Cargando…
Latozinemab, a novel progranulin-elevating therapy for frontotemporal dementia
BACKGROUND: Heterozygous loss-of-function mutations in the progranulin (PGRN) gene (GRN) cause a reduction in PGRN and lead to the development of frontotemporal dementia (FTD-GRN). PGRN is a secreted lysosomal chaperone, immune regulator, and neuronal survival factor that is shuttled to the lysosome...
Autores principales: | Kurnellas, Michael, Mitra, Ananya, Schwabe, Tina, Paul, Robert, Arrant, Andrew E., Roberson, Erik D., Ward, Michael, Yeh, Felix, Long, Hua, Rosenthal, Arnon |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268535/ https://www.ncbi.nlm.nih.gov/pubmed/37322482 http://dx.doi.org/10.1186/s12967-023-04251-y |
Ejemplares similares
-
Impaired β-glucocerebrosidase activity and processing in frontotemporal dementia due to progranulin mutations
por: Arrant, Andrew E., et al.
Publicado: (2019) -
Preclinical Interventions in Mouse Models of Frontotemporal Dementia Due to Progranulin Mutations
por: Kashyap, Shreya N., et al.
Publicado: (2023) -
Effects of Exercise on Progranulin Levels and Gliosis in Progranulin-Insufficient Mice1,2,3
por: Arrant, Andrew E., et al.
Publicado: (2015) -
Recent Insights into the Involvement of Progranulin in Frontotemporal Dementia
por: Sun, Li, et al.
Publicado: (2011) -
Partial Tmem106b reduction does not correct abnormalities due to progranulin haploinsufficiency
por: Arrant, Andrew E., et al.
Publicado: (2018)