Surrogate gene therapy for muscular dystrophy

An engineered truncated gene derived from the dystrophin-related protein (utrophin), prevents pathology without an immune response in an animal model of Duchenne muscular dystrophy (DMD) gene therapy.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Davies, KE, Chamberlain, JS
Μορφή: Journal article
Γλώσσα:English
Έκδοση: Springer Nature 2019
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author Davies, KE
Chamberlain, JS
author_facet Davies, KE
Chamberlain, JS
author_sort Davies, KE
collection OXFORD
description An engineered truncated gene derived from the dystrophin-related protein (utrophin), prevents pathology without an immune response in an animal model of Duchenne muscular dystrophy (DMD) gene therapy.
first_indexed 2024-03-07T01:28:31Z
format Journal article
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institution University of Oxford
language English
last_indexed 2024-03-07T01:28:31Z
publishDate 2019
publisher Springer Nature
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spelling oxford-uuid:92c93d21-c69b-4c06-9d3c-8b72e0aa5a052022-03-26T23:28:01ZSurrogate gene therapy for muscular dystrophyJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:92c93d21-c69b-4c06-9d3c-8b72e0aa5a05EnglishSymplectic ElementsSpringer Nature2019Davies, KEChamberlain, JSAn engineered truncated gene derived from the dystrophin-related protein (utrophin), prevents pathology without an immune response in an animal model of Duchenne muscular dystrophy (DMD) gene therapy.
spellingShingle Davies, KE
Chamberlain, JS
Surrogate gene therapy for muscular dystrophy
title Surrogate gene therapy for muscular dystrophy
title_full Surrogate gene therapy for muscular dystrophy
title_fullStr Surrogate gene therapy for muscular dystrophy
title_full_unstemmed Surrogate gene therapy for muscular dystrophy
title_short Surrogate gene therapy for muscular dystrophy
title_sort surrogate gene therapy for muscular dystrophy
work_keys_str_mv AT davieske surrogategenetherapyformusculardystrophy
AT chamberlainjs surrogategenetherapyformusculardystrophy