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Volumn 98, Issue 9, 2001, Pages 2856-2858

A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTIC ACID; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX1; UNCLASSIFIED DRUG;

EID: 0035525785     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.V98.9.2856     Document Type: Article
Times cited : (108)

References (8)
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    • Osato M, Asou N, Abdalla E, et al. Biallelic and heterozygous point mutations in the Runt domain of the AML1/PEBP2αB gene associated with myeloblastic leukemias. Blood. 1999;93:1817-1824.
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    • Osato, M.1    Asou, N.2    Abdalla, E.3
  • 2
    • 0034667690 scopus 로고    scopus 로고
    • High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in MO acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
    • Preudhomme C, Warot-Loze D, Roumier C, et al. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in MO acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21. Blood. 2000;96:2862-2869.
    • (2000) Blood , vol.96 , pp. 2862-2869
    • Preudhomme, C.1    Warot-Loze, D.2    Roumier, C.3
  • 3
    • 0034332068 scopus 로고    scopus 로고
    • Mutations in myelodysplastic syndrome and their functional implications in leukemogenesis
    • Imai Y, Kurokawa M, Izutsu K, et al. Mutations in myelodysplastic syndrome and their functional implications in leukemogenesis. Blood. 2000;96:3154-3160.
    • (2000) Blood , vol.96 , pp. 3154-3160
    • Imai, Y.1    Kurokawa, M.2    Izutsu, K.3
  • 4
    • 0034012933 scopus 로고    scopus 로고
    • AML1 haploinsufficiency, gene dosage, and the predisposition to acute leukemia
    • Barton K, Nucifora G. AML1 haploinsufficiency, gene dosage, and the predisposition to acute leukemia. Bioessays. 2000;22:214-218.
    • (2000) Bioessays , vol.22 , pp. 214-218
    • Barton, K.1    Nucifora, G.2
  • 5
    • 0027049743 scopus 로고
    • Platelet storage pool deficiency, leukemia, and myelodysplastic syndromes
    • Gerrard JM, McNicol A. Platelet storage pool deficiency, leukemia, and myelodysplastic syndromes. Leuk Lymphoma. 1992;8:277-281.
    • (1992) Leuk Lymphoma , vol.8 , pp. 277-281
    • Gerrard, J.M.1    McNicol, A.2
  • 6
    • 8944224533 scopus 로고    scopus 로고
    • Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 22q22.1-22.2
    • Ho CY, Otterud B, Legare RD, et al. Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 22q22.1-22.2. Blood. 1996;87:5218-5224.
    • (1996) Blood , vol.87 , pp. 5218-5224
    • Ho, C.Y.1    Otterud, B.2    Legare, R.D.3
  • 7
    • 0032830638 scopus 로고    scopus 로고
    • Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
    • Song W-J, Sullivan MG, Legare RD, et al. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat Genet. 1999;23:166-175.
    • (1999) Nat Genet , vol.23 , pp. 166-175
    • Song, W.-J.1    Sullivan, M.G.2    Legare, R.D.3
  • 8
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    • The Ig fold of the core binding factor alpha Runt domain is a member of a family of structurally and functionally related Ig-fold DNA-binding domains
    • Berardi MJ, Sun C, Zehr M, et al. The Ig fold of the core binding factor alpha Runt domain is a member of a family of structurally and functionally related Ig-fold DNA-binding domains. Struct Fold Des. 1999;7:1247-1256.
    • (1999) Struct Fold Des , vol.7 , pp. 1247-1256
    • Berardi, M.J.1    Sun, C.2    Zehr, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.