Molecular biology of amyotrophic lateral sclerosis: insights from genetics

P Pasinelli, RH Brown - Nature Reviews Neuroscience, 2006 - nature.com
Amyotrophic lateral sclerosis (ALS) is a paralytic disorder caused by motor neuron
degeneration. Mutations in more than 50 human genes cause diverse types of motor neuron …

Axonal transport defects in neurodegenerative diseases

GA Morfini, M Burns, LI Binder, NM Kanaan… - Journal of …, 2009 - Soc Neuroscience
Adult-onset neurodegenerative diseases (AONDs) comprise a heterogeneous group of
neurological disorders characterized by a progressive, age-dependent decline in neuronal …

Autophagic and lysosomal defects in human tauopathies: analysis of post-mortem brain from patients with familial Alzheimer disease, corticobasal degeneration and …

A Piras, L Collin, F Grüninger, C Graff… - Acta neuropathologica …, 2016 - Springer
Introduction The accumulation of insoluble proteins within neurons and glia cells is a
pathological hallmark of several neurodegenerative diseases. Abnormal aggregation of the …

Impaired neurogenesis is an early event in the etiology of familial Alzheimer's disease in transgenic mice

M Demars, YS Hu, A Gadadhar… - Journal of neuroscience …, 2010 - Wiley Online Library
Formation of new neurons in the adult brain takes place in the subventricular zone and in
the subgranule layer of the dentate gyrus throughout life. Neurogenesis is thought to play a …

Pathogenic forms of tau inhibit kinesin-dependent axonal transport through a mechanism involving activation of axonal phosphotransferases

NM Kanaan, GA Morfini, NE LaPointe… - Journal of …, 2011 - Soc Neuroscience
Aggregated filamentous forms of hyperphosphorylated tau (a microtubule-associated
protein) represent pathological hallmarks of Alzheimer's disease (AD) and other …

Advances in the potential biomarkers of epilepsy

D Kobylarek, P Iwanowski, Z Lewandowska… - Frontiers in …, 2019 - frontiersin.org
Epilepsy is a group of chronic neurological disorders characterized by recurrent,
spontaneous, and unpredictable seizures. It is one of the most common neurological …

Microtubule-binding drugs offset tau sequestration by stabilizing microtubules and reversing fast axonal transport deficits in a tauopathy model

B Zhang, A Maiti, S Shively, F Lakhani… - Proceedings of the …, 2005 - National Acad Sciences
We tested the hypothesis that microtubule (MT)-binding drugs could be therapeutically
beneficial in tauopathies by functionally substituting for the MT-binding protein tau, which is …

Glycogen synthase kinase 3: a drug target for CNS therapies

RV Bhat, SL Budd Haeberlein… - Journal of …, 2004 - Wiley Online Library
Abstract Glycogen synthase kinase3 (GSK3) is emerging as a prominent drug target in the
CNS. The most exciting of the possibilities of GSK3 lies within the treatment of Alzheimer's …

HDAC6 regulates mitochondrial transport in hippocampal neurons

S Chen, GC Owens, H Makarenkova, DB Edelman - PloS one, 2010 - journals.plos.org
Background Tubulin is a major substrate of the cytoplasmic class II histone deacetylase
HDAC6. Inhibition of HDAC6 results in higher levels of acetylated tubulin and enhanced …

Long-term accumulation of amyloid-β, β-secretase, presenilin-1, and caspase-3 in damaged axons following brain trauma

XH Chen, R Siman, A Iwata, DF Meaney… - The American journal of …, 2004 - Elsevier
Plaques composed of amyloid β (Aβ) have been found within days following brain trauma in
humans, similar to the hallmark plaque pathology of Alzheimer's disease (AD). Here, we …