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482 Screening of defective cystic fibrosis (CF) genomes: Two different approaches, one to be favored

机译：482筛查缺陷性囊性纤维化（CF）基因组：两种不同的方法，一种值得推荐

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1. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Potentiator VX-770 (Ivacaftor) Opens the Defective Channel Gate of Mutant CFTR in a Phosphorylation-dependent but ATP-independent Manner [J] . Paul W. Eckford, Canhui Li, Mohabir Ramjeesingh, The Journal of biological chemistry . 2012,第44期

机译：囊性纤维化跨膜电导调节器（CFTR）电位器VX-770（IVACAFTOR）在依赖于磷酸化但ATP独立的方式中打开突变体CFTR的缺陷通道栅极
2. Intraclonal diversity of the Pseudomonas aeruginosa cystic fibrosis airway isolates TBCF10839 and TBCF121838: Distinct signatures of transcriptome, proteome, metabolome, adherence and pathogenicity despite an almost identical genome sequence [J] . Klockgether J, Miethke N, Kubesch P, Environmental microbiology . 2013,第1期

机译：铜绿假单胞菌囊性纤维化气道分离株TBCF10839和TBCF121838的克隆内多样性：尽管基因组序列几乎相同，但转录组，蛋白质组，代谢组，粘附和致病性的独特特征
3. Structural mechanisms for defective CFTR gating caused by the Q1412X mutation, a severe Class?VI pathogenic mutation in cystic fibrosis [J] . Yeh Jiunn‐Tyng, Yu Ying‐Chun, Hwang Tzyh‐Chang The Journal of Physiology . 2019,第2期

机译：Q1412X突变引起的缺陷CFTR门控的结构机制，严重的血纤粒术中的致血液致病性突变
4. Cystic fibrosis transmembrane conductance regulator gene mutations cause 'black' pigment gallstone formation: new insights from mouse models and implications for therapeutic interventions in cystic fibrosis [C] . A. L. BRODERICK, H. WITTENBURG, M. A. LYONS, Falk Symposium . 2004

机译：囊性纤维化跨膜电导调节剂基因突变引起'黑色'颜料胆结石形成：来自小鼠模型的新见解，以及对囊性纤维化治疗干预的影响
5. CFTR-associated ligand (CAL)-dependent post-Golgi trafficking of cystic fibrosis transmembrane conductance regulator (CFTR) is modulated by insulin-like growth factor 1 (IGF-1). [D] . Lee, Ha Won. 2012

机译：囊性纤维化跨膜电导调节剂（CFTR）的CFTR相关配体（CAL）依赖性高尔基体运输受到胰岛素样生长因子1（IGF-1）的调节。
6. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Potentiator VX-770 (Ivacaftor) Opens the Defective Channel Gate of Mutant CFTR in a Phosphorylation-dependent but ATP-independent Manner [O] . Paul D. W. Eckford, Canhui Li, Mohabir Ramjeesingh, 2012

机译：囊性纤维化跨膜电导调节剂（CFTR）增效剂VX-770（Ivacaftor）以依赖磷酸化但不依赖ATP的方式打开突变CFTR的缺陷通道门
7. 211 What physiotherapy is being carried out for infants with cystic fibrosis (CF) in the UK since the introduction of newborn screening? Results from a national physiotherapy survey conducted by the Cystic Fibrosis Trust [O] . Ferguson K.V., Old K. 2013

机译：211自从引入新生儿筛查以来，英国正在对患有囊性纤维化（CF）的婴儿进行哪些物理治疗？囊性纤维化信托基金进行的全国理疗调查的结果

482 Screening of defective cystic fibrosis (CF) genomes: Two different approaches, one to be favored

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