Gpcr Selectivity
GPCR Selectivity is a pharmacological property that refers to the capacity of a ligand to preferentially bind to or activate a specific G protein-coupled receptor subtype over other structurally or functionally related GPCR subtypes.
181
Publications
12.9K
Citations
1.3K
Authors
363
Institutions
Publications per year
2017–2026
71
Variants
G Protein-coupled Receptor Selectivity
Parents
181
Illuminating G-Protein-Coupling Selectivity of GPCRs
Asuka Inoue, Francesco Raimondi, Francois Marie Ngako Kadji et al. · Cell · 2019 · 679 citations · Full text
Selectivity determinants of GPCR–G-protein binding
Tilman Flock, Alexander S. Hauser, Nadia Lund et al. · Nature · 2017 · 399 citations · Full text
Douglas McHugh, Sherry S-J. Hu, Neta Rimmerman et al. · BMC Neuroscience · 2010 · 318 citations · Full text
PtdIns(4,5)P2 stabilizes active states of GPCRs and enhances selectivity of G-protein coupling
Hsin‐Yung Yen, Kin Kuan Hoi, Idlir Liko et al. · Nature · 2018 · 310 citations · Full text
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363
University of Copenhagen
Copenhagen, Denmark
14 h-index
43 publications
4.3K citations
Université de Montréal
Montreal, Canada
11 h-index
52 publications
4.8K citations

University of Glasgow
Glasgow, United Kingdom
11 h-index
47 publications
2.5K citations
Institute for Research in Immunology and Cancer
Montreal, Canada
10 h-index
49 publications
4.8K citations
Inserm
Paris, France
8 h-index
16 publications
1.3K citations
National Institute of Diabetes and Digestive and Kidney Diseases
Bethesda, United States
6 h-index
28 publications
2.7K citations
Pfizer (United States)
New York, United States
6 h-index
66 publications
2.2K citations

Tohoku University
Sendai, Japan
6 h-index
18 publications
7.3K citations
1–8 of 363
17 publications · 977 citations
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JBC · 8 publications · 693 citations
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7 publications · 322 citations
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PNAS · 7 publications · 510 citations
7
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JCIM · 5 publications · 150 citations
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