Functional analysis of a CDKN2A 5'UTR germline variant associated with pancreatic cancer development.

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Functional analysis of a CDKN2A 5'UTR germline variant associated with pancreatic cancer development.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Functional analysis of a CDKN2 ...... pancreatic cancer development.

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Functional analysis of a CDKN2 ...... pancreatic cancer development.

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Functional analysis of a CDKN2 ...... pancreatic cancer development.

@en

Functional analysis of a CDKN2 ...... pancreatic cancer development.

@nl

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Functional analysis of a CDKN2 ...... pancreatic cancer development.

@en

Functional analysis of a CDKN2 ...... pancreatic cancer development.

@nl

P1476

Functional analysis of a CDKN2 ...... pancreatic cancer development.

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P2093

Alberto Inga

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Giovanna Bianchi-Scarrà

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Giuseppe Fornarini

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Stefania Sciallero

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Virginia Andreotti

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P2860

TERT promoter mutations in familial and sporadic melanoma

Genetic predisposition to pancreatic cancer.

Role of non-coding sequence variants in cancer.

Whole genomes redefine the mutational landscape of pancreatic cancer.

Identification, genetic testing, and management of hereditary melanoma.

A single nucleotide polymorphism in the p53 pathway interacts with gender, environmental stresses and tumor genetics to influence cancer in humans.

The 5'-untranslated region of p16INK4a melanoma tumor suppressor acts as a cellular IRES, controlling mRNA translation under hypoxia through YBX1 binding.

Familial skin cancer syndromes: Increased melanoma risk.

CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment.

Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.

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e0189123

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scholarly article

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10.1371/JOURNAL.PONE.0189123

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English

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P478

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P577

2017-12-07T00:00:00Z

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29216274

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5720692

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