Similar articles for PMID: 11055897

Year	Number of Results
1924	1
1967	1
1988	2
1991	2
1992	2
1993	1
1994	5
1995	6
1996	3
1997	3
1998	3
1999	1
2000	7
2001	7
2002	3
2003	3
2004	5
2005	4
2006	5
2007	2
2008	3
2009	3
2010	6
2011	2
2012	5
2013	6
2014	3
2015	4
2016	6
2017	6
2018	2
2019	5
2020	5
2021	1
2022	4
2024	0

1

Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: an evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion.

Högenauer C, Santa Ana CA, Porter JL, Millard M, Gelfand A, Rosenblatt RL, Prestidge CB, Fordtran JS. Högenauer C, et al. Am J Hum Genet. 2000 Dec;67(6):1422-7. doi: 10.1086/316911. Epub 2000 Oct 30. Am J Hum Genet. 2000. PMID: 11055897 Free PMC article. Clinical Trial.

2

Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model.

Gabriel SE, Brigman KN, Koller BH, Boucher RC, Stutts MJ. Gabriel SE, et al. Science. 1994 Oct 7;266(5182):107-9. doi: 10.1126/science.7524148. Science. 1994. PMID: 7524148

3

Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes.

Sermet-Gaudelus I, Déchaux M, Vallée B, Fajac A, Girodon E, Nguyen-Khoa T, Marianovski R, Hurbain I, Bresson JL, Lenoir G, Edelman A. Sermet-Gaudelus I, et al. Am J Respir Crit Care Med. 2005 May 1;171(9):1026-31. doi: 10.1164/rccm.200406-740OC. Epub 2005 Feb 11. Am J Respir Crit Care Med. 2005. PMID: 15709055

4

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

5

CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.

Bonadia LC, de Lima Marson FA, Ribeiro JD, Paschoal IA, Pereira MC, Ribeiro AF, Bertuzzo CS. Bonadia LC, et al. Gene. 2014 May 1;540(2):183-90. doi: 10.1016/j.gene.2014.02.040. Epub 2014 Feb 26. Gene. 2014. PMID: 24583165

6

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

7

β-adrenergic sweat secretion as a diagnostic test for cystic fibrosis.

Quinton P, Molyneux L, Ip W, Dupuis A, Avolio J, Tullis E, Conrad D, Shamsuddin AK, Durie P, Gonska T. Quinton P, et al. Am J Respir Crit Care Med. 2012 Oct 15;186(8):732-9. doi: 10.1164/rccm.201205-0922OC. Epub 2012 Aug 2. Am J Respir Crit Care Med. 2012. PMID: 22859523

8

Role of CFTR mutation analysis in the diagnostic algorithm for cystic fibrosis.

Ratkiewicz M, Pastore M, McCoy KS, Thompson R, Hayes D Jr, Sheikh SI. Ratkiewicz M, et al. World J Pediatr. 2017 Apr;13(2):129-135. doi: 10.1007/s12519-017-0015-8. Epub 2017 Feb 15. World J Pediatr. 2017. PMID: 28194692

9

Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.

Johnson LG, Boyles SE, Wilson J, Boucher RC. Johnson LG, et al. J Clin Invest. 1995 Mar;95(3):1377-82. doi: 10.1172/JCI117789. J Clin Invest. 1995. PMID: 7533790 Free PMC article.

10

Induction of a cAMP-stimulated chloride secretion in regenerating poorly differentiated airway epithelial cells by adenovirus-mediated CFTR gene transfer.

Dupuit F, Chinet T, Zahm JM, Pierrot D, Hinnrasky J, Kaplan H, Bonnet N, Puchelle E. Dupuit F, et al. Hum Gene Ther. 1997 Aug 10;8(12):1439-50. doi: 10.1089/hum.1997.8.12-1439. Hum Gene Ther. 1997. PMID: 9287144

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