Tezacaftor/Ivacaftor in Subjects with Cystic Fibrosis and F508del/F508del-CFTR or F508del/G551D-CFTR-Reference-Cited by-同舟云学术

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

Published:2018-01-15 Issue:2 Volume:197 Page:214-224
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

Donaldson Scott H.¹,Pilewski Joseph M.²,Griese Matthias³,Cooke Jon⁴,Viswanathan Lakshmi⁵,Tullis Elizabeth⁶,Davies Jane C.⁷,Lekstrom-Himes Julie A.⁴,Wang Linda T.⁵

Affiliation:

1. University of North Carolina School of Medicine, Chapel Hill, North Carolina

2. University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania

3. Department of Pediatric Pneumology, Dr. von Hauner Children’s Hospital, Ludwig-Maximilians-University, Munich, Germany

4. Vertex Pharmaceuticals (Europe) Limited, London, United Kingdom

5. Vertex Pharmaceuticals Incorporated, Boston, Massachusetts

6. St. Michael’s Hospital and Keenan Research Centre, Li Ka Shing Knowledge Institute, University of Toronto, Toronto, Ontario, Canada; and

7. Paediatric Respiratory Medicine, Imperial College and Royal Brompton and Harefield Foundation Trust, London, United Kingdom

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Link

http://www.atsjournals.org/doi/pdf/10.1164/rccm.201704-0717OC

Reference27 articles.

1. Cystic fibrosis genetics: from molecular understanding to clinical application

2. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

3. Identification of the Cystic Fibrosis Gene: Genetic Analysis

4. Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping

5. Targeting a genetic defect: cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis

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