147 related articles for article (PubMed ID: 7678968)
1. Cystic fibrosis gene and protein expression during fetal lung development.
McGrath SA; Basu A; Zeitlin PL
Am J Respir Cell Mol Biol; 1993 Feb; 8(2):201-8. PubMed ID: 7678968
[TBL] [Abstract][Full Text] [Related]
2. Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis.
Chu CS; Trapnell BC; Curristin SM; Cutting GR; Crystal RG
J Clin Invest; 1992 Sep; 90(3):785-90. PubMed ID: 1381723
[TBL] [Abstract][Full Text] [Related]
3. Regional expression of CFTR in developing human respiratory tissues.
Tizzano EF; O'Brodovich H; Chitayat D; Bènichou JC; Buchwald M
Am J Respir Cell Mol Biol; 1994 Apr; 10(4):355-62. PubMed ID: 7510983
[TBL] [Abstract][Full Text] [Related]
4. Molecular physiology of CFTR Cl- channels in heart.
Hume JR; Hart P; Levesque PC; Collier ML; Geary Y; Warth J; Chapman T; Horowitz B
Jpn J Physiol; 1994; 44 Suppl 2():S177-82. PubMed ID: 7752524
[TBL] [Abstract][Full Text] [Related]
5. Expression and localization of CFTR in the rhesus monkey surface airway epithelium.
Dupuit F; Bout A; Hinnrasky J; Fuchey C; Zahm JM; Imler JL; Pavirani A; Valerio D; Puchelle E
Gene Ther; 1995 Mar; 2(2):156-63. PubMed ID: 7536618
[TBL] [Abstract][Full Text] [Related]
6. Cationic lipids for reporter gene and CFTR transfer to rat pulmonary epithelium.
Logan JJ; Bebok Z; Walker LC; Peng S; Felgner PL; Siegal GP; Frizzell RA; Dong J; Howard M; Matalon
Gene Ther; 1995 Jan; 2(1):38-49. PubMed ID: 7536114
[TBL] [Abstract][Full Text] [Related]
7. Developmental differences of cystic fibrosis transmembrane conductance regulator functional expression in isolated rat fetal distal airway epithelial cells.
MacLeod RJ; Hamilton JR; Kopelman H; Sweezey NB
Pediatr Res; 1994 Jan; 35(1):45-9. PubMed ID: 7510872
[TBL] [Abstract][Full Text] [Related]
8. Expression of cystic fibrosis transmembrane conductance regulator in human gallbladder epithelial cells.
Dray-Charier N; Paul A; Veissiere D; Mergey M; Scoazec JY; Capeau J; Brahimi-Horn C; Housset C
Lab Invest; 1995 Dec; 73(6):828-36. PubMed ID: 8558844
[TBL] [Abstract][Full Text] [Related]
9. Quantitative expression patterns of multidrug-resistance P-glycoprotein (MDR1) and differentially spliced cystic-fibrosis transmembrane-conductance regulator mRNA transcripts in human epithelia.
Bremer S; Hoof T; Wilke M; Busche R; Scholte B; Riordan JR; Maass G; Tümmler B
Eur J Biochem; 1992 May; 206(1):137-49. PubMed ID: 1375156
[TBL] [Abstract][Full Text] [Related]
10. 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
Hum Mutat; 1992; 1(5):380-7. PubMed ID: 1284540
[TBL] [Abstract][Full Text] [Related]
11. Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice.
Whitsett JA; Dey CR; Stripp BR; Wikenheiser KA; Clark JC; Wert SE; Gregory RJ; Smith AE; Cohn JA; Wilson JM
Nat Genet; 1992 Sep; 2(1):13-20. PubMed ID: 1284640
[TBL] [Abstract][Full Text] [Related]
12. Localization of cystic fibrosis transmembrane conductance regulator mRNA in human fetal lung tissue by in situ hybridization.
McCray PB; Wohlford-Lenane CL; Snyder JM
J Clin Invest; 1992 Aug; 90(2):619-25. PubMed ID: 1379613
[TBL] [Abstract][Full Text] [Related]
13. CFTR chloride channels in human and simian heart.
Warth JD; Collier ML; Hart P; Geary Y; Gelband CH; Chapman T; Horowitz B; Hume JR
Cardiovasc Res; 1996 Apr; 31(4):615-24. PubMed ID: 8689654
[TBL] [Abstract][Full Text] [Related]
14. Expression of CFTR and a cAMP-stimulated chloride secretory current in cultured human fetal alveolar epithelial cells.
McCray PB; Bettencourt JD; Bastacky J; Denning GM; Welsh MJ
Am J Respir Cell Mol Biol; 1993 Dec; 9(6):578-85. PubMed ID: 7504926
[TBL] [Abstract][Full Text] [Related]
15. A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations.
Highsmith WE; Burch LH; Zhou Z; Olsen JC; Boat TE; Spock A; Gorvoy JD; Quittel L; Friedman KJ; Silverman LM
N Engl J Med; 1994 Oct; 331(15):974-80. PubMed ID: 7521937
[TBL] [Abstract][Full Text] [Related]
16. A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis.
Will K; Dörk T; Stuhrmann M; Meitinger T; Bertele-Harms R; Tümmler B; Schmidtke J
J Clin Invest; 1994 Apr; 93(4):1852-9. PubMed ID: 7512993
[TBL] [Abstract][Full Text] [Related]
17. Cystic fibrosis transmembrane conductance regulator (CFTR) dependent cytoskeletal tension during lung organogenesis.
Cohen JC; Larson JE
Dev Dyn; 2006 Oct; 235(10):2736-48. PubMed ID: 16906518
[TBL] [Abstract][Full Text] [Related]
18. In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium.
Rosenfeld MA; Yoshimura K; Trapnell BC; Yoneyama K; Rosenthal ER; Dalemans W; Fukayama M; Bargon J; Stier LE; Stratford-Perricaudet L
Cell; 1992 Jan; 68(1):143-55. PubMed ID: 1370653
[TBL] [Abstract][Full Text] [Related]
19. Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells.
Wei X; Eisman R; Xu J; Harsch AD; Mulberg AE; Bevins CL; Glick MC; Scanlin TF
J Cell Physiol; 1996 Aug; 168(2):373-84. PubMed ID: 8707873
[TBL] [Abstract][Full Text] [Related]
20. Expression and characterization of the cystic fibrosis transmembrane conductance regulator.
Gregory RJ; Cheng SH; Rich DP; Marshall J; Paul S; Hehir K; Ostedgaard L; Klinger KW; Welsh MJ; Smith AE
Nature; 1990 Sep; 347(6291):382-6. PubMed ID: 1699127
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
