Invited review: decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the art.
about
Immunoprecipitation and mass spectrometry defines an extensive RBM45 protein-protein interaction networkRNA-Binding Proteins in the Regulation of miRNA Activity: A Focus on Neuronal FunctionsAsparaginase treatment side-effects may be due to genes with homopolymeric Asn codons (Review-Hypothesis)The role of TREX in gene expression and diseaseComparison of Sirtuin 3 Levels in ALS and Huntington's Disease-Differential Effects in Human Tissue Samples vs. Transgenic Mouse Models.SRSF1-dependent nuclear export inhibition of C9ORF72 repeat transcripts prevents neurodegeneration and associated motor deficits.The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis.Expression of hsrω-RNAi transgene prior to heat shock specifically compromises accumulation of heat shock-induced Hsp70 in Drosophila melanogaster.An Intrabody Drug (rAAV6-INT41) Reduces the Binding of N-Terminal Huntingtin Fragment(s) to DNA to Basal Levels in PC12 Cells and Delays Cognitive Loss in the R6/2 Animal ModelCurrent developments in gene therapy for amyotrophic lateral sclerosis.Liver X receptors: from cholesterol regulation to neuroprotection-a new barrier against neurodegeneration in amyotrophic lateral sclerosis?Structures of RNA repeats associated with neurological diseases.Protein sequestration as a normal function of long noncoding RNAs and a pathogenic mechanism of RNAs containing nucleotide repeat expansions.Calpain-dependent disruption of nucleo-cytoplasmic transport in ALS motor neurons.The ALS-linked E102Q mutation in Sigma receptor-1 leads to ER stress-mediated defects in protein homeostasis and dysregulation of RNA-binding proteins.Genome-wide scan in Hispanics highlights candidate loci for brain white matter hyperintensities.Body Mass Index and Amyotrophic Lateral Sclerosis: A Study of US Military Veterans.RNA Nuclear Export: From Neurological Disorders to Cancer.Amyotrophic lateral sclerosisLocalization of RNAi Machinery to Axonal Branch Points and Growth Cones Is Facilitated by Mitochondria and Is Disrupted in ALS
P2860
Q26765391-62994DB5-359F-494B-9FC4-44BCD3BF5F10Q26782020-B5962596-A168-4E8E-B4BF-50BFD3D58709Q26801165-4B588252-D77F-44C0-AECB-71705B44478CQ28078160-2A459766-B20A-4FE3-B9C5-16E2B3537768Q33729341-9B28B5D5-8873-4060-8316-2EB24604A84AQ33891056-762C5BD1-930C-4B75-A093-F1005245454BQ35501931-DDE693C9-4D83-4AB7-9F9A-24ACBD41EB97Q36373552-8C5EF115-896F-4E4E-B8AD-EF69E780995BQ37198517-418B7E12-EA98-4125-B330-488931ED4158Q38470242-CFE74D60-FBAD-4A9B-B38A-C472F2615051Q38924052-021A09B1-B2A0-4002-A33D-C584CAEA807BQ38994216-F4325B39-9527-4FAE-A6FE-989A598C766DQ39292842-D7F57B5F-FE6D-469D-97B1-81F01A1CF8ECQ40548161-1808458C-A3B4-4161-AA0F-26F1C051EEF9Q41636922-DE6C8924-B4FC-4B11-B93F-CCCA013C9953Q42366365-0FB84640-63E9-4EA8-BC3A-357A97955A87Q45326900-1CF95E40-8B9A-4A79-95D0-DD445C568A16Q47907249-EC397CE9-4E1E-4F94-8C51-A6AF4AEF7EEAQ56531747-7282AF60-DB0D-4E62-BE10-71212A13C6BEQ58762951-A85D0F77-C462-42B1-986F-BB573C8C6B80
P2860
Invited review: decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the art.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Invited review: decoding the p ...... the current state of the art.
@en
type
label
Invited review: decoding the p ...... the current state of the art.
@en
prefLabel
Invited review: decoding the p ...... the current state of the art.
@en
P2093
P2860
P50
P356
P1476
Invited review: decoding the p ...... the current state of the art.
@en
P2093
Guillaume M Hautbergue
Jennifer E Dodd
Matthew J Stopford
Matthew J Walsh
P2860
P304
P356
10.1111/NAN.12187
P5008
P577
2015-02-01T00:00:00Z