CFTR and Cystic Fibrosis: From Structure to Function - Couverture souple

Farinha, Carlos M. M.

Couverture souple

ISBN 10 : 3319654934 ISBN 13 : 9783319654935

Editeur : Springer, 2017

Synopsis

Discusses the relationship between the CFTR protein and cystic fibrosis

Explains how the protein structure and structure-defects affect the function of CFTR

Presents CFTR-based and independent therapies to correct the basic defect

A propos du livre

À propos de l?auteur

Carlos M Farinha obtained his Ph.D. (2003) and Habilitation (2015) in Biochemistry from the University of Lisbon. He has worked at the National Institute of Health Dr. Ricardo Jorge and at the Faculty of Sciences, University of Lisbon with training periods at the Johns Hopkins University School of Medicine, Baltimore, MD, USA and at the University of Pittsburgh School of Medicine - Children's Hospital of Pittsburgh, Pittsburgh, PA, USA. Currently, he is Assistant Professor with habilitation at the Faculty of Sciences, University of Lisbon, and Principal Investigator at BioISI - Biosystems and Integrative Sciences Institute. His research focuses on the molecular mechanisms of cystic fibrosis (CF), in particular the endoplasmic reticulum retention and early degradation of CFTR's most common mutant and characterization of the role of CFTR interacting proteins. He received the 2012 ERS Romain Pauwels Research Award from the European Respiratory Society for "research into the different aspects of CFTR biology".

Détails de l'édition

• Éditeur: Springer
• Date d'édition: 2017
• Langue: anglais
• ISBN 10: 3319654934
• ISBN 13: 9783319654935
• Reliure: Broché
• Numéro d'édition: 1
• Nombre de pages: 76
• Coordonnées du fabricant: Springer Nature Customer Service Center GmbH; ProductSafety@springernature.com; ; Europaplatz 3,69115 Heidelberg, Germany; Heidelberg; 69115; Allemagne