Results 161 to 170 of about 1,208,918 (256)

Cystic Fibrosis and Primary Ciliary Dyskinesia Share Extensive Similarities: Is It Time to Place Them Under a Common Umbrella?

Pediatric Pulmonology, Volume 60, Issue 11, November 2025.
Andreas M. Matthaiou, Panayiotis Kouis, Pinelopi Anagnostopoulou, Panayiotis K. Yiallouros   +3 more
wiley   +1 more source

Current strategies for the long-term assessment, monitoring, and management of cystic fibrosis patients treated with CFTR modulator therapy [PDF]

, 2016
J.S. Elborn, Jane C. Davies, Marcus Mall, Patrick A. Flume, Barry J. Plant   +4 more
openalex   +1 more source

P031 Perspectives for gene therapy with the use of CFTR modulators in patients with cystic fibrosis [PDF]

, 2023
Luana da Silva Baptista Arpini, Fernanda Mayrink Gonçalves Liberato, R.d.C.N.C. Melotti, Sabrina da Silva Santos, Gina Torres Rego Monteiro   +4 more
openalex   +1 more source

P-84 HAVE CFTR MODULATORS CHANGED THE NEED FOR LIVER TRANSPLANTATION AMONG PATIENTS WITH CYSTIC FIBROSIS? AN ANALYSIS OF THE UNOS DATABASE

Annals of Hepatology
Conflict of interest: No Introduction and Objectives: The impact of cystic fibrosis (CF) transmembrane conductance regulator (CFTR) modulators on the natural history of liver disease is unknown.
MANUEL MENDIZABAL, Claire Cywes, Nicolas Muñoz, Amay Banker, Christian Bermudez, Denis Hadjiliadis, Peter Abt   +6 more
doaj   +1 more source

Code supporting "Phenotyping ciliary dynamics and coordination in response to CFTR-modulators in Cystic Fibrosis respiratory epithelial cells"

, 2019
Luigi Feriani, Pietro Cicuta
openalex   +1 more source

87: Characterization of pediatric and adolescent patients at risk for adverse reactions related to triple combination CFTR modulator therapy

, 2021
Jenna M. Rosano, Marie E. Egan
openalex   +1 more source

Using a systems approach to identify the mechanism of action of correctors [PDF]

, 2018
Tese de doutoramento, Biologia (Biologia de Sistemas), Universidade de Lisboa, Faculdade de Ciências, 2018Cystic Fibrosis (CF), the most common life-shortening genetic disorder among Caucasians, is caused by mutations in the gene encoding the Cystic ...
Awatade, Nikhil T
core  

Chaperones as integrators of cellular networks: Changes of cellular integrity in stress and diseases

, 2008
Cellular networks undergo rearrangements during stress and diseases. In un-stressed state the yeast protein-protein interaction network (interactome) is highly compact, and the centrally organized modules have a large overlap.
Albanese, Albert, Almaas, Arita, Barabasi, Barabasi, Batada, Batada, Batagelj, Bertin, Bobula, Colizza, Csermely, Csermely, Csermely, Csermely, Derenyi, Ekman, Gasch, Goldberger, Guimerá, Han, Kim, Komurov, Korcsmaros, Korcsmáros, Lewandowska, Linding, Luscombe, Macario, Maslov, McAuley, McClellan, Ng, Palla, Papp, Pál, Ravasz, Rutherford, Sales-Pardo, Shorter, Song, Soti, Soti, Soti, Szabadkai, Szalay, Tanaka, Taxis, Vigh, Wang, Watts, Xu, Yu, Zhu   +54 more
core   +2 more sources

176 Cystic fibrosis airway inflammation enhances the efficacy of CFTR modulators

, 2023
Carla M. P. Ribeiro, John T. Minges, Nancy L. Quinney, Susan E. Boyles, Kenichi Okuda, Deborah M. Cholon, Charles R. Esther, M. Gentzsch   +7 more
openalex   +1 more source

Profile of tezacaftor/ivacaftor combination and its potential in the treatment of cystic fibrosis

Therapeutics and Clinical Risk Management, 2019
Dejene Shiferaw,* Shoaib Faruqi*Department of Respiratory Medicine, Hull University Teaching Hospitals NHS Trust, Cottingham HU16 5JQ, UK *These authors contributed equally to this workCorrespondence: Shoaib FaruqiDepartment of Respiratory Medicine ...
Shiferaw D, Faruqi S
doaj