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Volumn 61, Issue 4, 2007, Pages 502-505

Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; NUCLEOTIDE; SODIUM CHLORIDE COTRANSPORTER;

EID: 34147100659     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/01.pdr.0000265051.26718.b5     Document Type: Article
Times cited : (16)

References (13)
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  • 2
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    • Inherited primary renal tubular hypokalemic alkalosis: A review of Gitelman and Bartter syndromes
    • Shaer AJ 2001 Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes. Am J Med Sci 322:316-332
    • (2001) Am J Med Sci , vol.322 , pp. 316-332
    • Shaer, A.J.1
  • 3
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    • Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life
    • Cruz DN, Shaer AJ, Bia MJ, Lifton RP, Simon DB 2001 Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life. Kidney Int 59:710-717
    • (2001) Kidney Int , vol.59 , pp. 710-717
    • Cruz, D.N.1    Shaer, A.J.2    Bia, M.J.3    Lifton, R.P.4    Simon, D.B.5
  • 6
    • 0033852423 scopus 로고    scopus 로고
    • Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease
    • Igarashi T, Inatomi J, Ohara T, Kuwahara T, Shimadzu M, Thakker RV 2000 Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease. Kidney Int 58:520-527
    • (2000) Kidney Int , vol.58 , pp. 520-527
    • Igarashi, T.1    Inatomi, J.2    Ohara, T.3    Kuwahara, T.4    Shimadzu, M.5    Thakker, R.V.6
  • 7
    • 33745991117 scopus 로고    scopus 로고
    • The urinary sediment beyond light microscopical examination
    • Colucci G, Floege J, Schena FP 2006 The urinary sediment beyond light microscopical examination. Nephrol Dial Transplant 21:1482-1485
    • (2006) Nephrol Dial Transplant , vol.21 , pp. 1482-1485
    • Colucci, G.1    Floege, J.2    Schena, F.P.3
  • 8
    • 33744805113 scopus 로고    scopus 로고
    • The effect of immunosuppressive therapy on the messenger RNA expression of target genes in the urinary sediment of patients with active lupus nephritis
    • Chan RW, Lai FM, Li EK, Tam LS, Chow KM, Li PK, Szeto CC 2006 The effect of immunosuppressive therapy on the messenger RNA expression of target genes in the urinary sediment of patients with active lupus nephritis. Nephrol Dial Transplant 21:1534-1540
    • (2006) Nephrol Dial Transplant , vol.21 , pp. 1534-1540
    • Chan, R.W.1    Lai, F.M.2    Li, E.K.3    Tam, L.S.4    Chow, K.M.5    Li, P.K.6    Szeto, C.C.7
  • 9
    • 33746224027 scopus 로고    scopus 로고
    • Applying nonsense-mediated mRNA decay research to the clinic: Progress and challenges
    • Kuzmiak HA, Maquat LE 2006 Applying nonsense-mediated mRNA decay research to the clinic: progress and challenges. Trends Mol Med 12:306-316
    • (2006) Trends Mol Med , vol.12 , pp. 306-316
    • Kuzmiak, H.A.1    Maquat, L.E.2
  • 10
    • 0037041395 scopus 로고    scopus 로고
    • An extensive network of coupling among gene expression machines
    • Maniatis T, Reed R 2002 An extensive network of coupling among gene expression machines. Nature 416:499-506
    • (2002) Nature , vol.416 , pp. 499-506
    • Maniatis, T.1    Reed, R.2
  • 11
    • 30344489013 scopus 로고    scopus 로고
    • Gitelman syndrome: Genetic and expression analysis of the thiazide-sensitive sodium-chloride transporter in blood cells
    • Riancho JA, Saro G, Sanudo C, Izquierdo MJ, Zarrabeitia MT 2006 Gitelman syndrome: genetic and expression analysis of the thiazide-sensitive sodium-chloride transporter in blood cells. Nephrol Dial Transplant 21:217-220
    • (2006) Nephrol Dial Transplant , vol.21 , pp. 217-220
    • Riancho, J.A.1    Saro, G.2    Sanudo, C.3    Izquierdo, M.J.4    Zarrabeitia, M.T.5
  • 13
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    • Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy
    • Shiga N, Takeshima Y, Sakamoto H, Inoue K, Yokota Y, Yokoyama M, Matsuo M 1997 Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy. J Clin Invest 100:2204-2210
    • (1997) J Clin Invest , vol.100 , pp. 2204-2210
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.