Use of Caenorhabditis elegans as a model to study Alzheimer's disease and other neurodegenerative diseases

AG Alexander, V Marfil, C Li - Frontiers in genetics, 2014 - frontiersin.org
Advances in research and technology has increased our quality of life, allowed us to combat
diseases, and achieve increased longevity. Unfortunately, increased longevity is …

Modeling neurodegeneration in Caenorhabditiselegans

KA Caldwell, CW Willicott… - Disease Models & …, 2020 - journals.biologists.com
The global burden of neurodegenerative diseases underscores the urgent need for
innovative strategies to define new drug targets and disease-modifying factors. The …

ER–mitochondria associations are regulated by the VAPB–PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43

R Stoica, KJ De Vos, S Paillusson, S Mueller… - Nature …, 2014 - nature.com
Mitochondria and the endoplasmic reticulum (ER) form tight structural associations and
these facilitate a number of cellular functions. However, the mechanisms by which regions of …

Lactate and pyruvate promote oxidative stress resistance through hormetic ROS signaling

A Tauffenberger, H Fiumelli, S Almustafa… - Cell death & …, 2019 - nature.com
L-lactate was long considered a glycolytic by-product but is now being recognized as a
signaling molecule involved in cell survival. In this manuscript, we report the role of L-lactate …

Nearly 30 years of animal models to study amyotrophic lateral sclerosis: a historical overview and future perspectives

T Bonifacino, RA Zerbo, M Balbi, C Torazza… - International journal of …, 2021 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a fatal, multigenic, multifactorial, and non-cell
autonomous neurodegenerative disease characterized by upper and lower motor neuron …

TARDBP and FUS Mutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update

S Lattante, GA Rouleau, E Kabashi - Human mutation, 2013 - Wiley Online Library
Mutations in the TAR DNA B inding P rotein gene (TARDBP), encoding the protein TDP‐43,
were identified in amyotrophic lateral sclerosis (ALS) patients. Interestingly, TDP‐43 positive …

Drug discovery: Insights from the invertebrate Caenorhabditis elegans

S Giunti, N Andersen, D Rayes… - Pharmacology …, 2021 - Wiley Online Library
Therapeutic drug development is a long, expensive, and complex process that usually takes
12–15 years. In the early phases of drug discovery, in particular, there is a growing need for …

TDP‐43 loss of function increases TFEB activity and blocks autophagosome–lysosome fusion

Q Xia, H Wang, Z Hao, C Fu, Q Hu, F Gao, H Ren… - The EMBO …, 2016 - embopress.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that is
characterized by selective loss of motor neurons in brain and spinal cord. TAR DNA‐binding …

Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. elegans

M Therrien, GA Rouleau, PA Dion, JA Parker - PloS one, 2013 - journals.plos.org
An expansion of the hexanucleotide GGGGCC repeat in the first intron of C9ORF72 gene
was recently linked to amyotrophic lateral sclerosis. It is not known if the mutation results in a …

Expression of ALS‐linked TDP‐43 mutant in astrocytes causes non‐cell‐autonomous motor neuron death in rats

J Tong, C Huang, F Bi, Q Wu, B Huang, X Liu… - The EMBO …, 2013 - embopress.org
Mutation of Tar DNA‐binding protein 43 (TDP‐43) is linked to amyotrophic lateral sclerosis.
Although astrocytes have important roles in neuron function and survival, their potential …