Lap-Chee Tsui
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, PathologyWebsite:
https://www.ourhkfoundation.org.hk/en/node/784Google:
"Lap-Chee Tsui"Bio:
https://www4.hku.hk/hongrads/graduates/professor-lap-chee-tsui
https://presidentoffice.hku.hk/LCTsui/LapCheeTsuiCV.pdf
http://www.science.ca/scientists/scientistprofile.php?pID=19
http://www.cdnmedhall.org/inductees/lapcheetsui
Parents
Sign in to add mentor| Roger W. Hendrix | grad student | 1974-1979 | University of Pittsburgh (Microtree) |
| Manuel Buchwald | post-doc | 1981-1983 | University of Toronto |
Children
Sign in to add trainee| Daphne R. Goring | grad student | 1985-1990 | University of Toronto |
| Henry H. Heng | grad student | 1990-1994 | University of Toronto |
| David S. Sinasac | grad student | 2003 | University of Toronto |
| John L. Teem | post-doc | 1990-1992 | University of Toronto |
| Lucy Osborne | post-doc | 1993-1998 | University of Toronto (GenetiTree) |
BETA: Related publications
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Publications
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| Tsui LC, Dorfman R. (2013) The cystic fibrosis gene: a molecular genetic perspective. Cold Spring Harbor Perspectives in Medicine. 3: a009472 |
| Dorfman R, Li W, Sun L, et al. (2009) Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results. Human Genetics. 126: 763-78 |
| Aznarez I, Barash Y, Shai O, et al. (2008) 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 |
| Dorfman R, Sandford A, Taylor C, et al. (2008) Complex two-gene modulation of lung disease severity in children with cystic fibrosis. The Journal of Clinical Investigation. 118: 1040-9 |
| Zielenski J, Markiewicz D, Lin S, et al. (2008) Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family. Clinical Genetics. 47: 125-132 |
| Saheki T, Iijima M, Li MX, et al. (2007) Citrin/mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiency. The Journal of Biological Chemistry. 282: 25041-52 |
| Aznarez I, Zielenski J, Rommens JM, et al. (2007) 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 |
| Wilschanski M, Dupuis A, Ellis L, et al. (2006) Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials. American Journal of Respiratory and Critical Care Medicine. 174: 787-94 |
| Moriyama M, Li MX, Kobayashi K, et al. (2006) Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice. Journal of Hepatology. 44: 930-8 |
| Heng HH, Windle B, Tsui LC. (2005) High-resolution FISH analysis. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 4.5 |