Total RNAseq in the sporadic ALS and healthy control motor cortex

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the degeneration of upper and lower motor neurons leading to progressive muscle weakness, wasting and paralysis that result in death within a few years from disease onset. In order to characterize RNA alterations in ALS, total RNAseq was performed in the ALS motor cortex, which is an early and vulnerable region in ALS.

Type: Other
Archiver: European Genome-Phenome Archive (EGA)

1 Dataset 1 Publication

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID	Description	Technology	Samples
EGAD00001006022	The motor cortex is the earliest affected brain region in ALS. This dataset contains total RNA sequencing (stranded, 2x101bp) data derived from the motor cortex of 11 sporadic ALS patients and 8 healthy controls.		19

Publications	Citations
Motor cortex transcriptome reveals microglial key events in amyotrophic lateral sclerosis. Dols-Icardo O, Montal V, Sirisi S, López-Pernas G, Cervera-Carles L, Querol-Vilaseca M, Muñoz L, Belbin O, Belbin O, Alcolea D, Molina-Porcel L, Pegueroles J, Turón-Sans J, Blesa R, Lleó A, Fortea J, Fortea J, Rojas-García R, Clarimón J. Neurol Neuroimmunol Neuroinflamm 7: 2020 e829	37