Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control (Q64087937)

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English	Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control	article

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title

Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control (English)

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author

Jacques Simard

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12

object named as

Jacques Simard

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Daniel Sinnett

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10

object named as

Daniel Sinnett

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author name string

Yosr Hamdi

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1

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Martin Leclerc

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2

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Martine Dumont

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3

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Stéphane Dubois

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4

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Martine Tranchant

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5

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Guy Reimnitz

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6

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Penny Soucy

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7

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Pauline Cassart

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8

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Manon Ouimet

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9

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M'Hamed Lajmi Lakhal Chaieb

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11

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language of work or name

English

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publication date

28 February 2019

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published in

Genes

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volume

10

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issue

3

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page(s)

186

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copyright license

Creative Commons Attribution 4.0 International

start time

28 February 2019

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April 2022 Public Data File from Crossref

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copyrighted

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cites work

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Wnt/beta-catenin signaling

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A New Statistical Method for Haplotype Reconstruction from Population Data

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Characterization of Glis2, a novel gene encoding a Gli-related, Krüppel-like transcription factor with transactivation and repressor functions. Roles in kidney development and neurogenesis

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The structure of haplotype blocks in the human genome

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Abundant raw material for cis-regulatory evolution in humans

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Polymorphisms in DNA repair genes and associations with cancer risk

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You Wnt some, you lose some: oncogenes in the Wnt signaling pathway

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Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

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https://pubmed.ncbi.nlm.nih.gov/30823486

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Functional analysis of human promoter polymorphisms.

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Functional analysis of polymorphisms in the promoter regions of genes on 22q11.

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Haploview: analysis and visualization of LD and haplotype maps

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Cdc7 inhibition reveals a p53-dependent replication checkpoint that is defective in cancer cells

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MatInspector and beyond: promoter analysis based on transcription factor binding sites

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https://pubmed.ncbi.nlm.nih.gov/30823486

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ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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The Krüppel-like zinc finger protein Glis2 functions as a negative modulator of the Wnt/beta-catenin signaling pathway

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Association between common variation in 120 candidate genes and breast cancer risk

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Functional profiling of uncommon VCAM1 promoter polymorphisms prevalent in African American populations

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https://pubmed.ncbi.nlm.nih.gov/30823486

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An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)

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beta-Catenin signaling in biological control and cancer.

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RAP80 and RNF8, key players in the recruitment of repair proteins to DNA damage sites

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Cdc7-Dbf4 kinase overexpression in multiple cancers and tumor cell lines is correlated with p53 inactivation

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Overexpression of cell division cycle 7 homolog is associated with gene amplification frequency in breast cancer.

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PubMed

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Selection and evaluation of Tag-SNPs using Tagger and HapMap

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Genomewide association studies and assessment of the risk of disease

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12 December 2020

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Promoter polymorphisms and transcript levels of nicotinic receptor CHRNA5.

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12 December 2020

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Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

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12 December 2020

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Principles for the post-GWAS functional characterization of cancer risk loci

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12 December 2020

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Unraveling the mechanism of BRCA2 in homologous recombination

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https://pubmed.ncbi.nlm.nih.gov/30823486

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Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Genome-wide association analysis identifies three new breast cancer susceptibility loci

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PubMed

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12 December 2020

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Functional analyses of human DNA repair proteins important for aging and genomic stability using yeast genetics

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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BRCA1 tumor suppressor network: focusing on its tail

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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RAP80 is critical in maintaining genomic stability and suppressing tumor development

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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DNA repair and genome maintenance in Bacillus subtilis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Systematic localization of common disease-associated variation in regulatory DNA

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Large-scale genotyping identifies 41 new loci associated with breast cancer risk

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

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12 December 2020

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Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

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Two decades after BRCA: setting paradigms in personalized cancer care and prevention

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12 December 2020

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Global view of enhancer-promoter interactome in human cells.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Breast-Cancer Risk in Families with Mutations in PALB2

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Prediction of breast cancer risk based on profiling with common genetic variants

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Hereditary breast and ovarian cancer: new genes in confined pathways

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https://pubmed.ncbi.nlm.nih.gov/30823486

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12 December 2020

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Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.

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12 December 2020

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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30823486

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VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis

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Identifiers

DOI

10.3390/GENES10030186

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PMC publication ID

6470759

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PubMed publication ID

30823486

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