Association of sweat chloride concentration at time of diagnosis and CFTR genotype with mortality and cystic fibrosis phenotype

McKone Edward F.; Velentgas Priscilla; Swenson Anna J.; Goss Christopher H.

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Association of sweat chloride concentration at time of diagnosis and CFTR genotype with mortality and cystic fibrosis phenotype

机译：诊断时汗液氯化物浓度和CFTR基因型与死亡率和囊性纤维化表型的关系

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Background: The extent to which sweat chloride concentration predicts survival and clinical phenotype independently of CFTR genotype in cystic fibrosis is not well understood.

机译：背景：在囊性纤维化中，汗液中氯化物的浓度预测生存率和临床表型与CFTR基因型无关的程度尚不清楚。

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《Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society》 |2015年第5期|共7页
作者
McKone Edward F.; Velentgas Priscilla; Swenson Anna J.; Goss Christopher H.;
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正文语种 eng
中图分类泌尿科学（泌尿生殖系疾病）;
关键词
Cystic fibrosis; Survival analysis; Respiratory function; Genetics;

机译：囊性纤维化;生存分析;呼吸功能;遗传学;

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1. Association of sweat chloride concentration at time of diagnosis and CFTR genotype with mortality and cystic fibrosis phenotype [J] . McKone Edward F., Velentgas Priscilla, Swenson Anna J., Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society . 2015,第5期

机译：诊断时汗液氯化物浓度和CFTR基因型与死亡率和囊性纤维化表型的关系
2. Conductivity determined by a new sweat analyzer compared with chloride concentrations for the diagnosis of cystic fibrosis. [J] . Barben J, Ammann RA, Metlagel A, The Journal of pediatrics . 2005,第2期

机译：用新型汗液分析仪测定的电导率与氯化物浓度进行比较，以诊断囊性纤维化。
3. The relationship between sweat chloride levels and mortality in cystic fibrosis varies by individual genotype [J] . Julia C. Espel, Hannah L. Palac, Ankit Bharat, Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society . 2018,第1期

机译：患者氯化物水平与囊性纤维化中死亡率之间的关系因个体基因型而异
4. NEW PHARMACOLOGICAL TARGETS FOR CYSTIC FIBROSIS TREATMENT FROM EXTENSIVE PROTEOMIC PROFILING OF ?F508-CFTR EXPRESSING CELLS [C] . Clarissa Braccia, Valeria Tomati, Nicoletta Pedemonte, International Mass Spectrometry Conference . 2018

机译：新的药理纤维化治疗来自αF508-CFTR的广泛蛋白质组学分析
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. Chronic cough with normal sweat chloride: Phenotypic descriptions of two rare cystic fibrosis genotypes [O] . Hemang Yadav, Kaiser G. Lim 2016

机译：慢性咳嗽伴正常的汗液氯化物：两种罕见的囊性纤维化基因型的表型描述
7. Diagnosis of cystic fibrosis in the kindred of an infant with CFTR -related metabolic syndrome: Importance of follow-up that includes monitoring sweat chloride concentrations over time [O] . Sophia N. Williams, Eliezer Nussbaum, Terry W. Chin, 2013

机译：诊断患有CFTR相关代谢综合征的婴儿的囊泡纤维化：随访的重要性，包括监测禽类浓度随着时间的推移

Association of sweat chloride concentration at time of diagnosis and CFTR genotype with mortality and cystic fibrosis phenotype

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