cystic fibrosis transmembrane regulator
- cystic fibrosis transmembrane regulator
- (CFTR), cystic fibrosis transmembrane conductance regulator a transmembrane protein produced by the CFTR gene, primarily functioning as a cAMP-regulated chloride channel that also regulates other ion channels, and found in cell membranes of the respiratory epithelium, pancreas, salivary glands, sweat glands, intestines, and reproductive tract. Numerous mutations, particularly a deletion causing omission of a phenylalanine residue from the protein, have been associated with cystic fibrosis.
Medical dictionary.
2011.
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cystic fibrosis transmembrane regulator — cystic fibrosis transmembrane regulator. См. трансмембранный регулятор муковисцидоза. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
cystic fibrosis transmembrane regulator protein — cystic fibrosis transmembrane regulator … Medical dictionary
Cystic fibrosis transmembrane conductance regulator — (ATP binding cassette sub family C, member 7) NBD1 of human CFTR complexed with ATP. PDB rendering based on 1xmi … Wikipedia
Cystic Fibrosis Transmembrane Conductance Regulator — Vorhandene Strukturdaten … Deutsch Wikipedia
cystic fibrosis transmembrane conductance regulator — (= CFTR) Gene believed to be defective in cystic fibrosis. Gene encodes a chloride channel, homologous to a family of proteins that actively transport small solutes in an ATP dependent manner (ABC proteins) … Dictionary of molecular biology
Cystic fibrosis — One of the most common grave genetic (inherited) diseases, CF affects the exocrine glands and is characterized by the production of abnormal secretions, leading to mucous build up. This accumulation of mucus can impair the pancreas and,… … Medical dictionary
Cystic fibrosis — Classification and external resources A breathing treatment for cystic fibrosis, using a mask nebuliser and a ThAIRapy Vest ICD 10 E … Wikipedia
cystic fibrosis — Pathol. a hereditary chronic disease of the exocrine glands, characterized by the production of viscid mucus that obstructs the pancreatic ducts and bronchi, leading to infection and fibrosis. [1950 55] * * * ▪ pathology also called… … Universalium
cystic fibrosis — fibrocystic disease of the pancreas; = mucoviscidosis a hereditary disease affecting cells of the exocrine glands (including mucus secreting glands, sweat glands, and others). The faulty gene responsible for the most common form of the disease… … The new mediacal dictionary
Дегенерация Фибрознокистозная (Cystic Fibrosis), Дегенерация Поджелудочной Железы Фиброзно-Кистозная (Fibrocystic Disease Of The Pancreas), Муковисцидоз (Mucoviscidosis) — наследственное заболевание, при котором поражаются клетки экзокринных желез (в том числе слизистых, потовых и некоторых других). Дефектный ген, отвечающий за развитие этой болезни, находится в хромосоме № 7 и является рецессивным, т.е. оба… … Медицинские термины
