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Volumn 32, Issue 6, 2008, Pages 995-997

Mutation analysis of AML1 gene in pediatric primary myelodysplastic syndrome and juvenile myelomonocytic leukemia

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; TRANSCRIPTION FACTOR POLYOMAVIRUS ENHANCER BINDING PROTEIN 2; TRANSCRIPTION FACTOR RUNX1; UNCLASSIFIED DRUG;

EID: 40849086140     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2007.09.004     Document Type: Letter
Times cited : (2)

References (6)
  • 1
    • 0025746321 scopus 로고
    • t(8;21) breakpoints in chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene AML1
    • Miyoshi Y., Shimizu K., Kozu T., Maseki N., Kaneko Y., and Ohki M. t(8;21) breakpoints in chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene AML1. Proc Natl Acad Sci USA 88 (1991) 10431-10434
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 10431-10434
    • Miyoshi, Y.1    Shimizu, K.2    Kozu, T.3    Maseki, N.4    Kaneko, Y.5    Ohki, M.6
  • 2
    • 0029100157 scopus 로고
    • Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia
    • Miyoshi H., Ohira M., Shimizu K., Mitani K., Hirai H., Imai T., et al. Alternative splicing and genomic structure of the AML1 gene involved in acute myeloid leukemia. Nucl Acids Res 23 (1995) 2762-2769
    • (1995) Nucl Acids Res , vol.23 , pp. 2762-2769
    • Miyoshi, H.1    Ohira, M.2    Shimizu, K.3    Mitani, K.4    Hirai, H.5    Imai, T.6
  • 3
    • 2942667930 scopus 로고    scopus 로고
    • Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia
    • Osato M. Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia. Oncogene 23 (2004) 4284-4296
    • (2004) Oncogene , vol.23 , pp. 4284-4296
    • Osato, M.1
  • 4
    • 0037438508 scopus 로고    scopus 로고
    • Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia
    • Harada H., Harada Y., Tanaka H., Kimura A., and Inaba T. Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia. Blood 101 (2003) 673-680
    • (2003) Blood , vol.101 , pp. 673-680
    • Harada, H.1    Harada, Y.2    Tanaka, H.3    Kimura, A.4    Inaba, T.5
  • 5
    • 1542373639 scopus 로고    scopus 로고
    • High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia
    • Harada H., Harada Y., Niimi H., Kyo T., Kimura A., and Inaba T. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood 103 (2004) 2316-2324
    • (2004) Blood , vol.103 , pp. 2316-2324
    • Harada, H.1    Harada, Y.2    Niimi, H.3    Kyo, T.4    Kimura, A.5    Inaba, T.6
  • 6
    • 4444302228 scopus 로고    scopus 로고
    • Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation
    • Christiansen D.H., Anderson M.K., and Pedersen-Bjergaard J. Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation. Blood 104 (2004) 1474-1481
    • (2004) Blood , vol.104 , pp. 1474-1481
    • Christiansen, D.H.1    Anderson, M.K.2    Pedersen-Bjergaard, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.