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 …

Disturbed mitochondrial dynamics and neurodegenerative disorders

F Burté, V Carelli, PF Chinnery… - Nature reviews …, 2015 - nature.com
Mitochondria form a highly interconnected tubular network throughout the cell via a dynamic
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 …

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

EM Scott, A Halees, Y Itan, EG Spencer, Y He… - Nature …, 2016 - nature.com
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 …

The axonal transport of mitochondria

WM Saxton, PJ Hollenbeck - Journal of cell science, 2012 - journals.biologists.com
Vigorous transport of cytoplasmic components along axons over substantial distances is
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 …

[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 …

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 …

[HTML][HTML] Axonal endoplasmic reticulum Ca2+ content controls release probability in CNS nerve terminals

J de Juan-Sanz, GT Holt, ER Schreiter, F de Juan… - Neuron, 2017 - cell.com
Although the endoplasmic reticulum (ER) extends throughout axons and axonal ER
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 …