Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

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FANCI and FANCD2 have common as well as independent functions during the cellular replication stress response.Recent advances in understanding hematopoiesis in Fanconi Anemia.Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi Anemia

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P2860

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

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http://www.wikidata.org/entity/Q51286905

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

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name

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

@en

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

@nl

type

Item

label

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

@en

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

@nl

prefLabel

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

@en

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

@nl

P1476

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

@en

P2093

Glen D Raffel

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

Nathan A Manalo

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

Ronny R Racine

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

Sakiko Suzuki

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

Sharon B Cantor

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

P2860

Why does the bone marrow fail in Fanconi anemia?

Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models

Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice

p53-Independent apoptosis disrupts early organogenesis in embryos lacking both ataxia-telangiectasia mutated and Prkdc

Genomic characterization of the inherited bone marrow failure syndromes.

Neonatal manifestations of inherited bone marrow failure syndromes.

Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1.

Telomere dysfunction induces metabolic and mitochondrial compromise.

Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice.

Maternal aldehyde elimination during pregnancy preserves the fetal genome

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scholarly article

P356

10.1016/J.EXPHEM.2016.11.006

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2016-11-30T00:00:00Z

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27915139

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Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

about

P2860

P2860

Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P932