Recent insights into inherited bone marrow failure syndromes. - Wikidata - awgldk - TriplyDB

Recent insights into inherited bone marrow failure syndromes.

Recent insights into inherited bone marrow failure syndromes.

http://www.wikidata.org/entity/Q37589103

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Secondary myeloid neoplasms: bone marrow cytogenetic and histological features may be relevant to prognosis.Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in THPO.Global transcriptome analyses of human and murine terminal erythroid differentiation.Advances in genetic studies of inherited bone marrow failure syndromes and their associated malignancies.Current insights into the diagnosis and treatment of inherited bone marrow failure syndromes in China.Genetic predispositions to childhood leukemia.Cytokine production by bone marrow mononuclear cells in inherited bone marrow failure syndromes Concise Review: Getting to the Core of Inherited Bone Marrow Failures.Acute Myeloid Leukemia With Myelodysplasia-Related Changes.Upregulated LINE-1 Activity in the Fanconi Anemia Cancer Susceptibility Syndrome Leads to Spontaneous Pro-inflammatory Cytokine Production.Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene.

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Recent insights into inherited bone marrow failure syndromes.

http://www.wikidata.org/entity/Q37589103

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 February 2012

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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

Recent insights into inherited bone marrow failure syndromes.

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Recent insights into inherited bone marrow failure syndromes.

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type

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Recent insights into inherited bone marrow failure syndromes.

@en

Recent insights into inherited bone marrow failure syndromes.

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prefLabel

Recent insights into inherited bone marrow failure syndromes.

@en

Recent insights into inherited bone marrow failure syndromes.

@nl

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Current Opinion in Pediatrics

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Recent insights into inherited bone marrow failure syndromes.

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Monica Bessler

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Shefali Parikh

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Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients

A syndrome with congenital neutropenia and mutations in G6PC3

A conserved WD40 protein binds the Cajal body localization signal of scaRNP particles

The ribosomal basis of Diamond-Blackfan Anemia: mutation and database update

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Congenital neutropenia: diagnosis, molecular bases and patient management.

Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations

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