Cargando…
Siah-1-interacting protein regulates mutated huntingtin protein aggregation in Huntington’s disease models
BACKGROUND: Huntington’s disease (HD) is a neurodegenerative disorder whereby mutated huntingtin protein (mHTT) aggregates when polyglutamine repeats in the N-terminal of mHTT exceeds 36 glutamines (Q). However, the mechanism of this pathology is unknown. Siah1-interacting protein (SIP) acts as an a...
Autores principales: | Latoszek, Ewelina, Wiweger, Małgorzata, Ludwiczak, Jan, Dunin-Horkawicz, Stanisław, Kuznicki, Jacek, Czeredys, Magdalena |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8934500/ https://www.ncbi.nlm.nih.gov/pubmed/35305696 http://dx.doi.org/10.1186/s13578-022-00755-0 |
Ejemplares similares
-
Molecular Components of Store-Operated Calcium Channels in the Regulation of Neural Stem Cell Physiology, Neurogenesis, and the Pathology of Huntington’s Disease
por: Latoszek, Ewelina, et al.
Publicado: (2021) -
Huntingtin-Associated Protein 1A Regulates Store-Operated Calcium Entry in Medium Spiny Neurons From Transgenic YAC128 Mice, a Model of Huntington’s Disease
por: Czeredys, Magdalena, et al.
Publicado: (2018) -
localpdb—a Python package to manage protein structures and their annotations
por: Ludwiczak, Jan, et al.
Publicado: (2022) -
Expression of genes encoding the calcium signalosome in cellular and transgenic models of Huntington's disease
por: Czeredys, Magdalena, et al.
Publicado: (2013) -
pLM-BLAST: distant homology detection based on direct comparison of sequence representations from protein language models
por: Kaminski, Kamil, et al.
Publicado: (2023)