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Items: 8

1.

miRNA profile in lumbar spinal cord homogenate of SOD-miR155 Tg mice

(Submitter supplied) Amyotrophic lateral sclerosis (ALS) is a paralytic degenerative disease of the nervous system. In the SOD1 mouse model of ALS we found loss of the molecular and functional microglia signature associated with pronounced expression of miR-155 in SOD1 mice. We also found increased expression of miR-155 in the spinal cord of ALS subjects. Genetic ablation of miR-155 increased survival in SOD1 mice and reversed the abnormal microglial and monocyte molecular signature. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL18014
6 Samples
Download data: RCC
Series
Accession:
GSE52898
ID:
200052898
2.

Nanostring Mouse miRNA Assay Kit (mirBase 15)

(Submitter supplied) according to the manufacturer’s protocol
Organism:
Mus musculus
2 Series
6 Samples
Download data
Platform
Accession:
GPL18014
ID:
100018014
3.

SOD 155 -/- (2)

Organism:
Mus musculus
Source name:
Lumbar spinal cord homogenate
Platform:
GPL18014
Series:
GSE52898 GSE52947
Download data: RCC
Sample
Accession:
GSM1277671
ID:
301277671
4.

SOD 155 -/- (1)

Organism:
Mus musculus
Source name:
Lumbar spinal cord homogenate
Platform:
GPL18014
Series:
GSE52898 GSE52947
Download data: RCC
Sample
Accession:
GSM1277670
ID:
301277670
5.

SOD 155+/- (2)

Organism:
Mus musculus
Source name:
Lumbar spinal cord homogenate
Platform:
GPL18014
Series:
GSE52898 GSE52947
Download data: RCC
Sample
Accession:
GSM1277669
ID:
301277669
6.

SOD 155+/- (1)

Organism:
Mus musculus
Source name:
Lumbar spinal cord homogenate
Platform:
GPL18014
Series:
GSE52898 GSE52947
Download data: RCC
Sample
Accession:
GSM1277668
ID:
301277668
7.

WT 155+/- (2)

Organism:
Mus musculus
Source name:
Lumbar spinal cord homogenate
Platform:
GPL18014
Series:
GSE52898 GSE52947
Download data: RCC
Sample
Accession:
GSM1277667
ID:
301277667
8.

WT 155+/- (1)

Organism:
Mus musculus
Source name:
Lumbar spinal cord homogenate
Platform:
GPL18014
Series:
GSE52898 GSE52947
Download data: RCC
Sample
Accession:
GSM1277666
ID:
301277666
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Supplemental Content

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