Cargando…
The Respiratory Phenotype of Pompe Disease Mouse Models
Pompe disease is a glycogen storage disease caused by a deficiency in acid α-glucosidase (GAA), a hydrolase necessary for the degradation of lysosomal glycogen. This deficiency in GAA results in muscle and neuronal glycogen accumulation, which causes respiratory insufficiency. Pompe disease mouse mo...
Autores principales: | Fusco, Anna F., McCall, Angela L., Dhindsa, Justin S., Zheng, Lucy, Bailey, Aidan, Kahn, Amanda F., ElMallah, Mai K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139647/ https://www.ncbi.nlm.nih.gov/pubmed/32214050 http://dx.doi.org/10.3390/ijms21062256 |
Ejemplares similares
-
Glycogen accumulation in smooth muscle of a Pompe disease mouse
model
por: McCall, Angela L., et al.
Publicado: (2021) -
The Respiratory Phenotype of Rodent Models of Amyotrophic Lateral Sclerosis and Spinocerebellar Ataxia
por: Fusco, Anna F., et al.
Publicado: (2019) -
Motor axonopathies in a mouse model of Duchenne muscular dystrophy
por: Dhindsa, Justin S., et al.
Publicado: (2020) -
Macroglossia, Motor Neuron Pathology, and Airway Malacia Contribute to Respiratory Insufficiency in Pompe Disease: A Commentary on Molecular Pathways and Respiratory Involvement in Lysosomal Storage Diseases
por: McCall, Angela L., et al.
Publicado: (2019) -
Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7
por: Fusco, Anna F., et al.
Publicado: (2021)