Tsui LC - Search Results

1

Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus.

Hamosh A, King TM, Rosenstein BJ, Corey M, Levison H, Durie P, Tsui LC, McIntosh I, Keston M, Brock DJ, et al. Hamosh A, et al. Among authors: tsui lc. Am J Hum Genet. 1992 Aug;51(2):245-50. Am J Hum Genet. 1992. PMID: 1379413 Free PMC article.

2

Genetic determination of exocrine pancreatic function in cystic fibrosis.

Kristidis P, Bozon D, Corey M, Markiewicz D, Rommens J, Tsui LC, Durie P. Kristidis P, et al. Among authors: tsui lc. Am J Hum Genet. 1992 Jun;50(6):1178-84. Am J Hum Genet. 1992. PMID: 1376016 Free PMC article.

3

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

Kerem E, Corey M, Kerem BS, Rommens J, Markiewicz D, Levison H, Tsui LC, Durie P. Kerem E, et al. Among authors: tsui lc. N Engl J Med. 1990 Nov 29;323(22):1517-22. doi: 10.1056/NEJM199011293232203. N Engl J Med. 1990. PMID: 2233932 Free article.

4

DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis.

Kerem BS, Buchanan JA, Durie P, Corey ML, Levison H, Rommens JM, Buchwald M, Tsui LC. Kerem BS, et al. Among authors: tsui lc. Am J Hum Genet. 1989 Jun;44(6):827-34. Am J Hum Genet. 1989. PMID: 2567116 Free PMC article.

5

Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?

Dorfman R, Nalpathamkalam T, Taylor C, Gonska T, Keenan K, Yuan XW, Corey M, Tsui LC, Zielenski J, Durie P. Dorfman R, et al. Among authors: tsui lc. Clin Genet. 2010 May;77(5):464-73. doi: 10.1111/j.1399-0004.2009.01351.x. Epub 2009 Jan 6. Clin Genet. 2010. PMID: 20059485

6

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein.

Cutting GR, Kasch LM, Rosenstein BJ, Zielenski J, Tsui LC, Antonarakis SE, Kazazian HH Jr. Cutting GR, et al. Among authors: tsui lc. Nature. 1990 Jul 26;346(6282):366-9. doi: 10.1038/346366a0. Nature. 1990. PMID: 1695717

7

Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease.

Cutting GR, Kasch LM, Rosenstein BJ, Tsui LC, Kazazian HH Jr, Antonarakis SE. Cutting GR, et al. Among authors: tsui lc. N Engl J Med. 1990 Dec 13;323(24):1685-9. doi: 10.1056/NEJM199012133232407. N Engl J Med. 1990. PMID: 2233965 Free article. No abstract available.

8

Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus.

Kerem E, Corey M, Kerem B, Durie P, Tsui LC, Levison H. Kerem E, et al. Among authors: tsui lc. J Pediatr. 1989 May;114(5):767-73. doi: 10.1016/s0022-3476(89)80134-9. J Pediatr. 1989. PMID: 2715890

9

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.

Wilschanski M, Zielenski J, Markiewicz D, Tsui LC, Corey M, Levison H, Durie PR. Wilschanski M, et al. Among authors: tsui lc. J Pediatr. 1995 Nov;127(5):705-10. doi: 10.1016/s0022-3476(95)70157-5. J Pediatr. 1995. PMID: 7472820

10

Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Zielenski J, Markiewicz D, Chen HS, Schappert K, Seller A, Durie P, Corey M, Tsui LC. Zielenski J, et al. Among authors: tsui lc. Hum Mutat. 1995;5(1):43-7. doi: 10.1002/humu.1380050106. Hum Mutat. 1995. PMID: 7537150

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