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

article

Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.3390/GENES10030186
P932PMC publication ID6470759
P698PubMed publication ID30823486

P50authorJacques SimardQ64516110
Daniel SinnettQ47451414
P2093author name stringPenny Soucy
Stéphane Dubois
Manon Ouimet
Yosr Hamdi
Martine Dumont
Pauline Cassart
Martin Leclerc
Martine Tranchant
Guy Reimnitz
M'Hamed Lajmi Lakhal Chaieb
P2860cites workOverexpression of cell division cycle 7 homolog is associated with gene amplification frequency in breast cancer.Q53361331
Functional analysis of human promoter polymorphisms.Q53652155
Screening for germ line TP53 mutations in breast cancer patientsQ58048740
Breast-Cancer Risk in Families with Mutations in PALB2Q59238239
Functional profiling of uncommon VCAM1 promoter polymorphisms prevalent in African American populationsQ80152805
Selection and evaluation of Tag-SNPs using Tagger and HapMapQ82857274
Prediction of breast cancer risk based on profiling with common genetic variantsQ36583004
Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancersQ36742577
Genome-wide association analysis identifies three new breast cancer susceptibility lociQ36842233
beta-Catenin signaling in biological control and cancer.Q36939963
RAP80 and RNF8, key players in the recruitment of repair proteins to DNA damage sitesQ37190148
Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.Q37367871
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.Q37684672
VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysisQ38814549
Hereditary breast and ovarian cancer: new genes in confined pathwaysQ38925408
Global patterns of cis variation in human cells revealed by high-density allelic expression analysisQ39786256
Cdc7-Dbf4 kinase overexpression in multiple cancers and tumor cell lines is correlated with p53 inactivationQ39949011
Functional analysis of polymorphisms in the promoter regions of genes on 22q11.Q40540996
The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsQ41226231
Promoter polymorphisms and transcript levels of nicotinic receptor CHRNA5.Q42928495
Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genomeQ43559819
The Krüppel-like zinc finger protein Glis2 functions as a negative modulator of the Wnt/beta-catenin signaling pathwayQ24296279
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 studiesQ24531993
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility geneQ24615080
A New Statistical Method for Haplotype Reconstruction from Population DataQ27860495
The structure of haplotype blocks in the human genomeQ27860500
Haploview: analysis and visualization of LD and haplotype mapsQ27860955
Unraveling the mechanism of BRCA2 in homologous recombinationQ28242443
Cdc7 inhibition reveals a p53-dependent replication checkpoint that is defective in cancer cellsQ28286189
Genomewide association studies and assessment of the risk of diseaseQ28288414
Characterization of Glis2, a novel gene encoding a Gli-related, Krüppel-like transcription factor with transactivation and repressor functions. Roles in kidney development and neurogenesisQ28508527
Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening studyQ28743906
Large-scale genotyping identifies 41 new loci associated with breast cancer riskQ29416989
Systematic localization of common disease-associated variation in regulatory DNAQ29614895
MatInspector and beyond: promoter analysis based on transcription factor binding sitesQ29616314
Association between common variation in 120 candidate genes and breast cancer riskQ33279162
Global view of enhancer-promoter interactome in human cells.Q33694443
Two decades after BRCA: setting paradigms in personalized cancer care and preventionQ33820594
Wnt/beta-catenin signalingQ34013834
Abundant raw material for cis-regulatory evolution in humansQ34157325
Polymorphisms in DNA repair genes and associations with cancer riskQ34166386
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility allelesQ34546389
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)Q34623703
You Wnt some, you lose some: oncogenes in the Wnt signaling pathwayQ35062431
Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting GenesQ35207476
BRCA1 tumor suppressor network: focusing on its tailQ35861690
Functional analyses of human DNA repair proteins important for aging and genomic stability using yeast geneticsQ35869772
Principles for the post-GWAS functional characterization of cancer risk lociQ35887461
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.Q35940158
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancerQ35996692
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.Q36178189
DNA repair and genome maintenance in Bacillus subtilisQ36194928
RAP80 is critical in maintaining genomic stability and suppressing tumor developmentQ36352398
Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expressionQ36354441
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue3
P407language of work or nameEnglishQ1860
P304page(s)186
P577publication date2019-02-28
P1433published inGenesQ5532699
P1476titleFunctional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control
P478volume10

Reverse relations

cites work (P2860)
Q101148678DICER1-Associated Embryonal Rhabdomyosarcoma and Adenosarcoma of the Gynecologic Tract: Pathology, Molecular Genetics and Indications for Molecular Testing
Q90325395Genome Dashboards: Framework and Examples

Search more.