Lap-Chee Tsui - Publications

Affiliations: 
1988-2006 University of Toronto, Toronto, ON, Canada 
 2002-2014 University of Hong Kong, Downingtown, Hong Kong Island, Hong Kong 
Area:
Genetics, Molecular Biology, Pathology
Website:
https://www.ourhkfoundation.org.hk/en/node/784

114 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
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  0.96
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  0.96
2008 Li J, Xiang YY, Ye L, Tsui LC, Macdonald JF, Hu J, Lu WY. Nonsteroidal anti-inflammatory drugs upregulate function of wild-type and mutant CFTR. The European Respiratory Journal. 32: 334-43. PMID 18385167 DOI: 10.1183/09031936.00168007  0.96
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  0.96
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  0.96
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  0.96
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  0.6
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  0.6
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  0.96
2003 Sheth S, Shea JC, Bishop MD, Chopra S, Regan MM, Malmberg E, Walker C, Ricci R, Tsui LC, Durie PR, Zielenski J, Freedman SD. Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis. Human Genetics. 113: 286-92. PMID 12783301 DOI: 10.1007/S00439-003-0963-Z  0.96
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  0.6
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  0.96
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  0.6
2002 Faiyaz-Ul-Haque M, Ahmad W, Wahab A, Haque S, Azim AC, Zaidi SH, Teebi AS, Ahmad M, Cohn DH, Siddique T, Tsui LC. Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia. American Journal of Medical Genetics. 111: 31-7. PMID 12124730 DOI: 10.1002/ajmg.10501  0.96
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  0.6
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  0.6
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  0.6
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  0.96
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.6
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  0.96
1998 Hegele RA, Harris SB, Connelly PW, Hanley AJG, Tsui LC, Zinman B, Scherer SW. Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-Cree Clinical Genetics. 54: 394-399. PMID 9842991 DOI: 10.1111/J.1399-0004.1998.Tb03752.X  0.96
1998 Hegele RA, Harris SB, Zinman B, Wang J, Cao H, Hanley AJ, Tsui LC, Scherer SW. Variation in the AU(AT)-rich element within the 3'-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal Canadians. The Journal of Clinical Endocrinology and Metabolism. 83: 3980-3. PMID 9814479 DOI: 10.1210/Jcem.83.11.5219  0.6
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  0.32
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  0.96
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  0.6
1998 Crackower MA, Motoyama J, Tsui L. Defect in the Maintenance of the Apical Ectodermal Ridge in the Dactylaplasia Mouse Developmental Biology. 201: 78-89. PMID 9733575 DOI: 10.1006/Dbio.1998.8938  0.6
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  0.96
1998 Boright AP, Connelly PW, Brunt JH, Scherer SW, Tsui LC, Hegele RA. Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites Atherosclerosis. 139: 131-136. PMID 9699900 DOI: 10.1016/S0021-9150(98)00071-9  0.96
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  0.6
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  0.96
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  0.6
1998 Gosselin D, Stevenson MM, Cowley EA, Griesenbach U, Eidelman DH, Boule M, Tam MF, Kent G, Skamene E, Tsui LC, Radzioch D. Impaired ability of Cftr knockout mice to control lung infection with Pseudomonas aeruginosa American Journal of Respiratory and Critical Care Medicine. 157: 1253-1262. PMID 9563748 DOI: 10.1164/Ajrccm.157.4.9702081  0.96
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  0.96
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  0.32
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  0.96
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  0.96
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  0.96
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  0.96
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  0.6
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  0.96
1997 Orozco L, Zielenski J, Markiewicz D, Villarreal T, Tsui LC, Lezana JL, del Angel RM. Two novel frameshift deletions (1924del7, 2055del9-->A) in the CFTR gene in Mexican cystic fibrosis patients. Human Mutation. 10: 239-40. PMID 9298826 DOI: 10.1002/(Sici)1098-1004(1997)10:3<239::Aid-Humu11>3.0.Co;2-0  0.96
1997 Hegele RA, Connelly PW, Scherer SW, Hanley AJG, Harris SB, Tsui LC, Zinman B. Paraoxonase-2 G148 variant in an aboriginal Canadian girl with non-insulin-dependent diabetes [7] Lancet. 350: 785. PMID 9298006 DOI: 10.1016/S0140-6736(05)62570-6  0.96
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  0.96
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  0.6
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  0.96
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  0.96
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  0.6
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  0.96
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  0.96
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  0.96
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  0.6
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  0.6
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  0.6
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  0.6
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1996 Rozmahel R, Wilschanski M, Matin A, Plyte S, Oliver M, Auerbach W, Moore A, Forstner J, Durie P, Nadeau J, Bear C, Tsui LC. Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor Nature Genetics. 12: 280-287. PMID 8589719 DOI: 10.1038/Ng0396-280  0.96
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  0.96
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  0.32
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  0.96
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  0.96
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  0.6
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1993 Gurrieri F, Trask BJ, van den Engh G, Krauss CM, Schinzel A, Pettenati MJ, Schindler D, Dietz-Band J, Vergnaud G, Scherer SW. Physical mapping of the holoprosencephaly critical region on chromosome 7q36. Nature Genetics. 3: 247-51. PMID 8485580 DOI: 10.1038/Ng0393-247  0.96
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  0.96
1993 Heng HH, Tsui LC. Modes of DAPI banding and simultaneous in situ hybridization. Chromosoma. 102: 325-32. PMID 8325164 DOI: 10.1007/bf00661275  0.96
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  0.96
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  0.96
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  0.96
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  0.64
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  0.56
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  0.96
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  0.96
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  0.56
1991 Fried MD, Durie PR, Tsui LC, Corey M, Levison H, Pencharz PB. The cystic fibrosis gene and resting energy expenditure. The Journal of Pediatrics. 119: 913-6. PMID 1960606 DOI: 10.1016/S0022-3476(05)83042-2  0.96
1991 Strong TV, Smit LS, Turpin SV, Cole JL, Hon CT, Markiewicz D, Petty TL, Craig MW, Rosenow EC, Tsui LC. Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels. The New England Journal of Medicine. 325: 1630-4. PMID 1944451 DOI: 10.1056/Nejm199112053252307  0.96
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  0.96
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  0.96
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  0.56
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  0.96
1989 Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science (New York, N.Y.). 245: 1059-65. PMID 2772657 DOI: 10.1126/Science.2772657  0.96
1989 Kerem E, Corey M, Kerem B, Durie P, Tsui LC, Levison H. Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus. The Journal of Pediatrics. 114: 767-73. PMID 2715890 DOI: 10.1016/S0022-3476(89)80134-9  0.96
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  0.56
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  0.96
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  0.96
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  0.56
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  0.96
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  0.56
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  0.96
1985 Tsui L, Breitman ML. Replication of pSV2-gpt in COS-1 cells: stability of plasmid DNA in the presence and absence of biochemical selection. Somatic Cell and Molecular Genetics. 11: 167-176. PMID 2984789 DOI: 10.1007/Bf01534705  0.56
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  0.56
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  0.96
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  1
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  0.96
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  0.96
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