Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia. - Wikidata - wikimedia - TriplyDB

Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia.

Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia.

http://www.wikidata.org/entity/Q37225823

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The emerging roles of the DDX41 protein in immunity and diseases.Targeting Cancer Stem Cells with Natural Killer Cell Immunotherapy.Nucleic acid sensing pattern recognition receptors in the development of colorectal cancer and colitis.Myeloid neoplasms with germline DDX41 mutation.Familial Acute Myeloid Leukemia and Myelodysplasia in Hungary.Re-emergence of acute myeloid leukemia in donor cells following allogeneic transplantation in a family with a germline DDX41 mutation.How I diagnose and manage individuals at risk for inherited myeloid malignancies.

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Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia.

http://www.wikidata.org/entity/Q37225823

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 02 May 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Germline heterozygous DDX41 va ...... ia and acute myeloid leukemia.

@en

Germline heterozygous DDX41 va ...... ia and acute myeloid leukemia.

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type

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Germline heterozygous DDX41 va ...... ia and acute myeloid leukemia.

@en

Germline heterozygous DDX41 va ...... ia and acute myeloid leukemia.

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Germline heterozygous DDX41 va ...... ia and acute myeloid leukemia.

@en

Germline heterozygous DDX41 va ...... ia and acute myeloid leukemia.

@nl

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Germline heterozygous DDX41 va ...... ia and acute myeloid leukemia.

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A Ellison

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A J Walne

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G Ryan

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DEAD box RNA helicase functions in cancer

Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.

Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.

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