Nusinersen Modulates Proteomics Profiles of Cerebrospinal Fluid in Spinal Muscular Atrophy Type 1 Patients.
ASO
apolipoprotein A1
apolipoprotein E
carbonyl groups
haptoglobin
neuromuscular disease
nusinersen
oxidized proteins
spinal muscular atrophy type 1
survival motor neuron (SMN)
transthyretin
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
21 Apr 2021
21 Apr 2021
Historique:
received:
01
04
2021
accepted:
19
04
2021
entrez:
30
4
2021
pubmed:
1
5
2021
medline:
20
5
2021
Statut:
epublish
Résumé
Spinal muscular atrophy (SMA) type 1 is a severe infantile autosomal-recessive neuromuscular disorder caused by a survival motor neuron 1 gene (
Identifiants
pubmed: 33919289
pii: ijms22094329
doi: 10.3390/ijms22094329
pmc: PMC8122268
pii:
doi:
Substances chimiques
Oligonucleotides
0
Oligonucleotides, Antisense
0
Proteome
0
nusinersen
5Z9SP3X666
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
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