Spastin recovery in hereditary spastic paraplegia by preventing neddylation-dependent degradation.
Animals
Carrier Proteins
/ metabolism
Disease Models, Animal
Gene Expression Regulation
/ genetics
HeLa Cells
Humans
Mice
Mice, Knockout
Microtubules
/ metabolism
Mutation
Neurites
/ metabolism
Neurodegenerative Diseases
/ metabolism
Neurons
/ metabolism
Protein Serine-Threonine Kinases
/ metabolism
Proteolysis
Spastic Paraplegia, Hereditary
/ metabolism
Spastin
/ metabolism
Synapses
/ metabolism
Ubiquitination
Journal
Life science alliance
ISSN: 2575-1077
Titre abrégé: Life Sci Alliance
Pays: United States
ID NLM: 101728869
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
28
05
2020
revised:
14
10
2020
accepted:
14
10
2020
entrez:
27
10
2020
pubmed:
28
10
2020
medline:
14
7
2021
Statut:
epublish
Résumé
Hereditary Spastic Paraplegia (HSP) is a neurodegenerative disease most commonly caused by autosomal dominant mutations in the
Identifiants
pubmed: 33106322
pii: 3/12/e202000799
doi: 10.26508/lsa.202000799
pmc: PMC7652396
pii:
doi:
Substances chimiques
Carrier Proteins
0
HIPK2 protein, human
EC 2.7.1.-
Hipk2 protein, mouse
EC 2.7.1.-
Protein Serine-Threonine Kinases
EC 2.7.11.1
Spastin
EC 3.6.4.3
SPAST protein, human
EC 5.6.1.1
Spast protein, mouse
EC 5.6.1.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© 2020 Sardina et al.
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