Hereditary gastrointestinal stromal tumors sharing the KIT Exon 17 germline mutation p.Asp820Tyr develop through different cytogenetic progression pathways (Q62122383)

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scientific article published on 21 October 2009

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English	Hereditary gastrointestinal stromal tumors sharing the KIT Exon 17 germline mutation p.Asp820Tyr develop through different cytogenetic progression pathways	scientific article published on 21 October 2009

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10 February 2020

Hereditary gastrointestinal stromal tumors sharing the KIT Exon 17 germline mutation p.Asp820Tyr develop through different cytogenetic progression pathways (English)

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10 February 2020

Manuela Pinheiro

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10 February 2020

Manuel R. Teixeira

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10 February 2020

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Mara Silva

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10 February 2020

Marta Soares

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Hugo Duarte

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Camila Coutinho

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10 February 2020

Carlos Lopes

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10 February 2020

Lúcio Santos

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10 February 2020

Artur L Bastos

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10 February 2020

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1 February 2010

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10 February 2020

Genes, Chromosomes and Cancer

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10 February 2020

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91-98

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10 February 2020

Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa

1 reference

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1 reference

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Polyclonal nature of diffuse proliferation of interstitial cells of Cajal in patients with familial and multiple gastrointestinal stromal tumours

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Imatinib inhibits various types of activating mutant kit found in gastrointestinal stromal tumors

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7 January 2021

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Evolution from heterozygous to homozygous KIT mutation in gastrointestinal stromal tumor correlates with the mechanism of mitotic nondisjunction and significant tumor progression.

1 reference

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PDGFRA germline mutation in a family with multiple cases of gastrointestinal stromal tumor

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Molecular pathobiology of gastrointestinal stromal sarcomas.

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KIT mutations are common in incidental gastrointestinal stromal tumors one centimeter or less in size

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Diagnostic morphological features of PDGFRA-mutated gastrointestinal stromal tumors: molecular genetic and histologic analysis of 60 cases of gastric gastrointestinal stromal tumors

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Cause of familial and multiple gastrointestinal autonomic nerve tumors with hyperplasia of interstitial cells of Cajal is germline mutation of the c-kit gene

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Germline-activating mutation in the kinase domain of KIT gene in familial gastrointestinal stromal tumors

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A new familial GIST identified

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Clinical significance of oncogenic KIT and PDGFRA mutations in gastrointestinal stromal tumours

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Familial gastrointestinal stromal tumor with hyperpigmentation: association with a germline mutation of the c-kit gene

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A mouse model of a human multiple GIST family with KIT-Asp820Tyr mutation generated by a knock-in strategy

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Familial gastrointestinal stromal tumours with germline mutation of the KIT gene

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The location of KIT and PDGFRA gene mutations in gastrointestinal stromal tumours is site and phenotype associated

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Pleomorphic characteristics of a germ-line KIT mutation in a large kindred with gastrointestinal stromal tumors, hyperpigmentation, and dysphagia

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Identifiers

10.1002/GCC.20720

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10 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

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10 February 2020

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