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Robert J. Lefkowitz

Researcher at Howard Hughes Medical Institute

Publications -  867
Citations -  153371

Robert J. Lefkowitz is an academic researcher from Howard Hughes Medical Institute. The author has contributed to research in topics: Receptor & G protein-coupled receptor. The author has an hindex of 214, co-authored 860 publications receiving 147995 citations. Previous affiliations of Robert J. Lefkowitz include University of Nice Sophia Antipolis & University of Stuttgart.

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Defective lymphocyte chemotaxis in β-arrestin2- and GRK6-deficient mice

TL;DR: Results indicate that β-arrestin2 and GRK6 actually play positive regulatory roles in mediating the chemotactic responses of T and B lymphocytes to CXCL12.
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Regulation of β-Adrenergic Receptor Signaling by S-Nitrosylation of G-Protein-Coupled Receptor Kinase 2

TL;DR: It is shown in mice that SNOs increase beta- AR expression and prevent agonist-stimulated receptor downregulation; and in cells, SNOs decrease GRK2-mediated beta-AR phosphorylation and subsequent recruitment of beta-arrestin to the receptor, resulting in the attenuation of receptor desensitization and internalization.
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β-Arrestin-Mediated Localization of Smoothened to the Primary Cilium

TL;DR: It is demonstrated that β-arrestins mediate the activity-dependent interaction of Smo and the kinesin motor protein Kif3A and suggested roles for β-Arrestins in mediating the intracellular transport of a 7TMR to its obligate subcellular location for signaling.
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Structure of the adrenergic and related receptors.

TL;DR: The isolation and sequencing of a number of G protein-coupled receptors has now provided extensive primary structure information for this family of homologous proteins, suggesting that the family of proteins may grow to include receptors for many neurotransmitters and perhaps many peptide hormones.
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ACTH Receptors in the Adrenal: Specific Binding of ACTH-125I and Its Relation to Adenyl Cyclase

TL;DR: This study demonstrates directly the binding of ACTH to its biologically significant site in direct proportion to their biological activity.