[HTML][HTML] Mitochondrial Dyshomeostasis as an Early Hallmark and a Therapeutic Target in Amyotrophic Lateral Sclerosis

NV Belosludtseva, LA Matveeva… - International Journal of …, 2023 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a fatal multisystem disease characterized by
progressive death of motor neurons, loss of muscle mass, and impaired energy metabolism …

[HTML][HTML] Application of the Yamanaka Transcription Factors Oct4, Sox2, Klf4, and c-Myc from the Laboratory to the Clinic

M Aguirre, M Escobar, S Forero Amézquita, D Cubillos… - Genes, 2023 - mdpi.com
The transcription factors Oct4, Sox2, Klf4, and c-Myc enable the reprogramming of somatic
cells into induced pluripotent cells. Reprogramming generates newly differentiated cells for …

[HTML][HTML] Susceptibility and disease modifier genes in amyotrophic lateral sclerosis: from genetic associations to therapeutic implications

SW Willemse, MA van Es - Current Opinion in Neurology, 2023 - journals.lww.com
Technological and methodological advances are enabling researchers to unravel the
genetics of ALS. Both causal mutations and genetic modifiers are viable therapeutic targets …

Optimal Therapeutic Strategy of Bone Marrow-Originated Autologous Mesenchymal Stromal/Stem Cells for ALS

SH Kim, KW Oh, MY Noh… - Stem Cells Translational …, 2024 - academic.oup.com
Amyotrophic lateral sclerosis (ALS) is characterized by selective and progressive
neurodegenerative changes in motor neural networks. Given the system complexity …

[HTML][HTML] Rapid and robust multi-phenotypic assay system for ALS using human iPS cells with mutations in causative genes

T Kondo, I Ebinuma, H Tanaka, Y Nishikawa… - International journal of …, 2023 - mdpi.com
Amyotrophic lateral sclerosis (ALS) is a major life-threatening disease caused by motor
neuron degeneration. More effective treatments through drug discovery are urgently …

The role of human pluripotent stem cells in amyotrophic lateral sclerosis: from biological mechanism to practical implications

L Ceccarelli, L Verriello, G Pauletto… - FRONTIERS IN …, 2024 - iris.uniroma1.it
Abstract Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disorder, characterized
by progressive loss of both upper and lower motor neurons, resulting in clinical features …

In Vivo Reprogramming Using Yamanaka Factors in the CNS: A Scoping Review

HE Cho, S Lee, JH Seo, SW Kang, WA Choi, SR Cho - Cells, 2024 - mdpi.com
Central nervous system diseases, particularly neurodegenerative disorders, pose significant
challenges in medicine. These conditions, characterized by progressive neuronal loss, have …

Meta-analysis of differential gene expression in lower motor neurons isolated by laser capture microdissection from post-mortem ALS spinal cords

WR Swindell - Frontiers in Genetics, 2024 - frontiersin.org
Introduction ALS is a fatal neurodegenerative disease for which underlying mechanisms are
incompletely understood. The motor neuron is a central player in ALS pathogenesis but …

Standardisation is the key to the sustained, rapid and healthy development of stem cell‐based therapy

J Zhang, M Suo, J Wang, X Liu, H Huang… - Clinical and …, 2024 - Wiley Online Library
Background Stem cell‐based therapy (SCT) is an important component of regenerative
therapy that brings hope to many patients. After decades of development, SCT has made …

Protein aggregation and therapeutic strategies in SOD1-and TDP-43-linked ALS

M Tsekrekou, M Giannakou… - Frontiers in Molecular …, 2024 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with severe socio-
economic impact. A hallmark of ALS pathology is the presence of aberrant cytoplasmic …