Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis - Wikidata - awgldk - TriplyDB

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

http://www.wikidata.org/entity/Q28943435

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Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci Association between Tumor Necrosis Factor- α-308 G/A Polymorphism and Multiple Sclerosis: A Systematic Review and Meta-Analysis Epistasis and immunity: the role of genetic interactions in autoimmune diseases A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis Mechanical dynamics in live cells and fluorescence-based force/tension sensors Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients.Alternative splicing and transcriptome profiling of experimental autoimmune encephalomyelitis using genome-wide exon arrays.Role of single nucleotide polymorphisms of KIF1B gene in HBV-associated viral hepatitis An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene.Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis.TRAIL/TRAIL receptor system and susceptibility to multiple sclerosis IL7Rα contributes to experimental autoimmune encephalomyelitis through altered T cell responses and nonhematopoietic cell lineages Perspectives on the use of multiple sclerosis risk genes for prediction Primary progressive multiple sclerosis: part of the MS disease spectrum or separate disease entity?Advances and challenges in biomarker development for type 1 diabetes prediction and prevention using omic technologies A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis.Progress in multiple sclerosis research in the last year.Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis.Abundant kif21b is associated with accelerated progression in neurodegenerative diseases.Pax6 interactions with chromatin and identification of its novel direct target genes in lens and forebrain Identification of shared genes and pathways: a comparative study of multiple sclerosis susceptibility, severity and response to interferon beta treatment.Association of SNPs of CD40 gene with multiple sclerosis in Russians.Contribution of genome-wide association studies to scientific research: a pragmatic approach to evaluate their impact.Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.When is the absence of evidence, evidence of absence? Use of equivalence-based analyses in genetic epidemiology and a conclusion for the KIF1B rs10492972*C allelic association in multiple sclerosis.No association between identified multiple sclerosis non-MHC risk loci and neuromyelitis optica.Genetic determinants of risk and progression in multiple sclerosis.Multiple sclerosis pharmacogenetics: personalized approach towards tailored therapeutics.Dissecting the genetic make-up of North-East Sardinia using a large set of haploid and autosomal markers.A hypermorphic SP1-binding CD24 variant associates with risk and progression of multiple sclerosis.Multiple sclerosis-associated CLEC16A controls HLA class II expression via late endosome biogenesis Multiple sclerosis: getting personal with induced pluripotent stem cells.Progress in multiple sclerosis genetics.IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci.TRPV1 gates tissue access and sustains pathogenicity in autoimmune encephalitis.Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility Pathway and network-based analysis of genome-wide association studies in multiple sclerosis.

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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

http://www.wikidata.org/entity/Q28943435

description

2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

articolo scientifico

@it

artículu científicu espublizáu en 2008

@ast

im Dezember 2008 veröffentlichter wissenschaftlicher Artikel

@de

scientific journal article

@en

wetenschappelijk artikel (gepubliceerd op 2008/12/01)

@nl

наукова стаття, опублікована в грудні 2008

@uk

مقالة علمية (نشرت في ديسمبر 2008)

@ar

name

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

@ast

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

@en

type

label

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

@ast

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

@en

prefLabel

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

@ast

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

@en

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Nature Genetics

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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

@en

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A. Dessa Sadovnick

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

Ben A. Oostra

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

Eva Greiner

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

George C. Ebers

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

Ilse A. Hoppenbrouwers

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

Jan Hillert

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

Jurgen Del-Favero

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

Linda Broer

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

Naghmeh Jafari

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

Rogier Q. Hintzen

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

P2860

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondria

Risk alleles for multiple sclerosis identified by a genomewide study

Molecular changes in neurons in multiple sclerosis: altered axonal expression of Nav1.2 and Nav1.6 sodium channels and Na+/Ca2+ exchanger

Pathogenesis of axonal and neuronal damage in multiple sclerosis.

Mitochondria on the move.

Environmental factors and multiple sclerosis.

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.

Mitochondrial dysfunction as a cause of axonal degeneration in multiple sclerosis patients.

Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis

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P304

1402–1403

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scholarly article

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10.1038/NG.251

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P407

P433

12

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P478

40

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Christine Van Broeckhoven

Cornelia M. van Duijn

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2008-12-01T00:00:00Z

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18997785

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multiple sclerosis