Erythro-megakaryocytic transcription factors associated with hereditary anemia - Test2 - elhamkhani - TriplyDB

Erythro-megakaryocytic transcription factors associated with hereditary anemia

Erythro-megakaryocytic transcription factors associated with hereditary anemia

http://www.wikidata.org/entity/Q28236415

about

Origins of the Vertebrate Erythro/Megakaryocytic System Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia.Inducible Gata1 suppression expands megakaryocyte-erythroid progenitors from embryonic stem cells.GATA factor mutations in hematologic disease.Defective acid hydrolase secretion in RUNX1 haplodeficiency: Evidence for a global platelet secretory defect.Combined loss of the GATA4 and GATA6 transcription factors in male mice disrupts testicular development and confers adrenal-like function in the testes.Altered chromatin occupancy of master regulators underlies evolutionary divergence in the transcriptional landscape of erythroid differentiation Robust hematopoietic progenitor cell commitment in the presence of a conflicting cue GATA factors in endocrine neoplasia Erythropoietin and IGF-1 signaling synchronize cell proliferation and maturation during erythropoiesis The Poly(C) Binding Protein Pcbp2 and Its Retrotransposed Derivative Pcbp1 Are Independently Essential to Mouse Development.A novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemias A Child With Dyserythropoietic Anemia and Megakaryocyte Dysplasia Due to a Novel 5'UTR GATA1s Splice Mutation.Differential miRNA Expression in the Liver of Balb/c Mice Protected by Vaccination during Crisis of Plasmodium chabaudi Blood-Stage Malaria.GATA1 Activity Governed by Configurations of cis-Acting Elements.Hsp90 chaperones hemoglobin maturation in erythroid and nonerythroid cells.Unexpected role for p19INK4d in posttranscriptional regulation of GATA1 and modulation of human terminal erythropoiesis.GATA1 insufficiencies in primary myelofibrosis and other hematopoietic disorders: consequences for therapy.GATA1 Is a Sensitive and Specific Nuclear Marker for Erythroid and Megakaryocytic Lineages.Erythropoiesis: insights into pathophysiology and treatments in 2017.

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

http://www.wikidata.org/entity/Q28236415

description

2014 nî lūn-bûn

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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Erythro-megakaryocytic transcription factors associated with hereditary anemia

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

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type

label

Erythro-megakaryocytic transcription factors associated with hereditary anemia

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

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prefLabel

Erythro-megakaryocytic transcription factors associated with hereditary anemia

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

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Erythro-megakaryocytic transcription factors associated with hereditary anemia

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A user's guide to the encyclopedia of DNA elements (ENCODE)

An integrated encyclopedia of DNA elements in the human genome

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

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts

GATA-1 forms distinct activating and repressive complexes in erythroid cells

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

Codanin-1, mutated in the anaemic disease CDAI, regulates Asf1 function in S-phase histone supply

A palindromic regulatory site within vertebrate GATA-1 promoters requires both zinc fingers of the GATA-1 DNA-binding domain for high-affinity interaction

Transcription factor NF-E2 is required for platelet formation independent of the actions of thrombopoietin/MGDF in megakaryocyte development

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