Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis. - Wikidata - wikimedia - TriplyDB

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

http://www.wikidata.org/entity/Q35137159

about

SCT for severe autoimmune diseases: consensus guidelines of the European Society for Blood and Marrow Transplantation for immune monitoring and biobanking Chronic cerebrospinal venous insufficiency and multiple sclerosis SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients.Copy number variation in African Americans.CD4 T-Cell-mediated immune response to prostatic proteins in HLA-DRB1*1503 transgenic mice and identification of a novel HLA-DRB1*1503-restricted T-cell epitope from human prostatic acid phosphatase.CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.Multiple sclerosis susceptibility alleles in African Americans.Refining the association of MHC with multiple sclerosis in African Americans.Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.Exomic sequencing of immune-related genes reveals novel candidate variants associated with alopecia universalis.Electrostatic modifications of the human leukocyte antigen-DR P9 peptide-binding pocket and susceptibility to primary sclerosing cholangitis A single-nucleotide polymorphism in serine-threonine kinase 11, the gene encoding liver kinase B1, is a risk factor for multiple sclerosis Genomic instability of human embryonic stem cell lines using different passaging culture methods.Association between the Advanced Glycosylation End Product-Specific Receptor Gene and Cardiovascular Death in Older Men Myelin basic protein-specific TCR/HLA-DRB5*01:01 transgenic mice support the etiologic role of DRB5*01:01 in multiple sclerosis.The immunogenetics of multiple sclerosis: A comprehensive review.Variation within DNA repair pathway genes and risk of multiple sclerosis.TRPV1 gates tissue access and sustains pathogenicity in autoimmune encephalitis.Genetic risk variants in African Americans with multiple sclerosis Shared Genetic Etiology of Autoimmune Diseases in Patients from a Biorepository Linked to De-identified Electronic Health Records.The killer immunoglobulin-like receptor KIR3DL1 in combination with HLA-Bw4 is protective against multiple sclerosis in African Americans From genes to function: the next challenge to understanding multiple sclerosis.Multiple sclerosis genetics--is the glass half full, or half empty?Bridging the gap from genetic association to functional understanding: the next generation of mouse models of multiple sclerosis.The genetics of multiple sclerosis: an up-to-date review.Molecular mechanisms for contribution of MHC molecules to autoimmune diseases Identifying patient subtypes in multiple sclerosis and tailoring immunotherapy: challenges for the future.Transcriptional dysregulation of Interferome in experimental and human Multiple Sclerosis.Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array.Heterogeneity in multiple sclerosis: scratching the surface of a complex disease.Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel.Altered expression of the plasminogen activation pathway in peripheral blood mononuclear cells in multiple sclerosis: possible pathomechanism of matrix metalloproteinase activation.Combined microRNA and mRNA expression analysis in pediatric multiple sclerosis: an integrated approach to uncover novel pathogenic mechanisms of the disease.Suppressed oligodendrocyte steroidogenesis in multiple sclerosis: Implications for regulation of neuroinflammation.Smoking and two human leukocyte antigen genes interact to increase the risk for multiple sclerosis.HLA-DRB1*15:01 and multiple sclerosis: a female association?Influence of HLA-DRB1 allele heterogeneity on disease risk and clinical course in a West Australian MS cohort: a high-resolution genotyping study.Necrotizing meningoencephalitis of Pug dogs associates with dog leukocyte antigen class II and resembles acute variant forms of multiple sclerosis.A functional p.82G>S polymorphism in the RAGE gene is associated with multiple sclerosis in the Chinese population.Association of Gene Polymorphism with Predisposition to Optic Neuritis and Optic Neuritis Together with Multiple Sclerosis

P2860

Q26853573-659A8F44-1740-43A6-B5A6-0415F8F97135 Q28278945-559BCCDB-59A6-415A-96DC-0FA6BAEDF611 Q30514239-CCFB3607-9DC8-4919-9F2A-17B3B6B14B8C Q33421551-07820E86-418A-4369-84AE-1BBF647009AD Q33707921-BC287FD2-FD7E-4F3F-A2D4-47B5CC222EE2 Q33832877-23A4DCBA-8884-4FF5-BC6A-CA32CE7DBFEB Q33892035-6AE217AA-FD43-4DE8-9D79-F778586EDA0F Q33980298-A5782756-1FD4-4BB1-8399-3D9C9B7E96F7 Q34184766-C497F8AC-65A3-454E-8217-AF145D37C9D0 Q34551587-B76AF6D7-145A-4CC3-9C33-8842976CE52E Q35083983-5F446AB5-CD14-47F4-936E-D948A47E841D Q35126302-C95EF58B-8E47-4317-AEA0-8C8092425E42 Q35686581-3EE4C4FE-537C-4F28-82D1-965D0F4133E1 Q35727237-8EEED2C2-7CD1-40B1-8E4F-7D236F359695 Q36218461-9296297A-968B-45D4-8CF6-93B068EA9CE2 Q36394834-2CFFAA19-114A-499F-A0B2-C512A5EF3E13 Q36856159-B7A8CB55-E0F5-45CB-81B8-AF1BC8D29B92 Q37100271-42A36519-0BCF-4331-9749-C66BE6961D83 Q37163271-C5115553-7197-43FC-BB65-E24686C64984 Q37351905-583D4E83-6C1A-405B-A5DF-5BB278E102B0 Q37409286-281D3C2B-01CD-4476-A06C-5CB9A126D252 Q37483492-85355ACE-844F-4D03-B985-A02118352AF9 Q37772077-2D7DC65B-6DE6-457E-BAA7-0C3E50A09BB7 Q38020955-9BD69C84-73E1-428C-8935-42FB5FBB542B Q38020959-7861B6E9-4CD8-4B06-A335-A2A560B98D86 Q38248679-D6FD7371-935F-40E5-9BDE-1BFFB53000E7 Q39802246-19DB0E22-281B-4E53-86B1-A5E14C0B7525 Q40085017-5D9623DD-DDDC-4E06-8569-21109F84CBC7 Q41189386-D24A30EA-7507-4D2F-8FB4-0CCC7FCBF411 Q41295973-60A63A6D-8B89-456E-B152-0A2EF993F12A Q43504710-17ECD0A0-40D1-4B31-B3E3-30DB24C0B80E Q46149675-A4740CE4-525D-4214-8F82-D48B47604DC4 Q47395782-9B572E98-0636-421D-AA3A-AD1084544305 Q48126920-25AE2851-D0CF-479C-B890-780EBB7333BA Q50787621-11259B78-FCBE-4C0D-9A53-7AB9B9A7E29D Q51381791-941835C9-3182-43FA-B56A-B808964107E3 Q51579145-A36769CB-5997-4D8F-BDFC-8968266E74C0 Q51703579-3F1D543A-2C24-40F4-8E72-86B0AE0EE542 Q54376586-5E39B665-42F8-4981-8E07-E067EF8EA1CA Q57825618-9BAD6D0F-F0A1-4A9E-B0AA-7312D15455A7

P2860

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

http://www.wikidata.org/entity/Q35137159

description

2008 nî lūn-bûn

@nan

2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

@ast

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

@en

type

label

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

@ast

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

@en

prefLabel

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

@ast

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

@en

P1433

Q35137159-12D959F0-2038-4814-8266-D326D739F8E2

P1476

Q35137159-53F8B504-3B99-4F40-8D0C-026EE649086F

P2093

Q35137159-0B454001-9CBB-45E1-9A5F-3730ABE3B7E4

Q35137159-0F547E86-AB9C-4B3B-8D4B-90074F25BEA4

Q35137159-121F03B8-146C-4CD1-BA55-6F6725D9FC7B

Q35137159-25A1E3C6-31DC-4C79-95A3-D8B796AB4A19

Q35137159-527DE8DC-F0F0-48C5-8320-592128CAEC08

Q35137159-53C1A762-A568-4D23-B50D-D831BABC52B8

Q35137159-73F992F9-6A45-46E4-B0B7-2EC84D79119C

Q35137159-826FABC7-FA06-4FDC-9890-EFA7F053721E

Q35137159-8D4D8C1E-B02C-42D9-B2E8-629EF21A1333

Q35137159-92895EBE-EAE4-44DB-B5CA-00DB2C1A51A1

P2860

Q35137159-01B230D3-4360-42BA-B531-83E2847255E6

Q35137159-19059214-B4CA-4B58-8BD8-75C548E7FCC1

Q35137159-1BED52A4-F461-481F-824C-C9F5E52ABE64

Q35137159-23BFCD9B-09FB-42F3-9BAB-93D0FA906910

Q35137159-25AC4AD4-FCAB-40DD-98FD-BF11763F73AD

Q35137159-2A5A4D15-3F1A-4B12-BED7-464CD6F4340D

Q35137159-33F0400D-5915-4380-88A2-3CD75D6B6516

Q35137159-35A13876-ECAD-4C3B-B65E-F1C86AC4ECE4

Q35137159-36D6A0ED-DDBC-4580-B737-CA3AC54EBF93

Q35137159-3879DC01-E4EA-4283-834F-FB1E63A1A14D

P304

Q35137159-4BAEEDCD-F23A-442E-9A2C-0B9B43EAE4D1

P31

Q35137159-00B9F159-4F44-4B99-9601-E7594D7E00B9

P356

Q35137159-84412C60-EF25-4859-B64A-A7A40B5ABCCE

P407

Q35137159-B81DDD91-9C80-4C72-9EA9-7F4FB9FEB0EB

P433

Q35137159-B79D46A2-AEEE-4C4D-B7AD-011F304C2536

P478

Q35137159-86560E2F-A56A-4A7E-AE9C-72BA95295A6E

P577

Q35137159-906F9B27-975A-46AB-9592-C9FDFF8722AA

P5875

Q35137159-A197400B-D26E-44C6-BD22-490EEA918749

P698

Q35137159-EBBBBC29-2937-4EE1-B27E-81066D88DA42

P921

Q35137159-2F3DBE86-7D82-4E82-94DA-DCBDEB04A9DC

P932

Q35137159-F475F612-14D9-48FA-A81B-3BE25C1A9C3E

P356

JIMMUNOL.181.8.5473

P1433

Journal of Immunology

P1476

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.

@en

P2093

Bruce A C Cree

http://www.w3.org/2001/XMLSchema#string

Farren Briggs

http://www.w3.org/2001/XMLSchema#string

Jorge R Oksenberg

http://www.w3.org/2001/XMLSchema#string

Lisa F Barcellos

http://www.w3.org/2001/XMLSchema#string

Marcelo Fernandez-Viña

http://www.w3.org/2001/XMLSchema#string

Omar Khan

http://www.w3.org/2001/XMLSchema#string

Patricia P Ramsay

http://www.w3.org/2001/XMLSchema#string

Sergio E Baranzini

http://www.w3.org/2001/XMLSchema#string

Stacy J Caillier

http://www.w3.org/2001/XMLSchema#string

Stephen L Hauser

http://www.w3.org/2001/XMLSchema#string

P2860

RAGE mediates a novel proinflammatory axis: a central cell surface receptor for S100/calgranulin polypeptides

Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis

Methods for high-density admixture mapping of disease genes

Cloning and expression of a cell surface receptor for advanced glycosylation end products of proteins

RAGE and amyloid-beta peptide neurotoxicity in Alzheimer's disease

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.

Redundancy in antigen-presenting function of the HLA-DR and -DQ molecules in the multiple sclerosis-associated HLA-DR2 haplotype

A functional and structural basis for TCR cross-reactivity in multiple sclerosis

Haploview: analysis and visualization of LD and haplotype maps

DQB1*0602 allele shows a strong association with multiple sclerosis in patients in Malaga, Spain

P304

5473-5480

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.4049/JIMMUNOL.181.8.5473

http://www.w3.org/2001/XMLSchema#string

P407

P433

8

http://www.w3.org/2001/XMLSchema#string

P478

181

http://www.w3.org/2001/XMLSchema#string

P577

2008-10-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

23297272

http://www.w3.org/2001/XMLSchema#string

P698

18832704

http://www.w3.org/2001/XMLSchema#string

P921

multiple sclerosis

P932

4346327

http://www.w3.org/2001/XMLSchema#string