(Q33467074)

27 July 2017

title

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 (English)

1 reference

27 July 2017

1 reference

Sylvie Desjardins

1

1 reference

27 July 2017

Joly Charles Beauparlant

2

1 reference

27 July 2017

Yvan Labrie

3

1 reference

27 July 2017

Geneviève Ouellette

4

1 reference

27 July 2017

Francine Durocher

5

1 reference

27 July 2017

INHERIT BRCAs

6

1 reference

27 July 2017

language of work or name

English

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publication date

12 June 2009

1 reference

27 July 2017

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27 July 2017

volume

9

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27 July 2017

page(s)

181

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A field synopsis on low-penetrance variants in DNA repair genes and cancer susceptibility

27 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Fine temporal analysis of DHT transcriptional modulation of the ATM/Gadd45g signaling pathways in the mouse uterus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

A potential link between alternative splicing of the NBS1 gene and DNA damage/environmental stress

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Functional analysis of the Myostatin gene promoter in sheep

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

WHAP: haplotype-based association analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Infrequent mutation of ATBF1 in human breast cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Mild Nijmegen breakage syndrome phenotype due to alternative splicing

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Impaired DNA double strand break repair in cells from Nijmegen breakage syndrome patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

ATBF1-a messenger RNA expression is correlated with better prognosis in breast cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

The role of Cdx proteins in intestinal development and cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Single nucleotide polymorphisms in breast cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Susceptibility to killer T cells of gastric cancer cells enhanced by Mitomycin-C involves induction of ATBF1 and activation of p21 (Waf1/Cip1) promoter.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

ESEfinder: A web resource to identify exonic splicing enhancers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Cancer biology. A matter of dosage

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Radiosensitivity of ataxia telangiectasia and Nijmegen breakage syndrome homozygotes and heterozygotes as determined by three-color FISH chromosome painting

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Double-strand breaks and tumorigenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

DNA double strand break repair and chromosomal translocation: lessons from animal models

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Myb-interacting protein, ATBF1, represses transcriptional activity of Myb oncoprotein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Improved splice site detection in Genie

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instability.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

A human alpha-fetoprotein enhancer-binding protein, ATBF1, contains four homeodomains and seventeen zinc fingers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

Nijmegen Breakage Syndrome mutations and risk of breast cancer

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Breast cancer risk is associated with the genes encoding the DNA double-strand break repair Mre11/Rad50/Nbs1 complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Cancer risk of heterozygotes with the NBN founder mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Polymorphisms in DNA repair genes, medical exposure to ionizing radiation, and breast cancer risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Association of ionizing radiation-induced foci of NBS1 with chromosomal instability and breast cancer susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

The R215W mutation in NBS1 impairs gamma-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Chromosomal aberrations in tire plant workers and interaction with polymorphisms of biotransformation and DNA repair genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Haploinsufficient prostate tumor suppression by Nkx3.1: a role for chromatin accessibility in dosage-sensitive gene regulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

The emerging landscape of breast cancer susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-9-181

Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL).

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702391

NBS1 variant I171V and breast cancer risk

31 October 2018

1 reference

12 December 2020

Chromosome instability and nibrin protein variants in NBS heterozygotes

1 reference

12 December 2020

Polygenic inheritance of breast cancer: Implications for design of association studies

1 reference

12 December 2020

First case of aplastic anemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2407-9-181

1 reference

Dimensions Publication ID

27 July 2017

0 references

1 reference

27 July 2017

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