Cargando…
Modeling Lysosomal Storage Diseases in the Zebrafish
Lysosomal storage diseases (LSDs) are a family of 70 metabolic disorders characterized by mutations in lysosomal proteins that lead to storage material accumulation, multiple-organ pathologies that often involve neurodegeneration, and early mortality in a significant number of patients. Along with t...
Autores principales: | Zhang, T., Peterson, R. T. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7218095/ https://www.ncbi.nlm.nih.gov/pubmed/32435656 http://dx.doi.org/10.3389/fmolb.2020.00082 |
Ejemplares similares
-
Pre-clinical Mouse Models of Neurodegenerative Lysosomal Storage Diseases
por: Favret, Jacob M., et al.
Publicado: (2020) -
Reproduction in Animal Models of Lysosomal Storage Diseases: A Scoping Review
por: Vuolo, Daniela, et al.
Publicado: (2021) -
Human iPSC-Based Models for the Development of Therapeutics Targeting Neurodegenerative Lysosomal Storage Diseases
por: Luciani, Marco, et al.
Publicado: (2020) -
CNS-Targeting Therapies for Lysosomal Storage Diseases: Current Advances and Challenges
por: Edelmann, Mariola J., et al.
Publicado: (2020) -
Lysosomal Diseases and Neuropsychiatry: Opportunities to Rebalance the Mind
por: Cox, Timothy M.
Publicado: (2020)