[HTML][HTML] Neuroprotection in glaucoma: mechanisms beyond intraocular pressure lowering
Glaucoma is a common, complex, multifactorial neurodegenerative disease characterized
by progressive dysfunction and then loss of retinal ganglion cells, the output neurons of the …
by progressive dysfunction and then loss of retinal ganglion cells, the output neurons of the …
[HTML][HTML] Axonal transport defects and neurodegeneration: molecular mechanisms and therapeutic implications
Because of the extremely polarized morphology, the proper functioning of neurons largely
relies on the efficient cargo transport along the axon. Axonal transport defects have been …
relies on the efficient cargo transport along the axon. Axonal transport defects have been …
Genome-wide analyses identify KIF5A as a novel ALS gene
To identify novel genes associated with ALS, we undertook two lines of investigation. We
carried out a genome-wide association study comparing 20,806 ALS cases and 59,804 …
carried out a genome-wide association study comparing 20,806 ALS cases and 59,804 …
Motor proteins at the mitochondria–cytoskeleton interface
AJ Kruppa, F Buss - Journal of cell science, 2021 - journals.biologists.com
Mitochondria are multifunctional organelles that not only produce energy for the cell, but are
also important for cell signalling, apoptosis and many biosynthetic pathways. In most cell …
also important for cell signalling, apoptosis and many biosynthetic pathways. In most cell …
Recent updates on the genetics of amyotrophic lateral sclerosis and frontotemporal dementia
L Kirola, A Mukherjee, M Mutsuddi - Molecular Neurobiology, 2022 - Springer
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) primarily affect the
motor and frontotemporal areas of the brain, respectively. These disorders share clinical …
motor and frontotemporal areas of the brain, respectively. These disorders share clinical …
Disease-modifying therapies in amyotrophic lateral sclerosis
A Chiò, L Mazzini, G Mora - Neuropharmacology, 2020 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder of adult life, causing
weakness and wasting of voluntary muscles, associated in about 50% of cases with a …
weakness and wasting of voluntary muscles, associated in about 50% of cases with a …
The axonal cytoskeleton: from organization to function
JT Kevenaar, CC Hoogenraad - Frontiers in molecular neuroscience, 2015 - frontiersin.org
The axon is the single long fiber that extends from the neuron and transmits electrical
signals away from the cell body. The neuronal cytoskeleton, composed of microtubules …
signals away from the cell body. The neuronal cytoskeleton, composed of microtubules …
Genetic convergence brings clarity to the enigmatic red line in ALS
C Cook, L Petrucelli - Neuron, 2019 - cell.com
Amyotrophic lateral sclerosis (ALS) is an aggressive neurodegenerative disorder that
orchestrates an attack on the motor nervous system that is unrelenting. Recent discoveries …
orchestrates an attack on the motor nervous system that is unrelenting. Recent discoveries …
Intertwined and finely balanced: endoplasmic reticulum morphology, dynamics, function, and diseases
HT Perkins, V Allan - Cells, 2021 - mdpi.com
The endoplasmic reticulum (ER) is an organelle that is responsible for many essential
subcellular processes. Interconnected narrow tubules at the periphery and thicker sheet-like …
subcellular processes. Interconnected narrow tubules at the periphery and thicker sheet-like …
Anterograde axonal transport in neuronal homeostasis and disease
L Guillaud, SE El-Agamy, M Otsuki… - Frontiers in molecular …, 2020 - frontiersin.org
Neurons are highly polarized cells with an elongated axon that extends far away from the
cell body. To maintain their homeostasis, neurons rely extensively on axonal transport of …
cell body. To maintain their homeostasis, neurons rely extensively on axonal transport of …