Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients

被引：0
|
作者：
Deanna M Green
Kathryn E McDougal
Scott M Blackman
Patrick R Sosnay
Lindsay B Henderson
Kathleen M Naughton
J Michael Collaco
Garry R Cutting
机构：
[1] Johns Hopkins University School of Medicine,Division of Pediatric Respiratory Sciences
[2] Johns Hopkins University,Department of Epidemiology, Bloomberg School of Public Health
[3] Johns Hopkins University School of Medicine,McKusick
[4] Johns Hopkins University School of Medicine,Nathans Institute of Genetic Medicine
来源：
Respiratory Research | / 11卷
关键词：
Cystic Fibrosis; Lung Function; Genetic Modifier; Cystic Fibrosis Patient; Methicillin Resistant Staphylococcus Aureus;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [41] Respiratory impairment in multiple sclerosis: a study of respiratory function in wheelchair-bound patients
    Levy, J.
    Bensmail, D.
    Brotier-Chomienne, A.
    Butel, S.
    Joussain, C.
    Hugeron, C.
    Prigent, H.
    EUROPEAN JOURNAL OF NEUROLOGY, 2017, 24 (03) : 497 - 502
  • [42] NASAL POTENTIAL DIFFERENCE IN SUSPECTED CF PATIENTS WITH 5T POLYMORPHISM - CFTR FUNCTION TESTING AND FOLLOW UP
    Aalbers, B. L.
    Bronsveld, I
    Yaakov, Y.
    Wilschanski, M.
    PEDIATRIC PULMONOLOGY, 2013, 48 : 268 - 268
  • [43] CFTR MESSENGER-RNA TRANSCRIPTS ARE DECREASED IN RESPIRATORY EPITHELIA OF PATIENTS WITH NONSENSE MUTATIONS IN THE CYSTIC-FIBROSIS GENE
    HAMOSH, A
    TRAPNELL, BC
    MONTROSERAFIZADEH, C
    ZEITLIN, PL
    ROSENSTEIN, BJ
    CRYSTAL, RG
    CUTTING, GR
    PEDIATRIC RESEARCH, 1991, 29 (04) : A130 - A130
  • [44] In vivo and in vitro ivacaftor response in cystic fibrosis patients with residual CFTR function: N-of-1 studies
    McGarry, Meghan E.
    Illek, Beate
    Ly, Ngoc P.
    Zlock, Lorna
    Olshansky, Sabrina
    Moreno, Courtney
    Finkbeiner, Walter E.
    Nielson, Dennis W.
    PEDIATRIC PULMONOLOGY, 2017, 52 (04) : 472 - 479
  • [45] EFFECT OF EARLY DERANGEMENTS IN GLUCOSE TOLERANCE MECHANISMS ON THE NUTRITIONAL STATUS & RESPIRATORY FUNCTION OF CF PATIENTS
    Battezzati, A.
    Alicandro, G.
    Zazzeron, L.
    Dacco, V.
    Battezzati, P.
    Costantini, D.
    Mari, A.
    Colombo, C.
    PEDIATRIC PULMONOLOGY, 2010, : 429 - 429
  • [46] INFLUENCE OF RESPIRATORY EXACERBATIONS ON LUNG-FUNCTION VARIABLES AND NUTRITIONAL-STATUS IN CF PATIENTS
    NEIJENS, HJ
    DUIVERMAN, EJ
    KERREBIJN, KF
    SINAASAPPEL, M
    ACTA PAEDIATRICA SCANDINAVICA, 1985, : 38 - 41
  • [47] The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells
    Stanke, Frauke
    van Barneveld, Andrea
    Hedtfeld, Silke
    Woelfl, Stefan
    Becker, Tim
    Tuemmler, Burkhard
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2014, 22 (05) : 660 - 666
  • [48] The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells
    Frauke Stanke
    Andrea van Barneveld
    Silke Hedtfeld
    Stefan Wölfl
    Tim Becker
    Burkhard Tümmler
    European Journal of Human Genetics, 2014, 22 : 660 - 666
  • [49] Co-infections of SARS-CoV-2 with multiple common respiratory pathogens in infected patients
    Dachuan Lin
    Lei Liu
    Mingxia Zhang
    Yunlong Hu
    Qianting Yang
    Jiubiao Guo
    Yongchao Guo
    Youchao Dai
    Yuzhong Xu
    Yi Cai
    Xinchun Chen
    Zheng Zhang
    Kaisong Huang
    Science China(Life Sciences) , 2020, (04) : 606 - 609
  • [50] Co-infections of SARS-CoV-2 with multiple common respiratory pathogens in infected patients
    Dachuan Lin
    Lei Liu
    Mingxia Zhang
    Yunlong Hu
    Qianting Yang
    Jiubiao Guo
    Yongchao Guo
    Youchao Dai
    Yuzhong Xu
    Yi Cai
    Xinchun Chen
    Zheng Zhang
    Kaisong Huang
    Science China Life Sciences, 2020, 63 : 606 - 609
12345