Cargando…

Identification of functional genetic variants associated with prostate cancer through analysis of genome-wide genetic and epigenetic datasets

Detalles Bibliográficos
Autores principales:	Tarway, McAnthony, Tang, Wei, Prokunina-Olsson, Ludmila
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2011
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3439059/ http://dx.doi.org/10.1186/gb-2011-12-s1-p24

Ejemplares similares

Whole transcriptome sequencing of normal and tumor bladder tissue samples
por: Tang, Wei, et al.
Publicado: (2011)

Prostate stem cell antigen (PSCA) and risk of bladder cancer: linking genotypes to functional mechanisms
por: Mumy, Adam, et al.
Publicado: (2011)

Detection of bladder, breast and prostate cancer using serum and tissue miRNA profiling
por: Porter-Gill, Patricia, et al.
Publicado: (2011)

Genetics of the Human Interferon Lambda Region
por: Prokunina-Olsson, Ludmila
Publicado: (2019)

Functional exploration of CCNE1 splicing forms as a possible link to bladder cancer susceptibility
por: Kohaar, Indu, et al.
Publicado: (2011)

A novel functional variant in 8q24 is associated with regulation of prostate stem cell antigen (PSCA) gene expression and bladder cancer risk
por: Fu, Yi-Ping, et al.
Publicado: (2011)

Joint analysis of genome-wide genetic variants associated with gene expression and disease susceptibility
por: Yu, Chen-Hsin, et al.
Publicado: (2011)

Identification of rare genetic variants in Juvenile Idiopathic Arthritis using whole exome sequencing
por: Sanchez, E, et al.
Publicado: (2015)

Variant CAPS in an adult- the use of genetics
por: Rozenbam, M, et al.
Publicado: (2015)

Common Genetic Variants in miR-1206 (8q24.2) and miR-612 (11q13.3) Affect Biogenesis of Mature miRNA Forms
por: Kim, Hye Kyung, et al.
Publicado: (2012)

Improving variant calling by incorporating known genetic variants into read alignment
por: Vo, Nam S, et al.
Publicado: (2015)

Genetic silencing of sGC β1 in cancer: role of epigenetic regulation
por: Sotolongo, Alex, et al.
Publicado: (2013)

Identification and characterization of disease causing genetic variant by conventional genotyping and whole genome sequencing in familial tooth agenesis
por: Sarkar, Tanmoy, et al.
Publicado: (2014)

A new set-valued system identification approach to identifying rare genetic variants for ordered categorical phenotype
por: Bi, Wenjian, et al.
Publicado: (2014)

Genetic diversity of Bertholletia excelsa, an Amazonian species of wide distribution
por: Sujii, Patrícia, et al.
Publicado: (2011)

Host genetic variants associated with community-acquired pneumonia
por: Salnikova, LE, et al.
Publicado: (2013)

Are genetic variants of Caspase-1 and Cryopyrin associated with systemic JIA?
por: Stock, CJ, et al.
Publicado: (2008)

Association of HLA DRB variants to genetic predisposition to rheumatoid arthritis
por: Jarullah, Bushra S
Publicado: (2014)

Influence of genetic variants in the susceptibility and outcome of influenza virus infection
por: Sole-Violan, J, et al.
Publicado: (2015)

P20-03. Identification of low frequency genetic variants during acute and early infection by parallel-allele specific sequencing
por: Pavlicek, JW, et al.
Publicado: (2009)

Genetic Variant as a Selection Marker for Anti–Prostate Stem Cell Antigen Immunotherapy of Bladder Cancer
por: Kohaar, Indu, et al.
Publicado: (2013)

Toward the identification of genetic determinants of breast cancer immune responsiveness
por: Simeone, Ines, et al.
Publicado: (2015)

Susceptibility to childhood onset rheumatoid arthritis: investigation of a weighted genetic risk score that integrates cumulative effects of five genetic risk variants
por: Prahalad, Sampath, et al.
Publicado: (2012)

Genetic variants in inflammatory cytokines and angiogenesis associated with diabetic nephropathy- A meta-analysis
por: Siddiqui, Khalid, et al.
Publicado: (2014)

Evaluation of galectin-3 genetic variants and lipid profile in RA patients in North Indian population
por: Kaur, Tarnjeet, et al.
Publicado: (2014)

Association between INADL genetic variant and a subgroup with high risk for TMD in the OPPERA study
por: Smith, Shad B, et al.
Publicado: (2014)

Genetic basis of common human disease: insight into the role of nonsynonymous SNPs from genome-wide association studies
por: Pal, Lipika R, et al.
Publicado: (2011)

Genome-wide analysis of An. gambiae s.s. reveal no genetic differences between indoor- and outdoor-biting populations in The Gambia
por: Fabrigar, Danica
Publicado: (2014)

Association of interleukin-10 promoter genetic variants with T-cell and B-cell activation in HIV-1 infection
por: Naicker, D, et al.
Publicado: (2012)

Genetic variants involved in specialized DNA replication and their relation with breast cancer risk, disease progression and patient prognosis
por: Brandalize, Ana PC, et al.
Publicado: (2013)

A transgenic in vitro cell model for the analysis of proinflammatory effects of naturally occurring genetic variants of caspase-1
por: Schulze, F, et al.
Publicado: (2015)

P072: Genetic environment and phenotypic analysis of a novel blaKPC variant produced by Klebsiella pneumonia
por: Mu, J-J
Publicado: (2013)

Pain in the network of genetic and epigenetic control
por: Lötsch, Jörn, et al.
Publicado: (2014)

Genetic and epigenetic changes in early carcinogenesis
por: Tlsty, TD
Publicado: (2005)

Association of haptoglobin genetic polymorphism with overall survival in advanced castration-resistant prostate cancer patients with personalized peptide vaccination
por: Komatsu, Nobukazu, et al.
Publicado: (2013)

P07-09. Contemporaneous transmission of genetically distinct HIV variants from a single donor to two recipients
por: English, S, et al.
Publicado: (2009)

Constraining neural microcircuits with surrogate physiological data and genetic algorithms
por: Eager, Michael A, et al.
Publicado: (2007)

Computer-guided discovery of epigenetics drugs: molecular modeling and identification of inhibitors of DNMT1
por: Yoo, Jakyung, et al.
Publicado: (2012)

Early identification of monogenic diabetes: implications on medical treatment and genetic counselling for an adolescent girl with MODY3
por: Wong, Wai-chun, et al.
Publicado: (2015)

Genome-wide mapping of chromatin marks from 1,000 cells to study epigenetic reprogramming in primordial germ cells
por: Brind’Amour, Julie, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_scuf21qdpg9ld9r3ksgif6gteq