Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1. - Wikidata - awgldk - TriplyDB

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

http://www.wikidata.org/entity/Q33367881

about

Biological Databases for Hematology Research Erythro-megakaryocytic transcription factors associated with hereditary anemia Transcription factor GATA-1 and Down syndrome leukemogenesis Analysis of disease-causing GATA1 mutations in murine gene complementation systems The University of Washington Health Sciences Library BioCommons: an evolving Northwest biomedical research information support infrastructure.Human phenotypes associated with GATA-1 mutations.Severe gastrointestinal bleeding and thrombocytopenia in a child with an anti-GATA1 autoantibody.Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1 (G208R) mutation.Current Strategies in Diagnosis of Inherited Storage Pool Defects Concomitant a novel ALAS2 mutation and GATA1 mutation in a newborn: a case report and review of the literature.Inherited platelet dysfunction and hematopoietic transcription factor mutations.Hematopoietic transcription factor mutations: important players in inherited platelet defects.Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach.Evolving insights into the synergy between erythropoietin and thrombopoietin and the bipotent erythroid/megakaryocytic progenitor cell.From the Cradle to the Grave: The Role of Macrophages in Erythropoiesis and Erythrophagocytosis.Novel GATA1 mutation in residue D218 leads to macrothrombocytopenia and clinical bleeding problems.Epigenetic dysregulation of GATA1 is involved in myelodysplastic syndromes dyserythropoiesis.GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II.Detection of mutations in GATA1 gene using automated denaturing high-performance liquid chromatography and direct sequencing in children with Down syndrome.GATA1 gene variants associated with thrombocytopenia and anemia.Genomics and transcriptomics of megakaryocytes and platelets: Implications for health and disease

P2860

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P2860

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

http://www.wikidata.org/entity/Q33367881

description

2005 nî lūn-bûn

@nan

2005 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

@ast

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

@en

type

label

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

@ast

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

@en

prefLabel

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

@ast

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

@en

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P2860

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P356

P1433

Acta Haematologica

P1476

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

@en

P2093

Attilio De Santis

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

Domenico De Mattia

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

Giovanni Carlo Del Vecchio

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

Lucia Giordani

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

P2860

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

X-linked thrombocytopenia caused by a novel mutation of GATA-1

X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction

Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation

Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1

A lineage-selective knockout establishes the critical role of transcription factor GATA-1 in megakaryocyte growth and platelet development.

Cloning of cDNA for the major DNA-binding protein of the erythroid lineage through expression in mammalian cells

The erythroid-specific transcription factor Eryf1: a new finger protein.

Distinct roles for the two cGATA-1 finger domains.

P304

113-116

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P31

scholarly article

P356

10.1159/000086586

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P433

2

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P478

114

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P577

2005-01-01T00:00:00Z

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P698

16103636

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P921

thrombocytopenia