Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia. (Q33419236)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25490895%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

title

Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia (English)

1 reference

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24 February 2020

1 reference

1 reference

4

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24 February 2020

Lucie Tosca

9

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24 February 2020

Gérard Tachdjian

10

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24 February 2020

Isabelle Plo

13

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24 February 2020

Mitchell J Weiss

16

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24 February 2020

Eric Solary

17

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24 February 2020

William Vainchenker

19

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24 February 2020

Hana Raslova

20

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24 February 2020

3

Nathalie Balayn

1 reference

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24 February 2020

12

Najet Debili

1 reference

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24 February 2020

author name string

Iléana Antony-Debré

1

1 reference

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24 February 2020

Vladimir T Manchev

2

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24 February 2020

Cécile Tomowiak

5

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24 February 2020

Céline Legrand

6

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24 February 2020

Thierry Langlois

7

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24 February 2020

Olivia Bawa

8

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24 February 2020

Bruno Leheup

11

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24 February 2020

Jason A Mills

14

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24 February 2020

Deborah L French

15

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24 February 2020

Remi Favier

18

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24 February 2020

language of work or name

English

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publication date

9 December 2014

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24 February 2020

1 reference

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24 February 2020

volume

125

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24 February 2020

issue

6

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24 February 2020

page(s)

930-940

1 reference

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Targeted correction of RUNX1 mutation in FPD patient-specific induced pluripotent stem cells rescues megakaryopoietic defects

24 February 2020

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1 reference

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Impaired hematopoietic differentiation of RUNX1-mutated induced pluripotent stem cells derived from FPD/AML patients

21 June 2018

1 reference

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Runx1 and Cbfβ regulate the development of Flt3+ dendritic cell progenitors and restrict myeloproliferative disorder.

21 June 2018

1 reference

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Utilization of the AAVS1 safe harbor locus for hematopoietic specific transgene expression and gene knockdown in human ES cells

21 June 2018

1 reference

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Transcription factor RUNX1 promotes survival of acute myeloid leukemia cells

21 June 2018

1 reference

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Clonal genetic and hematopoietic heterogeneity among human-induced pluripotent stem cell lines.

21 June 2018

1 reference

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Genome-wide profiling reveals transcriptional repression of MYC as a core component of NR4A tumor suppression in acute myeloid leukemia

21 June 2018

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21 June 2018

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Altered hematopoiesis in trisomy 21 as revealed through in vitro differentiation of isogenic human pluripotent cells

21 June 2018

1 reference

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RUNX1-induced silencing of non-muscle myosin heavy chain IIB contributes to megakaryocyte polyploidization

21 June 2018

1 reference

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Clinical effect of point mutations in myelodysplastic syndromes

21 June 2018

1 reference

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Somatic coding mutations in human induced pluripotent stem cells

21 June 2018

1 reference

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RUNX1 mutations in acute myeloid leukemia: results from a comprehensive genetic and clinical analysis from the AML study group

21 June 2018

1 reference

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Reduced NR4A gene dosage leads to mixed myelodysplastic/myeloproliferative neoplasms in mice

21 June 2018

1 reference

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Cell type of origin influences the molecular and functional properties of mouse induced pluripotent stem cells

21 June 2018

1 reference

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Epigenetic memory in induced pluripotent stem cells

21 June 2018

1 reference

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A common bipotent progenitor generates the erythroid and megakaryocyte lineages in embryonic stem cell-derived primitive hematopoiesis.

21 June 2018

1 reference

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Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter

21 June 2018

1 reference

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Diverse hematopoietic potentials of five human embryonic stem cell lines

21 June 2018

1 reference

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Integrative analysis of RUNX1 downstream pathways and target genes

21 June 2018

1 reference

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Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions

21 June 2018

1 reference

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Runx1 is involved in primitive erythropoiesis in the mouse

21 June 2018

1 reference

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Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

21 June 2018

1 reference

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Leukosialin (CD43) defines hematopoietic progenitors in human embryonic stem cell differentiation cultures

21 June 2018

1 reference

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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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 June 2018

1 reference

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Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture

21 June 2018

1 reference

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

21 June 2018

1 reference

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PU.1 functions in a cell-autonomous manner to control the differentiation of multipotential lymphoid-myeloid progenitors

21 June 2018

1 reference

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AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

21 June 2018

1 reference

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Prognostic score including gene mutations in chronic myelomonocytic leukemia.

21 June 2018

1 reference

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Human ESC-derived hemogenic endothelial cells undergo distinct waves of endothelial to hematopoietic transition

31 October 2018

1 reference

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C-terminal mutation of RUNX1 attenuates the DNA-damage repair response in hematopoietic stem cells.

31 October 2018

1 reference

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Down-regulation of the RUNX1-target gene NR4A3 contributes to hematopoiesis deregulation in familial platelet disorder/acute myelogenous leukemia.

31 October 2018

1 reference

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An accumulation of cytogenetic and molecular genetic events characterizes the progression from MDS to secondary AML: an analysis of 38 paired samples analyzed by cytogenetics, molecular mutation analysis and SNP microarray profiling.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4347283

Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.

31 October 2018

1 reference

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AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations.

31 October 2018

1 reference

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Restoration of Runx1 expression in the Tie2 cell compartment rescues definitive hematopoietic stem cells and extends life of Runx1 knockout animals until birth.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4347283

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4347283

Acute myeloid leukemia induced by graded reduction of a lineage-specific transcription factor, PU.1.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4347283

PU. 1 is not essential for early myeloid gene expression but is required for terminal myeloid differentiation.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4347283

Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

31 October 2018

1 reference

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Abrogation of nuclear receptors Nr4a3 and Nr4a1 leads to development of acute myeloid leukemia

31 October 2018

1 reference

12 December 2020

RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis

1 reference

12 December 2020

Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia

1 reference

12 December 2020

Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression

1 reference

12 December 2020

10.1182/BLOOD-2014-06-585513

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25490895%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25490895%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

PubMed publication ID

25490895

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25490895%20AND%20SRC:MED&resulttype=core&format=json