA, Danford TW, Gifford DK, Fraenkel E, Bell GI, Young RA. Core transcriptional regulatory circuitry in human hepatocytes. Molecular Systems Biology. 2: 2006.0017. PMID 16738562 DOI: 10.1038/Msb4100059  1
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  1
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  1
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  1
2005 Gunawardana SC, Hara M, Bell GI, Head WS, Magnuson MA, Piston DW. Imaging Beta cell development in real-time using pancreatic explants from mice with green fluorescent protein-labeled pancreatic Beta cells. In Vitro Cellular & Developmental Biology. Animal. 41: 7-11. PMID 15926862 DOI: 10.1290/0412080.1  1
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  1
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  1
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  1
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  1
2004 Otani K, Han DH, Ford EL, Garcia-Roves PM, Ye H, Horikawa Y, Bell GI, Holloszy JO, Polonsky KS. Calpain system regulates muscle mass and glucose transporter GLUT4 turnover. The Journal of Biological Chemistry. 279: 20915-20. PMID 15014085 DOI: 10.1074/Jbc.M400213200  1
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  1
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  1
2003 Weedon MN, Schwarz PEH, Horikawa Y, Iwasaki N, Illig T, Holle R, Rathmann W, Selisko T, Schulze J, Owen KR, Evans J, Del Bosque-Plata L, Hitman G, Walker M, Levy JC, ... ... Bell GI, et al. Meta-Analysis and a Large Association Study Confirm a Role for Calpain-10 Variation in Type 2 Diabetes Susceptibility American Journal of Human Genetics. 73: 1208-1212. PMID 14574648 DOI: 10.1086/379285  1
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  1
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  1
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  1
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  1
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  1
2002 Joost HG, Bell GI, Best JD, Birnbaum MJ, Charron MJ, Chen YT, Doege H, James DE, Lodish HF, Moley KH, Moley JF, Mueckler M, Rogers S, Schürmann A, Seino S, et al. Nomenclature of the GLUT/SLC2A family of sugar/polyol transport facilitators. American Journal of Physiology. Endocrinology and Metabolism. 282: E974-6. PMID 11882521 DOI: 10.1152/Ajpendo.00407.2001  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
1997 Chien EK, Tokuyama Y, Rouard M, Phillippe M, Bell GI. Identification of gestationally regulated genes in rat myometrium by use of messenger ribonucleic acid differential display. American Journal of Obstetrics and Gynecology. 177: 645-52. PMID 9322637 DOI: 10.1016/S0002-9378(97)70159-5  1
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  1
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  1
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  1
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  1
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  1
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  1
1996 Hino A, Tokuyama Y, Kobayashi M, Yano M, Weir B, Takeda J, Wang X, Bell GI, Macdonald RL. Increased expression of endothelin B receptor mRNA following subarachnoid hemorrhage in monkeys. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 16: 688-97. PMID 8964809 DOI: 10.1097/00004647-199607000-00020  1
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  1
1996 Lane RH, Flozak AS, Ogata ES, Bell GI, Simmons RA. Altered hepatic gene expression of enzymes involved in energy metabolism in the growth-retarded fetal rat. Pediatric Research. 39: 390-4. PMID 8929856 DOI: 10.1203/00006450-199603000-00003  1
1996 DeLisle S, Blondel O, Longo FJ, Schnabel WE, Bell GI, Welsh MJ. Expression of inositol 1,4,5-trisphosphate receptors changes the Ca2+ signal of Xenopus oocytes. The American Journal of Physiology. 270: C1255-61. PMID 8928753 DOI: 10.1152/Ajpcell.1996.270.4.C1255  1
1996 Hino A, Tokuyama Y, Weir B, Takeda J, Yano H, Bell GI, Macdonald RL. Changes in endothelial nitric oxide synthase mRNA during vasospasm after subarachnoid hemorrhage in monkeys. Neurosurgery. 39: 562-7; discussion 56. PMID 8875487 DOI: 10.1097/00006123-199609000-00026  1
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  1
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  1
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  1
1996 Reardon DB, Wood SL, Brautigan DL, Bell GI, Dent P, Sturgill TW. Activation of a protein tyrosine phosphatase and inactivation of Raf-1 by somatostatin. The Biochemical Journal. 314: 401-4. PMID 8670047 DOI: 10.1042/Bj3140401  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
1995 Buscail L, Estève JP, Saint-Laurent N, Bertrand V, Reisine T, O'Carroll AM, Bell GI, Schally AV, Vaysse N, Susini C. Inhibition of cell proliferation by the somatostatin analogue RC-160 is mediated by somatostatin receptor subtypes SSTR2 and SSTR5 through different mechanisms. Proceedings of the National Academy of Sciences of the United States of America. 92: 1580-4. PMID 7878022 DOI: 10.1073/Pnas.92.5.1580  1
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  0.44
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  0.4
1995 Tokuyama Y, Hara M, Jones EM, Fan Z, Bell GI. Cloning of rat and mouse P2Y purinoceptors. Biochemical and Biophysical Research Communications. 211: 211-8. PMID 7779087 DOI: 10.1006/Bbrc.1995.1798  1
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  1
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  0.36
1995 Tsaur ML, Menzel S, Lai FP, Espinosa R, Concannon P, Spielman RS, Hanis CL, Cox NJ, Le Beau MM, German MS. Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM. Diabetes. 44: 592-6. PMID 7729621 DOI: 10.2337/Diab.44.5.592  1
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  1
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  1
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  1
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  0.36
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  1
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  1
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  1
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  1
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  1
1994 Kong H, DePaoli AM, Breder CD, Yasuda K, Bell GI, Reisine T. Differential expression of messenger RNAs for somatostatin receptor subtypes SSTR1, SSTR2 and SSTR3 in adult rat brain: analysis by RNA blotting and in situ hybridization histochemistry. Neuroscience. 59: 175-84. PMID 8190266 DOI: 10.1016/0306-4522(94)90108-2  1
1994 Pérez J, Rigo M, Kaupmann K, Bruns C, Yasuda K, Bell GI, Lübbert H, Hoyer D. Localization of somatostatin (SRIF) SSTR-1, SSTR-2 and SSTR-3 receptor mRNA in rat brain by in situ hybridization. Naunyn-Schmiedeberg's Archives of Pharmacology. 349: 145-60. PMID 8170498 DOI: 10.1007/Bf00169831  1
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  1
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  1
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  1
1994 Takeda J, Blackburn CL, Menzel S, Yano H, Bell GI. Dinucleotide repeat polymorphism at D9S328E (EST hbc220). Human Molecular Genetics. 3: 387. PMID 8004124 DOI: 10.1093/Hmg/3.2.387  1
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  1
1994 Buscail L, Delesque N, Estève JP, Saint-Laurent N, Prats H, Clerc P, Robberecht P, Bell GI, Liebow C, Schally AV, Vaysse N, Susini C. Stimulation of tyrosine phosphatase and inhibition of cell proliferation by somatostatin analogues: Mediation by human somatostatin receptor subtypes SSTR1 and SSTR2 Proceedings of the National Academy of Sciences of the United States of America. 91: 2315-2319. PMID 7907795 DOI: 10.1073/Pnas.91.6.2315  1
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  0.36
1994 DePaoli AM, Hurley KM, Yasada K, Reisine T, Bell G. Distribution of kappa opioid receptor mRNA in adult mouse brain: an in situ hybridization histochemistry study. Molecular and Cellular Neurosciences. 5: 327-35. PMID 7804602 DOI: 10.1006/Mcne.1994.1039  1
1994 Tallent M, Dichter MA, Bell GI, Reisine T. The cloned kappa opioid receptor couples to an N-type calcium current in undifferentiated PC-12 cells. Neuroscience. 63: 1033-40. PMID 7700508 DOI: 10.1016/0306-4522(94)90570-3  1
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  0.36
1993 Stoffel M, Bell KL, Blackburn CL, Powell KL, Seo TS, Takeda J, Vionnet N, Xiang KS, Gidh-Jain M, Pilkis SJ. Identification of glucokinase mutations in subjects with gestational diabetes mellitus. Diabetes. 42: 937-40. PMID 8495817 DOI: 10.2337/Diab.42.6.937  1
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  1
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  0.52
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  1
1993 Yasuda K, Raynor K, Kong H, Breder CD, Takeda J, Reisine T, Bell GI. Cloning and functional comparison of kappa and delta opioid receptors from mouse brain. Proceedings of the National Academy of Sciences of the United States of America. 90: 6736-40. PMID 8393575 DOI: 10.1073/Pnas.90.14.6736  1
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  0.32
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  1
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  1
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  0.4
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  0.36
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  1
1992 Breder CD, Yamada Y, Yasuda K, Seino S, Saper CB, Bell GI. Differential expression of somatostatin receptor subtypes in brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 12: 3920-34. PMID 1403090 DOI: 10.1523/Jneurosci.12-10-03920.1992  1
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  1
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  1
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  1
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  1
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  1
1991 Bell GI. Molecular defects in diabetes mellitus Diabetes. 40: 413-422. PMID 2010042 DOI: 10.2337/Diab.40.4.413  1
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  1
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  1
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  1
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  1
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  1
1990 Nishi M, Bell GI, Steiner DF. Sequence of a cDNA encoding Syrian hamster islet amyloid polypeptide precursor Nucleic Acids Research. 18: 6726. PMID 2251153 DOI: 10.1093/Nar/18.22.6726  1
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  1
1990 Shapiro ET, Bell GI, Polonsky KS, Rubenstein AH, Kew MC, Tager HS. Tumor hypoglycemia: relationship to high molecular weight insulin-like growth factor-II. The Journal of Clinical Investigation. 85: 1672-9. PMID 2159026 DOI: 10.1172/Jci114619  1
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  1
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  1
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  1
1989 Sakurai A, Takeda K, Ain K, Ceccarelli P, Nakai A, Seino S, Bell GI, Refetoff S, DeGroot LJ. Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor β Proceedings of the National Academy of Sciences of the United States of America. 86: 8977-8981. PMID 2510172 DOI: 10.1073/Pnas.86.22.8977  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.56
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  0.44
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.72
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  1
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  1
1976 Bell GI, Valenzuela P, Rutter WJ. Phosphorylation of yeast RNA polymerases Nature. 261: 429-431. PMID 778627 DOI: 10.1038/261429A0  1
Show low-probability matches.