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Meeting the Vice-Chancellor and President > Curriculum Vitae

Publications: Papers in Refereed Journals

    1. Tsui L-C, Mark KK (1976).  The depression of endolysin synthesis in bacteria infected with high multiplicity of phage lambda. Molec Gen Genet 143: 269-278.
    2. Hendrix RW, Tsui L-C (1978).  Role of the host in virus assembly: Cloning of the Escherichia coli groE gene and identification of its protein product. Proc Natl Acad Sci USA 75:136-139.
    3. Tsui L-C, Hendrix RW (1980). The head-tail connector of bacteriophage lambda. J Molec Biol 142: 419-433.
    4. Breitman ML, Tsui L-C, Buchwald M, Siminovitch L (1982).  Introduction and recovery of a selectable bacterial gene from the genome of mammalian cells. Molec Cell Biol 8: 966-976.
    5. Tsui L-C, Breitman ML, Siminovitch L, Buchwald M (1982).  Persistence of a freely replicating SV40 recombinant molecule carrying a selectable marker in permissive simian cells. Cell 30: 499-508.
    6. Tsui L-C, Hendrix RW (1983).  Proteolytic processing of phage lambda tail protein gpH: Timing of the cleavage. Virology 125: 257-264.
    7. Tsui L-C, Hendrix RW (1983).  Role of gene T in phage lambda tail assembly. Virology 125: 265-273.
    8. Lok S, Tsui L-C, Shinohara T, Piatigorsky J, Gold RJM, Breitman ML (1984). Analysis of the mouse g-crystallin gene family: Assignment of multiple cDNAs to discrete genomic sequences and characterization of a representative gene. Nucleic Acids Res 12: 4517-4529.
    9. Breitman ML, Lok S, Wistow G, Piatigorsky J, Treton JA, Gold RJM, Tsui L-C  (1984). g-crystallin family of the mouse lens: Structural and evolutionary relationships. Proc Natl Acad Sci USA 81: 7762-7766.
    10. Tsui L-C, Breitman ML (1985).  Replication of pSV2-gpt in COS-1 cells: Stability of plasmid DNA in the presence and absence of biochemical selection. Somat Cell Molec Genet 11: 167-176.
    11. Meakin SO, Breitman ML, Tsui L-C (1985).  Structural and evolutionary relationship of five members of the human g-crystallin gene family. Molec Cell Biol 5: 1408-1414.
    12. Lok S, Breitman ML, Chepelinsky AB, Piatigorsky J, Gold RJM, Tsui L-C (1985).  Lens-specific promoter activity of a mouse g-crystallin gene. Molec Cell Biol 5: 2221-2230.
    13. Willard HF, Meakin S, Tsui L-C, Breitman ML (1985).  Assignment of the human g-crystallin multigene family to chromosome 2. Somat Cell Molec Genet 11: 511-516.
    14. Quan F, Korneluk RG, Macleod HL, Tsui L-C, Gravel RA (1985).  An RFLP associated with the human catalase gene.  Nucleic Acids Res 13: 8288.
    15. Tsui L-C, Cox DW, McAlpine PJ, Buchwald M (1985).  Cystic fibrosis: analysis of linkage of the disease locus to red cell and plasma protein markers. Cytogenet. Cell Genet. 39: 238-239.
    16. Tsui L-C, Buchwald M, Markiewicz D, Kao F-T, Cai G-Y, Law ML (1985).  Identification of a polymorphic DNA marker pDL32B and its localization to the long arm of chromosome 12, region q14.3-qter. Cytogenet Cell Genet 40: 764.
    17. Tsui L-C, Zsiga M, Kennedy D, Plavsic N, Markiewicz D, Buchwald M (1985).  Cystic fibrosis: progress in mapping the disease locus using polymorphic DNA markers. I. Cytogenet Cell Genet 39: 299-301.
    18. Naismith AB, Hoffman-Chudzik E, Tsui L-C, Riordan JR (1985).  Study on the expression of myelin proteolipid protein (lipophilin) using a cloned complementary DNA as probe. Nucleic Acids Res 13: 7413-7425.
    19. Tsui L-C, Buchwald M, Barker D, Braman JC, Knowlton RG, Schumm J, Eiberg H, Mohr J, Kennedy D, Plavsic N, Zsiga M, Markiewicz D, Akots G, Brown V, Helms C, Gravius T, Parker C, Rediker K, Donis-Keller H (1985).  Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker. Science 230: 1054-1057.
    20. Knowlton RG, Cohen-Haguenauer O, Nguyen Van Cong, Frezal J, Brown V, Barker D, Braman JC, Schumm JW, Tsui L-C, Buchwald M, Donis-Keller H (1985).  A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7. Nature 318: 380-382.
    21. Schmiegelow K, Eiberg H, Tsui L-C, Buchwald M, Phelan PD, Williamson R, Warwick W, Niebuhr E, Mohr J, Schwartz M, Koch C (1986).  Linkage between the loci for cystic fibrosis and paraoxonase. Clin Genet 29: 374-377.
    22. Buchwald M, Zsiga M, Markiewicz D, Plavsic N, Kennedy D, Zengerling S, Willard HF, Tsipouras P, Schmiegelow K, Schwartz M, Eiberg H, Mohr J, Barker D, Donis-Keller H, Tsui L-C (1986).  Linkage of cystic fibrosis to the proa2(I) collagen gene, COL1A2, on chromosome 7. Cytogenet Cell Genet 41: 234-239.
    23. Shiloh Y, Donlon T, Bruns G, Breitman ML, Tsui L-C (1986).  Assignment of the human g-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-q36. Human Genet 73: 17-19.
    24. Hogg D, Tsui L-C, Gorin M, Breitman ML (1986).  Characterization of the human b-crystallin gene HubA3/A1 reveals ancestral relationships among the bg-crystallin superfamily. J Biol Chem 261: 12420-12427.
    25. Law ML, Cai G-Y, Hartz J, Kao F-T, Hogg D, Breitman ML, Tsui L-C (1986).  Localization of a b-crystallin gene, HubA3/A1 (gene symbol:CRYB1), to the long arm of chromosome 17. Cytogenet. Cell. Genet. 42: 202-207.
    26. Beaudet A, Bowcock A, Buchwald M, Cavalli-Sforza LL, Farrall M, King M-C, Klinger K, Lalouel J-M, Lathrop M, Naylor S, Ott J, Tsui L-C, Wainwright B, Watkins P, White R, Williamson R (1986). Linkage of cystic fibrosis to two tightly linked DNA markers: Joint report from a collaborative study. Am J Hum Genet 39: 681-693.
    27. Tsui L-C, Buetow K, Buchwald M (1986).  Genetic analysis of cystic fibrosis using linked DNA markers. Am J Hum Genet 39: 720-728.
    28. Murer-Orlando M, Paterson RC, Lok S, Tsui L-C, Breitman ML (1987).  Differential regulation of g-crystallin genes during mouse lens development. Devel Biol 119: 260-267.
    29. Lubsen NH, Renwick JH, Tsui L-C, Breitman ML, Schoenmaker J (1987).  A locus for a human hereditary cataract is closely linked to the g-crystallin gene family.  Proc Natl Acad Sci USA 84: 489-492.
    30. Goring DR, Rossant J, Clapoff S, Breitman ML, Tsui L-C (1987).  In situ detection of b-galactosidase in lenses of transgenic mice with a g-crystallin/lacZ gene. Science 235: 456-458.
    31. Zengerling S, Tsui L-C, Grzeschik K-H, Olek K, Riordan JR, Buchwald M (1987).  Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7. Am J Hum Genet 40:228-236.
    32. Russell P, Garland D, Zigler Jr JS, Meakin SO, Tsui L-C, Breitman ML (1987).  Aging effects of vitamin C on a human lens protein produced in vitro. FESEB J. 1: 32-35.
    33. Meakin SO, Du RP, Tsui L-C, Breitman ML (1987).  g-crystallins of the human eye lens: Expression analysis of five members of the gene family.  Molec Cell Biol 7: 2671-2679.
    34. Russell P, Meakin SO, Hohman TC, Tsui L-C, Breitman ML (1987).  Relationship between proteins encoded by 3 human g-crystallin genes and distinct polypeptides in the eye lens.  Molec Cell Biol 7: 3320-3323.
    35. Quinlan P, Oda S-I, Breitman ML, Tsui L-C (1987).  The mouse eye lens obsolescence (Elo) mutant: studies on crystallin gene expression and linkage analysis between the mutant locus and the g-crystallin genes.  Genes & Develop 1: 637-644.
    36. Breitman ML, Clapoff S, Rossant J, Tsui L-C, Glode ML, Maxwell IH, Bernstein A (1987).   Genetic ablation: Targeted expression of a toxin gene causes microphthalmia in transgenic mice.  Science 238: 1563-1565.
    37. Farrall M, Lathrop M, Spence JE, Bowcock A, Klinger K, Tsui L-C (1987).  Further data on linkage between cystic fibrosis and 7C22 (D7S16).  Am J. Hum. Genet. 41: 286-287.
    38. Wainwright BJ, Tsui L-C, Leppert M, Buchwald M, Estivill X, O'Connell P, Lathrop M, Lalouel J-M, White R, Williamson R, Farrall M (1987).  Linkage of DNA probe B79a (D7S13) to cystic fibrosis.  Am J Hum Genet 41: 944-847.
    39. Kaiser R, Weber J, Grzeschik K-H, Edstrom JE, Driesel A, Zengerling S, Buchwald M, Tsui L-C, Olek K (1987).  Microdissection and microcloning of the long arm of human chromosome 7.  Molec Biol Rep 12: 3-6.
    40. Hogg D, Gorin MB, Heinzmann C, Zollman S, Mohandas T, Klisak I, Sparkes RS, Breitman ML, Tsui L-C, Horwitz J (1987).  Nucleotide sequence for the cDNA of the bovine bB2 crystallin and assignment of the orthologous human locus to chromosome 22.   Current Eye Res 6: 1335-1342.
    41. Rupert JL, Kuliszeski M, Tsui L-C, Breitman ML, Gold RJM (1988).  The mutant cataractogenic mutation, Cat Fraser, segregates independently of the g-crystallin genes.  Genet Res 51: 23-28.
    42. Musarella MA, Burghes A, Anson-Cartwright L, Mahtani MM, Tsui L-C, Worton RG (1988).  Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.  Am J Hum Genet 43: 484-494.
    43. Rommens JM, Zengerling S, Burns J, Melmer G, Kerem B, Plavsic N, Zsiga M, Kennedy D, Markiewicz D, Rozmahel R, Riordan JR, Buchwald M, Tsui L-C (1988).  Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.  Am J Hum Genet 43: 645-663.
    44. Duncan A, Buchwald M, Tsui L-C (1988).  Sublocalization of two cloned chromosome 7 sequences closely linked to the cystic fibrosis locus.  Cytogenet Cell Genet 49: 309-310.
    45. Meakin SO, Reddan JR, Tsui L-C, Breitman ML (1989).  A rabbit lens epithelial cell line supports expression of an exogenous crystallin gene characteristic of lens fiber cell differentiation.  Exp Eye Res 48: 131-137.
    46. Kerem E, Corey M, Kerem B, Durie P, Tsui L-C, Levison H (1989).  Are there clinical and genetical differences between cystic fibrosis with and without meconium ileus?  J Pediatr 114:767-773.
    47. Barker DF, Fain PR, Wright EC, Nguyen K, Tsui L-C (1989).  A rare PvuII RFLP at the CRYB1 locus (17q11.2-q12) Nucleic Acids Res 17: 826.
    48. Barker DF, Fain PR, Wright EC, Nguyen K, Tsui L-C (1989).  MspI RFLP at the CRYB1 locus (17q11.2-q12) Nucleic Acids Res 17: 827.
    49. Lok S, Stevens W, Breitman ML, Tsui L-C (1989).  Multiple regulatory elements of the murine g2-crystallin promoter.  Nucleic Acids Res 17: 3563-3582.
    50. Kerem B, Buchanan JA, Durie P, Corey M, Levison H, Buchwald M, Tsui L-C (1989).  DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis.  Am J Hum Genet 44: 827-834.
    51. Breitman ML, Bryce DM, Giddens E, Clapoff S, Goring D, Tsui L-C, Klinworth GK, Bernstein A (1989).  Analysis of lens cell fate and eye morphogenesis in transgenic mice ablated for cells of the lens lineage.  Development 106: 457-463.
    52. Ma NS-F, Watkins P, Tsui L-C (1989).  Owl monkey gene map: evidence for a homologous human chromosome 7 region containing the cystic fibrosis gene.  Genomics 5: 389-396.
    53. Lathrop GM, O'Connell P, Leppert M, Nakamura Y, Farrall M, Tsui L-C, Lalouel J-M, White R (1989).  Twenty-five loci from a continuous linkage map of markers for human chromosome 7.  Genomics 5, 866-873.
    54. Rommens JM, Zengerling-Lentes S, Kerem B, Melmer G, Buchwald M, Tsui L-C (1989).  Physical localization of two DNA markers closely linked to the cystic fibrosis by pulsed field gel electrophoresis.  Am J Hum Genet 45: 932-941.
    55. Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N, Zsiga M, Buchwald M, Riordan JR, Tsui L-C, Collins FS (1989).  Identification of the cystic fibrosis gene: chromosome walking and jumping.  Science 245: 1059-1065.
    56. Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou J-L, Drumm ML, Iannuzzi MC, Collin FS, Tsui L-C (1989).  Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.  Science 245: 1066-1073.
    57. Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, Buchwald M, Tsui L-C (1989).  Identification of the cystic fibrosis gene: genetic analysis.  Science 245: 1073-1080.
    58. Rosenbloom CL, Kerem B, Rommens JM, Tsui L-C, Wainwright B, Williamson R, O'Brien WE, Beaudet AL (1989).  DNA amplification for detection of the XV-2c polymorphism linked to cystic fibrosis.  Nucleic Acids Res 17: 17.
    59. Lemna WK, Feldman GL, Kerem B, Fernbach SD, Zevkovich EP, O'Brien WE, Collins FS, Tsui L-C, Beaudet AL (1990).  Mutation analysis for heterozygote detection and prenatal diagnosis of cystic fibrosis.  N Eng J Med 322: 291-296.
    60. Rommens J, Kerem B, Greer W, Chang P, Tsui L-C, Ray P (1990).  Rapid non-radioactive detection of the major CF mutation.  Am J Hum Genet 46: 395-396.
    61. Melmer G, Sood R, Rommens J, Rego D, Tsui L-C, Buchwald M (1990).  Isolation of clones on chromosome 7 that contain recognition sites for rare-cutting enzymes by oligonucleotide hybridization.  Genomics 7: 173-181.
    62. Cutting GR, Kasch LM, Rosenstein BJ, Zielenski J, Tsui L-C, Antonarakis SE, Kazazian HH Jr (1990).  A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein.  Nature 346: 366-369.
    63. The Cystic Fibrosis Genetic Analysis Consortium (1990).  Worldwide survey of the ∆F508 mutation– Report from the Cystic Fibrosis Genetic Analysis Consortium.  Am J Hum Genet 47: 354-359.  (note:  Tsui L-C served as the coordinator of this article with data from multiple contributors)
    64. Rozen R, Schwartz RH, Hilman BC, Stanislovitis P, Horn GT, Klinger K, Daigneault J, De Braekeleer M, Kerem B, Tsui L-C, Fujiwara TM, Morgan K (1990).  Cystic fibrosis mutations in North American populations of French Ancestry: Analysis of Quebec French-Canadian and Louisiana Acadian Families.  Am J Hum Genet 47: 606-610.
    65. Kerem E, Corey M, Kerem B, Rommens J, Markiewicz D, Levison H, Tsui L-C, Durie P (1990).  The relation between genotype and phenotype in cystic fibrosis– analysis of the most common mutation (∆F508).  N Eng J Med 323: 1517-1522.
    66. Kerem B, Zielenski J, Markiewicz D, Bozon D, Gazit E, Yahav J, Kennedy K, Riordan JR, Collins FS, Rommens JM, Tsui L-C (1990).  Identification of mutations in regions corresponding to the 2 putative nucleotide (ATP)-binding folds of the cystic fibrosis gene.  Proc Natl Acad Sci USA 87: 8447-8451.
    67. Cutting GR, Kasch LM, Rosenstein BJ, Tsui L-C, Kazazian HH Jr, Antonarakis SE (1990).  Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease.  N Eng J Med 323: 1685-1689.
    68. Drumm ML, Pope HA, Cliff WH, Rommens JM, Marvin SA, Tsui L-C, Collins FS, Frizzell RA, Wilson JM (1990).  Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.  Cell 62: 1227-1233.
    69. Yu CC-K, Tsui L-C, Breitman ML (1990).  Homologous and heterologous enhancers modulate spatial expression but not cell type-specificity of the murine gF-crystallin promoter.  Development 110: 131-139.
    70. Scherer SW, Otulakowski G, Robinson BH, Tsui L-C (1991).  Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31-q32.  Cytogenet Cell Genet 56: 176-177.
    71. Zielenski J, Rozmahel R, Bozon D, Kerem B, Grzelczak Z, Riordan JR, Rommens JM, Tsui L-C (1991).  Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.  Genomics 10: 214-228.
    72. Zielenski J, Bozon D, Kerem B, Markiewicz D, Durie P, Rommens JM, Tsui L-C (1991). Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.  Genomics 10: 229-235.
    73. Liu Q, Tini M, Tsui L-C, Breitman ML (1991).  Interaction of a lens cell transcription factor with the proximal domain of the mouse gF-crystallin promoter.  Molec Cell Biol 11: 1531-1537.
    74. Kartner N, Jensen TJ, Naismith AL, Sun S, Ackerley CA, Reyes EF, Tsui L-C, Rommens JM, Bear CE, Riordan JR (1991).  Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance.  Cell 64: 681-691.
    75. Yorifuji T, Lemna WK, Ballard CF, Rosenbloom CL, Rozmahel R, Plavsic N, Tsui L-C, Beaudet AL (1991).  Molecular cloning and sequence analysis of the murine cDNA for the cystic fibrosis transmembrane conductance regulator.  Genomics 10: 547-550.
    76. Rommens JM, Dho S, Bear CE, Kartner N, Kennedy D, Riordan JR, Tsui L-C, Forskett K (1991).  Cyclic-AMP-inducible chloride conductance in mouse fibroblast lines stably expressing human cystic fibrosis transmembrane conductance regulator.  Proc Natl Acad Sci USA 88: 7500-7504.
    77. Fried MD, Durie PR, Tsui L-C, Corey M, Levison H, Pencharz PB (1991).  The cystic fibrosis gene and resting energy expenditure.  J Pediatr 119: 913-916.
    78. Ng ISL, Pace R, Richard MV, Kobayashi K, Kerem B, Tsui L-C, Beaudet AL (1991).  Methods for analysis of multiple cystic fibrosis mutations.  Human Genet 87: 613-617.
    79. Zielenski J, Markiewicz D, Rininsland F, Rommens JM, Tsui L-C (1991). A cluster of highly polymorphic dinucleotide repeats in intron 17b of the CFTR gene.  Am J Hum Genet 49: 1256-1262.
    80. Strong TV, Smit LS, Turpin SV, Cole JL, Tom Hon C, Petty TL, Craig MW, Rosenaw EC, Tsui L-C, Iannuzzi MC, Knowles MR, Collins FS (1991).  Cystic fibrosis mutation in two sisters with mild disease and normal sweat electrolyte levels.  N Eng J Med 325: 1630-1634.
    81. Chou JL, Rozmahel R, Tsui L-C (1991).  Characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene.  J Biol Chem 266: 24471-24476.
    82. Morral N, Girbau E, Zielenski J, Nunes V, Casals T, Tsui L-C, Estivill X (1992).  Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.  Human Genet 88: 356.
    83. Dörk T, Neumann T, Wulbrand U, Wulf B, Krawczak M, Guillermit H, Ferec C, Maaß G, Kerem B, Zielenski J, Tsui L-C, Tümmler B. (1992).  Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.  Human Genet 88: 417-425.
    84. Mornet E, Chateau C, Simon-Buoy B, Boue J, Zielenski J, Tsui L-C, Boue A (1992).  Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphism.  Humam Genet 88: 479-481.
    85. Goring D, Breitman ML, Tsui L-C (1992).  Temporal regulation of the six g-crystallin genes during mouse lens development.  Exp. Eye Res. 54: 784-795.
    86. Scherer SW, Thompkins BJF, Tsui L-C (1992).  A human chromosome 7-specific genomic DNA library in yeast artificial chromosomes.  Mammalian Genome 3: 179-181.
    87. Kristidis P, Bozon D, Corey M, Markiewicz D, Rommens J, Tsui L-C, Durie P (1992).  Genetic determination of exocrine pancreatic function in cystic fibrosis.  Am J Hum Genet 50: 1178-1184.
    88. Hamosh A and 31 co-authors including Tsui L-C (1992).  Cystic fibrosis patients bearing both the common missense mutation GlyÆAsp at codon 551 and the ∆F508 mutation are clinically indistinguishable from ∆F508 homozygotes, except for decreased risk of meconium ileus.  Am J Hum Genet 51: 245-250.
    89. Cartier M, Breitman ML, Tsui L-C (1992).  A frame-shift mutation in the gE-crystallin gene of the Elo mouse.  Nature Genet 2: 42-45.
    90. Heng HHQ, Squire J, Tsui L-C (1992).  High resolution mapping of mammalian genes by in situ hybridization to free chromatin.  Proc Natl Acad Sci USA 89: 9509-9513.
    91. Gurrieri F, Trask BJ, van den Engh G, Krauss CM, Schinzel A, Pettenati MJ, Schindler D, Dietz-Band J, Vergnaud G,Scherer SW, Tsui L-C, Muenke M (1992).  Physical mapping of the holoprosencephaly critical region in 7q36.  Nature Genet 3: 247-251.
    92. Tini M, Otulakowski G, Breitman ML, Tsui L-C, Giguere V (1993).  An inverted repeat mediates retinoic acid induction of the gF-crystallin gene: Evidence of a direct role for retinoids in lens development.  Genes & Develop 7:295-307.
    93. Heng HHQ, Shi X-M, Tsui L-C (1993).  Fluorescence in situ hybridization of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3.  Cytogenet Cell Genet 62: 108-109.
    94. Zielenski J, Fujiwara TM, Markiewicz D, Paradis AJ, Anacleto AI, Richards B. Schwartz RH, Klinger KW, Tsui L-C, Morgan K (1993).  Identification of the M1101K mutation in the CFTR gene and complete detection of cystic fibrosis mutations in the Hutterite population.  Am J Hum Genet 52: 609-615.
    95. Scherer SW, Neufeld EJ, Lievens PM-J, Orkin SH, Kim J, Tsui L-C (1993).  Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybrids.  Genomics 15: 695-696.
    96. Bryce DM, Liu Q, Khoo W, Tsui L-C, Breitman ML (1993).  Progressive and recessive fate of lens tumors correlate with subtle differences in transgene expression in gF-crystallin-T-antigen transgenic mice.  Oncogene 8: 1611-1620.
    97. Kiesewetter S, Macek MJr, Davis C, Curristan SM, Chu C-S, Graham C, Shrimpton AE, Cashman SM, Tsui L-C, Mickle J, Amos J, Highsmith WE, Shuber A, Witt DR, Crystal RG, Cutting GR (1993).  A mutation in CFTR produces different phenotypes depending on chromosomal background.  Nature Genet 5: 274-278.
    98. Goring DR, Bryce DM, Tsui L-C, Breitman ML, Liu Q (1993).  Developmental regulation and cell type-specific expression of the murine gF-crystallin gene is mediated through a lens-specific element containing the gF-1 binding site.  Devel Dynamics 196: 143-152.
    99. Heng HHQ, Tsui L-C (1993).  Modes of DAPI banding and simultaneous in situ hybridization.  Chromosoma 102: 325-332.
    100. Teem JL, Berger HA, Ostedgaard LS, Rich DP, Tsui L-C, Welsh MJ (1993).  Identification of revertants for the cystic fibrosis ∆F508 mutation using STE6/CFTR chimeras in yeast.  Cell 73: 335-346.
    101. Zielenski J, Bozon D, Markiewicz D, Aubin G, Simard F, Rommens JM, Tsui L-C 1993).  Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621+1GÆT and 711+1GÆT mutations.  Human Molec Genet 2: 683-687.
    102. Scherer SW, Rommens JM, Soder S, Plavsic N, Tompkins BJF, Beattie A, Kim J, Tsui L-C (1993).  Refined localization and yeast artificial chromosome (YAC) contig-mapping of genes and DNA segments in the 7q21-q32 region.  Human Molec Genet 2: 751-760.
    103. Marsden PA, Heng HHQ, Scherer SW, Stewart RJ, Hall AV, Shi X-M, Tsui L-C, Schappert KT (1993).  Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene.  J Biol Chem 268: 17478-17488.
    104. Tabcharani JA, Rommens JM, Hou Y-X, Chang X-B, Tsui L-C, Riordan JR, Hanrahan JW (1993). Multi-ion pore behaviour in the CFTR channel.  Nature 366: 79-82.
    105. Heng HHQ, Xie B, Shi X-M, Tsui L-C, Mahuran DJ (1993).  Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-33.1, distal to the spinal muscular atrophy locus.  Genomics 18: 429-431.
    106. Ali ST, Duncan AMV, Schappert K, Heng HHQ, Tsui L-C, Chow W, Robinson BH (1993).  Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13.  Genomics 18: 435-439.
    107. O'Dowd BF, Heiber M, Chan A, Heng HHQ, Tsui L-C, Kennedy JL, Shi X, Petronis A, George S, Nguyen T (1993).  A human gene that shows identity with the angiotensin receptor is located on chromosome 11.  Gene 136: 355-360.
    108. Peichel CL, Scherer SW, Tsui L-C, Beier DR, Vogt TF (1993)  Mapping themidkine family of developmentally regulated signaling molecules.  Mammalian Genome 4: 632-638.
    109. The Cystic Fibrosis Genotype-Phenotype Consortium (1993).  Correlation between genotype and phenotype in patients with cystic fibrosis.  N. Eng. J. Med. 329: 1308-1313. (note:  Tsui L-C was one of the multiple contributors of this study)
    110. Bozon D, Zielenski J, Rininsland F, Tsui L-C (1994).  Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AAÆG.  Human Mutation 4: 3: 330-332.
    111. Heng HHQ, Shi X-M, Scherer SW, Andrulis IL, Tsui L-C (1994).  Localization of the human asparagine synthetase gene (ASNS) to chromosome 7q21.3 and characterization of the somatic hybrid cell line 4AF/106/KO15.  Cytogenet Cell Genet 66: 135-138.
    112. Heng HHQ, Xiao H, Shi X-M, Greenblatt J, Tsui L-C (1994).  Genes encoding general initiation factors for RNA polymerase II transcription are dispersed in the human genome.  Human Molec Genet 3: 61-64.
    113. Scherer SW, Poorkar P, Allen T, Kim J, Geshuri D, Nunez M, Soder S, Pagon R, Stephens K, Patton M, Rivera H, Berg MA, Pfeiffer RA, Naritomi K, Hughes H, Genuardi M, Gurrieri F, Neri G, Lovrein E, Magenis E, Tsui L-C, Evans JP (1994).  Fine mapping of the autosomal dominant split hand split foot malformation on chromosome 7 band q21.3-q22.1.  Am J Hum Genet 55: 12-20.
    114. Palmer S, Scherer S, Patton M, Homfrey T, Tsui L-C, Stephens K, Evans JP (1994).  Evidence for genetic heterogeneity in autosomal dominant split hand/split foot malformation: Linkage to 7q21-22 excluded in a single pedigree.  Am J Hum Genet 55: 21-26.
    115. Marsden PA, Heng HHQ, Duff CL, Shi X-M, Tsui L-C, Hall AV (1994).  Localization of the human gene for inducible nitric oxide synthase (NOS2) to chromosome 17q11.2-q12.  Genomics 19: 183-185.
    116. Powers PA, Scherer SW, Tsui L-C, Gregg RG, Hogan K (1994).  Localization of the gene encoding the a2/d subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromsosome 7q21-q22 by somatic cell hybrid analysis.  Genomics 19: 192-193.
    117. Iles DE, Lehmann-Horn F, Scherer SW, Tsui L-C, Olde Weghuis D, Suijkerbuijk RF, Heytens L, Mikala G, Schwartz A, Ellis FR, Stewart AD, Deufel T, Wieringa B (1994). Localization of the gene encoding the a2/d subunit of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families.  Human Molec Genet 3: 969-975.
    118. Kunz J, Scherer SW, Klawitz I, Soder S, Du Y-Z, Speich N, Kalff-Suske M, Heng H, Tsui L-C, Grzeschik K-H (1994).  Regional localization of 725 human chromosome 7-specific yeast artificial chromosome (YAC) clones.  Genomics 22: 439-448.
    119. The Cystic Fibrosis Genetic Analysis Consortium (1994).  Population variation of common cystic fibrosis mutations.  Human Mutation 4: 167-177.  (note: Tsui L-C coordinated the study and written the report)
    120. Scherer SW, Poorkaj P, Massa H, Soder S, Allen T, Nunes M, Geshuri D, Wong E, Belloni E, Little S, Zhou L, Becker D, Kere J, Ignatius J, Niikawa N, Fukushima Y, Hasegawa T, Weissenbach J, Boncinelli E, Trask B, Tsui L-C, Evans JP (1994).  Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly.  Human Molec Genet 3: 1345-1354.
    121. Zhang X-L, Lee KL, Heng HH, Tsui L-C, Parnes JR, Shepherd NS, Chamberlain JW (1994).  Isolation of P1 bacteriophage clones containing large contiguous segments of the human and mouse loci for the T-cell coreceptor molecule CD8.  Genet Anal Tech Appl 11:129-139.
    122. Feng G-S, Shen R, Heng HHQ, Tsui L-C, Kazlauskas A, Pawson T (1994).  Receptor-binding, tyrosine phosphorylation and chromosome localization of the mouse SH2-containing phosphotyrosine phosphatase Syp.  Oncogene 9: 1745-1750.
    123. Wu J, Salido EC, Yen PH, Mohandas TK, Heng HHQ, Shi X, Tsui L-C, Chapman VM, Shapiro (1994).  Mouse gene Xe169 escapes X-inactivation.  Nature Genet  7: 491-496.
    124. Becq F, Jensen TJ, Chang X-B, Savoia A, Rommens J, Tsui L-C, Buchwald M, Riordan JR, Hanrahan JW (1994).  Phosphatase inhibitors activate normal and defective CFTR channels.  Proc Natl Acad Sci USA 91: 9160-9164.
    125. Heng HHQ, Tsui L-C, Moens PB (1994).  Organization of heterologous DNA inserts on the mouse meiotic chromosome core.  Chromosoma 103: 401-407.
    126. Marchese A, Docherty J, Nguyen T, Heiber M, Cheng R, Heng HHQ, Tsui L-C, Shi X, George SR, O'Dowd BF (1994).  Cloning of human genes encoding novel G protein-coupled receptors.  Genomics 23: 609-618.
    127. Tini M, Tsui L-C, Giguere V (1994).  Heterodimeric interaction of the retinoic acid and thyroid hormone receptors in transcriptional regulation of the gF-crystallin everted retinoic acid response element.  Molec Endocrinol 8: 1494-1506.
    128. Ing YL, Leung IWL, Heng HHQ, Tsui L-C, Lassam NJ (1994).  MLK-3:  identification of a widely-expressed protein kinase bearing an SH3 domain and a leucine zipper-basic region domain.  Oncogene 9: 1745-1750.
    129. Zielenski J, Markiewicz D, Chen HS, Schappert K, Seller A, Durie P, Corey M, Tsui L-C (1995).  Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1098R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.  Human Mutation 5: 43-47.
    130. Thacker J, Tambini CE, Simpson PJ, Tsui L-C, Scherer SW (1995).  Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA damaging agents.  Human Molec Genet 4: 113-120.
    131. Zielenski J, Markiewicz D, Lin S-P, Huang F-Y, Yang-Feng TL, Tsui L-C (1995).  Skipping of exon 12 as a consequence of a point mutation (1898+5GÆT) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese CF family.  Clin Genet 47: 125-132.
    132. Heiber M, Docherty JM, Shah G, Nguyen T, Cheng R, Heng HHQ, Marchese A, Tsui L-C, Shi X, George SR, O'Dowd BF (1995).  Isolation of three novel human genes encoding G protein-coupled receptors.  DNA and Cell Biol 14: 25-35.
    133. Scherer SW, Heng HHQ, Robinson GW, Mahon KA, Evans JP, Tsui L-C (1995).  Assignment of the human homolog of mouse Dlx3 to chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situe hybridization.  Mammalian Genome 6: 310-311.
    134. O'Dowd B, Reisine T, Nguyen T, Marchese A, Cheng R, Heng HHQ, Tsui L-C, Shi X-M, Asa S, Puy L, George S (1995).  The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes expressed in discrete areas of the brian.  Genomics 28: 84-91.
    135. Jarvi K, Zielenski J, Wilchansky M, Durie P, Buckspan M, Tullis E, Markiewicz D, Tsui L-C (1995).  Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia.  Lancet 345: 1578.
    136. Wilchanski M, Zielenski J, Markiewicz D, Tsui L-C, Corey M, Levison H, Durie P (1995).  Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.  J Pediatr 127: 705-710.
    137. Zielenski J, Patrizio P, Corey M, Handelin B, Markiewicz D, Asch R, Tsui L-C (1995).  CFTR gene variant for patients with congenital absence of vas deferens.  Am J Hum Genet 57: 958-960.
    138. Barron-Casella EA, Torres MA, Scherer SW, Heng HHQ, Tsui L-C, and Casella JF (1995).  Sequence analysis and chromosome localization of human CapZ.  J Biol Chem 270: 1-8.
    139. Alley TL, Gray BA, Lee S, Scherer SW, Tsui L-C, Tint GS, Williams CA, Zori R, Wallace MR (1995).  Identification of a yeast artificial chromosome clone spanning the translocation breakpoint at 7q32 in a Smith-Laemli-Opitz syndrom patient.  Am J Hum Genet 56: 1411-1416.
    140. Torigoe K, Sato S, Kusaba H, Kohno K, Kuwano M, Okumura K, Green ED, Scherer SW, Tsui L-C, Schlessinger D, Wada M (1995).  A YAC-based 1.5 Mb contig spanning the human multi-drug resistance gene region and delimeating the amplification unit in two human multidrug resistant cell lines.  Genome Research 5: 233-244.
    141. Wu H-K, Heng HHQ, Shi X-M, Forsdyke DR, Tsui L-C, Mak TW, Minden MD, Siderovski DR (1995).  Differential expression of a basic helix-loop-helix phosphoprotein gene, GOS8, in acute leukemia and localization to human chromosome 1q31.  Leukemia 9: 1291-1298.
    142. Marchese A, Heiber M, Nguyen T, Heng HHQ, Saldivia VR, Cheng R, Murphy PM, Tsui L-C, Shi X, Gregor P, Geroge SR, O'Dowd BF, Docherty JM (1995).  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: 335-344.
    143. Takahara K, Osborne L, Elliott RW, Tsui L-C, Scherer SW, Greenspan DS (1996).  Fine mapping of the human and mouse genes for the type I procollagen COOH-terminal protease enhancer protein.  Genomics 31: 253-256.
    144. Petronis A, Heng HHQ, Tatuch Y, Shi X-M, Klempan TA, Tsui L-C, Ashizawa T, Surh LC, Holden JJA, Kennedy J (1996).  Direct detection of expanded trinucleotide repeats using DNA hybridization technique.  Am J Med Genet 67: 85-91.
    145. Zhang X-L, Heng HHQ, Yang Y, Tsui L-C, Parnes JR, Chamberlain JW (1996).  Chromosomal mapping of the second human CD8B gene locus.  Immunogenet 43: 220-226.
    146. Schanen N, Scherer SW, Tsui L-C, Francke U (1996).  Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A (HTR5A) gene to human chromosome band 7q36.1 with somatic cell hybrids.  Cytogenet Cell Genet 72: 187-188..
    147. Scherer SW, Duvoisin RM, Kuhn R, Heng HHQ, Belloni E, Tsui L-C (1996).  Localization of two metabotropic glutamate receptor genes, mGluR3 and mGluR8, to chromosome 7q.  Genomics 31: 230-233.
    148. Moral N, Dörk T, llevadot R, Dziadek V, Merceir B, Férec C, Costes B, Girodon E, Zielenski J, Tsui L-C, Tümmler B, Estivill X (1996).  Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers.  Human Mutation 8: 149-159.
    149. Barr CL, Wigg KG, Zovko E, Sandor P, Tsui L-C (1996).  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.  Am J Med Genet 67: 301-305.
    150. Höglund P, Haila S, Scherer SW, Tsui L-C, Green ED, Holmberg C, de la Chapelle A, Kere J (1996).  Positional candidate genes for congenital chloride diarrhea suggested by high resolution physical mapping in 7q31.  Genome Res 6: 202-210.
    151. Heng HHQ, Chamberlain J, Shi X-M, Spyropoulos B, Tsui L-C, Moens P (1996).  Regulation of meiotic chromatin loop size by chromosomal position.  Proc. Natl. Acad. Sci. USA 93: 2795-2800.
    152. Rozmahel R, Wilschanski M, Matin A, Plyte S, Oliver M, Auerbach W, Moore A, Forstner J, Durie P, Nadeau J, Bear CE, Tsui L-C (1996).  Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor.  Nature Genet 12: 280-287.
    153. Johnson EJ, Scherer SW, Osborne L, Tsui L-C, Oscier D, Mould S, Cotter F (1996).  Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia.  Blood 87: 3579-3586.
    154. Wilschanski M, Rozmahel R, Beharry S, Kent G, Tsui L-C, Bear CE (1996).  In vivo measurements of ion transport in long-living CF mice.  Biochim Biophys Res Commun 219: 753-760.
    155. Lei DC, Kunkelmann K, Koslowsky T, Yezzi MJ, Escobar LC, Xu Z, Ellison AR, Rommens JM, Tsui L-C, Tykoconski M, Gruenert DC (1996).  Episomal expression of wild-type CFTR corrects cAMP-dependent chloride transport in respiratory epithelial cells.  Gene Therapy 3: 427-436.
    156. Carlsson C, Jonsson M, Nordén B, Dulay MT, Zare RN, Noolandi J, Nielson PE, Tsui L-C, Zielenski J (1996).  Screening for genetic mutations (Scientific Correspondence: Rapid detection of single-base substitution by PNA-DNA hybridization in capillary electrophoresis).  Nature 380: 207.
    157. Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, Soder S, Cobben JM, Buys C, Hudgins L, Evans JP, Tsui L-C (1996).  Characterization of the split hand/ split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.  Human Molec Genet 5: 571-579.
    158. Scherer SW, Feinstein D, Oliveira L, Tsui L-C, Pittler SJ (1996).  Gene structure and chromosome localization to 7q21.3 of the human rod photoreceptor transducin g-subunit gene (GNGT1).  Genomics 35: 241-243.
    159. Rowles JC, Scherer SW, Xi T, Majer M, Nickle DC, Popov K, Harris RA, Riebow NL, Xia J, Rommens JM, Tsui L-C, Bogardus C, and Prochazka M (1996).  Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human.  J Biol Chem 271: 22376-22382.
    160. Osborne LR, Martindale D, Scherer SW., Shi X-M, Huizenga J, Heng HHQ, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui  L-C (1996).  Identification of genes from a 500 kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.  Genomics 36: 328-336.
    161. Eppert K, Scherer SW, Ozcelik H, Pirone R, Hoodless P, Kim H, Tsui L-C, Bapat B, Gallinger S, Andrulis IL, Wrana JL, Attisano L (1996).  MADR2 maps to 18q21 and encodes a TGFß regulated MAD-related protein that is functionally mutated in colorectal carcinoma.  Cell 86: 543-552.
    162. Lin JC, Scherer SW, Tougas L, Tsui L-C, Andrulis I, Jothy S, Park M (1996).  Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET.  Oncogene 13: 2001-2008.
    163. Mackay M, Fantes J, Scherer SW, Boyle S, West K, Tsui L-C, Belloni E, Lutz E, Van Heyningen V, Marmer AJ (1996).  Chromosome localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: A possible contributor to the holoprosencephaly 3 phenotype.  Genomics 37: 345-353.
    164. Malaney S, Heng HHQ, Tsui L-C, Shi X-M, Robinson BH (1996).  Localization of the human gene encoding the 13.3-kDA subunit of mitochondrial complex III (UQCRB) to 8q22 by in situ hybridization.  Cytogenet Cell Genet 73: 297-299.
    165. Belloni E, Muenke M, Roessler E, Mitchell HF, Siegel-Bartel J, Frumkin A, Traverso G, Donnis-Keller H, Helms C, Hing AV, Heng HHQ, Koop B, Martindale D, Rommens JM, Tsui L-C, Scherer SW (1996).  Identification of Sonic-Hedgehog (SHH) as a candidate gene responsible for holoprosencephaly HPE3.  Nature Genetics 14: 353-356.
    166. Roessler E, Belloni E, Gaudenz K, Jay P, Berta P, Scherer SW, Tsui L-C, Muenke M (1996).  Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.  Nature Genetics14: 357-360.
    167. Kim K-K, Youn B-S, Heng HHQ, Shi XM, Tsui L-C, Lee ZH, Pickard RT, Kwon BS (1996).  Genomic organization and FISH mapping of human Pmel 17, the putative silver locus.  Pigment Cell Res 9: 42-48.
    168. Rozman D, Stromsted M, Tsui L-C, Scherer SW, Waterman MR (1996).  Structure and mapping of the human lanosterol 14a-demthylase 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
    169. Prochazka M, Thompson DB, Elbein SC, Scherer SW, Tsui L-C, Furlong C, Knowler WC, Bennett PH, Bogardus C (1997).  A susceptibility locus for non-insulin-dependent diabetes mellitus (NIDDM) is located at 7q21.3-q22.1.  Diabetes 45: 42A.
    170. Nakabayashi K, Ogata T, Fujii M, Takahashi E, Tsui L-C, Scherer SW, Ayusawa D.  A panel of radiation hybrids defining 7q31-q32 region of human chromosome 7.   DNA Res 30: 181-183.
    171. Zielenski J, Patrizio P, Markiewicz D, Asch RH, Tsui L-C (1997).  Identification of two mutations (S50Y and 4137delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD).  Human Mutation 9: 183-184.
    172. Orozco L, Zielenski J, Markiewicz D, Villarreal T, Tsui L-C, Lezana JL, del Angel RM (1997).  Two novel frameshift deletions (1924del7, 2055del9ÆA) in the CFTR gene in Mexican cystic fibrosis patients.  Human Mutation 10: 239-240.
    173. Barr CL, Wigg KG, Zovko E, Sandor P, Tsui L-C (1997).  Linkage Study of the Dopamine D5 receptor and Gilles de la Tourette Syndrome.  Am J Med Genet 74: 58-61.
    174. Cohen D, Heng HHQ, Shi X-M, McIntosh EM, Tsui L-C, Pearlman R (1997).  Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21.1 by fluorescence in situ hybridization.  Genomics 40: 213-215.
    175. Mo R, Freer AM, Zinyk DL, Crackower MA, Michaud J, Heng HH-Q, Chik KW, Tsui L-C, Cheng SH, Joyner AL, Hui C-C (1997).  Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal paterning and development.  Development 124: 113-123
    176. Jerome CA, Scherer SW, Tsui L-C, Gietz RD, Triggs-Raine B (1997).  Assignment of Growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12.  Genomics 40: 215-216.
    177. Fischer K, Fröhling S, Scherer SW, McAllister Brown J, Scholl C, Stilgenbauer S, Tsui L-C, Lichter P, Döhner H (1997).  Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemia.  Blood 89: 2036-2041.
    178. Schmidt L, Duh FM, Chen F, Kishida T, Glenn G, Choke P, Zhang Z, Lubensky I, Dean M, Allkimets R, Chidambaram A, Bergerheim UR, Murrary J, Feltis JT, Casadevall C, Zamarron A, Richard S, Lips CJM, Walther MM, Scherer S, Tsui L-C, Geil L, Orcutt ML, Stackhouse T, Lipan J, Slife L, Brauch H, Deche J, Niehans G, Hughson MD, Moch H, Lerman MI, Linehan WM, Zbar B (1997).  Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinoma.  Nature Genet 16: 68-73.
    179. Tambini CE, George AM, Rommens JM, Tsui L-C, Scherer SW, Thacker J (1997).  The XRCC2 DNA repair gene: Identification of a positional candidate.  Genomics 41: 84-92.
    180. Zeng WR, Scherer SW, Koutsilieris M, Huizenga JJ, Filteau F, Tsui L-C, Nepveu A (1997).  Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas.  Oncogene 14: 2355- 2365.
    181. Edelson MI, Scherer SE. Tsui L-C, Welch W, Bell DA, Berkowitz RS, Mok SC (1997).  Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinoma.  Oncogene 14: 2979-2984.
    182. Rozmahel R, Gyömörey K, Plyte S, Nguyen V, Wilschanski M, Durie P, Bear CE, Tsui L-C (1997).  Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA.  Human Molec Genet 6: 1153-1162
    183. Osborne LR, Soder S, Shi X-M, Costa T, Scherer SW, Tsui L-C (1997).  Hemizygous deletion of syntaxin 1A gene in individuals with Williams syndrome.  Am J Human Genet 61: 449-452.
    184. Snow BE, Heng HHQ, Shi X-M, Zhou Y, Du K, Taub R, Tsui L-C, McInnes RR (1997).  Expression Analysis and Chromosomal Assignment of the Human SFRS5/SRp40 Gene.  Genomics 43: 165-170.
    185. Scherer SW, Soder S, Duvoisin RM, Huizenga JJ, Tsui L-C (1997).  The human metabotropic glutamate receptor 8 (GRM8) gene: A disproportionally large gene located at 7q31.1-q32.1.  Genomics 44: 232-236.
    186. Crackower MA, Scherer SW, Heng HHQ, Tsui L-C (1997).  Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human chromosome band 5q14. Mammalian Genomics 8:159-160.
    187. Crackower MA, Heng HHQ, Scherer SW, Tsui L-C (1997). Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6. Mammalian Genomics 8: 704.
    188. Osborne LR, Herbick J-A, Greavette T, Heng HHQ, Tsui L-C, Scherer SW (1997).  PMS2-related genes (hPMSR) flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics 45: 402-406.
    189. Krebs I, Weis I, Hudler M, Rommens JM, Roth H, Scherer SW, Tsui L-C, Füchtbauer E.M, Grzeschik K-H, Tsuji K, Kunz J (1997).  Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome.  Human Molec Genet 6: 1079-1086.
    190. Roessler E, Ward DE, Gaudenz K, Belloni E, Scherer SW, Donnai D, Siegel-Bartelt J, Tsui L-C, Muenke M (1997).  Cytogenetic rearrangments involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly.  Human Genet 100: 172-181.
    191. Hegele RA, Connelly PW, Scherer SW, Hanley AJG, Harris SB, Tsui L-C, Zinman B (1997).  Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus.  J Clin Endocrin Metab 82: 3373-3377.
    192. Linsdell P, Tabcharani JA, Rommens JM, Hou Y-X, Chang X-B, Tsui L-C, Riordan JR, Hanrahan JW (1997).  Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions.  J Gen Physiol 110: 355-364.
    193. Rozmahel R, Heng HHQ, Duncan A, X-M Shi, Rommens JM, Tsui L-C (1997).  Amplification of CFTR exon 9 sequences to multiple locations in the human genome. Genomics 45: 554-561.
    194. Hegele RA, Connelly PW, Scherer SW, Hanley AJG, Harris SB, Tsui L-C, Zinman B (1997).  Paraoxonase-2 G148 variant in an aborginal Canadian girl with non-insulin dependent diabetes.  Lancet 350: 785.
    195. Mak V, Jarvi KA, Zielenski J, Durie P, Tsui L-C (1997).  Higher proportion of intact exon 9 CFTR mRNA in nasal epithelium compared with vas deferens.  Human Molec Genet 6: 2099-2107.
    196. Wang A, Forman-Kay J, Luo Y, Luo M, Chow YH, Plumb J, Friesen JD, Tsui L-C, Heng HHQ, Woolford Jr JL, Hu J (1997).  Identification and characterization of human genes encoding hprp3p and hprp4p, interacting components of the spliceosome.  Human Molec Genet 6: 2117-2126.
    197. Windstetter D, Schaefer F, Schärer K, Reiter K, Eife R, Harms HK, Bertele-Harms R, Fielder F, Tsui L-C, Reitmeir P, Horster M, Hadorn HB (1997).  Renal function and renotropic effects of secretin in cystic fibrosis.  Eur J Med Res 2: 431-436.
    198. Duh F-M, Scherer SW, Tsui L-C, Lerman M, Zbar B, Schmidt L (1997). Gene structure of the human MET proto-oncogene.  Oncogene 15: 1583-1586.
    199. Alley TL, Scherer SW, Huizenga JJ, Tsui L-C, Wallace MR (1997).  Physical mapping of the chromosome 7 breakpoint region in an SLOS patient with t(7;20) (q32.1;q13.2).  Am J Med Genet 68: 279-281.
    200. Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick J-AS, Duncan A, Scherer SW, Tsui L-C, Loutradis-Anagnostou A, Cepko CL, Jacobson SG, Bhattacharya SS, McInnes RR (1997).  Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for survival of the mammalian photoreceptor.  Cell 91: 543-553.
    201. Dong WF, Heng HHQ, Lowsky R, Xu Y, DeCoteau JF, Shi X-M, Tsui L-C, Minden M (1997).  Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX Gene, hLim-1.  DNA and Cell Biol 16: 671-678.
    202. Kent G, Iles R, Bear CE, Huan L-J, Giesenbach U, McKerlie C, Frndova H, Ackerley C, Gosslin D, Radzioch D, O'Brodovich, Tsui L-C, Buchwald M, Tanswell AK (1997).  Lung disease in mice with cystic fibrosis. J Clin Invest 100: 3060-3069.
    203. Roessler E, Belloni E, Gaudenz K, Vargas F, Scherer SW, Tsui L-C, Muenke M (1997).  Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.  Human Molec Genet 6: 1847-1853.
    204. Alley TL, Scherer SW, Huizenga JJ, Tsui L-C, Wallace MR (1997).  Physicial mapping of the chromosome 7 breakpoint region in an SLOS patient with t(7;20)(q32.1;113.2).  Am J Med Genet 68: 279-281.
    205. Mueller H-W, Michel A, Heckel D, Fischer U, Tönnes M, Tsui L-C, Scherer SW, Zang KD, Meese E (1997).  Identification of an amplified gene cluster in glioma including two novel amplified genes isolated by exon trapping.  Human Genet 101: 190-197.
    206. Wilson DC, Ellis L, Zielenski J, Corey M, Ip W, Tsui L-C, Tullis E, Knowles MR, Durie P (1998).  Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurements.  J Pediatr 132: 596-599.
    207. Griesenbach U, Chonn A, Cassady R, Hannam V, Ackerley C, Post M, Tanswell AK, Olek K, O'Brodovich, Tsui L-C (1998).  Comparison between intratrcheal and intravenous administration of liposome/DNA complexes for cystic fibrosis lung gene therapy.  Gene Therapy 5: 181-188.
    208. Gosselin D, Stevenson MM, Cowley EA, Griesenbach U, Eidelman DH, Boulé M, Tam M-F, Kent G, Skamene E, Tsui L-C, Radzioch D (1998).  Impaired ability of Cftr-knockout mice to control lung infection with Pseudomonas aeruginosa.  Am J Respir Crit Care Med 157: 1253-1262.
    209. Nomiyama H, Osborne LR, Imai T, Kusuda J, Miura R, Tsui L-C, Yoshie O (1998).  Assignment of the human CC chemokine MPIF-2/Eotaxin-2 (SCYA24) to chromosome 7q11.23.  Genomics 49: 339-340.
    210. Pimenta AF, Tsui L-C, Heng HHQ, Levitt P (1998).  Assignment of the gene encoding the limbic system-associated membrane protein (LAMP) to mouse chromosome 16B5 and human chromosome 3q13.2-q21.  Genomics 49: 472-474.
    211. Onay T, Topaloglu O, Zielenski J, Gokgoz N, Kayserili H, Camcioglu Y, Cokugras H, Akcakaya N, Apak M, Tsui L-C, Kirdar B (1998).  Analysis of the CFTR gene in Turkish cystic fibrosis patients: Identification of three novel mutations (3172delAC, P1013L and M1028I).  Human Genet 102: 224-230.
    212. Crackower MA, Motoyama J, Tsui L-C (1998).  Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse.  Devel Biol 201: 78-89.
    213. Mishmar D, Rahat A, Scherer SW, Nyakatura G, Hinzmann B, Kohwi Y, Mandel-Gutfroind Y, Lee J, Drescher B, Sas DE, Margalit H, Platzer M, Weiss A, Tsui L-C, Rosenthal A, Kerem B (1998).  Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.  Proc Natl Acad Sci USA 95: 8141-8146.
    214. Vargas FR, Roessler E, Gaudenz K, Belloni E, Whitehead AS, Kirke PN, Mills JL, Hooper G, Stevenson RE, Cordeiro I, Correia P, Felix T, Gereige R, Cunningham ML, Canun S, Antonarakis SE, Strachan T, Tsui L-C, Scherer SW, Muenke M (1998). Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly.  Human Genet 102: 387-392.
    215. Torigoe K, Harada T, Kusaba H, Uchiumi T, Kohno K, Green ED, Scherer SW, Tsui L-C, Schlessinger D, Kuwano M, Wada M (1998).  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.
    216. Crackower MA, Heng HHQ, Tsui L-C (1998).  Assignment of mouse fibroblast growth factor 10 (Fgf10) gene to the telomeric region of chromosome 13.  Genomics 53: 247-248.
    217. Coyle B, Reardon W, Herbrick JA, Tsui L-C, Gausden E, Lee J, Coffey R, Grueters A, Grossman A, Phelps PD, Luxon L, Kendall-Taylor P, Scherer SW, Trembath RC (1998).  Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre).  Human Molec Genet 7: 1105-1112.
    218. Boright AP, Connelly PW, Brunt JH, Scherer SW, Tsui L-C, Hegele RA (1998). Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites.  Atherosclerosis 139: 131-136.
    219. Minassian BA, Lee J, Herbrick J, Huizenga J, Soder S, Mungall A, Dunham I, Gardner R, Fong CY, Carpenter S, Jardim L, Satishchandra P, Andermann E, Snead OC III, Lopes-Cendes I, Tsui L-C, Delgado-Escueta AV, Rouleau GA, Scherer SW (1998).  Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy. Nature Genet 20: 171-174.
    220. Hegele RA, Harris SB, Zinman B, Wang J, Cao H, Hanley AJG, Tsui L-C, Scherer SW (1998).  Variation in the AU(AT)-Rich Element within the 3'-Untranslated Region of PPP1R3 is associated with variation in Plasma Glucose in Aboriginal Canadians.  J Clin Endocr and Metab 83: 3980-3983.
    221. Jadayel DM, Osborne LR, Coignet LJA, Zani VJ, Tsui L-C, Scherer SW, Dyer MJS (1998). The BCL7 gene family: deletion of BCL7B in Williams syndrome.  Gene 224: 35-44.
    222. Egan S, Herbrick J-A, Tsui L-C, Cohen B, Flock G, Beatty B, Scherer SW (1998).  Mapping of the human lunatic fringe (LFNG) gene to 7p22 and manic fringe (MFNG) to 22q12.  Genomics 54: 576-577.
    223. Motoyama J, Heng H, Crackower MA, Takabatake T, Takeshima K, Tsui L-C, Hui C-C (1998).  Overlapping and non-overlapping Ptch2 expression with Shh during mouse embryogenesis.  Mechanisms of Development 78: 81-84.
    224. Glöckner G, Scherer SW, Schattevoy R, Boright A, Weber J, Tsui L-C, Rosenthal A (1998).  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 Res 8:1060-1073.
    225. Mochizuki H, Scherer SW, Xi T, Nickle DC, Majer M, Huizenga JJ, Tsui L-C, Prochazka M.  (1998).  Human PON2 gene at 7q21.3: cloning, multiple mRNA forms, and missense polymorphisms in the coding sequence.  Gene 213:149-157.
    226. Dohner K, Brown J, Hehmann U, Brown J, Lowther G, Schol C, Frohling S, Cuneo A, Tsui L-C, Lichter P, Dohner H (1998).  Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders.  Blood 92: 4031-4035.
    227. Jarvi K, McCallum S, Zielenski J, Durie P, Tullis E, Wilchanski M, Margolis M, Asch M, Ginzburg B, Martin S, Buckspan MB, Tsui L-C (1999). Heterogeneity of reproductive tract abnormalities in men with absence of the vas deferens: Role of cystic fibrosis transmembrane conductance regulator gene mutations.  Fertil Steril 70: 724-728.
    228. Hwang M-Y, Kang Y-J, Kim Y-H, Scherer SW, Tsui L-C, Sohn U (1999). Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymus.  Genome 42: 457-464.
    229. Crackower MA, Sinasac DS, Xia J, Motoyama J, Prochazka M, Rommens JM, Scherer SW, Tsui L-C (1999).  Cloning and characterization of two cytoplasmic dyenin intermediate chain genes in mouse and human.  Genomics 55:257-267.
    230. Osborne, RL, Campbell T, Daradich A, Scherer SW, Tsui L-C (1999).  Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.  Genomics 57:279-284.
    231. de Silva MG, Kantharidis P, Scherer SW, Rayeroux K, Campbell L, Tsui L-C, Zalcberg JR (1999).  Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype. Cancer Genet Cytogenet 110: 28-33.
    232. Barr CL, Wigg KG, Pakstis AJ, Kurlan R, Pauls D, Kidd KK, Tsui L-C, Sandor P (1999). Genome scan for linkage to Gilles de la Tourette syndrome.  Am J Med Genet 88: 437-445.
    233. Zielenski J, Corey M, Rozmahel R, Markiewicz D, Aznarez I, Casals T, Larriba S, Mercier B, Cutting G, Krebsova A, Macek M, Langfelder E, Marshall B, DeCelie-Germana, Claustres M, Palacio A, Bal J, Nowakowska A, Ferec C, Estivill X, Durie P, Tsui L-C (1999).  Detection of a cystic fibrosis modifier locus for meconium ileus on chromosome 19q13.  Nature Genet 22: 128-129.
    234. Mak V, Zielenski J, Tsui L-C, Durie P, Zini A, Martin S, Longley TB, Jarvi KA (1999). Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia.  JAMA 281: 2217-2224.
    235. 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 L-C, Scherer SW, Saheki T (1999).  The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein.  Nature Genet 22: 159-163.
    236. Crackower MA, Sinasac DS, Lee JR, Herbrick J-A, Tsui L-C, Scherer SW (1999).  Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24. Cytogenet Cell Genet 87: 197-198.
    237. Corcoran MM, Mould SJ, Orchard JA, Ibbotson RE, Chapman RM, Boright AP, Platt C, Tsui L-C, Scherer SW, Oscier DG (1999). Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations. Oncogene 18: 6271-6277.
    238. Sinasac DS, Crackower MA, Lee JR, Kobayashi K, Saheki T, Scherer SW, Tsui L-C, (1999).  Genomic structure of the adult-onset type II citullinemia gene, SLC25A13, and cloning and expression of its mouse momologue.  Genomics 62: 289-292.
    239. Nichol CJ, Zielenski J, Tsui L-C, Wells PG (2000).  An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis.  FASEB J 14: 111-127.
    240. Mak V, Zielenski J, Tsui L-C, Durie P, Zini A, Martin S, Longley TB, Jarvi KA (2000).  Cystic fibrosis gene mutations and infertile men with primary testicular failure. Hum Reprod 15: 436-439.
    241. Belloni E, Martucciello G, Verderio D, Ponti E, Seri M, Jasonni V, Torre M, Ferrari M, Tsui L-C, Scherer SW (2000).  Involvement of the HLXB9 homeobox gene in Currarino syndrome.  Am J Hum Genet 66: 312-319.
    242. Orozco L, Velazquez R, Zielenski J, Tsui L-C, Chavez M, Lezana JL, Saldana Y, Hermandez E, Carnevale A (2000).  Spectrum of CFTR mutations in Mexican cystic fibrosis patients: Identification of five novel mutations (W1098C, 846delT, P750L, 4160insGGGG and 297-1G- >A).  Human Genet 106: 360-365.
    243. Hellman A, Rahat A, Scherer SW, Darvasi A, Tsui L-C, Kerem B (2000). Replication delay along FRA7H, a common fragile site on human chromosome 7,  leads to chromosomal instability. Molec Cell Biol 20: 4420-4427. 
    244. Dork T, Macek M Jr, Mekus F, Tummler B, Tzountzouris J, Casals T, Krebsova A, Koudova M, Sakmaryova I, Macek M Sr, Vavrova V, Zemkova D, Ginter E, Petrova NV, Ivaschenko T, Baranov V, Witt M, Pogorzelski A, Bal J, Zekanowsky C, Wagner K, Stuhrmann M, Bauer I, Seydewitz HH, Neumann T, Jakubiczka S, Kraus C, Thamm B, Nechiporenko M, Livshits L, Mosse N, Tsukerman G, Kadasi L, Ravnik-Glavac M, Glavac D, Komel R, Vouk K, Kucinskas V, Krumina A, Teder M, Kocheva S, Efremov G, Onay T, Kirdar B, Malone G, Schwarz M, Zhou Z, Friedman K, Carles S, Claustres M, Bozon D, Verlingue C, Ferec C, Tzetis M, Kanavakis E, Cuppens H, Bombieri C, Pignatti PF, Sngiuolo F, Jordanova A, Kusic J, Radojkovic D, Sertic J, Richter D, Rukavina A, Bjorck E, Strandvik B, Cardoso H, Montgomery M, Nakielna B, Hughes D, Estivill X, Aznarez I, Tullis E, Tsui L-C, Zielenski J (2000).  Characterization of a novel 21-kb deletion, CFTRdele2, 3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe. Hum Genet 106: 259-268.
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    246. Bhatia E, Durie P, Zielenski J, Lam D, Sikora SS, Choudhuri G, Tsui L-C (2000).  Mutations in the cystic fibrosis transmembrane conductance regulator gene in patients with tropical calcific pancreatitis. Am J Gastroenterol 95: 3658-3659.
    247. Aznarez I, Bal J, Casals T, Estivill X, Moral N, Sands D, Nunes V, Sobczynska-Tomaszewska A, Tsui L-C, Zielenski J (2000). [Analysis of mutations in the CFTR gene in Polish cystic fibrosis patients identification of rare mutations]. Med Wieku Rozwoj. 4: 149-159.
    248. Wen X-Y, Stewart AK, Skaug J, Wei E, Tsui L-C (2001). Murine phosphotidylserine-specific phospholipase A1 (Ps-pla1) maps to chromosome 16 but distinct from the lpd (lipid defect) locus.  Mammalian Genome 12: 129-132.
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    250. Ye L, Chan S, Chow Y-H, Tsui L-C, Hu J (2001).  Regulated expression of the human CFTR gene in epithelial cells.  Molecular Therapy 3: 723-733.
    251. Onay T, Zielenski J, Topaloglu O, Gokgoz N, Kayserili H, Apak MY, Camcioglu Y, Cokugras H, Akcakaya N, Tsui L-C, Kirdar B (2001).  Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients.  Human Biol 73:191-203.
    252. Osborne LR, Li M, Pober B, Chitayat D, Bodurtha J, Mandel A, Costa T, Grebe T, Cox S, Tsui L-C, Scherer SW (2001).  A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.  Nature Genet 29:321-325.
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    257. Dong S, Leung KKH, Pelling AL, Lee PYT, Tang ASP, Heng HHQ, Tsui L-C, Tease C, Fisher G, Steel KP, Cheah KSE (2002). Circling, deafness, and yellow coat displayed by yellow submarine (ysb) and light coat and circling (lcc) mice with mutations on chromosome 3.  Genomics 79: 777-784.
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    260. Estivill X, Cheung J, Pujana MA, Nakabayashi K, Scherer S, Tsui L-C (2002). Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome. Hum Molec Genet. 11: 1987-1995.
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    273. Lo B, Faiyaz-Ul-Haque M, Kennedy S, Aviv R, Tsui L-C, Teebi AS (2003). Novel mutation in the gene encoding c-Abl-Binding Protein SH3BP2 causes Cherubism. Am J Med Genet 121: 37-40.
    274. Aznarez I, Chan E, Zielenski J, Blencowe B, Tsui L-C (2003). A pre-mRNA splicing enhancer signal in exon 13 of the cystic fibrosis transmembrane conductance regulator gene.  Human Molec Genet 12: 2031-2040.
    275. Chen L, Ma S, Li B, Fink T, Zachar V, Takahashi M, Cuttichia J, Tsui L-C, Ebbesen P, Liu X (2003). Transcriptional activation of immediate-early gene ETR101 by human T-cell leukaemia virus type I Tax. J Gen Virol 84: 3203-3214.
    276. Liu X, Li X, Li M, Acimovic YJ, Scherer SW, Estivill X, Tsui L-C (2004). Characterization of the segmental duplication LCR7-20 in the human genome.  Genomics 83: 262-269
    277. Lo B, Faiyaz-Ul-Haque M, Banwell B, Blaser S, Tsui L-C, Teebi AS (2004). The locus responsible for Horizontal Gaze Palsy/Progressive Scoliosis and Brainstem Hypoplasia is refined to a 9-cM region on chromosome 11q23.  Clin Genet 65: 137-142.
    278. Faiyaz-Ul-Haque M, Zaidi SHE, Al-Ali Mariam, Al-Mureikhi MS, Kennedy S, Al-Thani G, Tsui L-C, Teebi AS (2004).  A novel missense mutation in the Galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos Syndrome resembling the Progeroid.  A J Med Genet 128: 39-45.
    279. Sinasac DS, Moriyama M, Jalil MA, Begum L, Li MX, Iijima M, Horiuchi M, Robinson BH, Kobayashi K, Saheki T, Tsui L-C (2004). Slc25a13-Knockout Mice harbor metabolic deficits but fail to display hallmarks of Adult-Onset Type II Citrullinemia. Mol Cell Biol 24: 527-536.
    280. Faiyaz-Ul-Haque M, Ahmad W, Zaidi SHE, Hussain SS, Haque S, Cohn DH, Ahmad M, Tsui L-C (2004).  Novel mutations in the EXT1) gene in two large consanguineous families affected with multiple hereditary exostosis (familial osteochondromatosis). Clin Genet 66: 144-151.
    281. Eppert K, Wunder JS, Aneliunas V, Tsui L-C, Scherer SW, Andrulis IL (2005). Altered expression and deletion of RMO1 in osteosarcoma. Int J Can 114: 738-746.
    282. Faiyaz-Ul-Haque M, Zaidi SH, King LM, Haque S, Patel M, Ahmad M, Siddique T, Ahmad W, Tsui L-C, Cohn DH (2005). Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes. Clin Genet 67: 93-97.
    283. Rafiq MA, Faiyaz-Ul-Haque M, Ud Din MA, Malik S, Sohail M, Anwar M, Haque S, Paterson AD, Tsui L-C, Ahmad W (2005). A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1. J Invest Dermatol 124: 338-342.
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