231 related articles for article (PubMed ID: 12761627)
1. Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene.
Hayama A; Rai T; Sasaki S; Uchida S
Histochem Cell Biol; 2003 Jun; 119(6):485-93. PubMed ID: 12761627
[TBL] [Abstract][Full Text] [Related]
2. Generation and analyses of R8L barttin knockin mouse.
Nomura N; Tajima M; Sugawara N; Morimoto T; Kondo Y; Ohno M; Uchida K; Mutig K; Bachmann S; Soleimani M; Ohta E; Ohta A; Sohara E; Okado T; Rai T; Jentsch TJ; Sasaki S; Uchida S
Am J Physiol Renal Physiol; 2011 Aug; 301(2):F297-307. PubMed ID: 21593186
[TBL] [Abstract][Full Text] [Related]
3. Barttin increases surface expression and changes current properties of ClC-K channels.
Waldegger S; Jeck N; Barth P; Peters M; Vitzthum H; Wolf K; Kurtz A; Konrad M; Seyberth HW
Pflugers Arch; 2002 Jun; 444(3):411-8. PubMed ID: 12111250
[TBL] [Abstract][Full Text] [Related]
4. Treatment with 17-allylamino-17-demethoxygeldanamycin ameliorated symptoms of Bartter syndrome type IV caused by mutated Bsnd in mice.
Nomura N; Kamiya K; Ikeda K; Yui N; Chiga M; Sohara E; Rai T; Sakaki S; Uchida S
Biochem Biophys Res Commun; 2013 Nov; 441(3):544-9. PubMed ID: 24189473
[TBL] [Abstract][Full Text] [Related]
5. Barttin binds to the outer lateral surface of the ClC-K2 chloride channel.
Tajima M; Hayama A; Rai T; Sasaki S; Uchida S
Biochem Biophys Res Commun; 2007 Nov; 362(4):858-64. PubMed ID: 17767918
[TBL] [Abstract][Full Text] [Related]
6. Atypical Bartter syndrome with sensorineural deafness with G47R mutation of the beta-subunit for ClC-Ka and ClC-Kb chloride channels, barttin.
Miyamura N; Matsumoto K; Taguchi T; Tokunaga H; Nishikawa T; Nishida K; Toyonaga T; Sakakida M; Araki E
J Clin Endocrinol Metab; 2003 Feb; 88(2):781-6. PubMed ID: 12574213
[TBL] [Abstract][Full Text] [Related]
7. Disease-causing dysfunctions of barttin in Bartter syndrome type IV.
Janssen AG; Scholl U; Domeyer C; Nothmann D; Leinenweber A; Fahlke C
J Am Soc Nephrol; 2009 Jan; 20(1):145-53. PubMed ID: 18776122
[TBL] [Abstract][Full Text] [Related]
8. Mechanisms of Disease: the kidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and their clinical relevance.
Krämer BK; Bergler T; Stoelcker B; Waldegger S
Nat Clin Pract Nephrol; 2008 Jan; 4(1):38-46. PubMed ID: 18094726
[TBL] [Abstract][Full Text] [Related]
9. Human CLC-K Channels Require Palmitoylation of Their Accessory Subunit Barttin to Be Functional.
Steinke KV; Gorinski N; Wojciechowski D; Todorov V; Guseva D; Ponimaskin E; Fahlke C; Fischer M
J Biol Chem; 2015 Jul; 290(28):17390-400. PubMed ID: 26013830
[TBL] [Abstract][Full Text] [Related]
10. Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion.
Estévez R; Boettger T; Stein V; Birkenhäger R; Otto E; Hildebrandt F; Jentsch TJ
Nature; 2001 Nov; 414(6863):558-61. PubMed ID: 11734858
[TBL] [Abstract][Full Text] [Related]
11. Renal dysfunction and barttin expression in Bartter syndrome Type IV associated with a G47R mutation in BSND in a family.
Park CW; Lim JH; Youn DY; Chung S; Lim MH; Kim YK; Chang YS; Lee JH
Clin Nephrol; 2011 Feb; 75 Suppl 1():69-74. PubMed ID: 21269598
[TBL] [Abstract][Full Text] [Related]
12. Severe manifestation of Bartter syndrome Type IV caused by a novel insertion mutation in the BSND gene.
de Pablos AL; García-Nieto V; López-Menchero JC; Ramos-Trujillo E; González-Acosta H; Claverie-Martín F
Clin Nephrol; 2014 May; 81(5):363-8. PubMed ID: 23110775
[TBL] [Abstract][Full Text] [Related]
13. Role of zebrafish ClC-K/barttin channels in apical kidney chloride reabsorption.
Pérez-Rius C; Castellanos A; Gaitán-Peñas H; Navarro A; Artuch R; Barrallo-Gimeno A; Estévez R
J Physiol; 2019 Aug; 597(15):3969-3983. PubMed ID: 31177533
[TBL] [Abstract][Full Text] [Related]
14. ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
Andrini O; Keck M; Briones R; Lourdel S; Vargas-Poussou R; Teulon J
Am J Physiol Renal Physiol; 2015 Jun; 308(12):F1324-34. PubMed ID: 25810436
[TBL] [Abstract][Full Text] [Related]
15. Activation of renal ClC-K chloride channels depends on an intact N terminus of their accessory subunit barttin.
Wojciechowski D; Thiemann S; Schaal C; Rahtz A; de la Roche J; Begemann B; Becher T; Fischer M
J Biol Chem; 2018 Jun; 293(22):8626-8637. PubMed ID: 29674316
[TBL] [Abstract][Full Text] [Related]
16. Mutation G47R in the BSND gene causes Bartter syndrome with deafness in two Spanish families.
García-Nieto V; Flores C; Luis-Yanes MI; Gallego E; Villar J; Claverie-Martín F
Pediatr Nephrol; 2006 May; 21(5):643-8. PubMed ID: 16572343
[TBL] [Abstract][Full Text] [Related]
17. In vivo role of CLC chloride channels in the kidney.
Uchida S
Am J Physiol Renal Physiol; 2000 Nov; 279(5):F802-8. PubMed ID: 11053039
[TBL] [Abstract][Full Text] [Related]
18. Nephron specific regulation of chloride channel CLC-K2 mRNA in the rat.
Vitzthum H; Castrop H; Meier-Meitinger M; Riegger GA; Kurtz A; Krämer BK; Wolf K
Kidney Int; 2002 Feb; 61(2):547-54. PubMed ID: 11849395
[TBL] [Abstract][Full Text] [Related]
19. Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.
Cheng CJ; Lo YF; Chen JC; Huang CL; Lin SH
J Physiol; 2017 Aug; 595(16):5573-5586. PubMed ID: 28555925
[TBL] [Abstract][Full Text] [Related]
20. Carboxyl-terminal Truncations of ClC-Kb Abolish Channel Activation by Barttin Via Modified Common Gating and Trafficking.
Stölting G; Bungert-Plümke S; Franzen A; Fahlke C
J Biol Chem; 2015 Dec; 290(51):30406-16. PubMed ID: 26453302
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
