Cargando…
Dynactin Deficiency in the CNS of Humans with Sporadic ALS and Mice with Genetically Determined Motor Neuron Degeneration
Dynactin is a complex motor protein involved in the retrograde axonal transport disturbances of which may lead to amyotrophic lateral sclerosis (ALS). Mice with hSOD1G93A mutation develop ALS-like symptoms and are used as a model for the disease studies. Similar symptoms demonstrate Cra1 mice, with...
Autores principales: | Kuźma-Kozakiewicz, Magdalena, Chudy, Agnieszka, Kaźmierczak, Beata, Dziewulska, Dorota, Usarek, Ewa, Barańczyk-Kuźma, Anna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898179/ https://www.ncbi.nlm.nih.gov/pubmed/24078265 http://dx.doi.org/10.1007/s11064-013-1160-7 |
Ejemplares similares
-
Validation of qPCR reference genes in lymphocytes from patients with amyotrophic lateral sclerosis
por: Usarek, Ewa, et al.
Publicado: (2017) -
Mice with Mutation in Dynein Heavy Chain 1 Do Not Share the Same Tau Expression Pattern with Mice with SOD1-Related Motor Neuron Disease
por: Kuźma-Kozakiewicz, Magdalena, et al.
Publicado: (2011) -
Plasma profiling reveals three proteins associated to amyotrophic lateral sclerosis
por: Häggmark, Anna, et al.
Publicado: (2014) -
dnc-1/dynactin 1 Knockdown Disrupts Transport of Autophagosomes and Induces Motor Neuron Degeneration
por: Ikenaka, Kensuke, et al.
Publicado: (2013) -
Does the MUNIX Method Reflect Clinical Dysfunction in Amyotrophic Lateral Sclerosis: A Practical Experience
por: Gawel, Malgorzata, et al.
Publicado: (2016)