Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 1001

1.

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M.

Gastroenterology. 2004 Oct;127(4):1085-95.

PMID:
15480987
2.

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.

Mall M, Kreda SM, Mengos A, Jensen TJ, Hirtz S, Seydewitz HH, Yankaskas J, Kunzelmann K, Riordan JR, Boucher RC.

Gastroenterology. 2004 Jan;126(1):32-41.

PMID:
14699484
3.

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.

PMID:
10889152
4.

[Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].

Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E.

Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:6-9. Serbian.

PMID:
15637983
5.
6.

The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients.

Roth EK, Hirtz S, Duerr J, Wenning D, Eichler I, Seydewitz HH, Amaral MD, Mall MA.

PLoS One. 2011;6(8):e24445. doi: 10.1371/journal.pone.0024445. Epub 2011 Aug 31.

7.

CFTR-mediated inhibition of epithelial Na+ conductance in human colon is defective in cystic fibrosis.

Mall M, Bleich M, Kuehr J, Brandis M, Greger R, Kunzelmann K.

Am J Physiol. 1999 Sep;277(3 Pt 1):G709-16.

8.

Genotype-phenotype relationship for five CFTR mutations frequently identified in western France.

Duguépéroux I, De Braekeleer M; Participating Centres to the French National Cystic Fibrosis Registry.

J Cyst Fibros. 2004 Dec;3(4):259-63.

9.

Defective cholinergic Cl(-) secretion and detection of K(+) secretion in rectal biopsies from cystic fibrosis patients.

Mall M, Wissner A, Seydewitz HH, Kuehr J, Brandis M, Greger R, Kunzelmann K.

Am J Physiol Gastrointest Liver Physiol. 2000 Apr;278(4):G617-24.

10.
11.

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.

Pediatr Res. 2004 Jan;55(1):69-75. Epub 2003 Nov 6.

PMID:
14605249
12.

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.

Hepatology. 1999 Jun;29(6):1624-34.

PMID:
10347100
13.

Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data.

Derichs N, Sanz J, Von Kanel T, Stolpe C, Zapf A, Tümmler B, Gallati S, Ballmann M.

Thorax. 2010 Jul;65(7):594-9. doi: 10.1136/thx.2009.125088.

PMID:
20627915
14.

Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.

De Boeck K, Weren M, Proesmans M, Kerem E.

Pediatrics. 2005 Apr;115(4):e463-9. Epub 2005 Mar 16.

PMID:
15772171
15.

Understanding how cystic fibrosis mutations cause a loss of Cl- channel function.

Sheppard DN, Ostedgaard LS.

Mol Med Today. 1996 Jul;2(7):290-7. Review.

PMID:
8796909
16.

Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.

Sousa M, Servidoni MF, Vinagre AM, Ramalho AS, Bonadia LC, Felício V, Ribeiro MA, Uliyakina I, Marson FA, Kmit A, Cardoso SR, Ribeiro JD, Bertuzzo CS, Sousa L, Kunzelmann K, Ribeiro AF, Amaral MD.

PLoS One. 2012;7(10):e47708. doi: 10.1371/journal.pone.0047708. Epub 2012 Oct 17.

17.

Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype.

Beck S, Kühr J, Schütz VV, Seydewitz HH, Brandis M, Greger R, Kunzelmann K.

Pediatr Pulmonol. 1999 Apr;27(4):251-9.

PMID:
10230924
18.

In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study.

Sermet-Gaudelus I, Renouil M, Fajac A, Bidou L, Parbaille B, Pierrot S, Davy N, Bismuth E, Reinert P, Lenoir G, Lesure JF, Rousset JP, Edelman A.

BMC Med. 2007 Mar 29;5:5.

19.

[Cystic fibrosis from the exocrine pancreatic point of view].

Virgilis D.

Harefuah. 2004 Jan;143(1):67-72, 83. Review. Hebrew.

PMID:
14748292
20.

Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.

Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.

J Cyst Fibros. 2008 Mar;7(2):102-9. Epub 2007 Jul 27.

Supplemental Content

Support Center