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 *

313 related articles for article (PubMed ID: 17954289)

  • 1. Reduced urinary excretion of thiazide-sensitive Na-Cl cotransporter in Gitelman syndrome: preliminary data.
    Joo KW; Lee JW; Jang HR; Heo NJ; Jeon US; Oh YK; Lim CS; Na KY; Kim J; Cheong HI; Han JS
    Am J Kidney Dis; 2007 Nov; 50(5):765-73. PubMed ID: 17954289
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Generation and analysis of the thiazide-sensitive Na+ -Cl- cotransporter (Ncc/Slc12a3) Ser707X knockin mouse as a model of Gitelman syndrome.
    Yang SS; Lo YF; Yu IS; Lin SW; Chang TH; Hsu YJ; Chao TK; Sytwu HK; Uchida S; Sasaki S; Lin SH
    Hum Mutat; 2010 Dec; 31(12):1304-15. PubMed ID: 20848653
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Inactivation of the Na-Cl co-transporter (NCC) gene is associated with high BMD through both renal and bone mechanisms: analysis of patients with Gitelman syndrome and Ncc null mice.
    Nicolet-Barousse L; Blanchard A; Roux C; Pietri L; Bloch-Faure M; Kolta S; Chappard C; Geoffroy V; Morieux C; Jeunemaitre X; Shull GE; Meneton P; Paillard M; Houillier P; De Vernejoul MC
    J Bone Miner Res; 2005 May; 20(5):799-808. PubMed ID: 15824853
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of five novel variants in the thiazide-sensitive NaCl co-transporter gene in Chinese patients with Gitelman syndrome.
    Qin L; Shao L; Ren H; Wang W; Pan X; Zhang W; Wang Z; Shen P; Chen N
    Nephrology (Carlton); 2009 Feb; 14(1):52-8. PubMed ID: 19207868
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Problems in diagnosing atypical Gitelman's syndrome presenting with normomagnesaemia.
    Nakamura A; Shimizu C; Nagai S; Yoshida M; Aoki K; Kondo T; Miyoshi H; Wada N; Tajima T; Terauchi Y; Yoshioka N; Koike T
    Clin Endocrinol (Oxf); 2010 Feb; 72(2):272-6. PubMed ID: 19508680
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. [From gene to disease; mutations in the SLC12A3 gene as the cause of Gitelman's syndrome].
    Cornelissen EA; Bindels RJ; Hoefsloot LH; Knoers NV
    Ned Tijdschr Geneeskd; 2005 Jun; 149(24):1330-3. PubMed ID: 16008036
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Atypical Gitelman syndrome with L623P mutation of the thiazide-sensitive Na-Cl cotransporter gene exhibiting lack of hypocalciuria and increased proximal tubule salt reabsorption.
    Mizumori Y; Muto S; Uchida S; Sasaki S; Kusano E
    Nephrol Dial Transplant; 2006 Nov; 21(11):3340-1. PubMed ID: 16854846
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Localization of tubular adaptation to renal sodium loss in Gitelman syndrome.
    Favre GA; Nau V; Kolb I; Vargas-Poussou R; Hannedouche T; Moulin B
    Clin J Am Soc Nephrol; 2012 Mar; 7(3):472-8. PubMed ID: 22241817
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Increased expression of the sodium transporter BSC-1 in spontaneously hypertensive rats.
    Sonalker PA; Tofovic SP; Jackson EK
    J Pharmacol Exp Ther; 2004 Dec; 311(3):1052-61. PubMed ID: 15340004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease.
    Sabath E; Meade P; Berkman J; de los Heros P; Moreno E; Bobadilla NA; Vázquez N; Ellison DH; Gamba G
    Am J Physiol Renal Physiol; 2004 Aug; 287(2):F195-203. PubMed ID: 15068971
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.