Cargando…
Interaction between AP-5 and the hereditary spastic paraplegia proteins SPG11 and SPG15
The AP-5 complex is a recently identified but evolutionarily ancient member of the family of heterotetrameric adaptor proteins (AP complexes). It is associated with two proteins that are mutated in patients with hereditary spastic paraplegia, SPG11 and SPG15. Here we show that the four AP-5 subunits...
Autores principales: | Hirst, Jennifer, Borner, Georg H. H., Edgar, James, Hein, Marco Y., Mann, Matthias, Buchholz, Frank, Antrobus, Robin, Robinson, Margaret S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744948/ https://www.ncbi.nlm.nih.gov/pubmed/23825025 http://dx.doi.org/10.1091/mbc.E13-03-0170 |
Ejemplares similares
-
Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11
por: Renvoisé, Benoît, et al.
Publicado: (2014) -
An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15
por: Vander Stichele, Geert, et al.
Publicado: (2022) -
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
por: Regensburger, Martin, et al.
Publicado: (2022) -
Clinical analysis in patients with SPG11 hereditary spastic paraplegia
por: Kang, You-Ri, et al.
Publicado: (2023) -
Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia
por: Utz, Kathrin S., et al.
Publicado: (2022)