Cargando…

Absence of truncating BRIP1 mutations in chromosome 17q-linked hereditary prostate cancer families

BACKGROUND: In a genome-wide scan (GWS) of 175 multiplex prostate cancer (PCa) families from the University of Michigan Prostate Cancer Genetics Project (PCGP), linkage was observed to markers on chromosome 17q21–24, a region that includes two breast cancer susceptibility genes, BRCA1 and BRIP1. BRI...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ray, A M, Zuhlke, K A, Johnson, G R, Levin, A M, Douglas, J A, Lange, E M, Cooney, K A
Formato:	Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2009
Materias:	Genetics and Genomics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795448/ https://www.ncbi.nlm.nih.gov/pubmed/19935797 http://dx.doi.org/10.1038/sj.bjc.6605433

Ejemplares similares

A recurrent truncating germline mutation in the BRIP1/FANCJ gene and susceptibility to prostate cancer
por: Kote-Jarai, Z, et al.
Publicado: (2009)

Candidate target genes for loss of heterozygosity on human chromosome 17q21
por: DeMarchis, L, et al.
Publicado: (2004)

Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci
por: Brown, W M, et al.
Publicado: (2004)

High resolution chromosome 3p, 8p, 9q and 22q allelotyping analysis in the pathogenesis of gallbladder carcinoma
por: Wistuba, I I, et al.
Publicado: (2002)

A two-phase case–control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22
por: Abulí, A, et al.
Publicado: (2011)

Truncating mutations of PPM1D are found in blood DNA samples of lung cancer patients
por: Zajkowicz, A, et al.
Publicado: (2015)

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia
por: Schubert, Stephanie A, et al.
Publicado: (2017)

Cellular responses to ionising radiation of AT heterozygotes: differences between missense and truncating mutation carriers
por: Fernet, M, et al.
Publicado: (2004)

Germline truncating mutations in both MSH2 and BRCA2 in a single kindred
por: Thiffault, I, et al.
Publicado: (2004)

HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer
por: Benusiglio, P R, et al.
Publicado: (2006)

High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer
por: Pärssinen, J, et al.
Publicado: (2007)

MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression
por: Diosdado, B, et al.
Publicado: (2009)

A human cancer-associated truncation of MBD4 causes dominant negative impairment of DNA repair in colon cancer cells
por: Bader, S A, et al.
Publicado: (2007)

CHEK2 variants associate with hereditary prostate cancer
por: Seppälä, E H, et al.
Publicado: (2003)

SKCG-1: a new candidate growth regulatory gene at chromosome 11q23.2 in human sporadic Wilms tumours
por: Singh, K P, et al.
Publicado: (2006)

High-resolution genome-wide allelotype analysis identifies loss of chromosome 14q as a recurrent genetic alteration in astrocytic tumours
por: Hu, J, et al.
Publicado: (2002)

Genetic profiling of chromosome 1 in breast cancer: mapping of regions of gains and losses and identification of candidate genes on 1q
por: Orsetti, B, et al.
Publicado: (2006)

Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer
por: Ponz de Leon, M, et al.
Publicado: (2004)

Prospective study of DNA methylation at chromosome 8q24 in peripheral blood and prostate cancer risk
por: Barry, Kathryn Hughes, et al.
Publicado: (2017)

Gain of 17q in malignant fibrous histiocytoma is associated with a longer disease-free survival and a low risk of developing distant metastasis
por: Weng, W-H, et al.
Publicado: (2003)

MicroRNA-based molecular classification of non-BRCA1/2 hereditary breast tumours
por: Tanic, M, et al.
Publicado: (2013)

DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas
por: Kamieniak, M M, et al.
Publicado: (2013)

Chromosomal radiosensitivity in head and neck cancer patients: evidence for genetic predisposition?
por: De Ruyck, K, et al.
Publicado: (2008)

BRCA1 interactors, RAD50 and BRIP1, as prognostic markers for triple-negative breast cancer severity
por: Katheeja, Muhseena N., et al.
Publicado: (2023)

Smooth-muscle myosin mutations in hereditary non-polyposis colorectal cancer syndrome
por: Vickaryous, N, et al.
Publicado: (2008)

Empirical evaluation of the Q-Genie tool: a protocol for assessment of effectiveness
por: Sohani, Z N, et al.
Publicado: (2016)

Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes
por: Cowell, J K, et al.
Publicado: (2004)

Segmental chromosomal alterations have prognostic impact in neuroblastoma: a report from the INRG project
por: Schleiermacher, G, et al.
Publicado: (2012)

Chromosome aberrations in canine multicentric lymphomas detected with comparative genomic hybridisation and a panel of single locus probes
por: Thomas, R, et al.
Publicado: (2003)

Male breast cancer, age and sex chromosome aneuploidy
por: Jacobs, P A, et al.
Publicado: (2013)

Hereditary Cancer Syndrome in a Family with Double Mutation in BRIP1 and MUTYH Genes
por: D’Elia, Giovanna, et al.
Publicado: (2023)

Narrowing the wingless-2 mutation to a 227 kb candidate region on chicken chromosome 12
por: Webb, A E, et al.
Publicado: (2018)

Coarsening dynamics can explain meiotic crossover patterning in both the presence and absence of the synaptonemal complex
por: Fozard, John A, et al.
Publicado: (2023)

Frequent loss of the AXIN1 locus but absence of AXIN1 gene mutations in adenocarcinomas of the gastro-oesophageal junction with nuclear β-catenin expression
por: Koppert, L B, et al.
Publicado: (2004)

DNA copy number changes in young gastric cancer patients with special reference to chromosome 19
por: Varis, A, et al.
Publicado: (2003)

Multicolour-banding fluorescence in situ hybridisation (mbanding-FISH) to identify recurrent chromosomal alterations in breast tumour cell lines
por: Letessier, A, et al.
Publicado: (2005)

Increased level of chromosomal damage after irradiation of lymphocytes from BRCA1 mutation carriers
por: Kote-Jarai, Z, et al.
Publicado: (2006)

Allelic losses on chromosome 3p are accumulated in relation to morphological changes of lung adenocarcinoma
por: Iijima, H, et al.
Publicado: (2004)

Chromosomal analysis of non-small-cell lung cancer by multicolour fluorescent in situ hybridisation
por: Berrieman, H K, et al.
Publicado: (2004)

A novel gene ZNF862 causes hereditary gingival fibromatosis
por: Wu, Juan, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_v99fl6t81jum199bo5g6shlarc