200 related articles for article (PubMed ID: 24040112)
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; 8(9):e73905. PubMed ID: 24040112
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 23082198
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 20627915
[TBL] [Abstract][Full Text] [Related]
4. Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case-control study.
Bagheri-Hanson A; Nedwed S; Rueckes-Nilges C; Naehrlich L
BMC Pulm Med; 2014 Oct; 14():156. PubMed ID: 25280757
[TBL] [Abstract][Full Text] [Related]
5. Comparison of Nasal Potential Difference and Intestinal Current Measurements as Surrogate Markers for CFTR Function.
Wilschanski M; Yaakov Y; Omari I; Zaman M; Martin CR; Cohen-Cymberknoh M; Shoseyov D; Kerem E; Dasilva D; Sheth S; Uluer A; OʼSullivan BP; Freedman S
J Pediatr Gastroenterol Nutr; 2016 Nov; 63(5):e92-e97. PubMed ID: 27496797
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 23782101
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 21909392
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 10762616
[TBL] [Abstract][Full Text] [Related]
9. 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):G709-16. PubMed ID: 10484398
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 15463951
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 22553157
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 14699484
[TBL] [Abstract][Full Text] [Related]
13. Comparison of ex vivo and in vitro intestinal cystic fibrosis models to measure CFTR-dependent ion channel activity.
Zomer-van Ommen DD; de Poel E; Kruisselbrink E; Oppelaar H; Vonk AM; Janssens HM; van der Ent CK; Hagemeijer MC; Beekman JM
J Cyst Fibros; 2018 May; 17(3):316-324. PubMed ID: 29544685
[TBL] [Abstract][Full Text] [Related]
14. Forskolin-induced swelling of intestinal organoids correlates with disease severity in adults with cystic fibrosis and homozygous F508del mutations.
de Winter-de Groot KM; Berkers G; Marck-van der Wilt REP; van der Meer R; Vonk A; Dekkers JF; Geerdink M; Michel S; Kruisselbrink E; Vries R; Clevers H; Vleggaar FP; Elias SG; Heijerman HGM; van der Ent CK; Beekman JM
J Cyst Fibros; 2020 Jul; 19(4):614-619. PubMed ID: 31735562
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 10952679
[TBL] [Abstract][Full Text] [Related]
16. Measurement of ion transport function in rectal biopsies.
Hug MJ; Derichs N; Bronsveld I; Clancy JP
Methods Mol Biol; 2011; 741():87-107. PubMed ID: 21594780
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 10889152
[TBL] [Abstract][Full Text] [Related]
18. 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; 6():25. PubMed ID: 17018149
[TBL] [Abstract][Full Text] [Related]
19. Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis.
Veeze HJ; Sinaasappel M; Bijman J; Bouquet J; de Jonge HR
Gastroenterology; 1991 Aug; 101(2):398-403. PubMed ID: 2065916
[TBL] [Abstract][Full Text] [Related]
20. DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers.
Rowe SM; Pyle LC; Jurkevante A; Varga K; Collawn J; Sloane PA; Woodworth B; Mazur M; Fulton J; Fan L; Li Y; Fortenberry J; Sorscher EJ; Clancy JP
Pulm Pharmacol Ther; 2010 Aug; 23(4):268-78. PubMed ID: 20226262
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]