A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics - Wikidata - awgldk - TriplyDB

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

http://www.wikidata.org/entity/Q34015399

about

New genomic structure for prostate cancer specific gene PCA3 within BMCC1: implications for prostate cancer detection and progression A comparison of genetic risk score with family history for estimating prostate cancer risk East meets West: ethnic differences in prostate cancer epidemiology between East Asians and Caucasians Germline mutations in HOXB13 and prostate-cancer risk Prostate cancer susceptibility loci: finding the genes A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Genome-wide linkage analysis of inguinal hernia in pigs using affected sib pairs.Chromosomal regions associated with prostate cancer risk localize to lamin B-deficient microdomains and exhibit reduced gene transcription.Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.Mutational landscape of candidate genes in familial prostate cancer Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus Dysregulation of the homeobox transcription factor gene HOXB13: role in prostate cancer.Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease Mitochondrial haplogroups and polymorphisms reveal no association with sporadic prostate cancer in a southern European population.Familial testicular cancer: interest in genetic testing among high-risk family members.The expression level of miR-18b in hepatocellular carcinoma is associated with the grade of malignancy and prognosis.Common variation in the BRCA1 gene and prostate cancer risk.ARLTS1 and prostate cancer risk--analysis of expression and regulation.Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer.Fine-mapping the 2q37 and 17q11.2-q22 loci for novel genes and sequence variants associated with a genetic predisposition to prostate cancer Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance.GWAS SNP Replication among African American and European American men in the North Carolina-Louisiana prostate cancer project (PCaP)ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer Contribution of HPC1 (RNASEL) and HPCX variants to prostate cancer in a founder population.Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses.Germline Variants in Asporin Vary by Race, Modulate the Tumor Microenvironment, and Are Differentially Associated with Metastatic Prostate Cancer HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG The balance between heritable and environmental aetiology of human disease.What should a urologist know about hereditary predisposition to prostate cancer?HOXB13 mutations in a population-based, case-control study of prostate cancer.HOXB13 mutation and prostate cancer: studies of siblings and aggressive disease The role of the BRCA2 gene in susceptibility to prostate cancer revisited Prostate cancer risk-associated genetic markers and their potential clinical utility A population-based analysis of clustering identifies a strong genetic contribution to lethal prostate cancer HOXB13 and other high penetrant genes for prostate cancer.Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage Sequence variants at 22q13 are associated with prostate cancer risk.

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A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

http://www.wikidata.org/entity/Q34015399

description

2005 nî lūn-bûn

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2005 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2005 թվականի հունիսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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A combined genomewide linkage ...... m for prostate cancer genetics

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A combined genomewide linkage ...... m for prostate cancer genetics

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A combined genomewide linkage ...... m for prostate cancer genetics

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A combined genomewide linkage ...... m for prostate cancer genetics

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A combined genomewide linkage ...... m for prostate cancer genetics

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A combined genomewide linkage ...... m for prostate cancer genetics

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A combined genomewide linkage ...... m for prostate cancer genetics

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A combined genomewide linkage ...... m for prostate cancer genetics

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ACTANE Consortium

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Agnes Baffoe-Bonnie

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Alice S Whittemore

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Aubrey R Turner

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Bao-Li Chang

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Caroline E Mohai

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Charles M Ewing

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Chih-Lin Hsieh

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Chris Evans

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Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium

A candidate prostate cancer susceptibility gene at chromosome 17p

Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

Linkage of early-onset familial breast cancer to chromosome 17q21

Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search

Parametric and nonparametric linkage analysis: a unified multipoint approach

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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A genome screen of families with multiple cases of prostate cancer: evidence of genetic heterogeneity.

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Elaine Ostrander

Henrik Grönberg

Graham G. Giles

William D Foulkes

Kathleen A. Cooney

Joan Bailey-Wilson

Johanna Schleutker

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