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George Baillie on peptide array, a technique that transformed research on phosphodiesterases

George Baillie speaks to Francesca Lake (Managing Editor, Future Science OA): George Baillie is a Professor and PI within the Institute of Cardiovascular and Medical Sciences at the University of Glasgow (Glasgow, UK). His research over the last 15 years has examined many aspects of the cAMP signali...

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Autor principal: Baillie, George S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137849/
https://www.ncbi.nlm.nih.gov/pubmed/28031900
http://dx.doi.org/10.4155/fso.15.25
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author Baillie, George S
author_facet Baillie, George S
author_sort Baillie, George S
collection PubMed
description George Baillie speaks to Francesca Lake (Managing Editor, Future Science OA): George Baillie is a Professor and PI within the Institute of Cardiovascular and Medical Sciences at the University of Glasgow (Glasgow, UK). His research over the last 15 years has examined many aspects of the cAMP signaling pathway in disease and he has published over 140 papers on the subject. His major discovery was that phosphodiesterases are ‘compartmentalized’, and it is their location within cells that direct their function. The Baillie/Houslay laboratory was the first to discover a specific function for a single isoform of PDE4 (namely PDE4D5 with β-arrestin desensitizes the β2-adrenergic receptor). His laboratory has since gone on to ascribe functions to several other PDE4 isoforms. He is a founder and director of Sannox Therapeutics, a spin-out venture within University of Glasgow. He is also a member of the Editorial Board of Future Science OA and Co-Editor of Cellular Signalling.
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spelling pubmed-51378492016-12-28 George Baillie on peptide array, a technique that transformed research on phosphodiesterases Baillie, George S Future Sci OA Interview George Baillie speaks to Francesca Lake (Managing Editor, Future Science OA): George Baillie is a Professor and PI within the Institute of Cardiovascular and Medical Sciences at the University of Glasgow (Glasgow, UK). His research over the last 15 years has examined many aspects of the cAMP signaling pathway in disease and he has published over 140 papers on the subject. His major discovery was that phosphodiesterases are ‘compartmentalized’, and it is their location within cells that direct their function. The Baillie/Houslay laboratory was the first to discover a specific function for a single isoform of PDE4 (namely PDE4D5 with β-arrestin desensitizes the β2-adrenergic receptor). His laboratory has since gone on to ascribe functions to several other PDE4 isoforms. He is a founder and director of Sannox Therapeutics, a spin-out venture within University of Glasgow. He is also a member of the Editorial Board of Future Science OA and Co-Editor of Cellular Signalling. Future Science Ltd 2015-11-01 /pmc/articles/PMC5137849/ /pubmed/28031900 http://dx.doi.org/10.4155/fso.15.25 Text en © George Baillie This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Interview
Baillie, George S
George Baillie on peptide array, a technique that transformed research on phosphodiesterases
title George Baillie on peptide array, a technique that transformed research on phosphodiesterases
title_full George Baillie on peptide array, a technique that transformed research on phosphodiesterases
title_fullStr George Baillie on peptide array, a technique that transformed research on phosphodiesterases
title_full_unstemmed George Baillie on peptide array, a technique that transformed research on phosphodiesterases
title_short George Baillie on peptide array, a technique that transformed research on phosphodiesterases
title_sort george baillie on peptide array, a technique that transformed research on phosphodiesterases
topic Interview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137849/
https://www.ncbi.nlm.nih.gov/pubmed/28031900
http://dx.doi.org/10.4155/fso.15.25
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