Lysosomal dysfunction and glycosphingolipid dysregulation in rare and common neurodegenerative diseases
<p>Historically, the rare early-onset neurodegenerative lysosomal storage disorders (LSDs) have been studied as discrete metabolic diseases in their own right. However, in recent years links with more common late-onset neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS...
Главный автор: | Huebecker, M |
---|---|
Другие авторы: | Platt, F |
Формат: | Диссертация |
Язык: | English |
Опубликовано: |
2019
|
Предметы: |
Схожие документы
-
Glycosphingolipid dysregulation and lysosomal dysfunction in motor neuron disease
по: da Silva Santos, CS
Опубликовано: (2021) -
Early onset effects of single substrate accumulation recapitulate major features of LSD in patient-derived lysosomes
по: Gianluca Scerra, и др.
Опубликовано: (2021-07-01) -
Mucosal absorption of therapeutic peptides by harnessing the endogenous sorting of glycosphingolipids
по: Garcia-Castillo, Maria Daniela, и др.
Опубликовано: (2020) -
Dysregulated lysosomal exocytosis drives protease-mediated cartilage pathogenesis in multiple lysosomal disorders
по: Jen-Jie Lee, и др.
Опубликовано: (2024-04-01) -
Modern experimental biochemistry /
по: 324400 Boyer, Rodney F.
Опубликовано: (1993)