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Items: 1 to 20 of 166


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.


Role of K(V)LQT1 in cyclic adenosine monophosphate-mediated Cl(-) secretion in human airway epithelia.

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

Am J Respir Cell Mol Biol. 2000 Sep;23(3):283-9.


Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis.

Mall M, Hirtz S, Gonska T, Kunzelmann K.

J Cyst Fibros. 2004 Aug;3 Suppl 2:165-9. Review.


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.


Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.

Poulsen JH, Fischer H, Illek B, Machen TE.

Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5340-4.


Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice.

Clarke LL, Grubb BR, Yankaskas JR, Cotton CU, McKenzie A, Boucher RC.

Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):479-83.


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.


Isobutylmethylxanthine fails to stimulate chloride secretion in cystic fibrosis airway epithelia.

Grubb B, Lazarowski E, Knowles M, Boucher R.

Am J Respir Cell Mol Biol. 1993 Apr;8(4):454-60.

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