| cystic fibrosis transmembrane regulator p. |
a protein produced by the cystic fibrosis gene, consisting of a single peptide chain with 1480 amino acids; it is a transmembrane protein primarily functioning as a chloride channel, and found in cell membranes of the respiratory epithelium, pancreas, salivary glands, sweat glands, intestines, and reproductive tract. Numerous mutated forms of the gene, particularly one with a deletion causing omission of a phenylalanine residue from the protein, have been associated with clinical cystic fibrosis.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cystic g. |
one containing cysts formed by mucoid or colloid degeneration.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cystic h. |
a lymphangioma, usually in the neck area, composed of large, multilocular, thin-walled cysts. It may become large and exert pressure on adjacent structures. Called also cavernous or cystic lymphangioma.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cystic i. |
an infarct enclosed in a membrane.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| cystic k. |
one containing one or more cysts.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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