Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy. - Wikidata - awgldk - TriplyDB

Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy.

Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy.

http://www.wikidata.org/entity/Q37706412

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Ongoing developments in sporadic inclusion body myositis Sporadic inclusion body myositis: new insights and potential therapy.TDP-43 affects splicing profiles and isoform production of genes involved in the apoptotic and mitotic cellular pathways Amyotrophic lateral sclerosis and denervation alter sphingolipids and up-regulate glucosylceramide synthase Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy.Differentially expressed alternatively spliced genes in skeletal muscle from cancer patients with cachexia.Severe asymmetric muscle weakness revealing glycogenin-1 polyglucosan body myopathy.GNE-Myopathy in a Greek Romani Family with Unusual Calf Phenotype and Protein Aggregation Pathology.

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Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy.

http://www.wikidata.org/entity/Q37706412

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 December 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Widespread RNA metabolism impa ...... myositis TDP43-proteinopathy.

@en

Widespread RNA metabolism impa ...... myositis TDP43-proteinopathy.

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Widespread RNA metabolism impa ...... myositis TDP43-proteinopathy.

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Widespread RNA metabolism impa ...... myositis TDP43-proteinopathy.

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Widespread RNA metabolism impa ...... myositis TDP43-proteinopathy.

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Widespread RNA metabolism impa ...... myositis TDP43-proteinopathy.

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J.NEUROBIOLAGING.2013.12.029

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Neurobiology of Aging

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Widespread RNA metabolism impa ...... myositis TDP43-proteinopathy.

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Andrea Cortese

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Janice Holton

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Linda Greensmith

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Michael G Hanna

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Roberto Simone

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Rohan de Silva

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Stefen Brady

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Tammaryn Lashley

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P2860

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.

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

Exome sequencing reveals VCP mutations as a cause of familial ALS

Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

Linear models and empirical bayes methods for assessing differential expression in microarray experiments

Summaries of Affymetrix GeneChip probe level data

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: an important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing

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1491-1498

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scholarly article

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10.1016/J.NEUROBIOLAGING.2013.12.029

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6

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35

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Elizabeth M. C. Fisher

Vincent Plagnol

Abraham Acevedo-Arozena

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2013-12-30T00:00:00Z

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259916864

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24462217

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3988933

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