Results 81 to 90 of about 3,656,183 (130)
Lysosomal Storage Diseases: Is Impaired Apoptosis a Pathogenic Mechanism?*
International audienceLysosomal storage disorders are inborn diseases resulting from the lack or deficient activity of lysosomal hydrolases, transporters, or integral membrane proteins.
Tardy, Claudine +3 more
core +1 more source
Prevalence of lysosomal storage disorders
CONTEXT: Lysosomal storage disorders represent a group of at least 41 genetically distinct, biochemically related, inherited diseases. Individually, these disorders are considered rare, although high prevalence values have been reported in some ...
Hopwood, J. +3 more
core +1 more source
TFEB overexpression alleviates autophagy-lysosomal deficits caused by progranulin insufficiency
Progranulin is a pro-protein that is necessary for maintaining lysosomal function. Loss-of-function progranulin (GRN) mutations are a dominant cause of frontotemporal dementia (FTD).
Wren O. Nader +14 more
doaj +1 more source
Lysosomes and Storage diseases
info:eu-repo/semantics ...
Grégoire, Anne +3 more
openaire +1 more source
Lysosome storage dysfunction plays a central role in numerous human diseases, but a lack of appropriate tools has hindered lysosomal content profiling in clinical settings. In this issue of the JCI, Saarela et al. introduce a method called tagless LysoIP
Ali Shilatifard, Issam Ben-Sahra
doaj +1 more source
Nonimmune Hydrops Fetalis and Lysosomal Storage Diseases
Carlo Bellini
doaj +1 more source
Lysosomal Storage Diseases—Regulating Neurodegeneration
Rob U. Onyenwoke, Jay E. Brenman
doaj
Reply—Nonimmune Hydrops Fetalis and Lysosomal Storage Diseases
Ozge Surmeli-Onay, Ayse Korkmaz
doaj +1 more source
[Lysosomes and lysosomal storage diseases].
K K, Lie, S O, Lie
openaire +1 more source

