These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 29925901)

  • 21. Gitelman's syndrome: report of one case.
    Chan CF; Mu SC; Lau BH; Chang CJ; Lin SH
    Acta Paediatr Taiwan; 2008; 49(1):31-4. PubMed ID: 18581727
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Heterozygous mutations of the sodium chloride cotransporter in Chinese children: prevalence and association with blood pressure.
    Hsu YJ; Yang SS; Chu NF; Sytwu HK; Cheng CJ; Lin SH
    Nephrol Dial Transplant; 2009 Apr; 24(4):1170-5. PubMed ID: 19033254
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Rare mutations in SLC12A1 and SLC12A3 protect against hypertension by reducing the activity of renal salt cotransporters.
    Acuña R; Martínez-de-la-Maza L; Ponce-Coria J; Vázquez N; Ortal-Vite P; Pacheco-Alvarez D; Bobadilla NA; Gamba G
    J Hypertens; 2011 Mar; 29(3):475-83. PubMed ID: 21157372
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree.
    Chen Y; Zhang Z; Lin X; Pan Q; Zheng F; Li H
    BMC Med Genet; 2018 Jan; 19(1):17. PubMed ID: 29378538
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Gitelman's syndrome: towards genotype-phenotype correlations?
    Riveira-Munoz E; Chang Q; Bindels RJ; Devuyst O
    Pediatr Nephrol; 2007 Mar; 22(3):326-32. PubMed ID: 17061123
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evaluating PVALB as a candidate gene for SLC12A3-negative cases of Gitelman's syndrome.
    Riveira-Munoz E; Devuyst O; Belge H; Jeck N; Strompf L; Vargas-Poussou R; Jeunemaître X; Blanchard A; Knoers NV; Konrad M; Dahan K
    Nephrol Dial Transplant; 2008 Oct; 23(10):3120-5. PubMed ID: 18469313
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel compound heterozygous mutation of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome.
    Wang X; Ding Y; Liu Q; Yang G
    Endocrine; 2020 Mar; 67(3):673-677. PubMed ID: 31808035
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Structure-function relationships in the renal NaCl cotransporter (NCC).
    Moreno E; de Los Heros P; Plata C; Cutler C; Vega-Mateos A; Vázquez N; Gamba G
    Curr Top Membr; 2019; 83():177-204. PubMed ID: 31196605
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Case-control study of the role of the Gitelman's syndrome gene in essential hypertension.
    Aoi N; Nakayama T; Sato N; Kosuge K; Haketa A; Sato M; Soma M
    Endocr J; 2008 May; 55(2):305-10. PubMed ID: 18362449
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Spectrum of mutations in Gitelman syndrome.
    Vargas-Poussou R; Dahan K; Kahila D; Venisse A; Riveira-Munoz E; Debaix H; Grisart B; Bridoux F; Unwin R; Moulin B; Haymann JP; Vantyghem MC; Rigothier C; Dussol B; Godin M; Nivet H; Dubourg L; Tack I; Gimenez-Roqueplo AP; Houillier P; Blanchard A; Devuyst O; Jeunemaitre X
    J Am Soc Nephrol; 2011 Apr; 22(4):693-703. PubMed ID: 21415153
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A pedigree analysis of two homozygous mutant Gitelman syndrome cases.
    Luo J; Yang X; Liang J; Li W
    Endocr J; 2015; 62(1):29-36. PubMed ID: 25273610
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman's syndrome patients.
    Tavira B; Gómez J; Santos F; Gil H; Alvarez V; Coto E
    J Hum Genet; 2014 Jul; 59(7):376-80. PubMed ID: 24830959
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inheritance of an autosomal recessive disorder, Gitelman's syndrome, across two generations in one family.
    Yagi H; Yahata K; Usui T; Hasegawa C; Seta K; Sugawara A
    Intern Med; 2011; 50(11):1211-4. PubMed ID: 21628937
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Thiazide-sensitive Na+ -Cl- cotransporter (NCC) gene inactivation results in increased duodenal Ca2+ absorption, enhanced osteoblast differentiation and elevated bone mineral density.
    Hsu YJ; Yang SS; Cheng CJ; Liu ST; Huang SM; Chau T; Chu P; Salter DM; Lee HS; Lin SH
    J Bone Miner Res; 2015 Jan; 30(1):116-27. PubMed ID: 24984877
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.
    Riveira-Munoz E; Chang Q; Godefroid N; Hoenderop JG; Bindels RJ; Dahan K; Devuyst O;
    J Am Soc Nephrol; 2007 Apr; 18(4):1271-83. PubMed ID: 17329572
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes.
    Fava C; Montagnana M; Rosberg L; Burri P; Jönsson A; Wanby P; Wahrenberg H; Hulthén UL; Aurell M; Guidi GC; Melander O
    DNA Seq; 2007 Oct; 18(5):395-9. PubMed ID: 17654016
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Effects of chemical chaperones on partially retarded NaCl cotransporter mutants associated with Gitelman's syndrome in a mouse cortical collecting duct cell line.
    de Jong JC; Willems PH; Goossens M; Vandewalle A; van den Heuvel LP; Knoers NV; Bindels RJ
    Nephrol Dial Transplant; 2004 May; 19(5):1069-76. PubMed ID: 15102966
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome.
    Loffing J; Vallon V; Loffing-Cueni D; Aregger F; Richter K; Pietri L; Bloch-Faure M; Hoenderop JG; Shull GE; Meneton P; Kaissling B
    J Am Soc Nephrol; 2004 Sep; 15(9):2276-88. PubMed ID: 15339977
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review.
    Gu X; Su Z; Chen M; Xu Y; Wang Y
    Nephrology (Carlton); 2017 Aug; 22(8):652-655. PubMed ID: 28685938
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.