Transcriptional control of megakaryocyte development (Q30444726)

21 June 2017

1 reference

title

Transcriptional control of megakaryocyte development (English)

1 reference

21 June 2017

Goldfarb AN

1

1 reference

PubMed ID

17934486

21 June 2017

language of work or name

English

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publication date

1 October 2007

1 reference

21 June 2017

1 reference

21 June 2017

26

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21 June 2017

47

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21 June 2017

6795-6802

1 reference

Identification of Flt3+ lympho-myeloid stem cells lacking erythro-megakaryocytic potential a revised road map for adult blood lineage commitment.

21 June 2017

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

A clonogenic common myeloid progenitor that gives rise to all myeloid lineages

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Transcriptional regulation of erythropoiesis: an affair involving multiple partners

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Progression through key stages of haemopoiesis is dependent on distinct threshold levels of c-Myb.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Combinatorial interactions of Serpent, Lozenge, and U-shaped regulate crystal cell lineage commitment during Drosophila hematopoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Loss of Runx1 perturbs adult hematopoiesis and is associated with a myeloproliferative phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Fli-1 is required for murine vascular and megakaryocytic development and is hemizygously deleted in patients with thrombocytopenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Tel/Etv6 is an essential and selective regulator of adult hematopoietic stem cell survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

GATA1-mediated megakaryocyte differentiation and growth control can be uncoupled and mapped to different domains in GATA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Role of Cbfb in hematopoiesis and perturbations resulting from expression of the leukemogenic fusion gene Cbfb-MYH11

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Spatial and temporal expression pattern of Runx3 (Aml2) and Runx1 (Aml1) indicates non-redundant functions during mouse embryogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Zinc fingers as protein recognition motifs: structural basis for the GATA-1/friend of GATA interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

The tetramer structure of the Nervy homology two domain, NHR2, is critical for AML1/ETO's activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Role of RUNX1 in adult hematopoiesis: analysis of RUNX1-IRES-GFP knock-in mice reveals differential lineage expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Overexpression of Ets-1 in human hematopoietic progenitor cells blocks erythroid and promotes megakaryocytic differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Prospective isolation of human clonogenic common myeloid progenitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Transgene insertion in proximity to the c-myb gene disrupts erythroid-megakaryocytic lineage bifurcation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Differential requirements for the activation domain and FOG-interaction surface of GATA-1 in megakaryocyte gene expression and development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Maturation stage-specific regulation of megakaryopoiesis by pointed-domain Ets proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Congenital erythropoietic porphyria due to a mutation in GATA1: the first trans-acting mutation causative for a human porphyria

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

AML1 deletion in adult mice causes splenomegaly and lymphomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

c-Myb and p300 regulate hematopoietic stem cell proliferation and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Hemorrhage, impaired hematopoiesis, and lethality in mouse embryos carrying a targeted disruption of the Fli1 transcription factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Early block to erythromegakaryocytic development conferred by loss of transcription factor GATA-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Functional cross-antagonism between transcription factors FLI-1 and EKLF

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

The mediator complex functions as a coactivator for GATA-1 in erythropoiesis via subunit Med1/TRAP220

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Association of CBFA2 mutation with decreased platelet PKC-θ and impaired receptor-mediated activation of GPIIb-IIIa and pleckstrin phosphorylation: proteins regulated by CBFA2 play a role in GPIIb-IIIa activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFbeta dosage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Potential roles for RUNX1 and its orthologs in determining hematopoietic cell fate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Cooperation between the GATA and RUNX factors Serpent and Lozenge during Drosophila hematopoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Control of megakaryocyte-specific gene expression by GATA-1 and FOG-1: role of Ets transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Physical association of the patient-specific GATA1 mutants with RUNX1 in acute megakaryoblastic leukemia accompanying Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

A transcription-factor-binding surface of coactivator p300 is required for haematopoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

Cbf beta-SMMHC induces distinct abnormal myeloid progenitors able to develop acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

inferred from DOI database lookup

7 January 2021

based on heuristic

FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

inferred from DOI database lookup

7 January 2021

based on heuristic

Haploinsufficiency of AML1 results in a decrease in the number of LTR-HSCs while simultaneously inducing an increase in more mature progenitors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210762

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.ONC.1210762

1 reference

PubMed ID

17934486

Dimensions Publication ID

21 June 2017

0 references

1 reference

PubMed ID

17934486