메뉴 건너뛰기




Volumn 385, Issue 6, 2000, Pages 390-392

Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood

Author keywords

Constitutive activity; Mutation; Non autoimmune hyperthyroidism; TSHR

Indexed keywords

ANTITHYROID AGENT;

EID: 0033747056     PISSN: 14352443     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004230000145     Document Type: Article
Times cited : (26)

References (10)
  • 1
    • 0026743033 scopus 로고
    • The thyrotropin receptor and the regulation of thyrocyte function and growth
    • Vassart G, Dumont JE (1992) The thyrotropin receptor and the regulation of thyrocyte function and growth. Endocr Rev 13:596-611
    • (1992) Endocr Rev , vol.13 , pp. 596-611
    • Vassart, G.1    Dumont, J.E.2
  • 5
    • 0031772403 scopus 로고    scopus 로고
    • Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor
    • Grüters A, Schöneberg T, Biebermann H, Krude H, Krohn HP, Dralle H, Gudermann T (1998) Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor. J Clin Endocrinol Metab 83:1431-1436
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 1431-1436
    • Grüters, A.1    Schöneberg, T.2    Biebermann, H.3    Krude, H.4    Krohn, H.P.5    Dralle, H.6    Gudermann, T.7
  • 6
    • 0029874025 scopus 로고    scopus 로고
    • Microsatellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor gene
    • de Roux N, Misrahi M, Châtelain N, Gross B, Milgrom E (1996) Microsatellites and PCR primers for genetic studies and genomic sequencing of the human TSH receptor gene. Mol Cell Endocrinol 117:253-256
    • (1996) Mol Cell Endocrinol , vol.117 , pp. 253-256
    • Roux, N.1    Misrahi, M.2    Châtelain, N.3    Gross, B.4    Milgrom, E.5
  • 8
    • 0031406420 scopus 로고    scopus 로고
    • Congenital nonautoimmune hyperthyroidism in a nonidentical twin caused by a sporadic germline mutation in the thyrotropin receptor gene
    • Kopp P, Jameson JL, Roe TF (1997) Congenital nonautoimmune hyperthyroidism in a nonidentical twin caused by a sporadic germline mutation in the thyrotropin receptor gene. Thyroid 7:765-770
    • (1997) Thyroid , vol.7 , pp. 765-770
    • Kopp, P.1    Jameson, J.L.2    Roe, T.F.3
  • 9
    • 0031470487 scopus 로고    scopus 로고
    • Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism
    • Schwab KO, Gerlich M, Broecker M, Sohlemann P, Derwahl M, Lohse MJ (1997) Constitutively active germline mutation of the thyrotropin receptor gene as a cause of congenital hyperthyroidism. J Pediatr 131:899-904
    • (1997) J Pediatr , vol.131 , pp. 899-904
    • Schwab, K.O.1    Gerlich, M.2    Broecker, M.3    Sohlemann, P.4    Derwahl, M.5    Lohse, M.J.6
  • 10
    • 0030734932 scopus 로고    scopus 로고
    • Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism
    • Führer D, Wonerow P, Willgerodt H, Paschke R (1997) Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism. J Clin Endocrinol Metab 82:4234-4238
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 4234-4238
    • Führer, D.1    Wonerow, P.2    Willgerodt, H.3    Paschke, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.