4.7 Article

Tezacaftor/Ivacaftor in Subjects with Cystic Fibrosis and F508del/F508del-CFTR or F508del/G551D-CFTR

Related references

Note: Only part of the references are listed.
Article Respiratory System

An Observational Study of Outcomes and Tolerances in Patients with Cystic Fibrosis Initiated on Lumacaftor/Ivacaftor

Mark T. Jennings et al.

ANNALS OF THE AMERICAN THORACIC SOCIETY (2017)

Article Medicine, General & Internal

Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR

C. E. Wainwright et al.

NEW ENGLAND JOURNAL OF MEDICINE (2015)

Review Genetics & Heredity

Cystic fibrosis genetics: from molecular understanding to clinical application

Garry R. Cutting

NATURE REVIEWS GENETICS (2015)

Article Respiratory System

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)

Article Critical Care Medicine

Efficacy and Safety of Ivacaftor in Patients Aged 6 to 11 Years with Cystic Fibrosis with a G551D Mutation

Jane C. Davies et al.

AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2013)

Article Medicine, General & Internal

A CFTR Potentiator in Patients with Cystic Fibrosis and the G551D Mutation

Bonnie W. Ramsey et al.

NEW ENGLAND JOURNAL OF MEDICINE (2011)

Article Biochemistry & Molecular Biology

Most F508del-CFTR is targeted to degradation at an early folding checkpoint and independently of calnexin

CA Farinha et al.

MOLECULAR AND CELLULAR BIOLOGY (2005)