Potential Transfer of Polyglutamine and CAG-Repeat RNA in Extracellular Vesicles in Huntington's Disease: Background and Evaluation in Cell Culture.
about
Genetic variation in neurodegenerative diseases and its accessibility in the model organism Caenorhabditis elegans.Mutant huntingtin is secreted via a late endosomal/lysosomal unconventional secretory pathway.Achieving the Promise of Therapeutic Extracellular Vesicles: The Devil is in Details of Therapeutic Loading.Role of exosomes in the protection of cellular homeostasis.The Generation of Mouse and Human Huntington Disease iPS Cells Suitable for In vitro Studies on Huntingtin FunctionExtracellular Vesicles in Brain Tumors and Neurodegenerative Diseases.Mutant Huntingtin Inhibits αB-Crystallin Expression and Impairs Exosome Secretion from Astrocytes.Unconventional Secretion and Intercellular Transfer of Mutant Huntingtin.Bidirectional Microglia-Neuron Communication in Health and Disease
P2860
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P2860
Potential Transfer of Polyglutamine and CAG-Repeat RNA in Extracellular Vesicles in Huntington's Disease: Background and Evaluation in Cell Culture.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Potential Transfer of Polyglut ...... nd Evaluation in Cell Culture.
@en
type
label
Potential Transfer of Polyglut ...... nd Evaluation in Cell Culture.
@en
prefLabel
Potential Transfer of Polyglut ...... nd Evaluation in Cell Culture.
@en
P2093
P2860
P1476
Potential Transfer of Polyglut ...... nd Evaluation in Cell Culture.
@en
P2093
Erik R Abels
Jasmina S Redzic
Julia Margulis
Steve Finkbeiner
Xandra O Breakefield
Xuan Zhang
P2860
P2888
P304
P356
10.1007/S10571-016-0350-7
P577
2016-03-07T00:00:00Z
P6179
1013002979