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A multi-omics characterization reveals distinct molecular signatures in the human motor cortex and lumbar spinal cord in ALS

2026-07-28

Abstract excerpt

<h4>ABSTRACT</h4> Amyotrophic lateral sclerosis (ALS) is a debilitating neurodegenerative disease characterized by the loss of upper motor neurons in the motor cortex (MTC) and lower motor neurons in the spinal cord, leading to muscle atrophy and ultimately respiratory failure. While motor neurons (MNs) are the selectively vulnerable cell type, their interactions with glia contribute to the progression of ALS pat...

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Literature Corpus work
31774b78-df10-5fd5-82f7-a976645b3621
DOI
10.64898/2026.07.24.740361
Open publication

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