Item does not contain fulltextGap junctions are assemblies of intercellular channels that regulate a variety of physiologic and developmental processes through the exchange of small ions and signaling molecules. These channels consist of connexin family proteins that allow for diversity of channel composition and conductance properties. The human connexin 43 gene, or GJA1, is located at human chromosome 6q22-q23 within the candidate region for the oculodentodigital dysplasia locus. This autosomal dominant syndrome presents with craniofacial (ocular, nasal, and dental) and limb dysmorphisms, spastic paraplegia, and neurodegeneration. Syndactyly type III and conductive deafness can occur in some cases, and cardiac abnormalities are observed i...
AbstractGap junctions provide coupled cells with a direct pathway for sharing ions, nutrients, and s...
PurposeTo examine the mechanism by which a novel connexin 50 (Cx50) mutation, Cx50 V44A, in a Chines...
Aims More than 40 mutations in the GJA1 gene encoding connexin43 (Cx43) have been linked to oculo-de...
Gap junctions are assemblies of intercellular channels that regulate a variety of physiologic and de...
Gap junctions are assemblies of intercellular channels that regulate a variety of physiologic and de...
Gap junctions are assemblies of intercellular channels that regulate a variety of physiologic and de...
The predominantly autosomal dominant disorder, oculodentodigital dysplasia (ODDD) has high penetranc...
Contains fulltext : 80660.pdf (publisher's version ) (Closed access)The predominan...
AbstractThere are now at least 14 distinct diseases linked to germ line mutations in the 21 genes th...
Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant pleiotropic disorder, caused by muta...
Craniometaphyseal dysplasia (CMD) is a rare sclerosing skeletal disorder with progressive hyperostos...
The coordination of tissue function is mediated by gap junctions (GJs) that enable direct cell–cell ...
The coordination of tissue function is mediated by gap junctions (GJs) that enable direct cell–cell ...
AbstractThere are now at least 14 distinct diseases linked to germ line mutations in the 21 genes th...
© 2017 American Society for Bone and Mineral Research We present for the first time the generation o...
AbstractGap junctions provide coupled cells with a direct pathway for sharing ions, nutrients, and s...
PurposeTo examine the mechanism by which a novel connexin 50 (Cx50) mutation, Cx50 V44A, in a Chines...
Aims More than 40 mutations in the GJA1 gene encoding connexin43 (Cx43) have been linked to oculo-de...
Gap junctions are assemblies of intercellular channels that regulate a variety of physiologic and de...
Gap junctions are assemblies of intercellular channels that regulate a variety of physiologic and de...
Gap junctions are assemblies of intercellular channels that regulate a variety of physiologic and de...
The predominantly autosomal dominant disorder, oculodentodigital dysplasia (ODDD) has high penetranc...
Contains fulltext : 80660.pdf (publisher's version ) (Closed access)The predominan...
AbstractThere are now at least 14 distinct diseases linked to germ line mutations in the 21 genes th...
Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant pleiotropic disorder, caused by muta...
Craniometaphyseal dysplasia (CMD) is a rare sclerosing skeletal disorder with progressive hyperostos...
The coordination of tissue function is mediated by gap junctions (GJs) that enable direct cell–cell ...
The coordination of tissue function is mediated by gap junctions (GJs) that enable direct cell–cell ...
AbstractThere are now at least 14 distinct diseases linked to germ line mutations in the 21 genes th...
© 2017 American Society for Bone and Mineral Research We present for the first time the generation o...
AbstractGap junctions provide coupled cells with a direct pathway for sharing ions, nutrients, and s...
PurposeTo examine the mechanism by which a novel connexin 50 (Cx50) mutation, Cx50 V44A, in a Chines...
Aims More than 40 mutations in the GJA1 gene encoding connexin43 (Cx43) have been linked to oculo-de...