Neuronal and Network Dysfunction In Neurodegeneration

This feed focuses on neuronal and network dysfunction in neurodegenerative disorders and the effects of tauopathies on synapses and memory.

July 11, 2020

Complex I reductions in the nucleus basalis of Meynert in Lewy body dementia: the role of Lewy bodies

Acta Neuropathologica Communications
Christopher HattonDaniel Erskine
July 10, 2020
Review

Therapeutic applications of chelating drugs in iron metabolic disorders of the brain and retina

Journal of Neuroscience Research
Ali ShahandehChristine T O Nguyen
July 8, 2020
Review
Open Access

Dietary Antioxidants and Parkinson's Disease

Antioxidants
Han-A Park, Amy C Ellis
July 9, 2020
Open Access

Testing Amyloid Cross-Toxicity in the Vertebrate Brain

ACS Omega
Gabriela HenríquezMahesh Narayan
July 8, 2020
Review
Open Access

Effects of NAD+ in Caenorhabditis elegans Models of Neuronal Damage

Biomolecules
Yuri LeeKyung Won Kim
July 11, 2020

Dynamical system based compact deep hybrid network for classification of Parkinson disease related EEG signals

Neural Networks : the Official Journal of the International Neural Network Society
Syed Aamir Ali ShahAbdul Bais
July 11, 2020

PSP-FTD Complex: A Possible Variant of PSP

American Journal of Alzheimer's Disease and Other Dementias
Sunil Pradhan, Ruchika Tandon
July 10, 2020

Microdose Lithium Treatment Reduced Inflammatory Factors and Neurodegeneration in Organotypic Hippocampal Culture of Old SAMP-8 Mice

Cellular and Molecular Neurobiology
Mariana ToricelliTania Araujo Viel
July 11, 2020
Review
Open Access

Studying the Pathophysiology of Parkinson's Disease Using Zebrafish

Biomedicines
Lisa M BarnhillJeff M Bronstein
July 10, 2020

Neurofilament Light as a Biomarker in Traumatic Brain Injury

Neurology
Pashtun ShahimLeighton Chan
July 11, 2020

Expression of Mutant Ubiquitin and Proteostasis Impairment in Kii Amyotrophic Lateral Sclerosis/Parkinsonism-Dementia Complex Brains

Journal of Neuropathology and Experimental Neurology
Bert M VerheijenFred W van Leeuwen
July 12, 2020

Bassoon inhibits proteasome activity via interaction with PSMB4

Cellular and Molecular Life Sciences : CMLS
Carolina Montenegro-VenegasAnna Fejtova

Sign up to follow this feed and discover related papers.

Related Feeds

ALS

Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS here.

ALS & FTD: TDP-43

ALS shares with a considerable proportion of FTD cases the same neuropathological substrate, namely, inclusions of abnormally phosphorylated protein tdp-43 (ptdp-43). Here are the latest discoveries pertaining to ptdp-43 and these diseases.

ALS - Pathogenic Mechanisms

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. Here is the latest research investigating pathogenic mechanisms that underlie this genetically heterogeneous disorder.

ALS - Phenotypes

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. Here is the latest research investigating phenotypes associated with this genetically heterogeneous disorder.

ALS: Genetics

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. ALS is a genetically heterogeneous disorder with several causative genes. Here are the latest discoveries pertaining to the genetics of this disease.

ALS: Prions

Prions are misfolded proteins which characterize several fatal neurodegenerative diseases. Prion-like mechanisms are associated with the pathogenesis of Amyotrophic Lateral Sclerosis (ALS). Here are the latest discoveries pertaining to this disease.

ALS: Stress Granules

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease characterized by cytoplasmic protein aggregates within motor neurons. TDP-43 is an ALS-linked protein that is known to regulate splicing and storage of specific mRNAs into stress granules, which have been implicated in formation of ALS protein aggregates. Here is the latest research.

ALS: Therapies

Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS therapies here.

ALS: Transposon de-silencing

Transposon silencing is a form of transcriptional gene silencing. These gene silencing mechanisms are impaired in Amyotrophic lateral sclerosis (ALS). Here are the latest discoveries pertaining to transposon silencing and this disease.

Age-related Dementia

Age-related dementia (Alzheimer's disease) results from the destructive impact of the pulse on cerebral vasculature. Evidence is reviewed that the neuropathology of the dementia is caused by the breakdown of small cerebral vessels (silent microbleeds), that the microbleeds result from pulse-induced damage to the cerebral vessels, and that pulse becomes increasingly destructive with age, because of the age-related stiffening of the aorta and great arteries, which causes an increase in the intensity of the pressure pulse. Discover the latest research on age-related dementia here.

© 2020 Meta ULC. All rights reserved
/feed-previews/neuronal-and-network-dysfunction-in/506a6845-bc9d-4145-a3f0-201b860f7ea9