These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
218 related items for PubMed ID: 16798551
21. 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 [Abstract] [Full Text] [Related]
22. Future pharmacological treatment of cystic fibrosis. Zeitlin PL. Respiration; 2000 Nov; 67(4):351-7. PubMed ID: 10940786 [Abstract] [Full Text] [Related]
34. [From the laboratory to the clinic: CFTR and the therapeutic options for cystic fibrosis]. Mayol J, Alvarez de Arcaya Vicente A, Arbeo Escolar AM, Peña Soria MJ, Alvarez Fernández-Represa J. An Med Interna; 2000 Feb 01; 17(2):92-8. PubMed ID: 10829466 [Abstract] [Full Text] [Related]
35. The DeltaF508 cystic fibrosis mutation impairs domain-domain interactions and arrests post-translational folding of CFTR. Du K, Sharma M, Lukacs GL. Nat Struct Mol Biol; 2005 Jan 01; 12(1):17-25. PubMed ID: 15619635 [Abstract] [Full Text] [Related]
36. Correctors enhance maturation of DeltaF508 CFTR by promoting interactions between the two halves of the molecule. Loo TW, Bartlett MC, Clarke DM. Biochemistry; 2009 Oct 20; 48(41):9882-90. PubMed ID: 19761259 [Abstract] [Full Text] [Related]
37. A small-molecule modulator interacts directly with deltaPhe508-CFTR to modify its ATPase activity and conformational stability. Wellhauser L, Kim Chiaw P, Pasyk S, Li C, Ramjeesingh M, Bear CE. Mol Pharmacol; 2009 Jun 20; 75(6):1430-8. PubMed ID: 19339490 [Abstract] [Full Text] [Related]