相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。A helper-dependent adenoviral vector rescues CFTR to wild-type functional levels in cystic fibrosis epithelial cells harbouring class I mutations
Huibi Cao et al.
EUROPEAN RESPIRATORY JOURNAL (2020)
The CF Canada-Sick Kids Program in individual CF therapy: A resource for the advancement of personalized medicine in CF
Paul D. W. Eckford et al.
JOURNAL OF CYSTIC FIBROSIS (2019)
Airway Mucosal Host Defense Is Key to Genomic Regulation of Cystic Fibrosis Lung Disease Severity
Deepika Polineni et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2018)
A transcription factor network represses CFTR gene expression in airway epithelial cells
Michael J. Mutolo et al.
BIOCHEMICAL JOURNAL (2018)
Recent advances in developing therapeutics for cystic fibrosis
Lisa J. Strug et al.
HUMAN MOLECULAR GENETICS (2018)
Increased expression of ATP12A proton pump in cystic fibrosis airways
Paolo Scudieri et al.
JCI INSIGHT (2018)
Brushed nasal epithelial cells are a surrogate for bronchial epithelial CFTR studies
John J. Brewington et al.
JCI INSIGHT (2018)
A Joint Location-Scale Test Improves Power to Detect Associated SNPs, Gene Sets, and Pathways
David Soave et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
ΔF508 CFTR interactome remodelling promotes rescue of cystic fibrosis
Sandra Pankow et al.
NATURE (2015)
Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR
C. E. Wainwright et al.
NEW ENGLAND JOURNAL OF MEDICINE (2015)
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis
Harriet Corvol et al.
NATURE COMMUNICATIONS (2015)
The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells
Frauke Stanke et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2014)
Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation
Kris De Boeck et al.
JOURNAL OF CYSTIC FIBROSIS (2014)
Cathepsin B contributes to Na+ hyperabsorption in cystic fibrosis airway epithelial cultures
Chong Da Tan et al.
JOURNAL OF PHYSIOLOGY-LONDON (2014)
The joint graphical lasso for inverse covariance estimation across multiple classes
Patrick Danaher et al.
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY (2014)
The sva package for removing batch effects and other unwanted variation in high-throughput experiments
Jeffrey T. Leek et al.
BIOINFORMATICS (2012)
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis
Lei Sun et al.
NATURE GENETICS (2012)
Severe lung fibrosis requires an invasive fibroblast phenotype regulated by hyaluronan and CD44
Yuejuan Li et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2011)
Modulatory Effect of the SLC9A3 Gene on Susceptibility to Infections and Pulmonary Function in Children With Cystic Fibrosis
Ruslan Dorfman et al.
PEDIATRIC PULMONOLOGY (2011)
edgeR: a Bioconductor package for differential expression analysis of digital gene expression data
Mark D. Robinson et al.
BIOINFORMATICS (2010)
Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTR Mutation
Frank J. Accurso et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
AmiGO: online access to ontology and annotation data
Seth Carbon et al.
BIOINFORMATICS (2009)
Testing significance relative to a fold-change threshold is a TREAT
Davis J. McCarthy et al.
BIOINFORMATICS (2009)
Regulatory binding partners and complexes of NHE3
Mark Donowitz et al.
PHYSIOLOGICAL REVIEWS (2007)
分享论文
