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Molecular Cell|May 20, 2023
Structural snapshots uncover a key phosphorylation motif in GPCRs driving β-arrestin activationJagannath Maharana, Parishmita Sarma, Manish K Yadav, et al.
Nature Communications|November 10, 2016
Functional competence of a partially engaged GPCR-β-arrestin complexPunita Kumari, Ashish Srivastava, Ramanuj Banerjee, et al.
Nature Communications|March 2, 2024
Structure-guided engineering of biased-agonism in the human niacin receptor via single amino acid substitutionManish K Yadav, Parishmita Sarma, Jagannath Maharana, et al.
Nature Communications|March 29, 2025
Structural visualization of small molecule recognition by CXCR3 uncovers dual-agonism in the CXCR3-CXCR7 systemShirsha Saha, Fumiya K Sano, Saloni Sharma, et al.
Cell|October 18, 2023
Molecular basis of anaphylatoxin binding, activation, and signaling bias at complement receptorsManish K Yadav, Jagannath Maharana, Ravi Yadav, et al.
Science (New York, N.Y.)|January 4, 2024
Molecular insights into atypical modes of β-arrestin interaction with seven transmembrane receptorsJagannath Maharana, Fumiya K Sano, Parishmita Sarma, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 2026
Structural basis of complement anaphylatoxin receptor activation by an immunostimulant lead candidateAnnu Dalal, Manish K Yadav, Manisankar Ganguly, et al.
Nature Communications|August 8, 2022
Allosteric modulation of GPCR-induced β-arrestin trafficking and signaling by a synthetic intrabodyMithu Baidya, Madhu Chaturvedi, Hemlata Dwivedi-Agnihotri, et al.
Molecular Cell|September 28, 2021
Intrinsic bias at non-canonical, β-arrestin-coupled seven transmembrane receptorsShubhi Pandey, Punita Kumari, Mithu Baidya, et al.
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