(Q84962160)

English

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

scientific article published on 15 October 2009

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19946261%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

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

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19946261%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

acute myeloid leukemia

1 reference

based on heuristic

inferred from title

Catherine Carmichael

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19946261%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

15

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13 February 2020

Hamish S. Scott

17

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Europe PubMed Central

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13 February 2020

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M C J Jongmans

1

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13 February 2020

R P Kuiper

2

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13 February 2020

E J Wilkins

4

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13 February 2020

N Dors

5

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Europe PubMed Central

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13 February 2020

A Carmagnac

6

1 reference

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13 February 2020

A Y N Schouten-van Meeteren

7

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13 February 2020

X Li

8

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13 February 2020

M Stankovic

9

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13 February 2020

E Kamping

10

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13 February 2020

H Bengtsson

11

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13 February 2020

E F P M Schoenmakers

12

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13 February 2020

A Geurts van Kessel

13

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13 February 2020

P M Hoogerbrugge

14

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13 February 2020

P P Brons

16

1 reference

Europe PubMed Central

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13 February 2020

N Hoogerbrugge

18

1 reference

Europe PubMed Central

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13 February 2020

publication date

15 October 2009

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13 February 2020

1 reference

Europe PubMed Central

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13 February 2020

24

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13 February 2020

1

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13 February 2020

242-246

1 reference

Europe PubMed Central

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13 February 2020

https://scigraph.springernature.com/pub.10.1038/leu.2009.210

0 references

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.2009.210

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.210

7 January 2021

based on heuristic

inferred from DOI database lookup

Integrative analysis of RUNX1 downstream pathways and target genes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.210

7 January 2021

based on heuristic

inferred from DOI database lookup

Normal and transforming functions of RUNX1: a perspective

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.210

7 January 2021

based on heuristic

inferred from DOI database lookup

Cooperating gene mutations in acute myeloid leukemia: a review of the literature.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.210

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation?

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.210

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.2009.210

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.2009.210

7 January 2021

based on heuristic

inferred from DOI database lookup

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