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E-GEOD-16361 - Gene expression profiling of muscles from transgenic humanSODG93A mice at symptomatic stage

Status
Released on 4 March 2010, last updated on 3 September 2015
Organism
Mus musculus
Samples (20)
Array (1)
Protocols (8)
Description
The transgenic mice expressing the human mutated form (G93A) of the SOD1 gene represent a valuable model of Amyotrophic Lateral Sclerosis (ALS). SOD1 is one of the main causative genes of familial ALS which accounts for 10% of cases. These transgenic animals develop a motorneuronal pathology that recapitulates well the neuropatological features occuring in ALS patients, and the progression of the disease can be monitored by a series of motor tests. Gastrocnemius is first and most affected muscle in the disease, while triceps is relatively spared. Gene expression data of degenerating motor neurons at different disease stages are already available, while gene expression data on the muscle tissue are missing. Our aim is to define the role of muscle in motor neuron degeneration in ALS. Keywords: Single stage analysis (early symptomatic stage, 14 weeks-old mice) We considered two sets of muscle at symptomatic stage (14 weeks): gastrocnemius and triceps from 4 transgenic SOD1G93A and 4 non-transgenic mice (NTg). Gastrocnemius from 4 nerve-crushed mice were also considered as controls for the denervation process
Experiment type
transcription profiling by array 
Contacts
Antonia Ratti <antonia.ratti@unimi.it>, Manuela Volta, Stefano Calza
MIAME
PlatformsProtocolsVariablesProcessedRaw
Files
Investigation descriptionE-GEOD-16361.idf.txt
Sample and data relationshipE-GEOD-16361.sdrf.txt
Raw data (1)E-GEOD-16361.raw.1.zip
Processed data (1)E-GEOD-16361.processed.1.zip
Array designA-AFFY-36.adf.txt
Links