Huntingtin Lowering Strategies for Disease Modification in Huntington’s Disease-Reference-Cited by-同舟云学术

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Huntingtin Lowering Strategies for Disease Modification in Huntington’s Disease

Published:2019-03 Issue:5 Volume:101 Page:801-819
ISSN:0896-6273
Container-title:Neuron
language:en
Short-container-title:Neuron

Author:

Tabrizi Sarah J.,Ghosh Rhia,Leavitt Blair R.

Funder

Medical Research Council UK

Wellcome Trust

Rosetrees Trust

Takeda Pharmaceuticals

Cantervale Limited

NIHR North Thames Local Clinical Research Network

UK Dementia Research Institute

Wolfson Foundation for Neurodegeneration

CHDI Foundation

Medical Research Council, United Kingdom

Canadian Institutes of Health Research

Huntington Society of Canada

Teva

uniQure

Lifemax

Publisher

Elsevier BV

Subject

General Neuroscience

Reference150 articles.

1. Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis;Adams;N. Engl. J. Med.,2018

2. Deimmunization for gene therapy: host matching of synthetic zinc finger constructs enables long-term mutant Huntingtin repression in mice;Agustín-Pavón;Mol. Neurodegener.,2016

3. Structure and expression of the Huntington’s disease gene: evidence against simple inactivation due to an expanded CAG repeat;Ambrose;Somat. Cell Mol. Genet.,1994

4. RAN translation in Huntington disease;Bañez-Coronel;Neuron,2015

5. RNAi in moderation;Barik;Nat. Biotechnol.,2006

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