Cargando…
Transcriptional Profile of Muscle following Acute Induction of Symptoms in a Mouse Model of Kennedy's Disease/Spinobulbar Muscular Atrophy
BACKGROUND: Kennedy’s disease/Spinobulbar muscular atrophy (KD/SBMA) is a degenerative neuromuscular disease affecting males. This disease is caused by polyglutamine expansion mutations of the androgen receptor (AR) gene. Although KD/SBMA has been traditionally considered a motor neuron disease, eme...
Autores principales: | Halievski, Katherine, Mo, Kaiguo, Westwood, J. Timothy, Monks, Douglas A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4341878/ https://www.ncbi.nlm.nih.gov/pubmed/25719894 http://dx.doi.org/10.1371/journal.pone.0118120 |
Ejemplares similares
-
Muscle contractility in spinobulbar muscular atrophy
por: Dahlqvist, Julia R., et al.
Publicado: (2019) -
Microarray Analysis of Gene Expression by Skeletal Muscle of Three Mouse Models of Kennedy Disease/Spinal Bulbar Muscular Atrophy
por: Mo, Kaiguo, et al.
Publicado: (2010) -
The Use of Korean Medicine to Treat Patients with Spinobulbar Muscular Atrophy, Kennedy’s Disease - A Case Study
por: Lee, Seongjin, et al.
Publicado: (2017) -
Rapidly Worsening Bulbar Symptoms in a Patient with Spinobulbar Muscular Atrophy
por: Diaz-Abad, Montserrat, et al.
Publicado: (2013) -
Differences in F-Wave Characteristics between Spinobulbar Muscular Atrophy and Amyotrophic Lateral Sclerosis
por: Fang, Jia, et al.
Publicado: (2016)