DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.
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DNMT3A in haematological malignancies.DNMT3A in Leukemia.Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.High PRDM16 expression identifies a prognostic subgroup of pediatric acute myeloid leukaemia correlated to FLT3-ITD, KMT2A-PTD, and NUP98-NSD1: the results of the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-05 trial.DNMT3A mutations in Chinese childhood acute myeloid leukemia.NUP98-NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia.Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia.Clinical features and prognostic impact of PRDM16 expression in adult acute myeloid leukemia.ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis.
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DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.
description
2011 nî lūn-bûn
@nan
2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年學術文章
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2011年學術文章
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name
DNMT3A mutations are rare in c ...... nile myelomonocytic leukaemia.
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DNMT3A mutations are rare in c ...... nile myelomonocytic leukaemia.
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type
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DNMT3A mutations are rare in c ...... nile myelomonocytic leukaemia.
@en
DNMT3A mutations are rare in c ...... nile myelomonocytic leukaemia.
@nl
prefLabel
DNMT3A mutations are rare in c ...... nile myelomonocytic leukaemia.
@en
DNMT3A mutations are rare in c ...... nile myelomonocytic leukaemia.
@nl
P2093
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DNMT3A mutations are rare in c ...... enile myelomonocytic leukaemia
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Hirokazu Arakawa
Ichiro Tsukimoto
Keizo Horibe
Manabu Sotomatsu
Masahiro Tsuchida
Myoung-Ja Park
Norio Shiba
Ryoji Hanada
Souichi Adachi
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P304
P356
10.1111/J.1365-2141.2011.08879.X
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P577
2011-10-08T00:00:00Z