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Volumn 68, Issue 2, 2001, Pages 115-121

Genetic heterogeneity of primary familial and congenital polycythemia

Author keywords

Erythropoietin; Hematopolesis; Mutation; Receptor

Indexed keywords

ERYTHROPOIETIN; ERYTHROPOIETIN RECEPTOR;

EID: 0034839931     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajh.1162     Document Type: Article
Times cited : (57)

References (26)
  • 10
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    • Absence of polycythemia in a child with a unique erythropoietin receptor mutation in a family with autosomal dominant primary polycythemia
    • J Clin Invest
    • (1998) J Clin Invest , vol.102 , pp. 124-129
    • Kralovics, R.1    Sokol, L.2    Prchal, J.T.3
  • 21
    • 0031041432 scopus 로고    scopus 로고
    • In vitro erythropoiesis in polycythemia vera and other myeloproliferative disorders
    • Semin Hematol
    • (1997) Semin Hematol , vol.34 , pp. 64-69
    • Weinberg, R.S.1
  • 25
    • 0033050680 scopus 로고    scopus 로고
    • A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation
    • Exp Hematol
    • (1999) Exp Hematol , vol.27 , pp. 63-74
    • Arcasoy, M.O.1    Harris, K.W.2    Forget, B.G.3
  • 26
    • 0025633003 scopus 로고
    • Point mutation in the exoplasmic domain of the erythropoietin receptor resulting in hormone-independent activation and tumorigenicity
    • Nature
    • (1990) Nature , vol.348 , pp. 647-649
    • Yoshimura, A.1    Longmore, G.2    Lodish, H.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.