Cargando…
Heteromeric p97/p97(R155C) Complexes Induce Dominant Negative Changes in Wild-Type and Autophagy 9-Deficient Dictyostelium strains
Heterozygous mutations in the human VCP (p97) gene cause autosomal-dominant IBMPFD (inclusion body myopathy with early onset Paget’s disease of bone and frontotemporal dementia), ALS14 (amyotrophic lateral sclerosis with or without frontotemporal dementia) and HSP (hereditary spastic paraplegia). Mo...
Autores principales: | Arhzaouy, Khalid, Strucksberg, Karl-Heinz, Tung, Sze Man, Tangavelou, Karthikeyan, Stumpf, Maria, Faix, Jan, Schröder, Rolf, Clemen, Christoph S., Eichinger, Ludwig |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463532/ https://www.ncbi.nlm.nih.gov/pubmed/23056506 http://dx.doi.org/10.1371/journal.pone.0046879 |
Ejemplares similares
-
Correction: Heteromeric p97/p97(R155C) Complexes Induce Dominant Negative Changes in Wild-Type and Autophagy 9-Deficient Dictyostelium strains
por: Arhzaouy, Khalid, et al.
Publicado: (2018) -
Domain Organization of the UBX Domain Containing Protein 9 and Analysis of Its Interactions With the Homohexameric AAA + ATPase p97 (Valosin-Containing Protein)
por: Riehl, Jana, et al.
Publicado: (2021) -
Memorandum: comptability of P92 and P97
por: Kirkby, Jasper, et al.
Publicado: (1986) -
Inhibitors of the AAA+ Chaperone p97
por: Chapman, Eli, et al.
Publicado: (2015) -
The p97-FAF1 Protein Complex Reveals a Common Mode of p97 Adaptor Binding
por: Ewens, Caroline A., et al.
Publicado: (2014)