Transcriptomics

Dataset Information

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Expression data from V156D matn1 knock-in mouse rib chondrocytes at 5 days


ABSTRACT: V156D matn1 mutation (homologous to the V194D matn3 mutation causing Multiple Epiphyseal Dysplasia (MED)) was introduced by gene targetting in order to evaluate the potential of matrilin-1 to be a novel chondrodysplasia based on domain homology and aminoacid conservation. We used microarrays to analyse the differential expression of genes between wild type and mutant animals at day 5 (postnatal)

ORGANISM(S): Mus musculus

PROVIDER: GSE81880 | GEO | 2016/05/26

SECONDARY ACCESSION(S): PRJNA322836

REPOSITORIES: GEO

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