Lysosomes as dynamic regulators of cell and organismal homeostasis
A Ballabio, JS Bonifacino - Nature reviews Molecular cell biology, 2020 - nature.com
Exciting new discoveries have transformed the view of the lysosome from a static organelle
dedicated to the disposal and recycling of cellular waste to a highly dynamic structure that …
dedicated to the disposal and recycling of cellular waste to a highly dynamic structure that …
Programmed cell death in spinal cord injury pathogenesis and therapy
Z Shi, S Yuan, L Shi, J Li, G Ning, X Kong… - Cell …, 2021 - Wiley Online Library
Spinal cord injury (SCI) always leads to functional deterioration due to a series of processes
including cell death. In recent years, programmed cell death (PCD) is considered to be a …
including cell death. In recent years, programmed cell death (PCD) is considered to be a …
[HTML][HTML] Autophagy in neurodegenerative diseases: from mechanism to therapeutic approach
J Nah, J Yuan, YK Jung - Molecules and cells, 2015 - Elsevier
Autophagy is a lysosome-dependent intracellular degradation process that allows recycling
of cytoplasmic constituents into bioenergetic and biosynthetic materials for maintenance of …
of cytoplasmic constituents into bioenergetic and biosynthetic materials for maintenance of …
SOD1 function and its implications for amyotrophic lateral sclerosis pathology: new and renascent themes
RKA Bunton-Stasyshyn, RA Saccon… - The …, 2015 - journals.sagepub.com
The canonical role of superoxide dismutase 1 (SOD1) is as an antioxidant enzyme
protecting the cell from reactive oxygen species toxicity. SOD1 was also the first gene in …
protecting the cell from reactive oxygen species toxicity. SOD1 was also the first gene in …
[HTML][HTML] Resveratrol improves motoneuron function and extends survival in SOD1G93A ALS mice
Amyotrophic lateral sclerosis (ALS) is an adult onset neurodegenerative disease that causes
progressive paralysis and death due to degeneration of motoneurons in spinal cord …
progressive paralysis and death due to degeneration of motoneurons in spinal cord …
Brain disorders due to lysosomal dysfunction
Recent studies of autophagic and lysosomal pathways have significantly changed our
understanding of lysosomes; once thought to be simple degradative and recycling centers …
understanding of lysosomes; once thought to be simple degradative and recycling centers …
SQSTM1 mutations–bridging Paget disease of bone and ALS/FTLD
SL Rea, V Majcher, MS Searle, R Layfield - Experimental cell research, 2014 - Elsevier
Paget disease of bone (PDB) is a skeletal disorder common in Western Europe but
extremely rare in the Indian subcontinent and Far East. The condition has a strong genetic …
extremely rare in the Indian subcontinent and Far East. The condition has a strong genetic …
[HTML][HTML] Mitochondria: a Promising Convergent Target for the treatment of amyotrophic lateral sclerosis
T Cunha-Oliveira, L Montezinho, RF Simões… - Cells, 2024 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease
characterized by the progressive loss of motor neurons, for which current treatment options …
characterized by the progressive loss of motor neurons, for which current treatment options …
[HTML][HTML] Protein aggregation and dysfunction of autophagy-lysosomal pathway: a vicious cycle in lysosomal storage diseases
A Monaco, A Fraldi - Frontiers in Molecular Neuroscience, 2020 - frontiersin.org
Many neurodegenerative conditions are characterized by the deposition of protein
aggregates (mainly amyloid-like) in the central nervous system (CNS). In post-mitotic CNS …
aggregates (mainly amyloid-like) in the central nervous system (CNS). In post-mitotic CNS …
Mitophagy in neurodegenerative diseases
Neurodegenerative diseases, such as Parkinson's disease (PD), Alzheimer's disease (AD),
Huntington's disease (HD), and Amyotrophic Lateral Sclerosis (ALS), are a complex “family” …
Huntington's disease (HD), and Amyotrophic Lateral Sclerosis (ALS), are a complex “family” …