Neural cell cycle dysregulation and central nervous system diseases

W Wang, B Bu, M Xie, M Zhang, Z Yu, D Tao - Progress in neurobiology, 2009 - Elsevier
The cell cycle is a delicately manipulated process essential for the development,
differentiation, proliferation and death of cells. Inappropriate activation of cell cycle …

Protective role of anticancer drugs in neurodegenerative disorders: A drug repurposing approach

D Advani, R Gupta, R Tripathi, S Sharma… - Neurochemistry …, 2020 - Elsevier
The disease heterogeneity and little therapeutic progress in neurodegenerative diseases
justify the need for novel and effective drug discovery approaches. Drug repurposing is an …

Identification of novel trophoblast invasion-related genes: heme oxygenase-1 controls motility via peroxisome proliferator-activated receptor γ

M Bilban, P Haslinger, J Prast, F Klinglmüller… - …, 2009 - academic.oup.com
Invasion of cytotrophoblasts (CTBs) into uterine tissues is essential for placental
development. To identify molecules regulating trophoblast invasion, mRNA signatures of …

ALS-linked SOD1 mutants enhance neurite outgrowth and branching in adult motor neurons

Z Osking, JI Ayers, R Hildebrandt, K Skruber, H Brown… - Iscience, 2019 - cell.com
Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neurodegenerative disease
characterized by motor neuron cell death. However, not all motor neurons are equally …

Nutritional and exercise-based interventions in the treatment of amyotrophic lateral sclerosis

BP Patel, MJ Hamadeh - Clinical Nutrition, 2009 - Elsevier
BACKGROUND & AIMS: Disease pathogenesis in amyotrophic lateral sclerosis (ALS)
involves a number of interconnected mechanisms all resulting in the rapid deterioration of …

Mitochondrial involvement in amyotrophic lateral sclerosis: trigger or target?

SR Bacman, WG Bradley, CT Moraes - Molecular Neurobiology, 2006 - Springer
Despite numerous reports demonstrating mitochondrial abnormalities associated with
amyotrophic lateral sclerosis (ALS), the role of mitochondrial dysfunction in the disease …

Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model mice

P Zetterström, KS Graffmo, PM Andersen… - Journal of Biological …, 2011 - ASBMB
Mutant superoxide dismutase-1 (SOD1) has an unidentified toxic property that provokes
ALS. Several ALS-linked SOD1 mutations cause long C-terminal truncations, which …

Biochemical and molecular analyses of copper–zinc superoxide dismutase from a C4 plant Pennisetum glaucum reveals an adaptive role in response to oxidative …

S Mahanty, T Kaul, P Pandey, RA Reddy… - Gene, 2012 - Elsevier
Superoxide dismutases (SODs) form the foremost line of defense against ROS in aerobes.
Pennisetum glaucum cDNA library is constructed to isolate superoxide dismutase cDNA …

Using ALS to understand profilin 1's diverse roles in cellular physiology

HL Lindamood, TM Liu, TA Read, EA Vitriol - Cytoskeleton, 2024 - Wiley Online Library
Profilin is an actin monomer‐binding protein whose role in actin polymerization has been
studied for nearly 50 years. While its principal biochemical features are now well …

G93A SOD1 alters cell cycle in a cellular model of Amyotrophic Lateral Sclerosis

E Cova, A Ghiroldi, S Guareschi, G Mazzini… - Cellular signalling, 2010 - Elsevier
Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative multifactorial disease
characterized, like other diseases such as Alzheimer's disease (AD), Parkinson's disease …