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Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction

Cystic fibrosis is the most common autosomal recessive genetic disease in Caucasians and has been extensively studied for many decades. The cystic fibrosis transmembrane conductance regulator gene was identified in 1989. It encodes a complex protein which has numerous cellular functions. Our underst...

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Detalles Bibliográficos
Autores principales: Griesenbach, Uta, Alton, Eric W.F.W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculty of 1000 Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447040/
https://www.ncbi.nlm.nih.gov/pubmed/26097737
http://dx.doi.org/10.12703/P7-64
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author Griesenbach, Uta
Alton, Eric W.F.W.
author_facet Griesenbach, Uta
Alton, Eric W.F.W.
author_sort Griesenbach, Uta
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description Cystic fibrosis is the most common autosomal recessive genetic disease in Caucasians and has been extensively studied for many decades. The cystic fibrosis transmembrane conductance regulator gene was identified in 1989. It encodes a complex protein which has numerous cellular functions. Our understanding of cystic fibrosis pathophysiology and genetics is constantly expanding and being refined, leading to improved management of the disease and increased life expectancy in affected individuals.
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spelling pubmed-44470402015-06-19 Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction Griesenbach, Uta Alton, Eric W.F.W. F1000Prime Rep Review Article Cystic fibrosis is the most common autosomal recessive genetic disease in Caucasians and has been extensively studied for many decades. The cystic fibrosis transmembrane conductance regulator gene was identified in 1989. It encodes a complex protein which has numerous cellular functions. Our understanding of cystic fibrosis pathophysiology and genetics is constantly expanding and being refined, leading to improved management of the disease and increased life expectancy in affected individuals. Faculty of 1000 Ltd 2015-05-27 /pmc/articles/PMC4447040/ /pubmed/26097737 http://dx.doi.org/10.12703/P7-64 Text en © 2015 Faculty of 1000 Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode All F1000Prime Reports articles are distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Griesenbach, Uta
Alton, Eric W.F.W.
Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
title Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
title_full Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
title_fullStr Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
title_full_unstemmed Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
title_short Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
title_sort recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447040/
https://www.ncbi.nlm.nih.gov/pubmed/26097737
http://dx.doi.org/10.12703/P7-64
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