Splice isoform-specific suppression of the CaV2.1 variant underlying spinocerebellar ataxia type 6-Reference-Cited by-同舟云学术

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Splice isoform-specific suppression of the CaV2.1 variant underlying spinocerebellar ataxia type 6

Published:2011-09 Issue:3 Volume:43 Page:533-542
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Tsou Wei-Ling,Soong Bing-Wen,Paulson Henry L.,Rodríguez-Lebrón Edgardo

Funder

Fauver Family Ataxia Research Fund (HLP), University of Michigan Neurology Department Institutional Funds

National Science Council of Taiwan

Publisher

Elsevier BV

Subject

Neurology

Reference45 articles.

1. Allele-specific RNA silencing of mutant ataxin-3 mediates neuroprotection in a rat model of Machado-Joseph disease;Alves;PLoS One,2008

2. Experimental validation of the importance of seed complement frequency to siRNA specificity;Anderson;RNA.,2008

3. 3′ UTR seed matches, but not overall identity, are associated with RNAi off-targets;Birmingham;Nat. Methods,2006

4. Minimizing variables among hairpin-based RNAi vectors reveals the potency of shRNAs;Boudreau;RNA.,2008

5. Nonallele-specific silencing of mutant and wild-type huntingtin demonstrates therapeutic efficacy in Huntington's disease mice;Boudreau;Mol. Ther.,2009

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1. Consensus Paper: Strengths and Weaknesses of Animal Models of Spinocerebellar Ataxias and Their Clinical Implications;The Cerebellum;2021-08-10

2. Calcium channelopathies and intellectual disability: a systematic review;Orphanet Journal of Rare Diseases;2021-05-13

3. Commentary to: “The Pathophysiology and Clinical Manifestations of Spinocerebellar Ataxia Type 6” by Rentiya et al., Cerebellum 2020;19(3):459–464);The Cerebellum;2020-11-20

4. Recent advances in molecular therapies for neurological disease: triplet repeat disorders;Human Molecular Genetics;2019-06-22

5. Movement disorders in autoimmune encephalitis and paraneoplastic neurological syndromes;Revue Neurologique;2018-11

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