Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene. - Wikidata - awgldk - TriplyDB

Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene.

Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene.

http://www.wikidata.org/entity/Q53525497

about

Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis.Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia Heterozygous p.I171V mutation of the NBN gene as a risk factor for lung cancer development.NBS1 Heterozygosity and Cancer Risk.The MRN protein complex genes: MRE11 and RAD50 and susceptibility to head and neck cancers.NBN Gene Polymorphisms and Cancer Susceptibility: A Systemic Review.NBS1 Glu185Gln polymorphism and cancer risk: update on current evidence.Assessment of laryngeal cancer in patients younger than 40 years.NBS1 rs2735383 polymorphism is associated with an increased risk of laryngeal carcinoma.Genetic variants in ATM, H2AFX and MRE11 genes and susceptibility to breast cancer in the polish population.Association of polymorphisms and haplotypes of the NBN gene with laryngeal cancer and multiple primary tumors of the head and neck.

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Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene.

http://www.wikidata.org/entity/Q53525497

description

2007 nî lūn-bûn

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年學術文章

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2007年學術文章

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2007年學術文章

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name

Increased risk of larynx cance ...... 71V mutation of the NBS1 gene.

@en

Increased risk of larynx cance ...... 71V mutation of the NBS1 gene.

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type

label

Increased risk of larynx cance ...... 71V mutation of the NBS1 gene.

@en

Increased risk of larynx cance ...... 71V mutation of the NBS1 gene.

@nl

prefLabel

Increased risk of larynx cance ...... 71V mutation of the NBS1 gene.

@en

Increased risk of larynx cance ...... 71V mutation of the NBS1 gene.

@nl

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Increased risk of larynx cance ...... 171V mutation of the NBS1 gene

@en

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Iwona Ziólkowska

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Jerzy Nowak

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Maria Mosor

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Monika Pernak-Schwarz

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P2860

NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domain

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response

Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group

Heterozygous carriers of Nijmegen Breakage Syndrome have a distinct gene expression phenotype

Increased NBS1 expression is a marker of aggressive head and neck cancer and overexpression of NBS1 contributes to transformation

Polymorphisms of DNA repair genes and risk of non-small cell lung cancer.

Direct activation of the ATM protein kinase by the Mre11/Rad50/Nbs1 complex.

Second primary tumors in patients with head and neck squamous cell carcinoma.

Increased risk of gastrointestinal lymphoma in carriers of the 657del5 NBS1 gene mutation.

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11

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