Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Guillaume Van Beersel"'
Publikováno v:
The Open Pathology Journal. 7:16-27
The accumulation of pinocytosed sucrose in lysosomes constitutes a convenient mean to mimic a lysosomal storage and to study how such storage impacts the biology of the organelle and beyond. Several reports have shown that lysosomal storages can pert
Autor:
Michel Jadot, Guillaume Van Beersel, Thierry Arnould, Stéphane Demine, Isabelle Hamer, Eliane Tihon
Publikováno v:
Bioscience Reports
Bioscience Reports, Vol 33, Iss 2, p e00023 (2013)
Van Beersel, G, Tihon, E, Demine, S, Hamer, I, Jadot, M & Arnould, T 2013, ' Different molecular mechanisms involved in spontaneous and oxidative stress-induced mitochondrial fragmentation in tripeptidyl peptidase-1 (TPP-1)-deficient fibroblasts ', Bioscience reports, vol. 33, no. 2, pp. 243-258 . https://doi.org/10.1042/BSR20120104
Bioscience Reports, Vol 33, Iss 2, p e00023 (2013)
Van Beersel, G, Tihon, E, Demine, S, Hamer, I, Jadot, M & Arnould, T 2013, ' Different molecular mechanisms involved in spontaneous and oxidative stress-induced mitochondrial fragmentation in tripeptidyl peptidase-1 (TPP-1)-deficient fibroblasts ', Bioscience reports, vol. 33, no. 2, pp. 243-258 . https://doi.org/10.1042/BSR20120104
NCLs (neuronal ceroid lipofuscinoses) form a group of eight inherited autosomal recessive diseases characterized by the intralysosomal accumulation of autofluorescent pigments, called ceroids. Recent data suggest that the pathogenesis of NCL is assoc
Publikováno v:
Current drug metabolism. 13(10)
Lysosomes are cytoplasmic organelles delimited by a single membrane and filled with a variety of hydrolytic enzymes active at acidic pH and collectively capable to degrade the vast majority of macromolecules entering lysosomes via endocytosis, phagoc