Sporadic inclusion body myositis: the genetic contributions to the pathogenesis. - Wikidata - wikimedia - TriplyDB

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

http://www.wikidata.org/entity/Q33806912

about

Ongoing developments in sporadic inclusion body myositis Sporadic inclusion body myositis: new insights and potential therapy.The effects of an intronic polymorphism in TOMM40 and APOE genotypes in sporadic inclusion body myositis.Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis Development and evaluation of a standardized ELISA for the determination of autoantibodies against cN-1A (Mup44, NT5C1A) in sporadic inclusion body myositis.Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum.Genetics in inclusion body myositis.SEPARATING THE CAUSES AND CONSEQUENCES IN DISEASE TRANSCRIPTOME.Age-Related Changes in Skeletal Muscle of Cattle.

P2860

Q34519540-8E820ACC-7267-450F-A0E5-D3570410FC03 Q34591787-0C6CA76F-7693-4489-8243-342BD1530E0E Q35230251-1F670566-634D-4A10-B0A7-300AE7723182 Q37371636-4077C849-6A2B-4730-8248-9BE9961484FC Q37421042-F5712D57-CD6B-42C8-ADB5-CE39324C863C Q39021882-21607A72-0D80-45D8-A5D3-CA753B12AED7 Q40094784-51D6EB3D-4C38-4DA2-A065-1D5BD7F37781 Q40098415-A1D75A14-1EDD-4797-A7A4-24EAD82CE81C Q50260921-11E16DE6-9288-4BE0-8528-9EF2315FF087

P2860

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

http://www.wikidata.org/entity/Q33806912

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

@ast

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

@en

type

label

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

@ast

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

@en

prefLabel

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

@ast

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis.

@en

P1433

Q33806912-B9C4055A-7C8B-482C-87D1-5AE4BB8AC07D

P1476

Q33806912-54C5C69A-BDD6-45CA-B7FD-55E5FA4E106B

P2093

Q33806912-029A3DD4-3C7D-4C9D-9C23-8102D14E2956

Q33806912-10943460-D14D-4F17-9F7F-48575AB5B31C

Q33806912-A1B59F11-45F9-4897-B90B-F21A239D3D9B

P275

Q33806912-8FE1BEE3-2F65-47D6-BC19-FFA79C1CC97D

P2860

Q33806912-04DE38B8-B8E4-4D85-AEA2-A19940094E11

Q33806912-06BA94A2-E7ED-4FAA-B777-E414CDAAE428

Q33806912-06E2F520-6E78-48E6-98E4-E4657569955C

Q33806912-0D0F7440-5D03-4811-B40D-0B3B4ED73F72

Q33806912-11D4C92B-3F55-4C8F-B51A-8E1EA334CCB0

Q33806912-14ABE25E-8621-4F1E-B9CF-153485DC89BF

Q33806912-1F42696A-889A-441E-9072-1F92B7B1ABF2

Q33806912-2076E333-79A6-4719-90F4-29823B7B9B25

Q33806912-247C13DE-89D2-4F35-B918-A5A617D3B8DA

Q33806912-2855139C-D858-4E6C-96EB-99D9A7BBCF6F

P2888

Q33806912-8EEB9ED9-EBA2-47A2-8834-C50C23BE26BB

P304

Q33806912-89336322-4FC8-4F92-85CE-D8271853B2E1

P31

Q33806912-4B5EB9A7-109A-4FBB-A764-B8A3F58A3C02

P356

Q33806912-6FD7F597-9BB8-4CFC-8094-E3B6CDBD4309

P478

Q33806912-748B80A2-D485-4A85-B32B-9E62E2BB2D9E

P50

Q33806912-168FC3BD-52DF-453E-B9FF-CBE10217AA60

Q33806912-6940E801-F629-4F44-A921-960B2C63A512

P5008

Q33806912-B66D9CB8-676D-4A49-A3EB-199BEA02CAC3

P577

Q33806912-A39082B7-0B76-4742-AAB4-EF731A3BAF37

P5875

Q33806912-C5601E9C-D87D-4262-B6EC-AA50B97023C6

P6179

Q33806912-619F1EEE-F9E4-4D13-A4F3-C2A2B9B1D953

P698

Q33806912-5674E64F-4B6E-4319-9913-C609E8291D79

P921

Q33806912-1737E51E-2C04-4600-969E-48F0999D7B50

P932

Q33806912-0FBA54B0-9D30-4153-A636-B6F0D35BC43B

P356

P1433

Orphanet Journal of Rare Diseases

P1476

Sporadic inclusion body myositis: the genetic contributions to the pathogenesis

@en

P2093

Henry Houlden

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

Michael G Hanna

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

Qiang Gang

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

P275

Creative Commons Attribution 4.0 International

P2860

TREM2 Variants in Alzheimer's Disease

Altered ribostasis: RNA-protein granules in degenerative disorders

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis

HLA associations with inclusion body myositis

Update in inclusion body myositis

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

Autoantibodies against a 43 KDa muscle protein in inclusion body myositis

Prevalence of sporadic inclusion body myositis in Western Australia.

P2888

P304

88

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

P31

scholarly article

P356

10.1186/1750-1172-9-88

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

P478

9

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

P50

Pedro M Machado

P5008

P577

2014-06-19T00:00:00Z

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

P5875

263356588

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

P6179

1014569112

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

P698

24948216

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

P921

inclusion body myositis

P932

4071018

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