Cargando…
Brain cell type specific proteomics approach to discover pathological mechanisms in the childhood CNS disorder mucolipidosis type IV
Mucolipidosis IV (MLIV) is an ultra-rare, recessively inherited lysosomal disorder resulting from inactivating mutations in MCOLN1, the gene encoding the lysosomal cation channel TRPML1. The disease primarily affects the central nervous system (CNS) and manifests in the first year with cognitive and...
Autores principales: | Sangster, Madison, Shahriar, Sanjid, Niziolek, Zachary, Carisi, Maria Carla, Lewandowski, Michael, Budnik, Bogdan, Grishchuk, Yulia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440433/ https://www.ncbi.nlm.nih.gov/pubmed/37609073 http://dx.doi.org/10.3389/fnmol.2023.1215425 |
Ejemplares similares
-
Cross-sectional Observations on the Natural History of Mucolipidosis Type IV
por: Misko, Albert L., et al.
Publicado: (2022) -
Proteomics analysis of a human brain sample from a mucolipidosis type IV patient reveals pathophysiological pathways
por: Vardi, Ayelet, et al.
Publicado: (2021) -
Early evidence of delayed oligodendrocyte maturation in the mouse model of mucolipidosis type IV
por: Mepyans, Molly, et al.
Publicado: (2020) -
Peripheral Inflammatory Cytokine Signature Mirrors Motor Deficits in Mucolipidosis IV
por: Misko, Albert L., et al.
Publicado: (2022) -
The Dictyostelium Model for Mucolipidosis Type IV
por: Allan, Claire Y., et al.
Publicado: (2022)