Connective tissue disease, heritable
Connective tissue disease, heritable: See: Heritable connective tissue disease.
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- Connexin
Connexin: A subunit of connexon, a protein that forms a gap junction, a channel that permits ions and small molecules to move between adjacent cells. The connexins are important to intercellular communication. Historically, gap junctions were first characterized by EM (electron microscopy). They appeared to be specialized structures in the plasma membranes of cells in […]
- Connexin 26
Connexin 26: Also known as gap junction beta 2, or GJB2. See: GJB2. See also: Connexin.
- Connexon
Connexon: A special type of protein composed of an assembly of six subunits that are called connexins. A connexon of one cell is joined to that of an adjacent cell to form an intercellular channel consisting of 12 connexin subunits. Clusters of intercellular channels are known as a gap junction because of the minute extracellular […]
- Conor and Bruch disease
Conor and Bruch disease: African tick typhus, one of the tick-borne rickettsial diseases of the eastern hemisphere similar to Rocky Mountain spotted fever but less severe. Characteristic features include fever, a small ulcer (tache noire) at the site of the tick bite, swollen glands nearby (satellite lymphadenopathy), and a red raised (maculopapular) rash. Also called […]
- Conotoxin
Conotoxin: A toxin made by cone snails (Conidae), also called cone shells, which are fish-eating snails that inhabit tropical coral reefs, mangroves and associated habitats. Each of the 500 species of cone snail produces roughly 50 to 100 distinct conotoxins which they use to immobilize prey. These toxins are selective in their receptor binding sites. […]