Combinatorial treatment for spinal muscular atrophy-Reference-Cited by-同舟云学术

Combinatorial treatment for spinal muscular atrophy

Published:2020-02-14 Issue:2 Volume:153 Page:146-149
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Poletti Angelo¹^ORCID,Fischbeck Kenneth H.²^ORCID

Affiliation:

1. Dipartimento di Scienze Farmacologiche e Biomolecolari Centre of Excellence on Neurodegenerative Diseases Università degli Studi di Milano Milano Italy

2. Neurogenetics Branch National Institute for Neurological Disorders and Stroke National Institutes of Health Bethesda MD USA

Funder

National Institutes of Health

Fondazione Italiana di Ricerca per la Sclerosi Laterale Amiotrofica

Agenzia Italiana del Farmaco, Ministero della Salute

EU Joint Programme – Neurodegenerative Disease Research

Fondazione Telethon

Fondazione Cariplo

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jnc.14974

Reference15 articles.

1. Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy

2. Treatment of spinal muscular atrophy by sodium butyrate

3. Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy

4. LBH589 induces up to 10-fold SMN protein levels by several independent mechanisms and is effective even in cells from SMA patients non-responsive to valproate

5. Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse model

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