About: Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific journal article

Attributes	Values
rdf:type	Item
description	articolo scientifico (it) artículu científicu espublizáu en 2013 (ast) 2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в жовтні 2013 (uk) 2013 թվականի հոտեմբերին հրատարակված գիտական հոդված (hy) مقالة علمية (نشرت في أكتوبر 2013) (ar) wetenschappelijk artikel (gepubliceerd op 2013/10/01) (nl) scientific journal article (en) im Oktober 2013 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28943335-B8091E1B-93C1-49F9-B01D-2C22F7C40162
publication date	2013-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28943335-DD1AC2CB-2378-4FF5-9C09-71F01CDF5F87
language of work or name	English
cites work	wds:Q28943335-022B33B7-9125-4A87-A83C-C7E5441A31D2 wds:Q28943335-090574F9-F7D9-4601-AE50-54D2BE2B72CE wds:Q28943335-0E0DAF1C-F3D3-4A50-980C-1B5895894154 wds:Q28943335-11713194-FA4D-4CF5-806F-1D5C853B750F wds:Q28943335-15599B56-B6CB-4530-A2A6-6C9EC32319FC wds:Q28943335-1579AB38-828E-43EB-AA53-5AF154403EF1 wds:Q28943335-15CEA3BE-6A03-45A4-A5B3-255BD5AD475B wds:Q28943335-18E4B3D4-F361-43AA-9565-4A82E4AC0FD1 wds:Q28943335-1DA51D43-98C2-4F69-819B-3277745036BC wds:Q28943335-29495218-934A-4AD4-8841-AC3A2FBDB312 wds:Q28943335-2F00CB10-1969-40E8-83BA-430C455A020E wds:Q28943335-30D6F1D1-0BAA-4C69-8592-96904DD7C1B2 wds:Q28943335-313CFB0C-BA00-444D-B7E4-FA4BC1F1576C wds:Q28943335-32E06A0A-8D32-4EBE-B301-D60CBFA101BB wds:Q28943335-33401FC3-CDA0-4616-B572-EA0CDD07B667 wds:Q28943335-34D3DF4D-CBC7-4610-BF77-0AEE09184549 wds:Q28943335-366ABB6D-E8B4-46F0-B9BF-E34352AAEF9F wds:Q28943335-3A7EB81E-15A1-4DF5-A279-189C9D90BB37 wds:Q28943335-3AFD6052-50DF-4AF4-99E9-37FA064FD405 wds:Q28943335-440832D3-59EE-48DC-806F-E14C891B76C1 wds:Q28943335-5C501B79-D472-4516-8ED1-7F888383917F wds:Q28943335-5DA30305-9138-41AD-B217-488B6F784812 wds:Q28943335-600AD9BD-655A-4D9F-96FF-9AB7F549A3FD wds:Q28943335-670169E7-5E7C-42D9-B3A0-00716AB93263 wds:Q28943335-7B0AC380-1705-4AB0-B885-431C005C2F86 wds:Q28943335-814D1B07-7702-4362-A281-5D8E72575A7B wds:Q28943335-86852CE8-9B55-4C7D-B82A-9560E699AF33 wds:Q28943335-94C957DD-57CD-4F56-BF18-D2506CC81335 wds:Q28943335-99C5504C-E44E-4F16-9A14-4D578A22AFF6 wds:Q28943335-A7CB0B44-C0C9-45F8-9BCF-E4D745756AEE wds:Q28943335-AA94AB18-CC51-4052-91BB-83F04DE4DA8A wds:Q28943335-AE7B4542-7C76-44EC-8FD6-78EAF04CE244 wds:Q28943335-B8014C59-477E-48AD-AB78-9C598CEF44C6 wds:Q28943335-B85FF6BF-3B9A-451E-BFE2-B9D31B75DDEF wds:Q28943335-BE01B291-3539-45F8-AAB7-0953F64EFE11 wds:Q28943335-C5DBE319-FB5F-4149-B45E-758ADA264F65 wds:Q28943335-C902F736-3C1A-4B2E-83DC-6BD335124161 wds:Q28943335-D3B30D6A-285F-4B2F-A293-90E1F027987D wds:Q28943335-D67727A4-1097-4709-A06A-2A1FAF3E912F wds:Q28943335-D87FAEAD-359D-463B-B23D-F28E8820A35B wds:Q28943335-DA6D6E89-C219-4C5C-B215-5AD2729215EE wds:Q28943335-DE7B9BF1-BEEC-489C-B63C-C098C4EE1ED4 wds:Q28943335-DE7C61B4-3B09-409D-9881-A51DF83E9BA6 wds:Q28943335-E38CD5C6-59B1-479E-B6C2-B041B5513B59 wds:Q28943335-EE277B01-4CE8-41BA-A2E6-4D465CE290EC wds:Q28943335-F049C08D-A7C9-4B5B-8B1B-B190980B67AC wds:Q28943335-FA86BAC1-6398-4486-B73A-1E0A62701B7B wds:Q28943335-FEF8E7F3-81A0-437B-B640-EE55AFEE747E
cites work	METAL: fast and efficient meta-analysis of genomewide association scans A statistical method for predicting classical HLA alleles from SNP data International Myeloma Working Group molecular classification of multiple myeloma: spotlight review. HLA*IMP--an integrated framework for imputing classical HLA alleles from SNP genotypes Cohort profile: 1958 British birth cohort (National Child Development Study). Multiple Myeloma A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3) Discovery and characterization of chromatin states for systematic annotation of the human genome The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma PLINK: a tool set for whole-genome association and population-based linkage analyses The structure of haplotype blocks in the human genome Quantifying heterogeneity in a meta-analysis Principal components analysis corrects for stratification in genome-wide association studies Integration of global SNP-based mapping and expression arrays reveals key regions, mechanisms, and genes important in the pathogenesis of multiple myeloma Atacicept (TACI-Ig) inhibits growth of TACI(high) primary myeloma cells in SCID-hu mice and in coculture with osteoclasts A new multipoint method for genome-wide association studies by imputation of genotypes Common regulatory variation impacts gene expression in a cell type-dependent manner A fine-scale map of recombination rates and hotspots across the human genome The architecture of gene regulatory variation across multiple human tissues: the MuTHER study Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Facto Relative impact of nucleotide and copy number variation on gene expression phenotypes A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value Multiple myeloma. Role of polycomb group proteins in stem cell self-renewal and cancer. Population structure, differential bias and genomic control in a large-scale, case-control association study Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk Combining information regarding chromosomal aberrations t(4;14) and del(17p13) with the International Staging System classification allows stratification of myeloma patients undergoing autologous stem cell transplantation Patterns of cis regulatory variation in diverse human populations National study of colorectal cancer genetics Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma The clinical significance of cytogenetic studies in 100 patients with multiple myeloma, plasma cell leukemia, or amyloidosis Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. Loss of TACI causes fatal lymphoproliferation and autoimmunity, establishing TACI as an inhibitory BLyS receptor Role of the chromobox protein CBX7 in lymphomagenesis. Genome-wide associations of gene expression variation in humans First-line treatment with zoledronic acid as compared with clodronic acid in multiple myeloma (MRC Myeloma IX): a randomised controlled trial GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 195 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software