OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Quantifying Ligand Bias at Seven-Transmembrane Receptors
Sudarshan Rajagopal, Seungkirl Ahn, David H. Rominger, et al.
Molecular Pharmacology (2011) Vol. 80, Iss. 3, pp. 367-377
Open Access | Times Cited: 377

Showing 1-25 of 377 citing articles:

Structure-based discovery of opioid analgesics with reduced side effects
Aashish Manglik, Henry J. Lin, Dipendra K. Aryal, et al.
Nature (2016) Vol. 537, Iss. 7619, pp. 185-190
Open Access | Times Cited: 869

Regulation ofµ-Opioid Receptors: Desensitization, Phosphorylation, Internalization, and Tolerance
John T. Williams, Susan Ingram, Graeme Henderson, et al.
Pharmacological Reviews (2013) Vol. 65, Iss. 1, pp. 223-254
Open Access | Times Cited: 717

Signalling bias in new drug discovery: detection, quantification and therapeutic impact
Terry Kenakin, Arthur Christopoulos
Nature Reviews Drug Discovery (2012) Vol. 12, Iss. 3, pp. 205-216
Open Access | Times Cited: 684

Biased signalling: from simple switches to allosteric microprocessors
Jeffrey S. Smith, Robert J. Lefkowitz, Sudarshan Rajagopal
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 4, pp. 243-260
Open Access | Times Cited: 643

A G Protein-Biased Ligand at theμ-Opioid Receptor Is Potently Analgesic with Reduced Gastrointestinal and Respiratory Dysfunction Compared with Morphine
Scott M. DeWire, Dennis S. Yamashita, David H. Rominger, et al.
Journal of Pharmacology and Experimental Therapeutics (2013) Vol. 344, Iss. 3, pp. 708-717
Closed Access | Times Cited: 557

Molecular Mechanism of β-Arrestin-Biased Agonism at Seven-Transmembrane Receptors
Éric Reiter, Seungkirl Ahn, Arun K. Shukla, et al.
The Annual Review of Pharmacology and Toxicology (2011) Vol. 52, Iss. 1, pp. 179-197
Open Access | Times Cited: 545

Biased ligands at G-protein-coupled receptors: promise and progress
Jonathan D. Violin, Aimee L. Crombie, David G. Soergel, et al.
Trends in Pharmacological Sciences (2014) Vol. 35, Iss. 7, pp. 308-316
Closed Access | Times Cited: 336

Allosteric nanobodies reveal the dynamic range and diverse mechanisms of G-protein-coupled receptor activation
Dean P. Staus, Ryan T. Strachan, Aashish Manglik, et al.
Nature (2016) Vol. 535, Iss. 7612, pp. 448-452
Open Access | Times Cited: 322

Low intrinsic efficacy for G protein activation can explain the improved side effect profiles of new opioid agonists
Alexander Gillis, Arisbel B. Gondin, Andrea Kliewer, et al.
Science Signaling (2020) Vol. 13, Iss. 625
Open Access | Times Cited: 313

The role of kinetic context in apparent biased agonism at GPCRs
Carmen Klein Herenbrink, David A. Sykes, Prashant Donthamsetti, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 312

Fluorescence/Bioluminescence Resonance Energy Transfer Techniques to Study G-Protein-Coupled Receptor Activation and Signaling
Martin J. Lohse, Susanne Nuber, Carsten Hoffmann
Pharmacological Reviews (2012) Vol. 64, Iss. 2, pp. 299-336
Closed Access | Times Cited: 297

GPCR desensitization: Acute and prolonged phases
Sudarshan Rajagopal, Sudha K. Shenoy
Cellular Signalling (2017) Vol. 41, pp. 9-16
Open Access | Times Cited: 289

Recent developments in biased agonism
James W. Wisler, Kunhong Xiao, A. Thomsen, et al.
Current Opinion in Cell Biology (2013) Vol. 27, pp. 18-24
Open Access | Times Cited: 272

The β-Arrestins: Multifunctional Regulators of G Protein-coupled Receptors
Jeffrey S. Smith, Sudarshan Rajagopal
Journal of Biological Chemistry (2016) Vol. 291, Iss. 17, pp. 8969-8977
Open Access | Times Cited: 271

Spatial encoding of cyclic AMP signaling specificity by GPCR endocytosis
Nikoleta G. Tsvetanova, Mark von Zastrow
Nature Chemical Biology (2014) Vol. 10, Iss. 12, pp. 1061-1065
Open Access | Times Cited: 268

Mechanisms of Regulation of the Chemokine-Receptor Network
Martin J. Stone, Jenni A. Hayward, Cheng Huang, et al.
International Journal of Molecular Sciences (2017) Vol. 18, Iss. 2, pp. 342-342
Open Access | Times Cited: 251

Angiotensin Analogs with Divergent Bias Stabilize Distinct Receptor Conformations
Laura M. Wingler, Matthias Elgeti, Daniel Hilger, et al.
Cell (2019) Vol. 176, Iss. 3, pp. 468-478.e11
Open Access | Times Cited: 251

Biased agonism: An emerging paradigm in GPCR drug discovery
Zoran Ranković, Tarsis F. Brust, Laura Bohn
Bioorganic & Medicinal Chemistry Letters (2015) Vol. 26, Iss. 2, pp. 241-250
Open Access | Times Cited: 248

Biased Receptor Signaling in Drug Discovery
Terry Kenakin
Pharmacological Reviews (2019) Vol. 71, Iss. 2, pp. 267-315
Open Access | Times Cited: 247

Human Gain-of-Function MC4R Variants Show Signaling Bias and Protect against Obesity
Luca A. Lotta, Jacek Mokrosiński, Edson Mendes de Oliveira, et al.
Cell (2019) Vol. 177, Iss. 3, pp. 597-607.e9
Open Access | Times Cited: 241

Molecular basis of β-arrestin coupling to formoterol-bound β1-adrenoceptor
Yang Lee, Tony Warne, Rony Nehmé, et al.
Nature (2020) Vol. 583, Iss. 7818, pp. 862-866
Open Access | Times Cited: 233

Quantification of Ligand Bias for Clinically Relevant β2-Adrenergic Receptor Ligands: Implications for Drug Taxonomy
Emma T. van der Westhuizen, Billy Breton, Arthur Christopoulos, et al.
Molecular Pharmacology (2013) Vol. 85, Iss. 3, pp. 492-509
Closed Access | Times Cited: 223

Crystal Structures of a Stabilized β1-Adrenoceptor Bound to the Biased Agonists Bucindolol and Carvedilol
Tony Warne, Patricia C. Edwards, Andrew G. W. Leslie, et al.
Structure (2012) Vol. 20, Iss. 5, pp. 841-849
Open Access | Times Cited: 215

Advances in G Protein-Coupled Receptor Allostery: From Function to Structure
Arthur Christopoulos
Molecular Pharmacology (2014) Vol. 86, Iss. 5, pp. 463-478
Open Access | Times Cited: 213

Molecular mechanism of biased signaling in a prototypical G protein–coupled receptor
Carl‐Mikael Suomivuori, Naomi R. Latorraca, Laura M. Wingler, et al.
Science (2020) Vol. 367, Iss. 6480, pp. 881-887
Open Access | Times Cited: 211

Page 1 - Next Page

Scroll to top