Neuronal and Network Dysfunction in ND

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

January 20, 2021

The Structural Basis of Amyloid Strains in Alzheimer's Disease

ACS Biomaterials Science & Engineering
Lee Makowski
January 18, 2021

Vulnerability of subcellular structures to pathogenesis induced by rotenone in SH-SY5Y cells

Physiological Research
M PokusaA Kráľová-Trančíková
January 9, 2021
Open Access

Exosomes induce endolysosomal permeabilization as a gateway by which exosomal tau seeds escape into the cytosol

Acta Neuropathologica
Juan Carlos PolancoJürgen Götz
January 16, 2021

Effect of lipase incorporation on gelling properties of catfish (Clarias lazera) surimi and its mechanism

Journal of the Science of Food and Agriculture
Xidong JiaoDaming Fan
January 21, 2021

Homogentisic acid induces cytoskeleton and extracellular matrix alteration in alkaptonuric cartilage.

Journal of Cellular Physiology
Silvia GalderisiAnnalisa Santucci
January 16, 2021
Review

Brain lipidomics as a rising field in neurodegenerative contexts: Perspectives with Machine Learning approaches

Frontiers in Neuroendocrinology
Daniel Báez CastellanosJanneth González Santos
January 20, 2021

Indication of retrograde tau spreading along Braak stages and functional connectivity pathways

European Journal of Nuclear Medicine and Molecular Imaging
Joseph Seemillerand the Alzheimer’s Disease Neuroimaging Initiative
January 20, 2021
Open Access

Topographic patterns of white matter hyperintensities are associated with multimodal neuroimaging biomarkers of Alzheimer's disease.

Alzheimer's Research & Therapy
Malo GaubertMiranka Wirth
January 10, 2021

SOX21-AS1 modulates neuronal injury of MMP+ -treated SH-SY5Y cells via targeting miR-7-5p and inhibiting IRS2

Neuroscience Letters
Yang XieZuoxiao Li
January 20, 2021

Hyperhomocysteinemia and Dementia Associated With Severe Cortical Atrophy, but No Amyloid Burden

Journal of Geriatric Psychiatry and Neurology
Alessandro Reffo, Carlo Gabelli
January 9, 2021

Unique Subtype of Microglia in Degenerative Thalamus After Cortical Stroke

Stroke; a Journal of Cerebral Circulation
Zhijuan CaoGary K Steinberg
January 8, 2021

The interplay of emotional and social conceptual processes during moral reasoning in frontotemporal dementia

Brain : a Journal of Neurology
Cherie Strikwerda-BrownMuireann Irish

Sign up to follow this feed and discover related papers.

Related Feeds

3D Cellular Models of Brain and Neurodegeneration

Brain organoids are three-dimensional in vitro cellular models of the brain that can recapitulate many processes such as the neurodevelopment. In addition, these organoids can be combined with other cell types, such as neurons and astrocytes to study their interactions in assembloids. Disease processes can also be modeled by induced pluripotent stem cell-derived organoids and assembloids from patients with neurodegenerative disorders. Discover the latest research on the models here.

ALS & FTD: TDP-43

TAR DNA-binding protein 43 (TDP-43) is a pathological protein identified in sporadic Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD). Here are the latest discoveries pertaining to TDP-43 and these diseases.

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: Pathogenic Mechanisms

Amyotrophic Lateral Sclerosis 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 neurodegenerative disorder characterized phenotypically by progressive muscle weakness. Clinical phenotypes of ALS can be classified based on the pattern, level, and area of onset (e.g. bulbar, cervical, lumbar). Here is the latest research investigating phenotypes of ALS.

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 is the latest research on ALS and prions.

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 in this field.

ALS: Therapies

Amyotrophic Lateral Sclerosis (ALS) is associated with the death of neurons that control voluntary muscles. This feed followes the latest research into therapies for this progressive neurodegenerative disease.

Age-related Dementia

Dementias are a group of conditions, including Alzheimer's disease, vascular dementia, and frontotemporal dementia, characterized by deficiencies in cognitive abilities. Age-related dementia refers to dementias that occur in older individuals, usually 60+ years old, in contrast to early-onset dementia. Follow the latest research on age-related dementia here.

Alexander Disease

Alexander disease is a rare leukodystrophy caused by mutations in the astrocyte-specific intermediate filament protein glial fibrillary acidic protein (GFAP). Here is the latest research on this disease.

© 2021 Meta ULC. All rights reserved
/feed-previews/neuronal-and-network-dysfunction-in/506a6845-bc9d-4145-a3f0-201b860f7ea9