Strong TV - Search Results

1

Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Strong TV, Smit LS, Nasr S, Wood DL, Cole JL, Iannuzzi MC, Stern RC, Collins FS. Strong TV, et al. Hum Mutat. 1992;1(5):380-7. doi: 10.1002/humu.1380010506. Hum Mutat. 1992. PMID: 1284540 Free article.

2

Chloride conductance expressed by delta F508 and other mutant CFTRs in Xenopus oocytes.

Drumm ML, Wilkinson DJ, Smit LS, Worrell RT, Strong TV, Frizzell RA, Dawson DC, Collins FS. Drumm ML, et al. Among authors: strong tv. Science. 1991 Dec 20;254(5039):1797-9. doi: 10.1126/science.1722350. Science. 1991. PMID: 1722350

3

Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels.

Strong TV, Smit LS, Turpin SV, Cole JL, Hon CT, Markiewicz D, Petty TL, Craig MW, Rosenow EC 3rd, Tsui LC, et al. Strong TV, et al. N Engl J Med. 1991 Dec 5;325(23):1630-4. doi: 10.1056/NEJM199112053252307. N Engl J Med. 1991. PMID: 1944451 Free article. No abstract available.

4

Two frameshift mutations in the cystic fibrosis gene.

Iannuzzi MC, Stern RC, Collins FS, Hon CT, Hidaka N, Strong T, Becker L, Drumm ML, White MB, Gerrard B, et al. Iannuzzi MC, et al. Am J Hum Genet. 1991 Feb;48(2):227-31. Am J Hum Genet. 1991. PMID: 1990834 Free PMC article.

5

Localization of the cystic fibrosis transmembrane conductance regulator in human bile duct epithelial cells.

Cohn JA, Strong TV, Picciotto MR, Nairn AC, Collins FS, Fitz JG. Cohn JA, et al. Among authors: strong tv. Gastroenterology. 1993 Dec;105(6):1857-64. doi: 10.1016/0016-5085(93)91085-v. Gastroenterology. 1993. PMID: 7504645

6

Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization.

Strong TV, Boehm K, Collins FS. Strong TV, et al. J Clin Invest. 1994 Jan;93(1):347-54. doi: 10.1172/JCI116966. J Clin Invest. 1994. PMID: 7506713 Free PMC article.

7

Identification of a CFTR frameshift mutation (1013 delAA) in trans to delta F508 in a pancreatic sufficient cystic fibrosis patient.

Nasr SZ, Strong TV, Collins FS. Nasr SZ, et al. Among authors: strong tv. Hum Mol Genet. 1994 Nov;3(11):2063-4. Hum Mol Genet. 1994. PMID: 7533026 No abstract available.

8

Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance.

Strong TV, Wilkinson DJ, Mansoura MK, Devor DC, Henze K, Yang Y, Wilson JM, Cohn JA, Dawson DC, Frizzell RA, et al. Strong TV, et al. Hum Mol Genet. 1993 Mar;2(3):225-30. doi: 10.1093/hmg/2.3.225. Hum Mol Genet. 1993. PMID: 7684641

9

Molecular basis of defective anion transport in L cells expressing recombinant forms of CFTR.

Yang Y, Devor DC, Engelhardt JF, Ernst SA, Strong TV, Collins FS, Cohn JA, Frizzell RA, Wilson JM. Yang Y, et al. Among authors: strong tv. Hum Mol Genet. 1993 Aug;2(8):1253-61. doi: 10.1093/hmg/2.8.1253. Hum Mol Genet. 1993. PMID: 7691345

10

Missense mutation (G480C) in the CFTR gene associated with protein mislocalization but normal chloride channel activity.

Smit LS, Strong TV, Wilkinson DJ, Macek M Jr, Mansoura MK, Wood DL, Cole JL, Cutting GR, Cohn JA, Dawson DC, et al. Smit LS, et al. Among authors: strong tv. Hum Mol Genet. 1995 Feb;4(2):269-73. doi: 10.1093/hmg/4.2.269. Hum Mol Genet. 1995. PMID: 7757078

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