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Full record GDS1843

Cystic fibrosis transmembrane conductance regulator CFTR deficiency effect on lungs: time course

Expression profiling of lungs from animals lacking the cystic fibrosis transmembrane conductance regulator gene (CFTR). Animals examined at 3, 6, and 11 weeks of age. Mutations in CFTR cause cystic fibrosis, an autosomal recessive monogenic disorder.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 age, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE4513
10 Samples
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DataSet
Accession:
GDS1843
ID:
1843

GEO Profiles Analyze DataSet

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