Endoplasmic reticulum–mitochondria contacts: function of the junction
AA Rowland, GK Voeltz - Nature reviews Molecular cell biology, 2012 - nature.com
The most well-characterized organelle contact sites are those between the endoplasmic
reticulum (ER) and mitochondria. Increased understanding is being gained of how ER …
reticulum (ER) and mitochondria. Increased understanding is being gained of how ER …
Disturbed mitochondrial dynamics and neurodegenerative disorders
Mitochondria form a highly interconnected tubular network throughout the cell via a dynamic
process, with mitochondrial segments fusing and breaking apart continuously. Strong …
process, with mitochondrial segments fusing and breaking apart continuously. Strong …
Aging and functional brain networks
D Tomasi, ND Volkow - Molecular psychiatry, 2012 - nature.com
Aging is associated with changes in human brain anatomy and function and cognitive
decline. Recent studies suggest the aging decline of major functional connectivity hubs in …
decline. Recent studies suggest the aging decline of major functional connectivity hubs in …
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
Abstract The Greater Middle East (GME) has been a central hub of human migration and
population admixture. The tradition of consanguinity, variably practiced in the Persian Gulf …
population admixture. The tradition of consanguinity, variably practiced in the Persian Gulf …
The axonal transport of mitochondria
Vigorous transport of cytoplasmic components along axons over substantial distances is
crucial for the maintenance of neuron structure and function. The transport of mitochondria …
crucial for the maintenance of neuron structure and function. The transport of mitochondria …
The retromer complex–endosomal protein recycling and beyond
MNJ Seaman - Journal of cell science, 2012 - journals.biologists.com
The retromer complex is a vital element of the endosomal protein sorting machinery that is
conserved across all eukaryotes. Retromer is most closely associated with the endosome-to …
conserved across all eukaryotes. Retromer is most closely associated with the endosome-to …
[HTML][HTML] Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms
TL Giudice, F Lombardi, FM Santorelli, T Kawarai… - Experimental …, 2014 - Elsevier
Hereditary spastic paraplegia (HSP) is a group of clinically and genetically heterogeneous
neurological disorders characterized by pathophysiologic hallmark of length-dependent …
neurological disorders characterized by pathophysiologic hallmark of length-dependent …
Mitochondrial quality control: a matter of life and death for neurons
EI Rugarli, T Langer - The EMBO journal, 2012 - embopress.org
Neuronal survival critically depends on the integrity and functionality of mitochondria. A
hierarchical system of cellular surveillance mechanisms protects mitochondria against …
hierarchical system of cellular surveillance mechanisms protects mitochondria against …
[HTML][HTML] Axonal endoplasmic reticulum Ca2+ content controls release probability in CNS nerve terminals
Although the endoplasmic reticulum (ER) extends throughout axons and axonal ER
dysfunction is implicated in numerous neurological diseases, its role at nerve terminals is …
dysfunction is implicated in numerous neurological diseases, its role at nerve terminals is …
Hereditary spastic paraplegia: clinical and genetic hallmarks
PVS de Souza, WBV de Rezende Pinto… - The Cerebellum, 2017 - Springer
Hereditary spastic paraplegia comprises a wide and heterogeneous group of inherited
neurodegenerative and neurodevelopmental disorders resulting from primary retrograde …
neurodegenerative and neurodevelopmental disorders resulting from primary retrograde …