Global ETD Search
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Showing 1 to 1 of 1 for “"oculodentodigital dysplasia"”.
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FATE OF Cx43 IN CARDIAC AND EPIDERMAL TISSUES HARBOURING A DISEASE-LINKED Cx43 MUTANT
… in the GJA1 gene encoding Cx43 are linked to oculodentodigital dysplasia (ODDD), a pleiotropic, autosomal dominant disorder. We hypothesized that in the Gjal54 mouse model of ODDD there would be significant down-regulation of total Cx43 yet minimal compromise to cardiomyocyte or kératinocyte …