Fetal origins of hematopoietic failure in a murine model of Fanconi anemia - Wikidata - awgldk - TriplyDB

Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

http://www.wikidata.org/entity/Q36818532

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An abnormal bone marrow microenvironment contributes to hematopoietic dysfunction in Fanconi anemia.Fanconi anemia signaling and Mus81 cooperate to safeguard development and crosslink repair Maternal aldehyde elimination during pregnancy preserves the fetal genome Endogenous DNA Damage Leads to p53-Independent Deficits in Replicative Fitness in Fetal Murine Fancd2(-/-) Hematopoietic Stem and Progenitor Cells.Stress and DNA repair biology of the Fanconi anemia pathway Pregnancy outcomes in mothers of offspring with inherited bone marrow failure syndromes.The Fanconi anemia pathway is required for efficient repair of stress-induced DNA damage in haematopoietic stem cells Pluripotent cell models of fanconi anemia identify the early pathological defect in human hemoangiogenic progenitors.Metformin: treating the cause of Fanconi anemia?Loss of the homologous recombination gene rad51 leads to Fanconi anemia-like symptoms in zebrafish.Recent advances in understanding hematopoiesis in Fanconi Anemia.Metformin improves defective hematopoiesis and delays tumor formation in Fanconi anemia mice.Impairment of fetal hematopoietic stem cell function in the absence of Fancd2.Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi Anemia

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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

http://www.wikidata.org/entity/Q36818532

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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name

Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia

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Peter Kurre

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P2860

How the fanconi anemia pathway guards the genome

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

Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia

Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene

The purification and characterization of fetal liver hematopoietic stem cells.

Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage.

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

The journey of developing hematopoietic stem cells.

Fanconi anaemia and leukaemia - clinical and molecular aspects.

Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells.

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2008-2012

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Natalya Goloviznina

Ashley N Kamimae-Lanning

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234124255

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