[HTML][HTML] Fluid biomarkers for amyotrophic lateral sclerosis: a review

KE Irwin, U Sheth, PC Wong, TF Gendron - Molecular neurodegeneration, 2024 - Springer
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by
the loss of upper and lower motor neurons. Presently, three FDA-approved drugs are …

[HTML][HTML] Mesenchymal stem cell-derived extracellular vesicles: An emerging diagnostic and therapeutic biomolecules for neurodegenerative disabilities

M Kandeel, MA Morsy, KM Alkhodair, S Alhojaily - Biomolecules, 2023 - mdpi.com
Mesenchymal stem cells (MSCs) are a type of versatile adult stem cells present in various
organs. These cells give rise to extracellular vesicles (EVs) containing a diverse array of …

Endo-lysosomal dysfunction in neurodegenerative diseases: Opinion on current progress and future direction in the use of exosomes as biomarkers

M Herman, GW Randall, JL Spiegel… - … of the Royal …, 2024 - royalsocietypublishing.org
Over the past two decades, increased research has highlighted the connection between
endosomal trafficking defects and neurodegeneration. The endo-lysosomal network is an …

Exosomes in brain diseases: Pathogenesis and therapeutic targets

Q Si, L Wu, D Pang, P Jiang - MedComm, 2023 - Wiley Online Library
Exosomes are extracellular vesicles with diameters of about 100 nm that are naturally
secreted by cells into body fluids. They are derived from endosomes and are wrapped in …

[HTML][HTML] A machine learning approach for highlighting microRNAs as biomarkers linked to amyotrophic lateral sclerosis diagnosis and progression

G Lauria, R Curcio, P Tucci - Biomolecules, 2023 - mdpi.com
Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease characterized by
the progressive loss of motor neurons in the brain and spinal cord. The early diagnosis of …

[HTML][HTML] In vivo diagnosis of TDP-43 proteinopathies: in search of biomarkers of clinical use

JI López-Carbonero, I García-Toledo… - Translational …, 2024 - Springer
TDP-43 proteinopathies are a heterogeneous group of neurodegenerative disorders that
share the presence of aberrant, misfolded and mislocalized deposits of the protein TDP-43 …

The complexity of extracellular vesicles: Bridging the gap between cellular communication and neuropathology

S Tam, D Wear, CD Morrone… - Journal of …, 2024 - Wiley Online Library
Brain‐derived extracellular vesicles (EVs) serve a prominent role in maintaining
homeostasis and contributing to pathology in health and disease. This review establishes a …

Attenuation of amyotrophic lateral sclerosis via stem cell and extracellular vesicle therapy: An updated review

G Lockard, J Gordon, S Schimmel, B El Sayed… - …, 2023 - Wiley Online Library
Amyotrophic lateral sclerosis (ALS) is a rapidly fatal neurological disease characterized by
upper and lower motor neuron degeneration. Though typically idiopathic, familial forms of …

The endolysosomal pathway and ALS/FTD

TW Todd, W Shao, Y Zhang, L Petrucelli - Trends in neurosciences, 2023 - cell.com
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are considered to be
part of a disease spectrum that is associated with causative mutations and risk variants in a …

Interfering with hnRNPA2B1: ExoRNA interaction to challenge the quality of secreted extracellular vesicles

J Corsi - 2023 - iris.unitn.it
Amyotrophic lateral sclerosis (ALS) is a motor neuron disease. In ALS, RNA-binding proteins
(RBPs) accumulate and/or misfold and eventually associate with stress granules, leading to …