(Q44419404)

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Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

scientific article published in June 2003

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 December 2017

Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

1 reference

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juvenile myelomonocytic leukemia

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Marco Tartaglia

1

1 reference

Europe PubMed Central

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2 December 2017

8

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Europe PubMed Central

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2 December 2017

Alessandra Fragale

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Alessandra Fragale

3

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Bruce D Gelb

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author name string

Charlotte M Niemeyer

2

1 reference

Europe PubMed Central

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2 December 2017

Xiaoling Song

4

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Europe PubMed Central

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2 December 2017

Jochen Buechner

5

1 reference

Europe PubMed Central

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2 December 2017

Andreas Jung

6

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Europe PubMed Central

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2 December 2017

Karel Hählen

7

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2 December 2017

Jonathan D Licht

9

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2 December 2017

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publication date

1 June 2003

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2 December 2017

Nature Genetics

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2 December 2017

34

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2 December 2017

2

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2 December 2017

148-150

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2 December 2017

Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7. European Working Group on MDS in Childhood (EWOG-MDS)

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

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inferred from DOI database lookup

Juvenile myelomonocytic leukemia: molecular understanding and prospects for therapy

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

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Hypertelorism With Turner Phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

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%2FNG1156

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of priapism in children and adolescents with sickle cell anemia

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

based on heuristic

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Occurrence of myeloproliferative disorder in patients with Noonan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

based on heuristic

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Spontaneous remission of juvenile chronic myelomonocytic leukemia in an infant with Noonan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

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inferred from DOI database lookup

Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cells

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

based on heuristic

inferred from DOI database lookup

Crystal Structure of the Tyrosine Phosphatase SHP-2

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

based on heuristic

inferred from DOI database lookup

PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG1156

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

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