Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a
EVs
FTLD
GRN
LCLs
NCL
TDP-43
mutation
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:
09 Nov 2022
09 Nov 2022
Historique:
received:
29
10
2022
revised:
04
11
2022
accepted:
06
11
2022
entrez:
26
11
2022
pubmed:
27
11
2022
medline:
30
11
2022
Statut:
epublish
Résumé
Frontotemporal lobar degeneration (FTLD) is a complex disease, characterized by progressive degeneration of frontal and temporal lobes. Mutations in progranulin (
Identifiants
pubmed: 36430231
pii: ijms232213753
doi: 10.3390/ijms232213753
pmc: PMC9694984
pii:
doi:
Substances chimiques
DNA-Binding Proteins
0
GRN protein, human
0
Progranulins
0
TARDBP protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Italian Ministry of Health
ID : Ricerca Finalizzata RF-2016-02361492
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