Exploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response
Identifying ligands which activate the specific effectors driving particular in vivo drug effects remains challenging. Here, the authors apply unsupervised clustering of pharmacodynamic parameters to classify GPCR ligands into different categories with similar signaling profiles and shared frequency...
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Nature Portfolio
2019
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oai:doaj.org-article:c0db3f1cf110426bbd5f35d40fd3681b2021-12-02T16:57:41ZExploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response10.1038/s41467-019-11875-62041-1723https://doaj.org/article/c0db3f1cf110426bbd5f35d40fd3681b2019-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-11875-6https://doaj.org/toc/2041-1723Identifying ligands which activate the specific effectors driving particular in vivo drug effects remains challenging. Here, the authors apply unsupervised clustering of pharmacodynamic parameters to classify GPCR ligands into different categories with similar signaling profiles and shared frequency of report of side effects.Besma BenredjemJonathan GallionDennis PelletierPaul DallaireJohanie CharbonneauDarren CawkillKarim NagiMark GosinkViktoryia LukashevaStephen JenkinsonYong RenChristopher SompsBrigitte MuratEmma Van Der WesthuizenChristian Le GouillOlivier LichtargeAnne SchmidtMichel BouvierGraciela PineyroNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-15 (2019) |
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spellingShingle |
Science Q Besma Benredjem Jonathan Gallion Dennis Pelletier Paul Dallaire Johanie Charbonneau Darren Cawkill Karim Nagi Mark Gosink Viktoryia Lukasheva Stephen Jenkinson Yong Ren Christopher Somps Brigitte Murat Emma Van Der Westhuizen Christian Le Gouill Olivier Lichtarge Anne Schmidt Michel Bouvier Graciela Pineyro Exploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response |
description |
Identifying ligands which activate the specific effectors driving particular in vivo drug effects remains challenging. Here, the authors apply unsupervised clustering of pharmacodynamic parameters to classify GPCR ligands into different categories with similar signaling profiles and shared frequency of report of side effects. |
format |
article |
author |
Besma Benredjem Jonathan Gallion Dennis Pelletier Paul Dallaire Johanie Charbonneau Darren Cawkill Karim Nagi Mark Gosink Viktoryia Lukasheva Stephen Jenkinson Yong Ren Christopher Somps Brigitte Murat Emma Van Der Westhuizen Christian Le Gouill Olivier Lichtarge Anne Schmidt Michel Bouvier Graciela Pineyro |
author_facet |
Besma Benredjem Jonathan Gallion Dennis Pelletier Paul Dallaire Johanie Charbonneau Darren Cawkill Karim Nagi Mark Gosink Viktoryia Lukasheva Stephen Jenkinson Yong Ren Christopher Somps Brigitte Murat Emma Van Der Westhuizen Christian Le Gouill Olivier Lichtarge Anne Schmidt Michel Bouvier Graciela Pineyro |
author_sort |
Besma Benredjem |
title |
Exploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response |
title_short |
Exploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response |
title_full |
Exploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response |
title_fullStr |
Exploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response |
title_full_unstemmed |
Exploring use of unsupervised clustering to associate signaling profiles of GPCR ligands to clinical response |
title_sort |
exploring use of unsupervised clustering to associate signaling profiles of gpcr ligands to clinical response |
publisher |
Nature Portfolio |
publishDate |
2019 |
url |
https://doaj.org/article/c0db3f1cf110426bbd5f35d40fd3681b |
work_keys_str_mv |
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