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
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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Auteurs

Laura Bianchi (L)

Functional Proteomics Laboratory, Department of Life Sciences, University of Siena, 53100 Siena, Italy.

Maria Sframeli (M)

Nemo Sud Clinical Centre, 98125 Messina, Italy.

Lorenza Vantaggiato (L)

Functional Proteomics Laboratory, Department of Life Sciences, University of Siena, 53100 Siena, Italy.

Gian Luca Vita (GL)

Nemo Sud Clinical Centre, 98125 Messina, Italy.

Annamaria Ciranni (A)

Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Francesca Polito (F)

Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Rosaria Oteri (R)

Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Eloisa Gitto (E)

Neonatal and Paediatric Intensive Care Unit, Department of Human Pathology in Adult and Developmental Age, University of Messina, 98125 Messina, Italy.

Fabrizio Di Giuseppe (F)

Dentistry and Biotechnology, and Proteomics Unit, Centre of Advanced Studies and Technoloy, Department Medical, Oral & Biotechnological Sciences, "G. d'Annunzio", University of Chieti-Pescara, 66100 Chieti, Italy.

Stefania Angelucci (S)

Dentistry and Biotechnology, and Proteomics Unit, Centre of Advanced Studies and Technoloy, Department Medical, Oral & Biotechnological Sciences, "G. d'Annunzio", University of Chieti-Pescara, 66100 Chieti, Italy.

Antonio Versaci (A)

Intensive Care Unit, AOU Policlinico "G. Martino", 98125 Messina, Italy.

Sonia Messina (S)

Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Giuseppe Vita (G)

Nemo Sud Clinical Centre, 98125 Messina, Italy.
Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

Luca Bini (L)

Functional Proteomics Laboratory, Department of Life Sciences, University of Siena, 53100 Siena, Italy.

M'hammed Aguennouz (M)

Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, 98125 Messina, Italy.

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