Neurofilaments: neurobiological foundations for biomarker applications

AR Gafson, NR Barthélemy, P Bomont, RO Carare… - Brain, 2020 - academic.oup.com
Interest in neurofilaments has risen sharply in recent years with recognition of their potential
as biomarkers of brain injury or neurodegeneration in CSF and blood. This is in the context …

The HSP70 chaperone machinery: J proteins as drivers of functional specificity

HH Kampinga, EA Craig - Nature reviews Molecular cell biology, 2010 - nature.com
Heat shock 70 kDa proteins (HSP70s) are ubiquitous molecular chaperones that function in
a myriad of biological processes, modulating polypeptide folding, degradation and …

Population genetics of the coral Acropora millepora: Toward genomic prediction of bleaching

ZL Fuller, VJL Mocellin, LA Morris, N Cantin… - Science, 2020 - science.org
INTRODUCTION Coral reefs worldwide are suffering losses at an alarming rate as a result of
anthropogenic climate change. Increased seawater temperatures, even only slightly above …

Mitochondrial dynamics in neuronal injury, development and plasticity

KH Flippo, S Strack - Journal of cell science, 2017 - journals.biologists.com
Mitochondria fulfill numerous cellular functions including ATP production, Ca2+ buffering,
neurotransmitter synthesis and degradation, ROS production and sequestration, apoptosis …

[HTML][HTML] The role of mitochondrial dynamics in human cancers

Y Ma, L Wang, R Jia - American journal of cancer research, 2020 - ncbi.nlm.nih.gov
Mitochondria are crucial cellular organelles. Under extracellular stimulations, mitochondria
undergo constant fusion and fission dynamics to meet different cellular demands …

DNAJ Proteins in neurodegeneration: essential and protective factors

C Zarouchlioti, DA Parfitt, W Li… - … of the Royal …, 2018 - royalsocietypublishing.org
Maintenance of protein homeostasis is vitally important in post-mitotic cells, particularly
neurons. Neurodegenerative diseases such as polyglutamine expansion disorders—like …

Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)

M Girard, R Larivière, DA Parfitt… - Proceedings of the …, 2012 - National Acad Sciences
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a childhood-onset
neurological disease resulting from mutations in the SACS gene encoding sacsin, a 4,579 …

Ataxia in children: early recognition and clinical evaluation

P Pavone, AD Praticò, V Pavone, R Lubrano… - Italian Journal of …, 2017 - Springer
Background Ataxia is a sign of different disorders involving any level of the nervous system
and consisting of impaired coordination of movement and balance. It is mainly caused by …

The ARSACS disease protein sacsin controls lysosomal positioning and reformation by regulating microtubule dynamics

V Francis, W Alshafie, R Kumar, M Girard… - Journal of Biological …, 2022 - ASBMB
Autosomal recessive spastic ataxia of Charlevoix-Saguenay is a fatal brain disorder
featuring cerebellar neurodegeneration leading to spasticity and ataxia. This disease is …

Barcoding heat shock proteins to human diseases: looking beyond the heat shock response

V Kakkar, M Meister-Broekema… - Disease models & …, 2014 - journals.biologists.com
There are numerous human diseases that are associated with protein misfolding and the
formation of toxic protein aggregates. Activating the heat shock response (HSR)–and thus …