Limited relevance of the CHEK2 gene in hereditary breast cancer. - Wikidata - wikimedia - TriplyDB

Limited relevance of the CHEK2 gene in hereditary breast cancer.

Limited relevance of the CHEK2 gene in hereditary breast cancer.

http://www.wikidata.org/entity/Q47738885

about

Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer.The CHEK2 gene and inherited breast cancer susceptibility Linkage disequilibrium mapping of CHEK2: common variation and breast cancer risk.CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer.Current perspectives on CHEK2 mutations in breast cancer.Contribution of the Defective BRCA1, BRCA2 and CHEK2 Genes to the Familial Aggregation of Breast Cancer: a Simulation Study Based on the Swedish Family-Cancer Database Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma.Identification of Novel Susceptibility Genes for Breast Cancer - Genome-Wide Association Studies or Evaluation of Candidate Genes?Breast cancer susceptibility: current knowledge and implications for genetic counselling CHEK2 is a multiorgan cancer susceptibility gene.Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan.Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.Hereditary breast and ovarian cancer: new genes, new treatments, new concepts.Low prevalence of CHEK2 gene mutations in multiethnic cohorts of breast cancer patients in Malaysia.The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population.CHEK2 contribution to hereditary breast cancer in non-BRCA families Frequency of the CHEK2 1100delC mutation among women with early-onset and bilateral breast cancer.Pitfalls and caveats in BRCA sequencing.Functional single nucleotide polymorphism-based association studies.Clinical relevance of CHEK2 and NBN mutations in the macedonian population The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype.Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland.Genomics and breast cancer: the different levels of inherited susceptibility.CHEK2 I157T associates with familial and sporadic colorectal cancer.Irrelevance of CHEK2 variants to diagnosis of breast/ovarian cancer predisposition in Polish cohort.CHEK2*1100delC is not an important high-risk gene in families with hereditary prostate cancer in southern Sweden.A recurrent CHEK2 p.H371Y mutation is associated with breast cancer risk in Chinese women.

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P2860

Limited relevance of the CHEK2 gene in hereditary breast cancer.

http://www.wikidata.org/entity/Q47738885

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2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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2004年學術文章

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name

Limited relevance of the CHEK2 gene in hereditary breast cancer.

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Limited relevance of the CHEK2 gene in hereditary breast cancer.

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type

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Limited relevance of the CHEK2 gene in hereditary breast cancer.

@en

Limited relevance of the CHEK2 gene in hereditary breast cancer.

@nl

prefLabel

Limited relevance of the CHEK2 gene in hereditary breast cancer.

@en

Limited relevance of the CHEK2 gene in hereditary breast cancer.

@nl

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International Journal of Cancer

P1476

Limited relevance of the CHEK2 gene in hereditary breast cancer.

@en

P2093

Andrea Pietschmann

http://www.w3.org/2001/XMLSchema#string

Astrid Golla

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Beate Betz

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Caroline Nestle-Krämling

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Celia von Lindern

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Christine Hüttner

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Dieter Niederacher

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Katrin Bandick

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Kerstin Rhiem

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Marion Kiechle

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P2860

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

The ATM-Chk2-Cdc25A checkpoint pathway guards against radioresistant DNA synthesis

Frequency of CHEK2*1100delC in New York breast cancer cases and controls

Structural and functional versatility of the FHA domain in DNA-damage signaling by the tumor suppressor kinase Chk2

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

Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility

CHK2 kinase--a busy messenger.

Mutation analysis of the CHK2 gene in families with hereditary breast cancer.

CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer.

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320-325

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10.1002/IJC.20073

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3

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110

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Rita Schmutzler

Barbara Wappenschmidt

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2004-06-01T00:00:00Z

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8609018

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15095295

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