CFTR:蛋白
囊性纤维化跨膜传导调节因子(Cystic Fibrosis Transmembrane Regulator,简称CFTR)是一种在医学与生物学研究中广泛涉及的跨膜蛋白。为便于书写与交流,该专业术语在文献及临床应用中常以其缩写“CFTR”指代。这一蛋白质的功能涉及离子通道调节,其编码基因的突变与囊性纤维化等遗传性疾病的发生密切相关。
Cystic Fibrosis Transmembrane Regulator具体释义
Cystic Fibrosis Transmembrane Regulator的英文发音
例句
- Children with CF have an abnormality in the function of a cell protein called the cystic fibrosis transmembrane regulator.
- 患有囊性纤维化的儿童有异常的细胞蛋白(CFTR)功能,这个细胞蛋白(CFTR)叫囊性纤维化跨膜蛋白(CFTR)调节因子。
- The protective effects of cystic fibrosis transmembrane conductance regulator chloride channel on injured human alveolar epithelial cells
- 囊性纤维化跨膜调节因子氯离子通道在人肺泡上皮细胞损伤中的保护作用
- Butyl-p-hydroxybenzoate stimulates cystic fibrosis transmembrane conductance regulator Cl ~ - transport Preliminary study on the effect of transcription-coactivator OBF-1 protein upon the expression of p300
- 对羟基苯甲酸丁酯激活囊性纤维化跨膜电导调节因子氯离子通道开放转录共激活因子OBF-1调节p300表达的初步研究
- The cystic fibrosis transmembrane conductance regulator ( CFTR ) is a cAMP-activated and ATP-gated Cl ~ - channel expressed in the apical plasma membrane of epithelial cells in the airways, digestive and reproductive tracts.
- 囊性纤维化跨膜传导调节因子(CFTR)是一种cAMP激活的ATP门控性氯离子通道,表达于气道,消化道和生殖道上皮细胞的顶部质膜中。
- The etiology of CAVD is associated with the cystic fibrosis transmembrane conductance regulator ( CFTR ) gene and defects in the Wolffian duct, and frequently complicated by renal agenesis and other urogenital abnormalities.
- 研究表明,CAVD的发病与囊性纤维化跨膜转运调节物(CFTR)基因突变和中肾管发育缺陷有关。CAVD患者可合并肾发育不全和其他泌尿系统异常。
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