Correction of defective CFTR / EN aC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells-Reference-Cited by-同舟云学术

Correction of defective CFTR / EN aC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells

Published:2014-06-03 Issue:8 Volume:18 Page:1631-1643
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J. Cell. Mol. Med.

Author:

Carbone Annalucia¹²,Castellani Stefano²,Favia Maria³,Diana Anna⁴,Paracchini Valentina¹,Di Gioia Sante²,Seia Manuela¹,Casavola Valeria³,Colombo Carla⁵,Conese Massimo²

Affiliation:

1. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Medical Genetics Laboratory Milan Italy

2. Department of Medical and Surgical Sciences University of Foggia Foggia Italy

3. Department of Biosciences, Biotechnologies and Biopharmaceutics University of Bari Bari Italy

4. Cystic Fibrosis Regional Center Azienda Ospedaliero‐Universitaria Policlinico Bari Italy

5. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Cystic Fibrosis Center Milan Italy

Funder

Italian Cystic Fibrosis Research Foundation

Italian Ministry of Health, Ricerca Corrente and Law 548/93

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.12303

Reference60 articles.

1. Structure and Function of the CFTR Chloride Channel

2. Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease

3. CFTR regulation of ENaC;Donaldson SH;Methods Mol Med,2002

4. The Cystic Fibrosis Transmembrane Conductance Regulator Impedes Proteolytic Stimulation of the Epithelial Na+ Channel

5. Cystic fibrosis gene therapy: successes, failures and hopes for the future

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