Intraventricular Administration of Exosomes from Patients with Amyotrophic Lateral Sclerosis Provokes Motor Neuron Disease in Mice

Amyotrophic lateral sclerosis (ALS) is a severe disease of the central nervous system (CNS) characterized by motor neuron damage leading to death from respiratory failure. The neurodegenerative process in ALS is characterized by an accumulation of aberrant proteins (TDP-43, SOD1, etc.) in CNS cells....

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Vydané v:	Actanaturae Ročník 16; číslo 4; s. 73
Hlavní autori:	Stavrovskaya, A V, Voronkov, D N, Pavlova, A K, Olshanskiy, A S, Belugin, B V, Ivanova, M V, Zakharova, M N, Illarioshkin, S N
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	Russia (Federation) 01.10.2024
Predmet:	TDP43 motor neurons neurodegeneration amyotrophic lateral sclerosis exosomes
ISSN:	2075-8251
On-line prístup:	Zistit podrobnosti o prístupe
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