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Global transcriptional changes caused by an EDMD mutation correlate to tissue specific disease phenotypes in C. elegans

There are numerous heritable diseases associated with mutations in the LMNA gene. Most of these laminopathic diseases, including several muscular dystrophies, are autosomal dominant and have tissue-specific phenotypes. Our previous studies have shown that the globally expressed Emery-Dreifuss muscul...

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Библиографические подробности
Опубликовано в: :Nucleus
Главные авторы: Zuela, Noam, Dorfman, Jehudith, Gruenbaum, Yosef
Формат: Artigo
Язык:Inglês
Опубликовано: Taylor & Francis 2016
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5287205/
https://ncbi.nlm.nih.gov/pubmed/27673727
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19491034.2016.1238999
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