Amyotrophic lateral sclerosis. Homo sapiens

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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA87835

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Identification of amyotrophic lateral sclerosis (ALS) associated genes. Post mortem spinal cord grey matter from sporadic and familial ALS patients compared with controls. Keywords: other

创建时间：

2003-11-14

Amyotrophic Lateral Sclerosis. Homo sapiens

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease that affects the nerves in the brain and spinal cord, leading to muscle weakening and eventual paralysis and death. 10% of ALS cases

NIAID Data Ecosystem10

Expression profiling of motor cortex in sporadic amyotrophic lateral sclerosis. Homo sapiens

We used oligonucleotide microarrays to find differentially expressed genes between control subjects and those affected by sporadic amyotrophic lateral sclerosis. Keywords: disease state analysis Overa

NIAID Data Ecosystem20

Identification of circular RNAs in amyotrophic lateral sclerosis. Identification of circular RNAs in amyotrophic lateral sclerosis

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series

NIAID Data Ecosystem20

Whole-Exome Sequencing of Familial Amyotrophic Lateral Sclerosis. Homo sapiens

Amyotrophic Lateral Sclerosis (ALS) is a terminal late onset neurodegenerative disease characterized by the degeneration of both the upper and lower motor neurons. A family history of ALS, familial AL

NIAID Data Ecosystem20

Abnormal RNA stability in amyotrophic lateral sclerosis. Abnormal RNA stability in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) share key features, including accumulation of the RNA binding protein TDP-43. TDP-43 regulatesRNA homeostasis, but it remains uncl

NIAID Data Ecosystem20