Proteomics of protein post-translational modifications implicated in neurodegeneration - Wikidata - awgldk - TriplyDB

Proteomics of protein post-translational modifications implicated in neurodegeneration

Proteomics of protein post-translational modifications implicated in neurodegeneration

http://www.wikidata.org/entity/Q28088631

about

Clinical proteomics of enervated neurons Post-Translational Modifications of Cardiac Mitochondrial Proteins in Cardiovascular Disease: Not Lost in Translation X-ray crystallography over the past decade for novel drug discovery - where are we heading next?Insight of brain degenerative protein modifications in the pathology of neurodegeneration and dementia by proteomic profiling Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss Protein post-translational modifications: In silico prediction tools and molecular modeling.Redox proteomics: Methods for the identification and enrichment of redox-modified proteins and their applications.Degradomics in Neurotrauma: Profiling Traumatic Brain Injury.Cholinergic System and Post-translational Modifications: An Insight on the Role in Alzheimer's Disease Novel insights into redox system and the mechanism of redox regulation.Brain ureido degenerative protein modifications are associated with neuroinflammation and proteinopathy in Alzheimer's disease with cerebrovascular disease.A cluster of palmitoylated cysteines are essential for aggregation of cysteine-string protein mutants that cause neuronal ceroid lipofuscinosis.Changes in the detergent-insoluble brain proteome linked to amyloid and tau in Alzheimer's Disease progression.Global quantitative analysis of the human brain proteome in Alzheimer's and Parkinson's Disease.

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P2860

Proteomics of protein post-translational modifications implicated in neurodegeneration

http://www.wikidata.org/entity/Q28088631

description

2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Proteomics of protein post-translational modifications implicated in neurodegeneration

@ast

Proteomics of protein post-translational modifications implicated in neurodegeneration

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Proteomics of protein post-translational modifications implicated in neurodegeneration

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type

label

Proteomics of protein post-translational modifications implicated in neurodegeneration

@ast

Proteomics of protein post-translational modifications implicated in neurodegeneration

@en

Proteomics of protein post-translational modifications implicated in neurodegeneration

@nl

prefLabel

Proteomics of protein post-translational modifications implicated in neurodegeneration

@ast

Proteomics of protein post-translational modifications implicated in neurodegeneration

@en

Proteomics of protein post-translational modifications implicated in neurodegeneration

@nl

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Translational Neurodegeneration

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Proteomics of protein post-translational modifications implicated in neurodegeneration

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Allan I Levey

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

Gang Wang

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

Nicholas T Seyfried

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

Ru-Jing Ren

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P2860

Redox signalling directly regulates TDP-43 via cysteine oxidation and disulphide cross-linking

Lrrk2 phosphorylates alpha synuclein at serine 129: Parkinson disease implications

p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy

Purification of proteins associated with specific genomic Loci

A role for NBR1 in autophagosomal degradation of ubiquitinated substrates

Recognition of the polyubiquitin proteolytic signal

Conceptual evolution in Alzheimer's disease: implications for understanding the clinical phenotype of progressive neurodegenerative disease

Altered ribostasis: RNA-protein granules in degenerative disorders

Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS

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

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10.1186/2047-9158-3-23

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