Translation initiator EIF4G1 mutations in familial Parkinson disease
about
Ribosomal protein s15 phosphorylation mediates LRRK2 neurodegeneration in Parkinson's diseaseLoss of PINK1 attenuates HIF-1α induction by preventing 4E-BP1-dependent switch in protein translation under hypoxiaThe Genetic Basis of Cognitive Impairment and Dementia in Parkinson's DiseaseResearch in Parkinson's disease in India: A review.Genetic Profile, Environmental Exposure, and Their Interaction in Parkinson's DiseaseTargeting heat shock proteins to modulate α-synuclein toxicityGenetics of Parkinson's diseaseThe genetics and neuropathology of Parkinson's diseaseEvolutionary conservation and expression of human RNA-binding proteins and their role in human genetic diseaseHeterogeneity of leucine-rich repeat kinase 2 mutations: genetics, mechanisms and therapeutic implicationsIs inhibition of kinase activity the only therapeutic strategy for LRRK2-associated Parkinson's disease?Mitochondrial Biology and Neurological DiseasesIdentification of TMEM230 mutations in familial Parkinson's diseaseThe EIF4G1 gene and Parkinson's diseaseVPS35 regulates cell surface recycling and signaling of dopamine receptor D1Parkinson's disease genes VPS35 and EIF4G1 interact genetically and converge on α-synucleinGene and MicroRNA transcriptome analysis of Parkinson's related LRRK2 mouse modelsDNAJC13 mutations in Parkinson diseaseComprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Parkinson's Disease and Cognitive ImpairmentCaenorhabditis elegans: a model to investigate oxidative stress and metal dyshomeostasis in Parkinson's diseaseEIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population.Purinergic receptors P2RX4 and P2RX7 in familial multiple sclerosis.Systems-based analyses of brain regions functionally impacted in Parkinson's disease reveals underlying causal mechanismsRNA metabolism in the pathogenesis of Parkinson׳s diseaseGenetic analysis in neurology: the next 10 years.Signals from the lysosome: a control centre for cellular clearance and energy metabolism.The genetic background of Parkinson's disease: current progress and future prospects.Genome-Scale Networks Link Neurodegenerative Disease Genes to α-Synuclein through Specific Molecular Pathways.Analysis of EIF4G1 in ethnic Chinese.Genetic association of sirtuin genes and Parkinson's disease.Identification of synaptosomal proteins binding to monomeric and oligomeric α-synuclein.Evidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson's Disease.PINK1 and Parkin control localized translation of respiratory chain component mRNAs on mitochondria outer membrane.EIF4G1 mutations do not cause Parkinson's disease.Rapid genetic diagnosis in single-gene movement disordersCharacterization of the Expression of the RNA Binding Protein eIF4G1 and Its Clinicopathological Correlation with Serous Ovarian CancerTarget gene capture sequencing in Chinese population of sporadic Parkinson diseaseDrosophila as a model to study mitochondrial dysfunction in Parkinson's disease.Combination therapies: The next logical Step for the treatment of synucleinopathies?
P2860
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P2860
Translation initiator EIF4G1 mutations in familial Parkinson disease
description
2011 nî lūn-bûn
@nan
2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Translation initiator EIF4G1 mutations in familial Parkinson disease
@ast
Translation initiator EIF4G1 mutations in familial Parkinson disease
@en
Translation initiator EIF4G1 mutations in familial Parkinson disease
@nl
type
label
Translation initiator EIF4G1 mutations in familial Parkinson disease
@ast
Translation initiator EIF4G1 mutations in familial Parkinson disease
@en
Translation initiator EIF4G1 mutations in familial Parkinson disease
@nl
prefLabel
Translation initiator EIF4G1 mutations in familial Parkinson disease
@ast
Translation initiator EIF4G1 mutations in familial Parkinson disease
@en
Translation initiator EIF4G1 mutations in familial Parkinson disease
@nl
P2093
P2860
P50
P3181
P1476
Translation initiator EIF4G1 mutations in familial Parkinson disease
@en
P2093
Abba C Zubair
Alain Destée
Alexandra I Soto-Ortolaza
Alexandre Kreisler
Anna Krygowska-Wajs
Aurélie Duflot
Austen J Milnerwood
Bahareh Behrouz
Brett H Keeling
Christel Vanbesien-Mailliot
P2860
P304
P3181
P356
10.1016/J.AJHG.2011.08.009
P407
P50
P577
2011-09-09T00:00:00Z