CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

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Impaired hematopoiesis and leukemia development in mice with a conditional knock-in allele of a mutant splicing factor gene Proteomic analysis identifies transcriptional cofactors and homeobox transcription factors as TBX18 binding proteins

P2860

Q57465846-AFD561AA-D96C-4D65-B36E-B9CD79240E58 Q58803849-852E71C5-C892-4293-B448-B8C039411B4B

P2860

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

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http://www.wikidata.org/entity/Q42778080

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

@en

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

@nl

type

Item

label

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

@en

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

@nl

prefLabel

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

@en

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

@nl

P1476

Chd7 deficiency delays leukemogenesis in mice induced by Cbfb-MYH11

@en

P2093

Erika M Kwon

http://www.w3.org/2001/XMLSchema#string

Jingmei Hsu

http://www.w3.org/2001/XMLSchema#string

Lemlem Alemu

http://www.w3.org/2001/XMLSchema#string

Ling Zhao

http://www.w3.org/2001/XMLSchema#string

Nancy A Speck

http://www.w3.org/2001/XMLSchema#string

R Katherine Hyde

http://www.w3.org/2001/XMLSchema#string

Tao Zhen

http://www.w3.org/2001/XMLSchema#string

Ying Lu

http://www.w3.org/2001/XMLSchema#string

P2860

Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome

COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

The inv(16) encodes an acute myeloid leukemia 1 transcriptional corepressor

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

Acute Myeloid Leukemia

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

Hematopoiesis in the fetal liver is impaired by targeted mutagenesis of a gene encoding a non-DNA binding subunit of the transcription factor, polyomavirus enhancer binding protein 2/core binding factor

P304

2431-2442

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scholarly article

P356

10.1182/BLOOD-2017-04-780106

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P407

English

P433

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P478

130

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P50

P Paul Liu

P577

2017-10-10T00:00:00Z

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P698

29018080

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P921

RNA-Seq

P932

5709785

http://www.w3.org/2001/XMLSchema#string

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

about

P2860

P2860

CHD7 deficiency delays leukemogenesis in mice induced by CBFB-MYH11.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932