Similar articles for PMID: 11733566

Year	Number of Results
1946	1
1989	2
1990	3
1991	6
1992	7
1993	5
1994	1
1995	10
1996	13
1997	7
1998	1
1999	3
2000	7
2001	3
2002	7
2003	6
2004	4
2005	3
2006	1
2007	3
2008	2
2009	1
2010	5
2011	4
2012	4
2013	2
2014	2
2015	1
2016	1
2018	1
2020	2
2021	2
2023	1
2024	0

1

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings.

Bronsveld I, Mekus F, Bijman J, Ballmann M, de Jonge HR, Laabs U, Halley DJ, Ellemunter H, Mastella G, Thomas S, Veeze HJ, Tümmler B. Bronsveld I, et al. J Clin Invest. 2001 Dec;108(11):1705-15. doi: 10.1172/JCI12108. J Clin Invest. 2001. PMID: 11733566 Free PMC article.

2

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. Bronsveld I, et al. Gastroenterology. 2000 Jul;119(1):32-40. doi: 10.1053/gast.2000.8524. Gastroenterology. 2000. PMID: 10889152

3

Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation.

Sermet-Gaudelus I, Vallée B, Urbin I, Torossi T, Marianovski R, Fajac A, Feuillet MN, Bresson JL, Lenoir G, Bernaudin JF, Edelman A. Sermet-Gaudelus I, et al. Pediatr Res. 2002 Nov;52(5):628-35. doi: 10.1203/00006450-200211000-00005. Pediatr Res. 2002. PMID: 12409506

4

Cystic fibrosis transmembrane conductance regulator (CFTR)-mediated residual chloride secretion does not protect against early chronic Pseudomonas aeruginosa infection in F508del homozygous cystic fibrosis patients.

Derichs N, Mekus F, Bronsveld I, Bijman J, Veeze HJ, von der Hardt H, Tummler B, Ballmann M. Derichs N, et al. Pediatr Res. 2004 Jan;55(1):69-75. doi: 10.1203/01.PDR.0000100758.66805.CE. Epub 2003 Nov 6. Pediatr Res. 2004. PMID: 14605249

5

Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.

Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C. Dray-Charier N, et al. Hepatology. 1999 Jun;29(6):1624-34. doi: 10.1002/hep.510290634. Hepatology. 1999. PMID: 10347100

6

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive.

Denning GM, Anderson MP, Amara JF, Marshall J, Smith AE, Welsh MJ. Denning GM, et al. Nature. 1992 Aug 27;358(6389):761-4. doi: 10.1038/358761a0. Nature. 1992. PMID: 1380673

7

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.

French PJ, van Doorninck JH, Peters RH, Verbeek E, Ameen NA, Marino CR, de Jonge HR, Bijman J, Scholte BJ. French PJ, et al. J Clin Invest. 1996 Sep 15;98(6):1304-12. doi: 10.1172/JCI118917. J Clin Invest. 1996. PMID: 8823295 Free PMC article.

8

Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.

Dalemans W, Barbry P, Champigny G, Jallat S, Dott K, Dreyer D, Crystal RG, Pavirani A, Lecocq JP, Lazdunski M. Dalemans W, et al. Nature. 1991 Dec 19-26;354(6354):526-8. doi: 10.1038/354526a0. Nature. 1991. PMID: 1722027

9

Diversity of the basic defect of homozygous CFTR mutation genotypes in humans.

Stanke F, Ballmann M, Bronsveld I, Dörk T, Gallati S, Laabs U, Derichs N, Ritzka M, Posselt HG, Harms HK, Griese M, Blau H, Mastella G, Bijman J, Veeze H, Tümmler B. Stanke F, et al. J Med Genet. 2008 Jan;45(1):47-54. doi: 10.1136/jmg.2007.053561. J Med Genet. 2008. PMID: 18178635 Free article.

10

In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR.

Rubenstein RC, Egan ME, Zeitlin PL. Rubenstein RC, et al. J Clin Invest. 1997 Nov 15;100(10):2457-65. doi: 10.1172/JCI119788. J Clin Invest. 1997. PMID: 9366560 Free PMC article.

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