(Q47959794)

English

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

scientific article published on 23 April 2009

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scholarly article

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

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

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

1 reference

based on heuristic

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1 reference

based on heuristic

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author name string

T Ripperger

1

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

D Steinemann

2

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

G Göhring

3

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

J Finke

4

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

C M Niemeyer

5

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

B Strahm

6

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

B Schlegelberger

7

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

publication date

23 April 2009

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

23

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

7

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

1364-1366

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

https://scigraph.springernature.com/pub.10.1038/leu.2009.87

0 references

Point mutations of the RUNx1/AML1 gene in sporadic and familial myeloid leukemias

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.87

21 January 2018

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.2009.87

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.87

21 January 2018

MYB function in normal and cancer cells

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.87

21 January 2018

The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.87

21 January 2018

The c-myb proto-oncogene and microRNA-15a comprise an active autoregulatory feedback loop in human hematopoietic cells

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.87

21 January 2018

Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.87

21 January 2018

Identifiers

10.1038/LEU.2009.87

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

1 reference

Europe PubMed Central

7 February 2018

http://europepmc.org/abstract/MED/19387465

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