(Q42167156)

17 October 2017

title

Noonan syndrome, the SOS1 gene and embryonal rhabdomyosarcoma (English)

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Adrianus Henricus Maria Geurts van Kessel

17 October 2017

1 reference

1 reference

11

object named as

Ad Geurts van Kessel

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Nicoline Hoogerbrugge

13

object named as

Nicoline Hoogerbrugge

1 reference

17 October 2017

Marjolijn J L Ligtenberg

10

object named as

Marjolijn J L Ligtenberg

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17 October 2017

author name string

Marjolijn C J Jongmans

1

1 reference

17 October 2017

Peter M Hoogerbrugge

2

1 reference

17 October 2017

Linda Hilkens

3

1 reference

17 October 2017

Uta Flucke

4

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17 October 2017

Ineke van der Burgt

5

1 reference

17 October 2017

Kees Noordam

6

1 reference

17 October 2017

Martina Ruiterkamp-Versteeg

7

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17 October 2017

Helger G Yntema

8

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17 October 2017

Willy M Nillesen

9

1 reference

17 October 2017

Ad Geurts van Kessel

11

1 reference

17 October 2017

Roland P Kuiper

12

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17 October 2017

publication date

1 July 2010

1 reference

Genes, Chromosomes and Cancer

17 October 2017

published in

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17 October 2017

volume

49

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17 October 2017

issue

7

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17 October 2017

page(s)

635-641

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Pigmented villonodular synovitis in a patient with Noonan syndrome andSOS1gene mutation

17 October 2017

cites work

1 reference

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SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions

21 January 2018

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7 January 2021

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

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7 January 2021

Stops along the RAS pathway in human genetic disease

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7 January 2021

Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype

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7 January 2021

Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hybridization and fluorescence in situ hybridization: an intergroup rhabdomyosarcoma study

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7 January 2021

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7 January 2021

Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies

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7 January 2021

A restricted spectrum of NRAS mutations causes Noonan syndrome

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7 January 2021

Noonan Syndrome and Neuroblastoma

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7 January 2021

Soft-tissue sarcomas in children and adolescents with neurofibromatosis type 1

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7 January 2021

Tumor predisposition in Costello syndrome

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7 January 2021

A case of Noonan's syndrome with possible associated neuroblastoma

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7 January 2021

Orbital rhabdomyosarcoma in Noonan syndrome

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7 January 2021

Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome

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7 January 2021

Diverse biochemical properties of Shp2 mutants. Implications for disease phenotypes

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7 January 2021

Vaginal rhabdomyosarcoma in a patient with Noonan syndrome

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7 January 2021

Noonan syndrome with leukaemoid reaction and overproduction of catecholamines: a case report

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7 January 2021

A gain-of-function mutation of JAK2 in myeloproliferative disorders

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7 January 2021

Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia

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7 January 2021

Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome.

1 reference

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7 January 2021

High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression.

1 reference

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7 January 2021

Effects of RAS on the genesis of embryonal rhabdomyosarcoma.

1 reference

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7 January 2021

Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis

1 reference

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7 January 2021

Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors

1 reference

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7 January 2021

RAS signaling dysregulation in human embryonal Rhabdomyosarcoma

1 reference

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7 January 2021

The role of Shp2 (PTPN11) in cancer.

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7 January 2021

Rhabdomyosarcoma in a patient with Noonan syndrome phenotype and review of the literature

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7 January 2021

Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors

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7 January 2021

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20773

7 January 2021

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

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7 January 2021

Structural analysis of autoinhibition in the Ras activator Son of sevenless

1 reference

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7 January 2021

SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients

1 reference

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7 January 2021

Mutational analysis of SOS1 gene in acute myeloid leukemia

1 reference

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7 January 2021

Noonan syndrome and related disorders: genetics and pathogenesis

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Noonan, Costello and cardio-facio-cutaneous syndromes: dysregulation of the Ras-MAPK pathway

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20773

7 January 2021

Allelotype of pediatric rhabdomyosarcoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20773

7 January 2021

SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20773

7 January 2021

Wildtype Kras2 can inhibit lung carcinogenesis in mice

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20773

7 January 2021

Identifiers

DOI

10.1002/GCC.20773

1 reference

17 October 2017

1 reference