Deciphering the Complex Molecular Pathogenesis of Myotonic Dystrophy Type 1 through Omics Studies

Deciphering the Complex Molecular Pathogenesis of Myotonic Dystrophy Type 1 through Omics Studies

Omics studies are crucial to improve our understanding of myotonic dystrophy type 1 (DM1), the most common muscular dystrophy in adults. Employing tissue samples and cell lines derived from patients and animal models, omics approaches have revealed the myriad alterations in gene and microRNA express...

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Bibliographic Details
Main Authors: Jorge Espinosa-Espinosa, Anchel González-Barriga, Arturo López-Castel, Rubén Artero
Format: Article
Language:English
Published: MDPI AG 2022-01-01
Series:International Journal of Molecular Sciences
Subjects:
transcriptomics
proteomics
alternative splicing
alternative polyadenylation
expanded CUG repeats
gene expression
Online Access:https://www.mdpi.com/1422-0067/23/3/1441

Internet

https://www.mdpi.com/1422-0067/23/3/1441

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