(Q46402382)

21 December 2017

title

Hodgkin's lymphoma in a patient with Noonan syndrome with germ-line PTPN11 mutations (English)

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21 December 2017

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Fu-Sung Lo

1

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21 December 2017

Tseng-Tong Kuo

2

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21 December 2017

Chao-Jan Wang

3

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21 December 2017

Min-Tzu Kuo

4

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21 December 2017

Ming-Chung Kuo

5

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21 December 2017

publication date

30 August 2008

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21 December 2017

International Journal of Hematology

published in

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21 December 2017

volume

88

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21 December 2017

issue

3

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21 December 2017

page(s)

287-290

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21 December 2017

The 'Shp'ing news: SH2 domain-containing tyrosine phosphatases in cell signaling

cites work

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12 December 2020

Germline KRAS mutations cause Noonan syndrome

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12 December 2020

PTPN11 (protein-tyrosine phosphatase, nonreceptor-type 11) mutations in seven Japanese patients with Noonan syndrome

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12 December 2020

PTPN11 is the first identified proto-oncogene that encodes a tyrosine phosphatase

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12 December 2020

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

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12 December 2020

Activating mutations of the noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia

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12 December 2020

A revised European-American classification of lymphoid neoplasms: a proposal from the International Lymphoma Study Group

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12 December 2020

Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression

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12 December 2020

Contribution of the Epstein Barr virus to the molecular pathogenesis of Hodgkin lymphoma.

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12 December 2020

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

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12 December 2020

The role of Shp2 (PTPN11) in cancer.

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12 December 2020

Mutational analysis of PTPN11 gene in Taiwanese children with Noonan syndrome

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12 December 2020

New aspects in descriptive, etiologic, and molecular epidemiology of Hodgkin's lymphoma

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12 December 2020

Genotype-phenotype correlations in Noonan syndrome

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12 December 2020

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

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12 December 2020

A clinical study of Noonan syndrome

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12 December 2020

Germline gain-of-function mutations in SOS1 cause Noonan syndrome

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12 December 2020

Germ-line and somatic PTPN11 mutations in human disease

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12 December 2020

Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia

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12 December 2020

Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.

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12 December 2020

10.1007/S12185-008-0157-5

Identifiers

DOI

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21 December 2017

release_k5umrfzv4vdapdumb7yt2pla3a

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/k5umrfzv4vdapdumb7yt2pla3a

24 November 2022

mapped directly with Wikidata item

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21 December 2017