Cargando…

Analysis of Prostate Cancer Susceptibility Variants in South African Men: Replicating Associations on Chromosomes 8q24 and 10q11

Genome-wide association studies (GWAS) have implicated single nucleotide polymorphisms (SNPs) on chromosomes 2p15, 6q25, 7p15.2, 7q21, 8q24, 10q11, 10q26, 11q13, 17q12, 17q24, 19q13, and Xp11, with prostate cancer (PCa) susceptibility and/or tumour aggressiveness, in populations of African, European...

Descripción completa

Detalles Bibliográficos
Autores principales:	Fernandez, Pedro, Salie, Muneeb, du Toit, Danielle, van der Merwe, Andre
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549549/ https://www.ncbi.nlm.nih.gov/pubmed/26347821 http://dx.doi.org/10.1155/2015/465184

Ejemplares similares

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24
por: Jones, Angela M, et al.
Publicado: (2012)

Significance of common variants on human chromosome 8q24 in relation to the risk of prostate cancer in native Japanese men
por: Liu, Miao, et al.
Publicado: (2009)

Chromosome 15q24 microdeletion syndrome
por: Magoulas, Pilar L, et al.
Publicado: (2012)

Genome‐wide association study identifies gastric cancer susceptibility loci at 12q24.11‐12 and 20q11.21
por: Tanikawa, Chizu, et al.
Publicado: (2018)

Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

The X chromosome and sex-specific effects in infectious disease susceptibility
por: Schurz, Haiko, et al.
Publicado: (2019)

Chromosome 11q13 deletion syndrome
por: Kim, Yu-Seon, et al.
Publicado: (2016)

Chromosome 6q24-related diabetes mellitus
por: Yorifuji, Tohru, et al.
Publicado: (2018)

Germline variation at 8q24 and prostate cancer risk in men of European ancestry
por: Matejcic, Marco, et al.
Publicado: (2018)

Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21
por: Haiman, Christopher A., et al.
Publicado: (2011)

8q24 sequence variants in relation to prostate cancer risk among men of African descent: A case-control study
por: Benford, Marnita L, et al.
Publicado: (2010)

Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
por: Delorme, Richard, et al.
Publicado: (2010)

Identification of a Susceptibility Locus for Severe Adolescent Idiopathic Scoliosis on Chromosome 17q24.3
por: Miyake, Atsushi, et al.
Publicado: (2013)

Analysis of 2 men with t(8;22)(q13;q13) and t(8;14)(q13;q22) chromosomal translocation karyotypes
por: Sun, Qijia, et al.
Publicado: (2022)

ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer
por: Lin, Chun-Lin, et al.
Publicado: (2020)

de novo interstitial deletions at the 11q23.3-q24.2 region
por: Su, Jiasun, et al.
Publicado: (2016)

Previously Unreported Chromosomal Aberrations of t(3;3)(q29;q23), t(4;11)(q21;q23), and t(11;18)(q10;q10) in a Patient with Accelerated Phase Ph+ CML
por: Aydin, Cigdem, et al.
Publicado: (2014)

The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder
por: Hodgetts Morton, Victoria, et al.
Publicado: (2017)

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

Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
por: Zhang, Mingfeng, et al.
Publicado: (2016)

Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry
por: Matejcic, Marco, et al.
Publicado: (2019)

Variant Burkitt-type translocation (8;22)(q24;q11) in plasma cell myeloma
por: Kim, Hanah, et al.
Publicado: (2011)

Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation
por: Mishra, Divya, et al.
Publicado: (2014)

Region 2 of 8q24 is associated with the risk of aggressive prostate cancer in Caribbean men of African descent from Guadeloupe (French West Indies)
por: Cancel-Tassin, Geraldine, et al.
Publicado: (2015)

A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31
por: Barnekow, Elin, et al.
Publicado: (2023)

Frequent loss of heterozygosity on chromosome 17 at 17q11.2-q12 in Barrett's adenocarcinoma.
por: Swift, A., et al.
Publicado: (1995)

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects
por: Al-Zahrani, Jawaher, et al.
Publicado: (2011)

Mosaic duplication of 8q24.1q24.3 detected by chromosomal microarray but not karyotyping in two unrelated fetuses with cardiac defects
por: Lin, Shaobin, et al.
Publicado: (2021)

A duplication at chromosome 11q12.2–11q12.3 is associated with spinocerebellar ataxia type 20
por: Knight, Melanie A., et al.
Publicado: (2008)

New Complex Chromosomal Translocation in Chronic Myeloid Leukaemia: t(9;18;22)(q34;p11;q11)
por: El Andaloussi, Abdeljabar, et al.
Publicado: (2007)

Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2
por: Thye, Thorsten, et al.
Publicado: (2010)

Commentary on “Region 2 of 8q24 is associated with the risk of aggressive prostate cancer in Caribbean men of African descent from Guadeloupe (French West Indies)”
por: Koochekpour, Shahriar
Publicado: (2015)

A novel chromosome 2q24.3‐q32.1 microdeletion in a fetus with multiple malformations
por: Zhu, Mianmian, et al.
Publicado: (2022)

Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo
por: Ikram, M. Kamran, et al.
Publicado: (2010)

Childhood-onset schizophrenia case with 2.2 Mb deletion at chromosome 3p12.2–p12.1 and two large chromosomal abnormalities at 16q22.3–q24.3 and Xq23–q28
por: Rudd, Danielle, et al.
Publicado: (2015)

Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report
por: Mohammadi, Reza, et al.
Publicado: (2021)

A Novel Acquired t(2;4)(q36.1;q24) with a Concurrent Submicroscopic del(4)(q23q24) in An Adult with Polycythemia Vera
por: Kjeldsen, Eigil
Publicado: (2018)

Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population
por: Wang, Linyan, et al.
Publicado: (2018)

Correction: Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo
por: Ikram, M. Kamran, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_e6lndl3vl4hopm65vh4b6phf2a