CHEK2 mutations and the risk of papillary thyroid cancer. - Wikidata - wikimedia - TriplyDB

CHEK2 mutations and the risk of papillary thyroid cancer.

CHEK2 mutations and the risk of papillary thyroid cancer.

http://www.wikidata.org/entity/Q52976068

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DNA repair genes implicated in triple negative familial non-BRCA1/2 breast cancer predisposition.Rapid Detection Method for the Four Most Common CHEK2 Mutations Based on Melting Profile Analysis A new POT1 germline mutation-expanding the spectrum of POT1-associated cancers.Prevalence of the CHEK2 R95* germline mutation Cancerouspdomains: comprehensive analysis of cancer type-specific recurrent somatic mutations in proteins and domains.Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication.Investigating the association of rs2910164 with cancer predisposition in an Irish cohort.Inherited pancreatic cancer.Prognostic value of long non-coding RNA BLACAT1 in patients with papillary thyroid carcinoma.Molecular characterization of papillary thyroid carcinoma: a potential three-lncRNA prognostic signature Mutations of the CHEK2 gene in patients with cancer and their presence in the Latin American population Thyroid cancers of follicular origin in a genomic light: in-depth overview of common and unique molecular marker candidates

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P2860

CHEK2 mutations and the risk of papillary thyroid cancer.

http://www.wikidata.org/entity/Q52976068

description

2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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name

CHEK2 mutations and the risk of papillary thyroid cancer.

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CHEK2 mutations and the risk of papillary thyroid cancer.

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type

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CHEK2 mutations and the risk of papillary thyroid cancer.

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CHEK2 mutations and the risk of papillary thyroid cancer.

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CHEK2 mutations and the risk of papillary thyroid cancer.

@en

CHEK2 mutations and the risk of papillary thyroid cancer.

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International Journal of Cancer

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CHEK2 mutations and the risk of papillary thyroid cancer.

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P2093

Artur Kowalik

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Beata Kozak-Klonowska

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Dominika Wokołorczyk

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Katarzyna Lizis-Kolus

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Małgorzata Chłopek

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Monika Siołek

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Ping Sun

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Stanisław Góźdż

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Wojciech Kluźniak

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P2860

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

Finding the missing heritability of complex diseases

Ataxia telangiectasia-mutated phosphorylates Chk2 in vivo and in vitro

Mammalian Chk2 is a downstream effector of the ATM-dependent DNA damage checkpoint pathway

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

Chk1 and Chk2 kinases in checkpoint control and cancer

Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.

Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma.

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype.

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548-552

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scholarly article

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10.1002/IJC.29426

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3

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137

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Cezary Cybulski

Aldona Kowalska

Danuta Gąsior-Perczak

Steven A. Narod

Agnieszka Walczyk

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2015-01-28T00:00:00Z

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25583358

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