(Q83696129)

English

Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigrees

scientific article published on 20 March 2012

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Europe PubMed Central

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26 January 2020

Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigrees (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22430633%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

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A Buijs

1

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26 January 2020

M Poot

2

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26 January 2020

S van der Crabben

3

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26 January 2020

B van der Zwaag

4

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26 January 2020

E van Binsbergen

5

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26 January 2020

M J van Roosmalen

6

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26 January 2020

M Tavakoli-Yaraki

7

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26 January 2020

O de Weerdt

8

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26 January 2020

H K Nieuwenhuis

9

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26 January 2020

M van Gijn

10

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26 January 2020

W P Kloosterman

11

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26 January 2020

publication date

20 March 2012

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26 January 2020

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26 January 2020

26

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26 January 2020

9

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26 January 2020

2151-2154

1 reference

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26 January 2020

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Insights into familial platelet disorder with propensity to myeloid malignancy (FPD/AML)

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

Runx1-mediated hematopoietic stem-cell emergence is controlled by a Gata/Ets/SCL-regulated enhancer

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

The mouse Runx1 +23 hematopoietic stem cell enhancer confers hematopoietic specificity to both Runx1 promoters.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

MCAF1/AM is involved in Sp1-mediated maintenance of cancer-associated telomerase activity

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2012.79

7 January 2021

based on heuristic

inferred from DOI database lookup

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