Cargando…
Actin Mutations and Their Role in Disease
Actin is a widely expressed protein found in almost all eukaryotic cells. In humans, there are six different genes, which encode specific actin isoforms. Disease-causing mutations have been described for each of these, most of which are missense. Analysis of the position of the resulting mutated res...
Autores principales: | Parker, Francine, Baboolal, Thomas G., Peckham, Michelle |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247010/ https://www.ncbi.nlm.nih.gov/pubmed/32397632 http://dx.doi.org/10.3390/ijms21093371 |
Ejemplares similares
-
Disease mutations in striated muscle myosins
por: Parker, Francine, et al.
Publicado: (2020) -
A Combination of Diffusion and Active Translocation Localizes Myosin 10 to the Filopodial Tip
por: Baboolal, Thomas G., et al.
Publicado: (2016) -
Affimers and nanobodies as molecular probes and their applications in imaging
por: Cordell, Paul, et al.
Publicado: (2022) -
Hypertrophic cardiomyopathy mutations in the calponin-homology domain of ACTN2 affect actin binding and cardiomyocyte Z-disc incorporation
por: Haywood, Natalie J., et al.
Publicado: (2016) -
A1603P and K1617del, Mutations in β-Cardiac Myosin Heavy Chain that Cause Laing Early-Onset Distal Myopathy, Affect Secondary Structure and Filament Formation In Vitro and In Vivo
por: Parker, Francine, et al.
Publicado: (2018)