Detalhe da pesquisa
1.
The apical 70-pS potassium K channel in the thick ascending limb of Henle's loop is a large-conductance Na+-and Cl--activated, KNa1.1-like, channel.
Am J Physiol Renal Physiol
; 2024 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38269407
2.
Diversity of functional alterations of the ClC-5 exchanger in the region of the proton glutamate in patients with Dent disease 1.
Hum Mutat
; 42(5): 537-550, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33600050
3.
Defective bicarbonate reabsorption in Kir4.2 potassium channel deficient mice impairs acid-base balance and ammonia excretion.
Kidney Int
; 97(2): 304-315, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31870500
4.
A novel CLCN5 pathogenic mutation supports Dent disease with normal endosomal acidification.
Hum Mutat
; 39(8): 1139-1149, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29791050
5.
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.
Hum Mutat
; 36(8): 743-52, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25907713
6.
ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
Am J Physiol Renal Physiol
; 308(12): F1324-34, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25810436
7.
Characterization of the mouse ClC-K1/Barttin chloride channel.
Biochim Biophys Acta
; 1828(11): 2399-409, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23791703
8.
CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca2+ dependence of ClC-Kb channels.
Pflugers Arch
; 466(9): 1713-23, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24271511
9.
Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome.
Proc Natl Acad Sci U S A
; 108(25): 10361-6, 2011 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-21633011
10.
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression.
Hum Mutat
; 34(9): 1269-78, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23703872
11.
A calcium-permeable non-selective cation channel in the thick ascending limb apical membrane of the mouse kidney.
Biochim Biophys Acta
; 1818(5): 1135-41, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22230350
12.
ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.
Pflugers Arch
; 463(2): 247-56, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22083641
13.
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
Hum Mutat
; 32(4): 476-83, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21305656
14.
Voltage-dependent electrogenic chloride/proton exchange by endosomal CLC proteins.
Nature
; 436(7049): 424-7, 2005 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-16034422
15.
Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing.
Kidney Int
; 76(9): 999-1005, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19657328
16.
Renal Chloride Channels in Relation to Sodium Chloride Transport.
Compr Physiol
; 9(1): 301-342, 2018 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30549019
17.
[Blood pressure regulation: A crucial role of potassium intake]. / Régulation de la pression artérielle - Un rôle majeur de l'apport en potassium.
Med Sci (Paris)
; 38(8-9): 743-745, 2022.
Artigo
em Francês
| MEDLINE | ID: mdl-36094250
18.
How Bartter's and Gitelman's syndromes, and Dent's disease have provided important insights into the function of three renal chloride channels: ClC-Ka/b and ClC-5.
Nephron Physiol
; 103(1): p7-13, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16352917
19.
Dual regulation of the native ClC-K2 chloride channel in the distal nephron by voltage and pH.
J Gen Physiol
; 148(3): 213-26, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27574292
20.
Rattlesnake Phospholipase A2 Increases CFTR-Chloride Channel Current and Corrects ∆F508CFTR Dysfunction: Impact in Cystic Fibrosis.
J Mol Biol
; 428(14): 2898-915, 2016 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27241308