Feed Preview

Fast Growing

Organelles in Neurodegeneration

Organelles in Neurodegeneration diagram by Tefi, Shutterstock
Tefi, Shutterstock

Neurodegeneration is the progressive loss of neural structures and functions, including neuronal death. This feed focuses on dynamics of neuronal organelles in neurodegenerative diseases.

Top 20 most recent papers
Scientific Reports

Association of Insulin-like Growth Factor 1 Concentrations with Risk for and Prognosis of Amyotrophic Lateral Sclerosis - Results from the ALS Registry Swabia

Scientific ReportsJanuary 22, 2020
Gabriele NagelAlbert C Ludolph
Neuron

Aβ Puts the Alpha in Synuclein

NeuronJanuary 24, 2020
Casey Cook, Leonard Petrucelli
7
bioRxiv

Loss of function of the mitochondrial peptidase PITRM1 induces proteotoxic stress and Alzheimer's disease-like pathology in human cerebral organoids

bioRxivJanuary 27, 2020
Michela DeleidiCarlo Viscomi
Neuroscience Research

The PINK1-Parkin axis: An Overview

Neuroscience ResearchJanuary 27, 2020
Keiji Tanaka
3
The Journal of Immunology : Official Journal of the American Association of Immunologists

Size-Selective Phagocytic Clearance of Fibrillar α-Synuclein through Conformational Activation of Complement Receptor 4

The Journal of Immunology : Official Journal of the American Association of ImmunologistsJanuary 24, 2020
Kristian Juul-MadsenThomas Vorup-Jensen
2
Journal of Molecular Biology

Association between Atg5-independent alternative autophagy and neurodegenerative diseases

Journal of Molecular BiologyJanuary 25, 2020
Shinya HondaShigeomi Shimizu
Brain Structure & Function

Exclusive neuronal detection of KGDHC-specific subunits in the adult human brain cortex despite pancellular protein lysine succinylation

Brain Structure & FunctionJanuary 27, 2020
Arpad DobolyiChristos Chinopoulos
2
Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry

Huntington's Disease: A Review of the Known PET Imaging Biomarkers and Targeting Radiotracers

Molecules : a Journal of Synthetic Chemistry and Natural Product ChemistryJanuary 26, 2020
Klaudia CybulskaMark Rijpkema
3
bioRxiv

Vps13D is required for mitochondrial fission and mitophagy triggered by fission defects in Drosophila neurons

bioRxivJanuary 22, 2020
Ryan InsoleraCatherine A Collins
Molecular Neurobiology

Sephin1 Reduces Prion Infection in Prion-Infected Cells and Animal Model

Molecular NeurobiologyJanuary 26, 2020
Simrika ThapaHermann M Schatzl
3
International Journal of Molecular Sciences

Computer-Aided Drug Design of β-Secretase, γ-Secretase and Anti-Tau Inhibitors for the Discovery of Novel Alzheimer's Therapeutics

International Journal of Molecular SciencesJanuary 25, 2020
Varnavas D MouchlisAntreas Afantitis
Scientific Reports

Epothilone D alters normal growth, viability and microtubule dependent intracellular functions of cortical neurons in vitro

Scientific ReportsJanuary 24, 2020
J A ClarkC A Blizzard
Neurobiology of Aging

Modulation of neuroinflammation by cysteinyl leukotriene 1 and 2 receptors: implications for cerebral ischemia and neurodegenerative diseases

Neurobiology of AgingJanuary 28, 2020
Yuxi WangLihui Zhang
bioRxiv

Combining feature selection and shape analysis uncovers precise rules for miRNA regulation in Huntington's disease mice

bioRxivJanuary 25, 2020
Lucile MegretChristian Neri
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Für Pharmazeutische Verfahrenstechnik E.V

Current insights on lipid nanocarrier-assisted drug delivery in the treatment of neurodegenerative diseases

European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Für Pharmazeutische Verfahrenstechnik E.VJanuary 27, 2020
Maria Inês TeixeiraPaulo C Costa
2
Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry

White Matter and Neuroprotection in Alzheimer's Dementia

Molecules : a Journal of Synthetic Chemistry and Natural Product ChemistryJanuary 26, 2020
Luca LorenziniLuciana Giardino
2
Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry

Microglial Phenotypes and Their Relationship to the Cannabinoid System: Therapeutic Implications for Parkinson's Disease

Molecules : a Journal of Synthetic Chemistry and Natural Product ChemistryJanuary 25, 2020
Rachel KellyEilís Dowd
Toxicology

Glutamate affects cholesterol homeostasis within the brain via the up-regulation of CYP46A1 and ApoE

ToxicologyJanuary 26, 2020
Junjie ZhangJiang Yue
Journal of Neuroscience Research

Mirror neurons and their relationship with neurodegenerative disorders

Journal of Neuroscience ResearchJanuary 25, 2020
Elisabetta FarinaThierry Pozzo
4
Journal of Agricultural and Food Chemistry

Synthesis of Dithiolethiones and Identification of Potential Neuroprotective Agents via Activation of Nrf2-Driven Antioxidant Enzymes

Journal of Agricultural and Food ChemistryJanuary 28, 2020
Zi-Long SongJianguo Fang

See more papers from this feed

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.

ATP Synthases

ATP synthases are enzymes located in the inner mitochondrial membrane that catalyze the synthesis of ATP during cellular respiration. Discover the latest research on ATP synthases here.

© 2020 Meta ULC. All rights reserved
/feed-previews/organelles-in-neurodegeneration/bd19b26f-e529-49eb-a494-b9c1dc5e2624