受强制性开放获取政策约束的文章 - Ravi Chopra了解详情
可在其他位置公开访问的文章：14 篇
Oligonucleotide therapy mitigates disease in spinocerebellar ataxia type 3 mice
HS McLoughlin, LR Moore, R Chopra, R Komlo, M McKenzie, ...
Annals of neurology 84 (1), 64-77, 2018
强制性开放获取政策： US National Institutes of Health
Neuronal atrophy early in degenerative ataxia is a compensatory mechanism to regulate membrane excitability
JM Dell'Orco, AH Wasserman, R Chopra, MAC Ingram, YS Hu, V Singh, ...
Journal of Neuroscience 35 (32), 11292-11307, 2015
强制性开放获取政策： US National Institutes of Health
Coordinate regulation of mutant NPC1 degradation by selective ER autophagy and MARCH6-dependent ERAD
ML Schultz, KL Krus, S Kaushik, D Dang, R Chopra, L Qi, VG Shakkottai, ...
Nature communications 9 (1), 3671, 2018
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Targeting potassium channels to treat cerebellar ataxia
DD Bushart, R Chopra, V Singh, GG Murphy, H Wulff, VG Shakkottai
Annals of clinical and translational neurology 5 (3), 297-314, 2018
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Untangling the Dravet syndrome seizure network: the changing face of a rare genetic epilepsy: the paradox of Dravet syndrome
R Chopra, LL Isom
Epilepsy currents 14 (2), 86-89, 2014
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Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia
R Chopra, AH Wasserman, SM Pulst, CI De Zeeuw, VG Shakkottai
Human molecular genetics 27 (8), 1396-1410, 2018
强制性开放获取政策： US National Institutes of Health
Translating cerebellar Purkinje neuron physiology to progress in dominantly inherited ataxia
R Chopra, VG Shakkottai
Future neurology 9 (2), 187-196, 2014
强制性开放获取政策： US National Institutes of Health
Dendritic potassium channel dysfunction may contribute to dendrite degeneration in spinocerebellar ataxia type 1
R Chopra, DD Bushart, VG Shakkottai
PLoS One 13 (5), e0198040, 2018
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Altered Capicua expression drives regional Purkinje neuron vulnerability through ion channel gene dysregulation in spinocerebellar ataxia type 1
R Chopra, DD Bushart, JP Cooper, D Yellajoshyula, LM Morrison, ...
Human molecular genetics 29 (19), 3249-3265, 2020
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MTSS1/Src family kinase dysregulation underlies multiple inherited ataxias
AS Brown, P Meera, B Altindag, R Chopra, EM Perkins, S Paul, ...
Proceedings of the National Academy of Sciences 115 (52), E12407-E12416, 2018
强制性开放获取政策： US National Institutes of Health, Wellcome Trust
The role for alterations in neuronal activity in the pathogenesis of polyglutamine repeat disorders
R Chopra, VG Shakkottai
Neurotherapeutics 11 (4), 751-763, 2014
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Deriving early single-rosette brain organoids from human pluripotent stem cells
AM Tidball, W Niu, Q Ma, TN Takla, JC Walker, JL Margolis, ...
Stem Cell Reports 18 (12), 2498-2514, 2023
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Self-organizing single-rosette brain organoids from human pluripotent stem cells
AM Tidball, W Niu, Q Ma, TN Takla, JC Walker, JL Margolis, ...
Biorxiv, 2022.02. 28.482350, 2022
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BIOLOGICAL SCIENCES: Neuroscience, cell biology MTSS1/Src family kinase Dysregulation Underlies Multiple Inherited Ataxias
AS Brown, P Meera, B Altindag, R Chopra, E Perkins, S Paul, DR Scoles, ...
bioRxiv, 338046, 2018
强制性开放获取政策： Wellcome Trust
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