159 related articles for article (PubMed ID: 21071987)
1. Loop disorders: insights derived from defined genotypes.
Jeck N; Seyberth HW
Nephron Physiol; 2011; 118(1):p7-14. PubMed ID: 21071987
[TBL] [Abstract][Full Text] [Related]
2. Mouse model of type II Bartter's syndrome. II. Altered expression of renal sodium- and water-transporting proteins.
Wagner CA; Loffing-Cueni D; Yan Q; Schulz N; Fakitsas P; Carrel M; Wang T; Verrey F; Geibel JP; Giebisch G; Hebert SC; Loffing J
Am J Physiol Renal Physiol; 2008 Jun; 294(6):F1373-80. PubMed ID: 18322017
[TBL] [Abstract][Full Text] [Related]
3. Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.
Peters M; Jeck N; Reinalter S; Leonhardt A; Tönshoff B; Klaus G Gü; Konrad M; Seyberth HW
Am J Med; 2002 Feb; 112(3):183-90. PubMed ID: 11893344
[TBL] [Abstract][Full Text] [Related]
4. Analysis of renal tubular electrolyte transporter genes in seven patients with hypokalemic metabolic alkalosis.
Fukuyama S; Okudaira S; Yamazato S; Yamazato M; Ohta T
Kidney Int; 2003 Sep; 64(3):808-16. PubMed ID: 12911530
[TBL] [Abstract][Full Text] [Related]
5. Maxi-K channels contribute to urinary potassium excretion in the ROMK-deficient mouse model of Type II Bartter's syndrome and in adaptation to a high-K diet.
Bailey MA; Cantone A; Yan Q; MacGregor GG; Leng Q; Amorim JB; Wang T; Hebert SC; Giebisch G; Malnic G
Kidney Int; 2006 Jul; 70(1):51-9. PubMed ID: 16710355
[TBL] [Abstract][Full Text] [Related]
6. [Bartter's syndrome].
Daniluk U; Kaczmarski M; Wasilewska J; Matuszewska E; Semeniuk J; Sidor K; Krasnow A
Pol Merkur Lekarski; 2004 May; 16(95):484-9. PubMed ID: 15518434
[TBL] [Abstract][Full Text] [Related]
7. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Brochard K; Boyer O; Blanchard A; Loirat C; Niaudet P; Macher MA; Deschenes G; Bensman A; Decramer S; Cochat P; Morin D; Broux F; Caillez M; Guyot C; Novo R; Jeunemaître X; Vargas-Poussou R
Nephrol Dial Transplant; 2009 May; 24(5):1455-64. PubMed ID: 19096086
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Mouse model of type II Bartter's syndrome. I. Upregulation of thiazide-sensitive Na-Cl cotransport activity.
Cantone A; Yang X; Yan Q; Giebisch G; Hebert SC; Wang T
Am J Physiol Renal Physiol; 2008 Jun; 294(6):F1366-72. PubMed ID: 18385266
[TBL] [Abstract][Full Text] [Related]
10. Renal outer medullary potassium channel knockout models reveal thick ascending limb function and dysfunction.
Wang T
Clin Exp Nephrol; 2012 Feb; 16(1):49-54. PubMed ID: 22038261
[TBL] [Abstract][Full Text] [Related]
11. Potassium handling in health and disease: lessons from inherited tubulopathies.
Landau D
Pediatr Endocrinol Rev; 2004 Dec; 2(2):203-8. PubMed ID: 16429107
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes.
Shaer AJ
Am J Med Sci; 2001 Dec; 322(6):316-32. PubMed ID: 11780689
[TBL] [Abstract][Full Text] [Related]
14. Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
Kemter E; Rathkolb B; Bankir L; Schrewe A; Hans W; Landbrecht C; Klaften M; Ivandic B; Fuchs H; Gailus-Durner V; Hrabé de Angelis M; Wolf E; Wanke R; Aigner B
Am J Physiol Renal Physiol; 2010 Jun; 298(6):F1405-15. PubMed ID: 20219826
[TBL] [Abstract][Full Text] [Related]
15. [Bartter's syndromes].
Vantyghem MC; Douillard C; Binaut R; Provot F
Ann Endocrinol (Paris); 1999 Dec; 60(6):465-72. PubMed ID: 10617800
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Absence of small conductance K+ channel (SK) activity in apical membranes of thick ascending limb and cortical collecting duct in ROMK (Bartter's) knockout mice.
Lu M; Wang T; Yan Q; Yang X; Dong K; Knepper MA; Wang W; Giebisch G; Shull GE; Hebert SC
J Biol Chem; 2002 Oct; 277(40):37881-7. PubMed ID: 12130653
[TBL] [Abstract][Full Text] [Related]
18. Characterization of the mouse ClC-K1/Barttin chloride channel.
L'Hoste S; Diakov A; Andrini O; Genete M; Pinelli L; Grand T; Keck M; Paulais M; Beck L; Korbmacher C; Teulon J; Lourdel S
Biochim Biophys Acta; 2013 Nov; 1828(11):2399-409. PubMed ID: 23791703
[TBL] [Abstract][Full Text] [Related]
19. Heterozygous disruption of renal outer medullary potassium channel in rats is associated with reduced blood pressure.
Zhou X; Zhang Z; Shin MK; Horwitz SB; Levorse JM; Zhu L; Sharif-Rodriguez W; Streltsov DY; Dajee M; Hernandez M; Pan Y; Urosevic-Price O; Wang L; Forrest G; Szeto D; Zhu Y; Cui Y; Michael B; Balogh LA; Welling PA; Wade JB; Roy S; Sullivan KA
Hypertension; 2013 Aug; 62(2):288-94. PubMed ID: 23753405
[TBL] [Abstract][Full Text] [Related]
20. Pharmacotyping of hypokalaemic salt-losing tubular disorders.
Reinalter SC; Jeck N; Peters M; Seyberth HW
Acta Physiol Scand; 2004 Aug; 181(4):513-21. PubMed ID: 15283765
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]