Cargando…
Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells
Mucopolysaccharidosis type IIIA (MPS IIIA) is characterised by a progressive neurological decline leading to early death. It is caused by bi-allelic loss-of-function mutations in SGSH encoding sulphamidase, a lysosomal enzyme required for heparan sulphate glycosaminoglycan (HS GAG) degradation, that...
Autores principales: | Lehmann, Rebecca J., Jolly, Lachlan A., Johnson, Brett V., Lord, Megan S., Kim, Ha Na, Saville, Jennifer T., Fuller, Maria, Byers, Sharon, Derrick-Roberts, Ainslie L.K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531667/ https://www.ncbi.nlm.nih.gov/pubmed/34712574 http://dx.doi.org/10.1016/j.ymgmr.2021.100811 |
Ejemplares similares
-
Altered IHH signaling contributes to reduced chondrocyte proliferation in the growth plate of MPS VII mice
por: Jiang, Zhirui, et al.
Publicado: (2020) -
Substrate Deprivation Therapy to Reduce Glycosaminoglycan Synthesis Improves Aspects of Neurological and Skeletal Pathology in MPS I Mice
por: Derrick-Roberts, Ainslie L. K., et al.
Publicado: (2017) -
Lentiviral-mediated gene correction of mucopolysaccharidosis type IIIA
por: Anson, Donald S, et al.
Publicado: (2007) -
Retinal Degeneration in MPS-IIIA Mouse Model
por: Intartaglia, Daniela, et al.
Publicado: (2020) -
Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors
por: Premarathne, Susitha, et al.
Publicado: (2017)