| Year |
Citation |
Score |
| 2013 |
Tsui LC, Dorfman R. The cystic fibrosis gene: a molecular genetic perspective. Cold Spring Harbor Perspectives in Medicine. 3: a009472. PMID 23378595 DOI: 10.1101/cshperspect.a009472 |
0.303 |
|
| 2009 |
Dorfman R, Li W, Sun L, Lin F, Wang Y, Sandford A, Paré PD, McKay K, Kayserova H, Piskackova T, Macek M, Czerska K, Sands D, Tiddens H, Margarit S, ... ... Tsui LC, et al. Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results. Human Genetics. 126: 763-78. PMID 19662435 DOI: 10.1007/S00439-009-0724-8 |
0.31 |
|
| 2008 |
Aznarez I, Barash Y, Shai O, He D, Zielenski J, Tsui LC, Parkinson J, Frey BJ, Rommens JM, Blencowe BJ. A systematic analysis of intronic sequences downstream of 5' splice sites reveals a widespread role for U-rich motifs and TIA1/TIAL1 proteins in alternative splicing regulation. Genome Research. 18: 1247-58. PMID 18456862 DOI: 10.1101/Gr.073155.107 |
0.316 |
|
| 2008 |
Dorfman R, Sandford A, Taylor C, Huang B, Frangolias D, Wang Y, Sang R, Pereira L, Sun L, Berthiaume Y, Tsui LC, Paré PD, Durie P, Corey M, Zielenski J. Complex two-gene modulation of lung disease severity in children with cystic fibrosis. The Journal of Clinical Investigation. 118: 1040-9. PMID 18292811 DOI: 10.1172/Jci33754 |
0.317 |
|
| 2008 |
Zielenski J, Markiewicz D, Lin S, Huang F, Yang-Feng TL, Tsui L. Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family. Clinical Genetics. 47: 125-132. PMID 7543385 DOI: 10.1111/J.1399-0004.1995.Tb03944.X |
0.421 |
|
| 2007 |
Saheki T, Iijima M, Li MX, Kobayashi K, Horiuchi M, Ushikai M, Okumura F, Meng XJ, Inoue I, Tajima A, Moriyama M, Eto K, Kadowaki T, Sinasac DS, Tsui LC, et al. Citrin/mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiency. The Journal of Biological Chemistry. 282: 25041-52. PMID 17591776 DOI: 10.1074/Jbc.M702031200 |
0.725 |
|
| 2007 |
Aznarez I, Zielenski J, Rommens JM, Blencowe BJ, Tsui LC. Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X. Journal of Medical Genetics. 44: 341-6. PMID 17475917 DOI: 10.1136/Jmg.2006.045880 |
0.335 |
|
| 2006 |
Wilschanski M, Dupuis A, Ellis L, Jarvi K, Zielenski J, Tullis E, Martin S, Corey M, Tsui LC, Durie P. Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials. American Journal of Respiratory and Critical Care Medicine. 174: 787-94. PMID 16840743 DOI: 10.1164/Rccm.200509-1377Oc |
0.32 |
|
| 2006 |
Moriyama M, Li MX, Kobayashi K, Sinasac DS, Kannan Y, Iijima M, Horiuchi M, Tsui LC, Tanaka M, Nakamura Y, Saheki T. Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice. Journal of Hepatology. 44: 930-8. PMID 16458993 DOI: 10.1016/J.Jhep.2005.09.018 |
0.7 |
|
| 2005 |
Heng HH, Windle B, Tsui LC. High-resolution FISH analysis. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 4.5. PMID 18428380 DOI: 10.1002/0471142905.hg0405s44 |
0.529 |
|
| 2005 |
Bishop MD, Freedman SD, Zielenski J, Ahmed N, Dupuis A, Martin S, Ellis L, Shea J, Hopper I, Corey M, Kortan P, Haber G, Ross C, Tzountzouris J, Steele L, ... ... Tsui LC, et al. The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis. Human Genetics. 118: 372-81. PMID 16193325 DOI: 10.1007/S00439-005-0059-Z |
0.304 |
|
| 2005 |
Rafiq MA, Faiyaz-Ul-Haque M, Ud Din MA, Malik S, Sohail M, Anwar M, Haque S, Paterson AD, Tsui LC, Ahmad W. A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1. The Journal of Investigative Dermatology. 124: 338-42. PMID 15675952 DOI: 10.1111/J.0022-202X.2004.23594.X |
0.431 |
|
| 2005 |
Eppert K, Wunder JS, Aneliunas V, Tsui LC, Scherer SW, Andrulis IL. Altered expression and deletion of RMO1 in osteosarcoma. International Journal of Cancer. 114: 738-46. PMID 15609301 DOI: 10.1002/Ijc.20786 |
0.348 |
|
| 2004 |
Faiyaz-Ul-Haque M, Zaidi SH, Al-Ali M, Al-Mureikhi MS, Kennedy S, Al-Thani G, Tsui LC, Teebi AS. A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type. American Journal of Medical Genetics. Part A. 128: 39-45. PMID 15211654 DOI: 10.1002/Ajmg.A.30005 |
0.413 |
|
| 2004 |
Liu X, Li X, Li M, Acimovic YJ, Li Z, Scherer SW, Estivill X, Tsui LC. Characterization of the segmental duplication LCR7-20 in the human genome. Genomics. 83: 262-9. PMID 14706455 DOI: 10.1016/J.Ygeno.2003.08.003 |
0.358 |
|
| 2004 |
Sinasac DS, Moriyama M, Jalil MA, Begum L, Li MX, Iijima M, Horiuchi M, Robinson BH, Kobayashi K, Saheki T, Tsui LC. Slc25a13-knockout mice harbor metabolic deficits but fail to display hallmarks of adult-onset type II citrullinemia. Molecular and Cellular Biology. 24: 527-36. PMID 14701727 DOI: 10.1128/Mcb.24.2.527-536.2004 |
0.706 |
|
| 2003 |
Aznarez I, Chan EM, Zielenski J, Blencowe BJ, Tsui LC. Characterization of disease-associated mutations affecting an exonic splicing enhancer and two cryptic splice sites in exon 13 of the cystic fibrosis transmembrane conductance regulator gene. Human Molecular Genetics. 12: 2031-40. PMID 12913074 DOI: 10.1093/Hmg/Ddg215 |
0.353 |
|
| 2003 |
Wen XY, Hegele RA, Wang J, Wang DY, Cheung J, Wilson M, Yahyapour M, Bai Y, Zhuang L, Skaug J, Young TK, Connelly PW, Koop BF, Tsui LC, Stewart AK. Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans. Human Molecular Genetics. 12: 1131-43. PMID 12719377 DOI: 10.1093/Hmg/Ddg124 |
0.351 |
|
| 2003 |
Cheung J, Estivill X, Khaja R, MacDonald JR, Lau K, Tsui LC, Scherer SW. Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence. Genome Biology. 4: R25. PMID 12702206 DOI: 10.1186/Gb-2003-4-4-R25 |
0.333 |
|
| 2003 |
Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, ... ... Tsui LC, et al. Human chromosome 7: DNA sequence and biology. Science (New York, N.Y.). 300: 767-72. PMID 12690205 DOI: 10.1126/Science.1083423 |
0.765 |
|
| 2002 |
Haston CK, Corey M, Tsui LC. Mapping of genetic factors influencing the weight of cystic fibrosis knockout mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 614-8. PMID 12461646 DOI: 10.1007/S00335-002-2195-2 |
0.329 |
|
| 2002 |
Haston CK, McKerlie C, Newbigging S, Corey M, Rozmahel R, Tsui LC. Detection of modifier loci influencing the lung phenotype of cystic fibrosis knockout mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 605-13. PMID 12461645 DOI: 10.1007/S00335-002-2190-7 |
0.33 |
|
| 2002 |
Estivill X, Cheung J, Pujana MA, Nakabayashi K, Scherer SW, Tsui LC. Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome. Human Molecular Genetics. 11: 1987-95. PMID 12165560 DOI: 10.1093/Hmg/11.17.1987 |
0.397 |
|
| 2002 |
Wu YQ, Bejjani BA, Tsui LC, Mandel A, Osborne LR, Shaffer LG. Refinement of the genomic structure of STX1A and mutation analysis in nondeletion Williams syndrome patients. American Journal of Medical Genetics. 109: 121-4. PMID 11977160 DOI: 10.1002/Ajmg.10321 |
0.731 |
|
| 2001 |
Strandvik B, Björck E, Fallström M, Gronowitz E, Thountzouris J, Lindblad A, Markiewicz D, Wahlström J, Tsui LC, Zielenski J. Spectrum of mutations in the CFTR gene of patients with classical and atypical forms of cystic fibrosis from southwestern Sweden: identification of 12 novel mutations. Genetic Testing. 5: 235-42. PMID 11788090 DOI: 10.1089/10906570152742290 |
0.335 |
|
| 2001 |
Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW. Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31. Genomics. 78: 7-11. PMID 11707066 DOI: 10.1006/Geno.2001.6651 |
0.504 |
|
| 2001 |
Osborne LR, Li M, Pober B, Chitayat D, Bodurtha J, Mandel A, Costa T, Grebe T, Cox S, Tsui LC, Scherer SW. A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. Nature Genetics. 29: 321-5. PMID 11685205 DOI: 10.1038/Ng753 |
0.304 |
|
| 2001 |
Onay T, Zielenski J, Topaloglu O, Gokgoz N, Kayserili H, Apak MY, Camcioglu Y, Cokugras H, Akcakaya N, Tsui LC, Kirdar B. Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients. Human Biology. 73: 191-203. PMID 11446424 DOI: 10.1353/Hub.2001.0022 |
0.312 |
|
| 2001 |
Wilson MD, Riemer C, Martindale DW, Schnupf P, Boright AP, Cheung TL, Hardy DM, Schwartz S, Scherer SW, Tsui LC, Miller W, Koop BF. Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5 Nucleic Acids Research. 29: 1352-1365. PMID 11239002 DOI: 10.1093/Nar/29.6.1352 |
0.505 |
|
| 2001 |
Wen XY, Stewart AK, Skaug J, Wei E, Tsui LC. Murine phosphatidylserine-specific phospholipase A1 (Ps-pla1) maps to chromosome 16 but is distinct from the lpd (lipid defect) locus. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 129-32. PMID 11210182 DOI: 10.1007/s003350010256 |
0.363 |
|
| 2000 |
Bhatia E, Durie P, Zielenski J, Lam D, Sikora SS, Choudhuri G, Tsui LC. Mutations in the cystic fibrosis transmembrane regulator gene in patients with tropical calcific pancreatitis. The American Journal of Gastroenterology. 95: 3658-9. PMID 11151920 DOI: 10.1111/J.1572-0241.2000.03400.X |
0.357 |
|
| 2000 |
Hellman A, Rahat A, Scherer SW, Darvasi A, Tsui LC, Kerem B. Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability. Molecular and Cellular Biology. 20: 4420-7. PMID 10825205 DOI: 10.1128/Mcb.20.12.4420-4427.2000 |
0.409 |
|
| 2000 |
Mak V, Zielenski J, Tsui LC, Durie P, Zini A, Martin S, Longley TB, Jarvi KA. Cystic fibrosis gene mutations and infertile men with primary testicular failure. Human Reproduction (Oxford, England). 15: 436-9. PMID 10655318 DOI: 10.1093/Humrep/15.2.436 |
0.338 |
|
| 2000 |
Bhatia E, Durie P, Zielenski J, Lam D, Tsui L. Mutations of the cystic fibrosis transmembrane regulator gene in patients of fibrocalculous pancreatic diabetes Diabetes Research and Clinical Practice. 50: 95-96. DOI: 10.1016/S0168-8227(00)81781-7 |
0.325 |
|
| 2000 |
Bhatia E, Durie P, Zielenski J, Lam D, Sikora SS, Choudhuri G, Tsui L. Letter to the editorMutations in the cystic fibrosis transmembrane regulator gene in patients with tropical calcific pancreatitis The American Journal of Gastroenterology. 95. DOI: 10.1016/S0002-9270(00)02193-6 |
0.339 |
|
| 1999 |
Crackower MA, Sinasac DS, Lee JR, Herbrick JA, Tsui LC, Scherer SW. Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24. Cytogenetics and Cell Genetics. 87: 197-8. PMID 10702666 DOI: 10.1159/000015465 |
0.731 |
|
| 1999 |
Sinasac DS, Crackower MA, Lee JR, Kobayashi K, Saheki T, Scherer SW, Tsui LC. Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue. Genomics. 62: 289-92. PMID 10610724 DOI: 10.1006/Geno.1999.6006 |
0.759 |
|
| 1999 |
Hwang MY, Kang YJ, Kim YH, Scherer SW, Tsui LC, Sohn U. Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymus. Genome / National Research Council Canada = GéNome / Conseil National De Recherches Canada. 42: 457-64. PMID 10382293 DOI: 10.1139/G98-148 |
0.455 |
|
| 1999 |
Mak V, Zielenski J, Tsui LC, Durie P, Zini A, Martin S, Longley TB, Jarvi KA. Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia. Jama. 281: 2217-24. PMID 10376575 DOI: 10.1001/Jama.281.23.2217 |
0.337 |
|
| 1999 |
Kobayashi K, Sinasac DS, Iijima M, Boright AP, Begum L, Lee JR, Yasuda T, Ikeda S, Hirano R, Terazono H, Crackower MA, Kondo I, Tsui LC, Scherer SW, Saheki T. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein. Nature Genetics. 22: 159-63. PMID 10369257 DOI: 10.1038/9667 |
0.771 |
|
| 1999 |
Zielenski J, Corey M, Rozmahel R, Markiewicz D, Aznarez I, Casals T, Larriba S, Mercier B, Cutting GR, Krebsova A, Macek M, Langfelder-Schwind E, Marshall BC, DeCelie-Germana J, Claustres M, ... ... Tsui LC, et al. Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13. Nature Genetics. 22: 128-9. PMID 10369249 DOI: 10.1038/9635 |
0.433 |
|
| 1999 |
Osborne LR, Campbell T, Daradich A, Scherer SW, Tsui LC. Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome. Genomics. 57: 279-84. PMID 10198167 DOI: 10.1006/Geno.1999.5784 |
0.481 |
|
| 1999 |
Crackower MA, Sinasac DS, Xia J, Motoyama J, Prochazka M, Rommens JM, Scherer SW, Tsui LC. Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human. Genomics. 55: 257-67. PMID 10049579 DOI: 10.1006/Geno.1998.5665 |
0.764 |
|
| 1999 |
Mak V, Zielenski J, Tsui L, Durie P, Zini A, Longley TB, Martin S, Jarvi KA. Cystic Fibrosis Gene Mutations And Infertile Men With Primary Testicular Failure The Journal of Urology. 345. DOI: 10.1097/00005392-199904020-00383 |
0.334 |
|
| 1999 |
Mak V, Zielenski J, Tsui L, Durie P, Zini A, Longley TB, Martin S, Jarvi KA. Obstructive Azoospermia: Importance of Extensive Screening for Mutations in the Cftr Gene The Journal of Urology. 281. DOI: 10.1097/00005392-199904020-00127 |
0.344 |
|
| 1998 |
Egan S, Herbrick JA, Tsui LC, Cohen B, Flock G, Beatty B, Scherer SW. Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic Fringe (MFNG) to 22q12. Genomics. 54: 576-7. PMID 9878264 DOI: 10.1006/Geno.1998.5559 |
0.427 |
|
| 1998 |
Motoyama J, Heng H, Crackower MA, Takabatake T, Takeshima K, Tsui LC, Hui CC. Overlapping and non-overlapping Ptch2 expression with Shh during mouse embryogenesis Mechanisms of Development. 78: 81-84. PMID 9858693 DOI: 10.1016/S0925-4773(98)00149-X |
0.591 |
|
| 1998 |
Glöckner G, Scherer S, Schattevoy R, Boright A, Weber J, Tsui L, Rosenthal A. Large-scale sequencing of two regions in human chromosome 7q22: analysis of 650 kb of genomic sequence around the EPO and CUTL1 loci reveals 17 genes. Genome Research. 8: 1060-1073. PMID 9799793 DOI: 10.1101/Gr.8.10.1060 |
0.491 |
|
| 1998 |
Jarvi K, McCallum S, Zielenski J, Durie P, Tullis E, Wilchanski M, Margolis M, Asch M, Ginzburg B, Martin S, Buckspan MB, Tsui L. Heterogeneity of reproductive tract abnormalities in men with absence of the vas deferens: role of cystic fibrosis transmembrane conductance regulator gene mutations Fertility and Sterility. 70: 724-728. PMID 9797105 DOI: 10.1016/S0015-0282(98)00247-7 |
0.355 |
|
| 1998 |
Crackower MA, Heng HH, Tsui LC. Assignment of mouse fibroblast growth factor 10 (Fgf10) gene to the telomeric region of chromosome 13. Genomics. 53: 247-8. PMID 9790778 DOI: 10.1006/Geno.1998.5506 |
0.647 |
|
| 1998 |
Minassian BA, Lee JR, Herbrick JA, Huizenga J, Soder S, Mungall AJ, Dunham I, Gardner R, Fong CY, Carpenter S, Jardim L, Satishchandra P, Andermann E, Snead OC, Lopes-Cendes I, ... Tsui LC, et al. Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Nature Genetics. 20: 171-4. PMID 9771710 DOI: 10.1038/2470 |
0.414 |
|
| 1998 |
Mochizuki H, Scherer SW, Xi T, Nickle DC, Majer M, Huizenga JJ, Tsui LC, Prochazka M. Human PON2 gene at 7q21.3: Cloning, multiple mRNA forms, and missense polymorphisms in the coding sequence Gene. 213: 149-157. PMID 9714608 DOI: 10.1016/S0378-1119(98)00193-0 |
0.426 |
|
| 1998 |
Mishmar D, Rahat A, Scherer SW, Nyakatura G, Hinzmann B, Kohwi Y, Mandel-Gutfroind Y, Lee JR, Drescher B, Sas DE, Margalit H, Platzer M, Weiss A, Tsui LC, Rosenthal A, et al. Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proceedings of the National Academy of Sciences of the United States of America. 95: 8141-6. PMID 9653154 DOI: 10.1073/Pnas.95.14.8141 |
0.395 |
|
| 1998 |
Coyle B, Reardon W, Herbrick J, Tsui L, Gausden E, Lee J, Coffey R, Grueters A, Grossman A, Phelps PD, Luxon L, Kendall-Taylor P, Scherer SW, Trembath RC. Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre) Human Molecular Genetics. 7: 1105-1112. PMID 9618167 DOI: 10.1093/Hmg/7.7.1105 |
0.346 |
|
| 1998 |
Pimenta AF, Tsui LC, Heng HH, Levitt P. Assignment of the gene encoding the limbic system-associated membrane protein (LAMP) to mouse chromosome 16B5 and human chromosome 3q13.2-q21. Genomics. 49: 472-4. PMID 9615236 DOI: 10.1006/Geno.1998.5280 |
0.662 |
|
| 1998 |
Torigoe K, Harada T, Kusaba H, Uchiumi T, Kohno K, Green ED, Scherer SW, Tsui LC, Schlessinger D, Kuwano M, Wada M. Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1. Genomics. 49: 14-22. PMID 9570944 DOI: 10.1006/Geno.1997.5200 |
0.5 |
|
| 1997 |
Crackower MA, Scherer SW, Heng HH, Tsui LC. Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5ql4. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 159-60. PMID 27518309 DOI: 10.1007/s003359900380 |
0.591 |
|
| 1997 |
Mueller H, Michel A, Heckel D, Fischer U, Tönnes M, Tsui L, Scherer S, Zang KD, Meese E. Identification of an amplified gene cluster in glioma including two novel amplified genes isolated by exon trapping. Human Genetics. 101: 190-197. PMID 9402967 DOI: 10.1007/S004390050612 |
0.48 |
|
| 1997 |
Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, et al. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell. 91: 543-53. PMID 9390563 DOI: 10.1016/S0092-8674(00)80440-7 |
0.329 |
|
| 1997 |
Duh FM, Scherer SW, Tsui LC, Lerman MI, Zbar B, Schmidt L. Gene structure of the human MET proto-oncogene. Oncogene. 15: 1583-6. PMID 9380410 DOI: 10.1038/Sj.Onc.1201338 |
0.399 |
|
| 1997 |
Osborne LR, Herbrick JA, Greavette T, Heng HH, Tsui LC, Scherer SW. PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics. 45: 402-6. PMID 9344666 DOI: 10.1006/Geno.1997.4923 |
0.691 |
|
| 1997 |
Hegele RA, Connelly PW, Scherer SW, Hanley AJG, Harris SB, Tsui LC, Zinman B. Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus Journal of Clinical Endocrinology and Metabolism. 82: 3373-3377. PMID 9329371 DOI: 10.1210/Jcem.82.10.4289 |
0.326 |
|
| 1997 |
Mak V, Jarvi KA, Zielenski J, Durie P, Tsui L. Higher Proportion of Intact Exon 9 CFTR mRNA in Nasal Epithelium Compared with Vas Deferens Human Molecular Genetics. 6: 2099-2107. PMID 9328474 DOI: 10.1093/Hmg/6.12.2099 |
0.343 |
|
| 1997 |
Osborne LR, Soder S, Shi X, Pober B, Costa T, Scherer SW, Tsui L. Hemizygous Deletion of the Syntaxin 1A Gene in Individuals with Williams Syndrome American Journal of Human Genetics. 61: 449-452. PMID 9311751 DOI: 10.1086/514850 |
0.324 |
|
| 1997 |
Scherer SW, Soder S, Duvoisin RM, Huizenga JJ, Tsui LC. The human metabotropic glutamate receptor 8 (GRM8) gene: a disproportionately large gene located at 7q31.3-q32.1. Genomics. 44: 232-6. PMID 9299241 DOI: 10.1006/Geno.1997.4842 |
0.473 |
|
| 1997 |
Crackower MA, Heng HH, Shi X, Scherer SW, Tsui LC. Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to chromosome 6. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 704. PMID 9271682 DOI: 10.1007/S003359900629 |
0.654 |
|
| 1997 |
Roessler E, Ward DE, Gaudenz K, Belloni E, Scherer SW, Donnai D, Siegel-Bartelt J, Tsui LC, Muenke M. Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly. Human Genetics. 100: 172-81. PMID 9254845 DOI: 10.1007/s004390050486 |
0.429 |
|
| 1997 |
Snow BE, Heng HHQ, Shi XM, Zhou Y, Du K, Taub R, Tsui LC, McInnes RR. Expression analysis and chromosomal assignment of the human SFRS5/SRp40 gene Genomics. 43: 165-170. PMID 9244433 DOI: 10.1006/Geno.1997.4794 |
0.452 |
|
| 1997 |
Rozmahel R, Gyömörey K, Plyte S, Nguyen V, Wilschanski M, Durie P, Bear CE, Tsui LC. Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA. Human Molecular Genetics. 6: 1153-62. PMID 9215687 DOI: 10.1093/Hmg/6.7.1153 |
0.389 |
|
| 1997 |
Krebs I, Weis I, Hudler M, Rommens JM, Roth H, Scherer SW, Tsui L, Füchtbauer E, Grzeschik K, Tsuji K, Kunz J. Translocation Breakpoint Maps 5 kb 3′ from TWIST in a Patient Affected with Saethre-Chotzen Syndrome Human Molecular Genetics. 6: 1079-1086. PMID 9215678 DOI: 10.1093/Hmg/6.7.1079 |
0.511 |
|
| 1997 |
Dong WF, Heng HH, Lowsky R, Xu Y, DeCoteau JF, Shi XM, Tsui LC, Minden MD. Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1. Dna and Cell Biology. 16: 671-8. PMID 9212161 DOI: 10.1089/Dna.1997.16.671 |
0.668 |
|
| 1997 |
Zeng WR, Scherer SW, Koutsilieris M, Huizenga JJ, Filteau F, Tsui LC, Nepveu A. Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas. Oncogene. 14: 2355-65. PMID 9178912 DOI: 10.1038/Sj.Onc.1201076 |
0.365 |
|
| 1997 |
Tambini CE, George AM, Rommens JM, Tsui LC, Scherer SW, Thacker J. The XRCC2 DNA repair gene: Identification of a positional candidate Genomics. 41: 84-92. PMID 9126486 DOI: 10.1006/Geno.1997.4636 |
0.506 |
|
| 1997 |
Cohen D, Heng HH, Shi XM, McIntosh EM, Tsui LC, Pearlman RE. Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21. 1 by fluorescence in situ hybridization. Genomics. 40: 213-5. PMID 9070952 DOI: 10.1006/Geno.1996.4540 |
0.657 |
|
| 1997 |
Alley TL, Scherer SW, Huizenga JJ, Tsui L, Wallace MR. Physical mapping of the chromosome 7 breakpoint region in an SLOS patient with t(7;20) (q32.1;q13.2). American Journal of Medical Genetics. 68: 279-281. PMID 9024559 DOI: 10.1002/(Sici)1096-8628(19970131)68:3<279::Aid-Ajmg6>3.0.Co;2-H |
0.439 |
|
| 1997 |
Thacker J, Cartwright R, Tambini C, George A, Rommens J, Tsui L, Scherer S. O IX.2 Molecular cloning and functional characterization of the human XRCC2 DNA repair gene Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 379: S61. DOI: 10.1016/S0027-5107(97)82804-7 |
0.353 |
|
| 1996 |
Rozman D, Strömstedt M, Tsui L, Scherer SW, Waterman MR. Structure and Mapping of the Human Lanosterol 14α- Demethylase Gene (CYP51) Encoding the Cytochrome P450 Involved in Cholesterol Biosynthesis; Comparison of Exon/Intron Organization with other Mammalian and Fungal CYP Genes Genomics. 38: 371-381. PMID 8975714 DOI: 10.1006/Geno.1996.0640 |
0.44 |
|
| 1996 |
Nakabayashi K, Ogata T, Fujii M, Takahashi E, Ogino H, Michishita E, Scherer SW, Tsui L, Ayusawa D. A Panel of Radiation Hybrids Defining the 7q31-q32 Region of Human Chromosome 7 Dna Research. 3: 181-183. PMID 8905237 DOI: 10.1093/Dnares/3.3.181 |
0.468 |
|
| 1996 |
Roessler E, Belloni E, Gaudenz K, Jay P, Berta P, Scherer SW, Tsui LC, Muenke M. Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Nature Genetics. 14: 357-60. PMID 8896572 DOI: 10.1038/Ng1196-357 |
0.424 |
|
| 1996 |
Takahara K, Osborne L, Elliott RW, Tsui LC, Scherer SW, Greenspan DS. Fine mapping of the human and mouse genes for the type I procollagen COOH-terminal proteinase enhancer protein. Genomics. 31: 253-6. PMID 8824813 DOI: 10.1006/Geno.1996.0043 |
0.754 |
|
| 1996 |
Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC. Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients. Genomics. 36: 328-36. PMID 8812460 DOI: 10.1006/Geno.1996.0469 |
0.691 |
|
| 1996 |
Rowles J, Scherer SW, Xi T, Majer M, Nickle DC, Rommens JM, Popov KM, Harris RA, Riebow NL, Xia J, Tsui LC, Bogardus C, Prochazka M. Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human Journal of Biological Chemistry. 271: 22376-22382. PMID 8798399 DOI: 10.1074/Jbc.271.37.22376 |
0.383 |
|
| 1996 |
Eppert K, Scherer SW, Ozcelik H, Pirone R, Hoodless P, Kim H, Tsui LC, Bapat B, Gallinger S, Andrulis IL, Thomsen GH, Wrana JL, Attisano L. MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma. Cell. 86: 543-52. PMID 8752209 DOI: 10.1016/S0092-8674(00)80128-2 |
0.362 |
|
| 1996 |
Barr CL, Wigg KG, Zovko E, Sandor P, Tsui LC. No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families. American Journal of Medical Genetics. 67: 301-5. PMID 8725747 DOI: 10.1002/(Sici)1096-8628(19960531)67:3<301::Aid-Ajmg6>3.0.Co;2-P |
0.306 |
|
| 1996 |
Scherer SW, Feinstein DS, Oliveira L, Tsui LC, Pittler SJ. Gene structure and chromosome localization to 7q21.3 of the human rod photoreceptor transducin gamma-subunit gene (GNGT1). Genomics. 35: 241-3. PMID 8661128 DOI: 10.1006/Geno.1996.0346 |
0.504 |
|
| 1996 |
Heng HH, Chamberlain JW, Shi XM, Spyropoulos B, Tsui LC, Moens PB. Regulation of meiotic chromatin loop size by chromosomal position. Proceedings of the National Academy of Sciences of the United States of America. 93: 2795-800. PMID 8610120 DOI: 10.1073/Pnas.93.7.2795 |
0.638 |
|
| 1996 |
Zhang XL, Heng HH, Yang Y, Tsui LC, Parnes JR, Chamberlain JW. Chromosomal mapping of the second human CD8B gene locus. Immunogenetics. 43: 220-6. PMID 8575821 DOI: 10.1007/Bf00587303 |
0.671 |
|
| 1996 |
Johnson E, Scherer S, Osborne L, Tsui L, Oscier D, Mould S, Cotter F. Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia Blood. 87: 3579-3586. DOI: 10.1182/Blood.V87.9.3579.Bloodjournal8793579 |
0.723 |
|
| 1995 |
Marchese A, Heiber M, Nguyen T, Heng HH, Saldivia VR, Cheng R, Murphy PM, Tsui LC, Shi X, Gregor P. Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors. Genomics. 29: 335-44. PMID 8666380 DOI: 10.1006/Geno.1995.9996 |
0.626 |
|
| 1995 |
Heiber M, Docherty JM, Shah G, Nguyen T, Cheng R, Heng HH, Marchese A, Tsui LC, Shi X, George SR. Isolation of three novel human genes encoding G protein-coupled receptors. Dna and Cell Biology. 14: 25-35. PMID 7832990 DOI: 10.1089/Dna.1995.14.25 |
0.667 |
|
| 1995 |
Thacker J, Tambini CE, Simpson PJ, Tsui L, Scherer SW. Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA-damaging agents Human Molecular Genetics. 4: 113-120. PMID 7711722 DOI: 10.1093/Hmg/4.1.113 |
0.493 |
|
| 1995 |
Barron-Casella EA, Torres MA, Scherer SW, Heng HH, Tsui LC, Casella JF. Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families. The Journal of Biological Chemistry. 270: 21472-9. PMID 7665558 DOI: 10.1074/Jbc.270.37.21472 |
0.601 |
|
| 1995 |
O'Dowd BF, Scheideler MA, Nguyen T, Cheng R, Rasmussen JS, Marchese A, Zastawny R, Heng HH, Tsui LC, Shi X. The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes, GPR7 and GPR8, expressed in discrete areas of the brain. Genomics. 28: 84-91. PMID 7590751 DOI: 10.1006/Geno.1995.1109 |
0.646 |
|
| 1995 |
Wilschanski M, Zielenski J, Markiewicz D, Tsui LC, Corey M, Levison H, Durie PR. Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations. The Journal of Pediatrics. 127: 705-10. PMID 7472820 DOI: 10.1016/S0022-3476(95)70157-5 |
0.345 |
|
| 1994 |
Powers PA, Scherer SW, Tsui LC, Gregg RG, Hogan K. Localization of the Gene Encoding the α2/δ Subunit (CACNL2A) of the Human Skeletal Muscle Voltage-Dependent Ca2+ Channel to Chromosome 7q21-q22 by Somatic Cell Hybrid Analysis Genomics. 19: 192-193. PMID 8188232 DOI: 10.1006/Geno.1994.1044 |
0.352 |
|
| 1994 |
Wu J, Salido EC, Yen PH, Mohandas TK, Heng HH, Tsui LC, Park J, Chapman VM, Shapiro LJ. The murine Xe169 gene escapes X-inactivation like its human homologue. Nature Genetics. 7: 491-6. PMID 7951318 DOI: 10.1038/Ng0894-491 |
0.664 |
|
| 1994 |
Heng HH, Tsui LC, Moens PB. Organization of heterologous DNA inserts on the mouse meiotic chromosome core. Chromosoma. 103: 401-7. PMID 7859560 DOI: 10.1007/Bf00362284 |
0.642 |
|
| 1994 |
Kunz J, Scherer SW, Klawitz I, Soder S, Du YZ, Speich N, Kalff-Suske M, Heng HH, Tsui LC, Grzeschik KH. Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clones. Genomics. 22: 439-48. PMID 7806232 DOI: 10.1006/Geno.1994.1407 |
0.66 |
|
| 1994 |
Zhang XL, Lee KL, Heng HH, Tsui LC, Parnes JR, Shepherd NS, Chamberlain JW. Isolation of P1 bacteriophage clones containing large contiguous segments of the human and mouse loci for the T-cell coreceptor molecule CD8. Genetic Analysis, Techniques and Applications. 11: 129-39. PMID 7710778 DOI: 10.1016/1050-3862(94)90033-7 |
0.565 |
|
| 1994 |
Bozon D, Zielenski J, Rininsland F, Tsui L. Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA→G Human Mutation. 3: 330-332. PMID 7517268 DOI: 10.1002/Humu.1380030329 |
0.332 |
|
| 1994 |
Marsden PA, Heng HHQ, Duff CL, Shi XM, Tsui LC, Hall AV. Localization of the Human Gene for Inducible Nitric Oxide Synthase (NOS2) to Chromosome 17q11.2-q12 Genomics. 19: 183-185. PMID 7514565 DOI: 10.1006/Geno.1994.1039 |
0.328 |
|
| 1994 |
Grzeschik K, Tsui L, Green ED. Report of the First International Workshop on Human Chromosome 7 Mapping 1993 Cytogenetic and Genome Research. 65: 51-73. DOI: 10.1159/000133602 |
0.401 |
|
| 1993 |
Goring DR, Bryce DM, Tsui LC, Breitman ML, Liu Q. Developmental regulation and cell type-specific expression of the murine gamma F-crystallin gene is mediated through a lens-specific element containing the gamma F-1 binding site. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 196: 143-52. PMID 8364223 DOI: 10.1002/Aja.1001960208 |
0.653 |
|
| 1993 |
Heng HH, Tsui LC. Modes of DAPI banding and simultaneous in situ hybridization. Chromosoma. 102: 325-32. PMID 8325164 DOI: 10.1007/bf00661275 |
0.557 |
|
| 1993 |
O'Dowd BF, Heiber M, Chan A, Heng HHQ, Tsui LC, Kennedy JL, Shi X, Petronis A, George SR, Nguyen T. A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11 Gene. 136: 355-360. PMID 8294032 DOI: 10.1016/0378-1119(93)90495-O |
0.474 |
|
| 1993 |
Heng HH, Xie B, Shi XM, Tsui LC, Mahuran DJ. Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locus. Genomics. 18: 429-31. PMID 8288250 DOI: 10.1006/Geno.1993.1491 |
0.662 |
|
| 1993 |
Peichel CL, Scherer SW, Tsui LC, Beier DR, Vogt TF. Mapping the midkine family of developmentally regulated signaling molecules. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 632-8. PMID 8281012 DOI: 10.1007/Bf00360899 |
0.471 |
|
| 1993 |
Zielenski J, Bozon D, Markiewicz D, Aubin G, Simard F, Rommens JM, Tsui LC. Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621 + 1G-->T and 711 + 1G-->T mutations. Human Molecular Genetics. 2: 683-7. PMID 7689008 DOI: 10.1093/Hmg/2.6.683 |
0.32 |
|
| 1993 |
Teem JL, Berger HA, Ostedgaard LS, Rich DP, Tsui LC, Welsh MJ. Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast. Cell. 73: 335-46. PMID 7682896 DOI: 10.1016/0092-8674(93)90233-G |
0.487 |
|
| 1992 |
Goring DR, Breitman ML, Tsui LC. Temporal regulation of six crystallin transcripts during mouse lens development. Experimental Eye Research. 54: 785-95. PMID 1623964 DOI: 10.1016/0014-4835(92)90034-P |
0.623 |
|
| 1992 |
Scherer SW, Tompkins BJ, Tsui LC. A human chromosome 7-specific genomic DNA library in yeast artificial chromosomes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: 179-81. PMID 1617225 DOI: 10.1007/Bf00352464 |
0.435 |
|
| 1992 |
Heng HH, Squire J, Tsui LC. High-resolution mapping of mammalian genes by in situ hybridization to free chromatin. Proceedings of the National Academy of Sciences of the United States of America. 89: 9509-13. PMID 1384055 DOI: 10.1073/Pnas.89.20.9509 |
0.633 |
|
| 1992 |
Cartier M, Breitman ML, Tsui LC. A frameshift mutation in the γE–crystallin gene of the Elo mouse Nature Genetics. 2: 42-45. PMID 1303247 DOI: 10.1038/Ng0992-42 |
0.447 |
|
| 1992 |
Cartier M, Breitman ML, Tsui L. Erratum: A frameshift mutation in the γE-crystallin gene of the Elo mouse Nature Genetics. 2: 343-343. DOI: 10.1038/Ng1292-343C |
0.392 |
|
| 1992 |
Liu Q, Tsui L, Breltman ML. Developmental regulation of γ-crystallin gene expression in the lens Experimental Eye Research. 55: 222. DOI: 10.1016/0014-4835(92)90993-3 |
0.357 |
|
| 1992 |
Cartier M, Breitman M, Tsui L. A frameshift mutation in the γE-crystallin gene of the Elo mice Experimental Eye Research. 55: 15. DOI: 10.1016/0014-4835(92)90266-U |
0.368 |
|
| 1991 |
Ng IS, Pace R, Richard MV, Kobayashi K, Kerem B, Tsui LC, Beaudet AL. Methods for analysis of multiple cystic fibrosis mutations. Human Genetics. 87: 613-7. PMID 1916764 DOI: 10.1007/Bf00209023 |
0.352 |
|
| 1991 |
Zielenski J, Bozon D, Kerem B, Markiewicz D, Durie P, Rommens JM, Tsui L. Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene Genomics. 10: 229-235. PMID 1710599 DOI: 10.1016/0888-7543(91)90504-8 |
0.396 |
|
| 1990 |
Lemna WK, Feldman GL, Kerem B, Fernbach SD, Zevkovich EP, O'Brien WE, Riordan JR, Collins FS, Tsui LC, Beaudet AL. Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis. The New England Journal of Medicine. 322: 291-6. PMID 2296270 DOI: 10.1056/Nejm199002013220503 |
0.444 |
|
| 1990 |
Kerem E, Corey M, Kerem BS, Rommens J, Markiewicz D, Levison H, Tsui LC, Durie P. The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508). The New England Journal of Medicine. 323: 1517-22. PMID 2233932 DOI: 10.1056/Nejm199011293232203 |
0.313 |
|
| 1990 |
Melmer G, Sood R, Rommens J, Rego D, Tsui LC, Buchwald M. Isolation of clones on chromosome 7 that contain recognition sites for rare-cutting enzymes by oligonucleotide hybridization. Genomics. 7: 173-81. PMID 2161402 DOI: 10.1016/0888-7543(90)90538-6 |
0.646 |
|
| 1989 |
Meakin SO, Reddan JR, Tsui LC, Breitman ML. A rabbit lens epithelial cell line supports expression of an exogenous crystallin gene characteristic of lens fiber cell differentiation Experimental Eye Research. 48: 131-137. PMID 2920780 DOI: 10.1016/0014-4835(89)90026-2 |
0.322 |
|
| 1988 |
Rupert JL, Kuliszewki M, Tsui L, Breitman ML, Gold RJM. The murine cataractogenic mutation, Cat Fraser, segregates independently of the gamma crystallin genes. Genetics Research. 51: 23-28. PMID 3366376 DOI: 10.1017/S0016672300023909 |
0.391 |
|
| 1987 |
Murer-Orlando M, Paterson RC, Lok S, Tsui LC, Breitman ML. Differential regulation of gamma-crystallin genes during mouse lens development. Developmental Biology. 119: 260-7. PMID 3792630 DOI: 10.1016/0012-1606(87)90227-2 |
0.385 |
|
| 1987 |
Breitman ML, Clapoff S, Rossant J, Tsui LC, Glode LM, Maxwell IH, Bernstein A. Genetic ablation: targeted expression of a toxin gene causes microphthalmia in transgenic mice. Science (New York, N.Y.). 238: 1563-5. PMID 3685993 DOI: 10.1126/Science.3685993 |
0.395 |
|
| 1987 |
Meakin SO, Du RP, Tsui LC, Breitman ML. Gamma-crystallins of the human eye lens: expression analysis of five members of the gene family Molecular and Cellular Biology. 7: 2671-2679. PMID 3670288 DOI: 10.1128/Mcb.7.8.2671 |
0.382 |
|
| 1987 |
Hogg D, Gorin MB, Heinzmann C, Zollman S, Mohandas T, Klisak I, Sparkes RS, Breitman M, Tsui LC, Horwitz J. Nucleotide sequence for the cDNA of the bovine beta B2 crystallin and assignment of the orthologous human locus to chromosome 22. Current Eye Research. 6: 1335-42. PMID 3427982 DOI: 10.3109/02713688708997559 |
0.485 |
|
| 1987 |
Goring DR, Rossant J, Clapoff S, Breitman ML, Tsui LC. In situ detection of beta-galactosidase in lenses of transgenic mice with a gamma-crystallin/lacZ gene. Science (New York, N.Y.). 235: 456-8. PMID 3099390 DOI: 10.1126/Science.3099390 |
0.666 |
|
| 1986 |
Shiloh Y, Donlon T, Bruns G, Breitman ML, Tsui LC. Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36. Human Genetics. 73: 17-9. PMID 3011643 DOI: 10.1007/Bf00292656 |
0.498 |
|
| 1985 |
Meakin SO, Breitman ML, Tsui LC. Structural and evolutionary relationships among five members of the human γ-crystallin gene family Molecular and Cellular Biology. 5: 1408-1414. PMID 4033658 DOI: 10.1128/Mcb.5.6.1408 |
0.442 |
|
| 1985 |
Lok S, Breitman ML, Chepelinsky AB, Piatigorsky J, Gold RJM, Tsui L. Lens-specific promoter activity of a mouse gamma-crystallin gene. Molecular and Cellular Biology. 5: 2221-2230. PMID 3837188 DOI: 10.1128/Mcb.5.9.2221 |
0.4 |
|
| 1985 |
Knowlton RG, Cohen-Haguenauer O, Van Cong N, Frézal J, Brown VA, Barker D, Braman JC, Schumm JW, Tsui LC, Buchwald M, Donis-Keller H. A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7 Nature. 318: 380-382. PMID 2999611 DOI: 10.1038/318380A0 |
0.598 |
|
| 1984 |
Lok S, Tsui L, Shinohara T, Piatigorsky J, Gold R, Breitman M. Analysis of the mouse γ-crystallin gene family: assignment of multiple cDNAs to discrete genomic sequences and characterization of a representative gene Nucleic Acids Research. 12: 4517-4529. PMID 6330674 DOI: 10.1093/Nar/12.11.4517 |
0.451 |
|
| 1984 |
Breitman ML, Lok S, Wistow G, Piatigorsky J, Treton JA, Gold RJM, Tsui L. Gamma-crystallin family of the mouse lens: structural and evolutionary relationships Proceedings of the National Academy of Sciences of the United States of America. 81: 7762-7766. PMID 6096855 DOI: 10.1073/Pnas.81.24.7762 |
0.337 |
|
| 1983 |
Tsui LC, Hendrix RW. Role of gene T in phage λ tail assembly Virology. 125: 265-273. PMID 6220514 DOI: 10.1016/0042-6822(83)90200-3 |
0.534 |
|
| 1983 |
Tsui LC, Hendrix RW. Proteolytic processing of phage λ tail protein gpH: timing of the cleavage Virology. 125: 257-264. PMID 6220513 DOI: 10.1016/0042-6822(83)90199-X |
0.493 |
|
| 1982 |
Tsui LC, Breitman ML, Siminovitch L, Buchwald M. Persistence of freely replicating SV40 recombinant molecules carrying a selectable marker in permissive simian cells. Cell. 30: 499-508. PMID 6291772 DOI: 10.1016/0092-8674(82)90247-1 |
0.586 |
|
| 1978 |
Hendrix RW, Tsui L. Role of the host in virus assembly: Cloning of the Escherichia coli groE gene and identification of its protein product Proceedings of the National Academy of Sciences of the United States of America. 75: 136-139. PMID 343102 DOI: 10.1073/Pnas.75.1.136 |
0.602 |
|
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