Cargando…
Hsp70 Chaperones and Type I PRMTs Are Sequestered at Intranuclear Inclusions Caused by Polyalanine Expansions in PABPN1
Genomic instability at loci with tandem arrays of simple repeats is the cause for many neurological, neurodegenerative and neuromuscular diseases. When located in coding regions, disease-associated expansions of trinucleotide repeats are translated into homopolymeric amino acid stretches of glutamin...
Autores principales: | Tavanez, João Paulo, Bengoechea, Rocio, Berciano, Maria T., Lafarga, Miguel, Carmo-Fonseca, Maria, Enguita, Francisco J. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2712759/ https://www.ncbi.nlm.nih.gov/pubmed/19641605 http://dx.doi.org/10.1371/journal.pone.0006418 |
Ejemplares similares
-
A polyalanine tract expansion in Arx forms intranuclear inclusions and results in increased cell death
por: Nasrallah, Ilya M., et al.
Publicado: (2004) -
Hsp110 Chaperones Control Client Fate Determination in the Hsp70–Hsp90 Chaperone System
por: Mandal, Atin K., et al.
Publicado: (2010) -
Biogenesis of the mitochondrial Hsp70 chaperone
por: Blamowska, Marta, et al.
Publicado: (2012) -
The Hsp70-Chaperone Machines in Bacteria
por: Mayer, Matthias P.
Publicado: (2021) -
The Hsp70/Hsp90 Chaperone Machinery in Neurodegenerative Diseases
por: Lackie, Rachel E., et al.
Publicado: (2017)