138 related articles for article (PubMed ID: 9596079)
1. Peripheral blood mononuclear cells express mutated NCCT mRNA in Gitelman's syndrome: evidence for abnormal thiazide-sensitive NaCl cotransport.
Abuladze N; Yanagawa N; Lee I; Jo OD; Newman D; Hwang J; Uyemura K; Pushkin A; Modlin RL; Kurtz I
J Am Soc Nephrol; 1998 May; 9(5):819-26. PubMed ID: 9596079
[TBL] [Abstract][Full Text] [Related]
2. Novel mutations in thiazide-sensitive Na-Cl cotransporter gene of patients with Gitelman's syndrome.
Monkawa T; Kurihara I; Kobayashi K; Hayashi M; Saruta T
J Am Soc Nephrol; 2000 Jan; 11(1):65-70. PubMed ID: 10616841
[TBL] [Abstract][Full Text] [Related]
3. Four novel mutations in the thiazide-sensitive Na-Cl co-transporter gene in Japanese patients with Gitelman's syndrome.
Maki N; Komatsuda A; Wakui H; Ohtani H; Kigawa A; Aiba N; Hamai K; Motegi M; Yamaguchi A; Imai H; Sawada K
Nephrol Dial Transplant; 2004 Jul; 19(7):1761-6. PubMed ID: 15069170
[TBL] [Abstract][Full Text] [Related]
4. Identification of a novel R642C mutation in Na/Cl cotransporter with Gitelman's syndrome.
Yahata K; Tanaka I; Kotani M; Mukoyama M; Ogawa Y; Goto M; Nakagawa M; Sugawara A; Tanaka K; Shimatsu A; Nakao K
Am J Kidney Dis; 1999 Nov; 34(5):845-53. PubMed ID: 10561140
[TBL] [Abstract][Full Text] [Related]
5. Novel NCCT gene mutations as a cause of Gitelman's syndrome and a systematic review of mutant and polymorphic NCCT alleles.
Reissinger A; Ludwig M; Utsch B; Prömse A; Baulmann J; Weisser B; Vetter H; Kramer HJ; Bokemeyer D
Kidney Blood Press Res; 2002; 25(6):354-62. PubMed ID: 12590198
[TBL] [Abstract][Full Text] [Related]
6. Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension.
Melander O; Orho-Melander M; Bengtsson K; Lindblad U; Râstam L; Groop L; Hulthén UL
Hypertension; 2000 Sep; 36(3):389-94. PubMed ID: 10988270
[TBL] [Abstract][Full Text] [Related]
7. Association of a mutation in thiazide-sensitive Na-Cl cotransporter with familial Gitelman's syndrome.
Takeuchi K; Kure S; Kato T; Taniyama Y; Takahashi N; Ikeda Y; Abe T; Narisawa K; Muramatsu Y; Abe K
J Clin Endocrinol Metab; 1996 Dec; 81(12):4496-9. PubMed ID: 8954067
[TBL] [Abstract][Full Text] [Related]
8. Gitelman's syndrome (Bartter's variant) maps to the thiazide-sensitive cotransporter gene locus on chromosome 16q13 in a large kindred.
Pollak MR; Delaney VB; Graham RM; Hebert SC
J Am Soc Nephrol; 1996 Oct; 7(10):2244-8. PubMed ID: 8915985
[TBL] [Abstract][Full Text] [Related]
9. Abnormal reabsorption of Na+/CI- by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome.
Colussi G; Rombolà G; Brunati C; De Ferrari ME
Am J Nephrol; 1997; 17(2):103-11. PubMed ID: 9096439
[TBL] [Abstract][Full Text] [Related]
10. Identification of novel mutations in Na-Cl cotransporter gene in a Korean patient with atypical Gitelman's syndrome.
Yoo TH; Lee SH; Yoon K; Baek H; Chung JH; Lee T; Ihm C; Kim M
Am J Kidney Dis; 2003 Dec; 42(6):E11-6. PubMed ID: 14655226
[TBL] [Abstract][Full Text] [Related]
11. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.
Simon DB; Nelson-Williams C; Bia MJ; Ellison D; Karet FE; Molina AM; Vaara I; Iwata F; Cushner HM; Koolen M; Gainza FJ; Gitleman HJ; Lifton RP
Nat Genet; 1996 Jan; 12(1):24-30. PubMed ID: 8528245
[TBL] [Abstract][Full Text] [Related]
12. Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndrome.
Lo YF; Nozu K; Iijima K; Morishita T; Huang CC; Yang SS; Sytwu HK; Fang YW; Tseng MH; Lin SH
Clin J Am Soc Nephrol; 2011 Mar; 6(3):630-9. PubMed ID: 21051746
[TBL] [Abstract][Full Text] [Related]
13. Three cases of Gitelman's syndrome possibly caused by different mutations in the thiazide-sensitive Na-Cl cotransporter.
Takeuchi K; Kato T; Taniyama Y; Tsunoda K; Takahashi N; Ikeda Y; Omata K; Imai Y; Saito T; Ito S; Abe K
Intern Med; 1997 Aug; 36(8):582-5. PubMed ID: 9260778
[TBL] [Abstract][Full Text] [Related]
14. Phenotype resembling Gitelman's syndrome in mice lacking the apical Na+-Cl- cotransporter of the distal convoluted tubule.
Schultheis PJ; Lorenz JN; Meneton P; Nieman ML; Riddle TM; Flagella M; Duffy JJ; Doetschman T; Miller ML; Shull GE
J Biol Chem; 1998 Oct; 273(44):29150-5. PubMed ID: 9786924
[TBL] [Abstract][Full Text] [Related]
15. Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure.
Fava C; Montagnana M; Rosberg L; Burri P; Almgren P; Jönsson A; Wanby P; Lippi G; Minuz P; Hulthèn LU; Aurell M; Melander O
Hum Mol Genet; 2008 Feb; 17(3):413-8. PubMed ID: 17981812
[TBL] [Abstract][Full Text] [Related]
16. The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.
Simon DB; Lifton RP
Am J Physiol; 1996 Nov; 271(5 Pt 2):F961-6. PubMed ID: 8945989
[TBL] [Abstract][Full Text] [Related]
17. A novel splice site mutation of the thiazide-sensitive NaCl cotransporter gene in a Japanese patient with Gitelman syndrome.
Iida K; Hanafusa M; Maekawa I; Kudo T; Takahashi K; Yoshioka S; Kishimoto M; Iguchi G; Tsukamoto T; Okimura Y; Kaji H; Chihara K
Clin Nephrol; 2004 Sep; 62(3):180-4. PubMed ID: 15481849
[TBL] [Abstract][Full Text] [Related]
18. Gitelman's syndrome (familial hypokalemia-hypomagnesemia).
Barakat AJ; Rennert OM
J Nephrol; 2001; 14(1):43-7. PubMed ID: 11281344
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome.
Kaito H; Nozu K; Fu XJ; Kamioka I; Fujita T; Kanda K; Krol RP; Suminaga R; Ishida A; Iijima K; Matsuo M
Pediatr Res; 2007 Apr; 61(4):502-5. PubMed ID: 17414160
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
