(Q46922192)

English

Characterization of acute myeloid leukemia with PTPN11 mutation: the mutation is closely associated with NPM1 mutation but inversely related to FLT3/ITD.

scientific article published in November 2007

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scholarly article

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Characterization of acute myeloid leukemia with PTPN11 mutation: the mutation is closely associated with NPM1 mutation but inversely related to FLT3/ITD. (English)

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

1 reference

based on heuristic

inferred from title

acute myeloid leukemia

1 reference

based on heuristic

inferred from title

author name string

Hou HA

1

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Chou WC

2

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Lin LI

3

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Chen CY

4

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Tang JL

5

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Tseng MH

6

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Huang CF

7

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Chiou RJ

8

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Lee FY

9

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Liu MC

10

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

Tien HF

11

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

publication date

1 November 2007

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

22

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

5

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

1075-1078

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

https://scigraph.springernature.com/pub.10.1038/sj.leu.2405005

0 references

Genetics of myeloid malignancies: pathogenetic and clinical implications

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2405005

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of myeloid leukemias

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2405005

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2405005

7 January 2021

based on heuristic

inferred from DOI database lookup

Acquisition of JAK2, PTPN11, and RAS mutations during disease progression in primary myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2405005

7 January 2021

based on heuristic

inferred from DOI database lookup

Nucleophosmin mutations in de novo acute myeloid leukemia: the age-dependent incidences and the stability during disease evolution

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2405005

7 January 2021

based on heuristic

inferred from DOI database lookup

RUNX1 gene mutation in primary myelodysplastic syndrome--the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2405005

7 January 2021

based on heuristic

inferred from DOI database lookup

Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2405005

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.LEU.2405005

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17972951

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