Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 100

1.

Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function.

Clancy JP, Szczesniak RD, Ashlock MA, Ernst SE, Fan L, Hornick DB, Karp PH, Khan U, Lymp J, Ostmann AJ, Rezayat A, Starner TD, Sugandha SP, Sun H, Quinney N, Donaldson SH, Rowe SM, Gabriel SE.

PLoS One. 2013 Sep 10;8(9):e73905. doi: 10.1371/journal.pone.0073905. eCollection 2013.

PMID:
24040112
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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.

PMID:
23082198
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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
[PubMed - indexed for MEDLINE]
4.

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.

PMID:
21909392
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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.

PMID:
10762616
[PubMed - indexed for MEDLINE]
Free Article
6.

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.

PMID:
10484398
[PubMed - indexed for MEDLINE]
Free Article
7.

Bioelectric characterization of epithelia from neonatal CFTR knockout ferrets.

Fisher JT, Tyler SR, Zhang Y, Lee BJ, Liu X, Sun X, Sui H, Liang B, Luo M, Xie W, Yi Y, Zhou W, Song Y, Keiser N, Wang K, de Jonge HR, Engelhardt JF.

Am J Respir Cell Mol Biol. 2013 Nov;49(5):837-44. doi: 10.1165/rcmb.2012-0433OC.

PMID:
23782101
[PubMed - indexed for MEDLINE]
8.

Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis.

Cohen-Cymberknoh M, Yaakov Y, Shoseyov D, Shteyer E, Schachar E, Rivlin J, Bentur L, Picard E, Aviram M, Israeli E, Kerem E, Wilschanski M.

Pediatr Pulmonol. 2013 Mar;48(3):229-35. doi: 10.1002/ppul.22586. Epub 2012 May 2.

PMID:
22553157
[PubMed - indexed for MEDLINE]
9.

Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers.

De Jonge HR, Ballmann M, Veeze H, Bronsveld I, Stanke F, Tümmler B, Sinaasappel M.

J Cyst Fibros. 2004 Aug;3 Suppl 2:159-63. Review.

PMID:
15463951
[PubMed - indexed for MEDLINE]
Free Article
10.

Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes.

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

Br J Pharmacol. 2000 Aug;130(8):1884-92.

PMID:
10952679
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

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
[PubMed - indexed for MEDLINE]
12.

Measurement of ion transport function in rectal biopsies.

Hug MJ, Derichs N, Bronsveld I, Clancy JP.

Methods Mol Biol. 2011;741:87-107. doi: 10.1007/978-1-61779-117-8_7.

PMID:
21594780
[PubMed - indexed for MEDLINE]
13.

Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation.

Rowe SM, Liu B, Hill A, Hathorne H, Cohen M, Beamer JR, Accurso FJ, Dong Q, Ordoñez CL, Stone AJ, Olson ER, Clancy JP; VX06-770-101 Study Group.

PLoS One. 2013 Jul 26;8(7):e66955. doi: 10.1371/journal.pone.0066955. Print 2013.

PMID:
23922647
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.

Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A.

BMC Pediatr. 2006 Oct 3;6:25.

PMID:
17018149
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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
[PubMed - indexed for MEDLINE]
16.

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
[PubMed - indexed for MEDLINE]
17.

Ex vivo biochemical analysis of CFTR in human rectal biopsies.

van Barneveld A, Stanke F, Ballmann M, Naim HY, Tümmler B.

Biochim Biophys Acta. 2006 Apr;1762(4):393-7. Epub 2006 Feb 13.

PMID:
16504487
[PubMed - indexed for MEDLINE]
Free Article
18.

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.

Gene. 2014 May 1;540(2):183-90. doi: 10.1016/j.gene.2014.02.040. Epub 2014 Feb 26.

PMID:
24583165
[PubMed - indexed for MEDLINE]
19.

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
[PubMed - indexed for MEDLINE]
20.

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
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk