Cargando…
Automated High-Content Live Animal Drug Screening Using C. elegans Expressing the Aggregation Prone Serpin α1-antitrypsin Z
The development of preclinical models amenable to live animal bioactive compound screening is an attractive approach to discovering effective pharmacological therapies for disorders caused by misfolded and aggregation-prone proteins. In general, however, live animal drug screening is labor and resou...
Autores principales: | Gosai, Sager J., Kwak, Joon Hyeok, Luke, Cliff J., Long, Olivia S., King, Dale E., Kovatch, Kevin J., Johnston, Paul A., Shun, Tong Ying, Lazo, John S., Perlmutter, David H., Silverman, Gary A., Pak, Stephen C. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980495/ https://www.ncbi.nlm.nih.gov/pubmed/21103396 http://dx.doi.org/10.1371/journal.pone.0015460 |
Ejemplares similares
-
Deficient and Null Variants of SERPINA1 Are Proteotoxic in a Caenorhabditis elegans Model of α1-Antitrypsin Deficiency
por: Cummings, Erin E., et al.
Publicado: (2015) -
α(1)-Antitrypsin and the serpins: variation and countervariation
por: Carrell, Robin, et al.
Publicado: (1985) -
Fluphenazine Reduces Proteotoxicity in C. elegans and Mammalian Models of Alpha-1-Antitrypsin Deficiency
por: Li, Jie, et al.
Publicado: (2014) -
An analog of glibenclamide selectively enhances autophagic degradation of misfolded α1-antitrypsin Z
por: Wang, Yan, et al.
Publicado: (2019) -
A Pro-Cathepsin L Mutant Is a Luminal Substrate for Endoplasmic-Reticulum-Associated Degradation in C. elegans
por: Miedel, Mark T., et al.
Publicado: (2012)