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GATA family transcriptional factors: emerging suspects in hematologic disorders

GATA family transcriptional factors: emerging suspects in hematologic disorders

http://www.wikidata.org/entity/Q26786487

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The genomics of inherited bone marrow failure: from mechanism to the clinic.SUMO5, a Novel Poly-SUMO Isoform, Regulates PML Nuclear Bodies.The sense behind retroviral anti-sense transcription.E2F and GATA switches turn off WD repeat domain 77 expression in differentiating cells.EP300-ZNF384 fusion gene product up-regulates GATA3 gene expression and induces hematopoietic stem cell gene expression signature in B-cell precursor acute lymphoblastic leukemia cells.Evolution of myeloid leukemia in children with Down syndrome.Epigenetic regulation of cellular and cytomegalovirus genes during myeloid cell development.GATA3 rs3824662 gene polymorphism as possible risk factor in a cohort of Egyptian patients with pediatric acute lymphoblastic leukemia and its prognostic impact.Nuclear features of infiltrating urothelial carcinoma are distinguished from low-grade noninvasive papillary urothelial carcinoma by image analysis.A population of hematopoietic stem cells derives from GATA4-expressing progenitors located in the placenta and lateral mesoderm of mice Genome-wide scan in Hispanics highlights candidate loci for brain white matter hyperintensities.SETBP1 mutations as a biomarker for myelodysplasia /myeloproliferative neoplasm overlap syndrome.GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II.GATA2 Deficiency and Epstein-Barr Virus Disease.Unexpected role for p19INK4d in posttranscriptional regulation of GATA1 and modulation of human terminal erythropoiesis.GATA-3-specific DNAzyme - A novel approach for stratified asthma therapy.Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary?UTX-mediated enhancer and chromatin remodeling suppresses myeloid leukemogenesis through noncatalytic inverse regulation of ETS and GATA programs

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GATA family transcriptional factors: emerging suspects in hematologic disorders

http://www.wikidata.org/entity/Q26786487

description

2015 nî lūn-bûn

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2015 թուականին հրատարակուած գիտական յօդուած

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

GATA family transcriptional factors: emerging suspects in hematologic disorders

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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type

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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Experimental Hematology & Oncology

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GATA family transcriptional factors: emerging suspects in hematologic disorders

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Juehua Gao

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LoAnn C Peterson

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Yi-Hua Chen

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P2860

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

GATA3 haplo-insufficiency causes human HDR syndrome

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

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

Transcriptional cofactors of the FOG family interact with GATA proteins by means of multiple zinc fingers

The genetic basis of early T-cell precursor acute lymphoblastic leukaemia.

Comprehensive molecular portraits of human breast tumours

Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature

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