589 related articles for article (PubMed ID: 10762539)
1. Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels.
Mickle JE; Milewski MI; Macek M; Cutting GR
Am J Hum Genet; 2000 May; 66(5):1485-95. PubMed ID: 10762539
[TBL] [Abstract][Full Text] [Related]
2. Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator.
Schwiebert EM; Morales MM; Devidas S; Egan ME; Guggino WB
Proc Natl Acad Sci U S A; 1998 Mar; 95(5):2674-9. PubMed ID: 9482946
[TBL] [Abstract][Full Text] [Related]
3. Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents.
Fulmer SB; Schwiebert EM; Morales MM; Guggino WB; Cutting GR
Proc Natl Acad Sci U S A; 1995 Jul; 92(15):6832-6. PubMed ID: 7542778
[TBL] [Abstract][Full Text] [Related]
4. A novel natural product compound enhances cAMP-regulated chloride conductance of cells expressing CFTR[delta]F508.
deCarvalho AC; Ndi CP; Tsopmo A; Tane P; Ayafor J; Connolly JD; Teem JL
Mol Med; 2002 Feb; 8(2):75-87. PubMed ID: 12080183
[TBL] [Abstract][Full Text] [Related]
5. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
Sharma H; Mavuduru RS; Singh SK; Prasad R
Mol Hum Reprod; 2014 Sep; 20(9):827-35. PubMed ID: 24958810
[TBL] [Abstract][Full Text] [Related]
6. A novel missense mutation A1081P in the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a Laotian patient with congenital bilateral absence of the vas deferens.
Ngukam A; Jacquemont ML; Souville I; Viel M; Beldjord C; Hubert D; Hughes JN; Bienvenu T
J Trop Pediatr; 2004 Aug; 50(4):239-40. PubMed ID: 15357566
[TBL] [Abstract][Full Text] [Related]
7. Molecular and functional characterization of CBAVD-causing mutations located in CFTR nucleotide-binding domains.
Grangeia A; Barro-Soria R; Carvalho F; Damas AM; Maurício AC; Kunzelmann K; Barros A; Sousa M
Cell Physiol Biochem; 2008; 22(1-4):79-92. PubMed ID: 18769034
[TBL] [Abstract][Full Text] [Related]
8. A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis.
Mickle JE; Macek M; Fulmer-Smentek SB; Egan MM; Schwiebert E; Guggino W; Moss R; Cutting GR
Hum Mol Genet; 1998 Apr; 7(4):729-35. PubMed ID: 9499426
[TBL] [Abstract][Full Text] [Related]
9. Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium.
Bronsveld I; Mekus F; Bijman J; Ballmann M; Greipel J; Hundrieser J; Halley DJ; Laabs U; Busche R; De Jonge HR; Tümmler B; Veeze HJ
Gastroenterology; 2000 Jul; 119(1):32-40. PubMed ID: 10889152
[TBL] [Abstract][Full Text] [Related]
10. Both CFTR and outwardly rectifying chloride channels contribute to cAMP-stimulated whole cell chloride currents.
Schwiebert EM; Flotte T; Cutting GR; Guggino WB
Am J Physiol; 1994 May; 266(5 Pt 1):C1464-77. PubMed ID: 7515570
[TBL] [Abstract][Full Text] [Related]
11. Structure and function of the cystic fibrosis transmembrane conductance regulator.
Morales MM; Capella MA; Lopes AG
Braz J Med Biol Res; 1999 Aug; 32(8):1021-8. PubMed ID: 10454765
[TBL] [Abstract][Full Text] [Related]
12. Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens.
Osborne LR; Lynch M; Middleton PG; Alton EW; Geddes DM; Pryor JP; Hodson ME; Santis GK
Hum Mol Genet; 1993 Oct; 2(10):1605-9. PubMed ID: 7505692
[TBL] [Abstract][Full Text] [Related]
13. Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.
De Braekeleer M; Férec C
Mol Hum Reprod; 1996 Sep; 2(9):669-77. PubMed ID: 9239681
[TBL] [Abstract][Full Text] [Related]
14. [Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].
Bienvenu T; Claustres M
Contracept Fertil Sex; 1996 Jun; 24(6):495-500. PubMed ID: 8766513
[TBL] [Abstract][Full Text] [Related]
15. Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens.
Radpour R; Gourabi H; Gilani MA; Dizaj AV; Rezaee M; Mollamohamadi S
Mol Hum Reprod; 2006 Nov; 12(11):717-21. PubMed ID: 16973827
[TBL] [Abstract][Full Text] [Related]
16. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.
Reddy MM; Quinton PM
JOP; 2001 Jul; 2(4 Suppl):212-8. PubMed ID: 11875262
[TBL] [Abstract][Full Text] [Related]
17. Inhibition of protein kinase CK2 closes the CFTR Cl channel, but has no effect on the cystic fibrosis mutant deltaF508-CFTR.
Treharne KJ; Xu Z; Chen JH; Best OG; Cassidy DM; Gruenert DC; Hegyi P; Gray MA; Sheppard DN; Kunzelmann K; Mehta A
Cell Physiol Biochem; 2009; 24(5-6):347-60. PubMed ID: 19910675
[TBL] [Abstract][Full Text] [Related]
18. Binding screen for cystic fibrosis transmembrane conductance regulator correctors finds new chemical matter and yields insights into cystic fibrosis therapeutic strategy.
Hall JD; Wang H; Byrnes LJ; Shanker S; Wang K; Efremov IV; Chong PA; Forman-Kay JD; Aulabaugh AE
Protein Sci; 2016 Feb; 25(2):360-73. PubMed ID: 26444971
[TBL] [Abstract][Full Text] [Related]
19. Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct.
Lu M; Dong K; Egan ME; Giebisch GH; Boulpaep EL; Hebert SC
Proc Natl Acad Sci U S A; 2010 Mar; 107(13):6082-7. PubMed ID: 20231442
[TBL] [Abstract][Full Text] [Related]
20. Structure-function analysis of a double-mutant cystic fibrosis transmembrane conductance regulator protein occurring in disorders related to cystic fibrosis.
Fanen P; Clain J; Labarthe R; Hulin P; Girodon E; Pagesy P; Goossens M; Edelman A
FEBS Lett; 1999 Jun; 452(3):371-4. PubMed ID: 10386624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
