Tsui LC - Search Results

1

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

2

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.

3

Cystic fibrosis: genotypic and phenotypic variations.

Zielenski J, Tsui LC. Zielenski J, et al. Among authors: tsui lc. Annu Rev Genet. 1995;29:777-807. doi: 10.1146/annurev.ge.29.120195.004021. Annu Rev Genet. 1995. PMID: 8825494 Review.

4

Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Morral N, Girbau E, Zielenski J, Nunes V, Casals T, Tsui LC, Estivill X. Morral N, et al. Among authors: tsui lc. Hum Genet. 1992 Jan;88(3):356. doi: 10.1007/BF00197276. Hum Genet. 1992. PMID: 1370810

5

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.

6

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Zielenski J, Rozmahel R, Bozon D, Kerem B, Grzelczak Z, Riordan JR, Rommens J, Tsui LC. Zielenski J, et al. Among authors: tsui lc. Genomics. 1991 May;10(1):214-28. doi: 10.1016/0888-7543(91)90503-7. Genomics. 1991. PMID: 1710598

7

Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Zielenski J, Bozon D, Kerem B, Markiewicz D, Durie P, Rommens JM, Tsui LC. Zielenski J, et al. Among authors: tsui lc. Genomics. 1991 May;10(1):229-35. doi: 10.1016/0888-7543(91)90504-8. Genomics. 1991. PMID: 1710599

8

Molecular genetics of cystic fibrosis.

Tsui LC, Rommens J, Kerem B, Rozmahel R, Zielenski J, Kennedy D, Markiewicz D, Plavsic N, Chou JL, Bozon D, et al. Tsui LC, et al. Adv Exp Med Biol. 1991;290:9-17; discussion 17-8. doi: 10.1007/978-1-4684-5934-0_2. Adv Exp Med Biol. 1991. PMID: 1719772 Review. No abstract available.

9

A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Zielenski J, Markiewicz D, Rininsland F, Rommens J, Tsui LC. Zielenski J, et al. Among authors: tsui lc. Am J Hum Genet. 1991 Dec;49(6):1256-62. Am J Hum Genet. 1991. PMID: 1720926 Free PMC article.

10

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

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