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- Report of a black South African child with oculodentodigital...
Related Articles Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation. - Cell-cell communication in the osteoblast/osteocyte lineage.
...junction protein in the skeleton is demonstrated by the skeletal malformations present in oculodentodigital dysplasia (ODDD), a disease linked... - Decreased levels of connexin43 result in impaired development of the...
Decreased levels of connexin43 result in impaired development of the mammary gland in a mouse model of oculodentodigital dysplasia. Dev Biol. - Ocular manifestations in oculodentodigital dysplasia resulting from...
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43). Eye. - Decreased Levels of Connexin43 Results in Impaired Development of
Isabelle, Plante , Dale W., Laird... - Some oculodentodigital dysplasia-associated Cx43 mutations cause
Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels. - Gap junction remodeling and cardiac arrhythmogenesis in a murine...
Related Articles Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia. - Closing the gap on autosomal dominant connexin-26 and connexin-43...
...in the GJA1 gene, which encodes Cx43, exhibit modest developmental disorders resulting in a disease termed oculodentodigital dysplasia. - A New GJA1 (Connexin 43) Mutation Causing Oculodentodigital...
Oculodentodigital dysplasia (ODDD) is an autosomal dominant disorder that includes a clinical spectrum of craniofacial, neurologic, limb, and ocular