Use of NanoBiT and NanoBRET to characterise interleukin-23 receptor dimer formation in living cells.

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Bibliographic Details
Title: Use of NanoBiT and NanoBRET to characterise interleukin-23 receptor dimer formation in living cells.
Authors: Lay CS; Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, University of Nottingham, Nottingham, UK.; Centre of Membrane Proteins and Receptors, University of Birmingham and Nottingham, The Midlands, UK.; Medicine Design, Medicinal Science and Technology, GlaxoSmithKline, Stevenage, UK., Kilpatrick LE; Centre of Membrane Proteins and Receptors, University of Birmingham and Nottingham, The Midlands, UK.; Division of Bimolecular Science and Medicinal Chemistry, School of Pharmacy, Biodiscovery Institute, University of Nottingham, Nottingham, UK., Craggs PD; Medicine Design, Medicinal Science and Technology, GlaxoSmithKline, Stevenage, UK.; Crick-GSK Biomedical Linklabs, GlaxoSmithKline, Stevenage, UK., Hill SJ; Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, University of Nottingham, Nottingham, UK.; Centre of Membrane Proteins and Receptors, University of Birmingham and Nottingham, The Midlands, UK.
Source: British journal of pharmacology [Br J Pharmacol] 2023 Jun; Vol. 180 (11), pp. 1444-1459. Date of Electronic Publication: 2023 Jan 10.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley Country of Publication: England NLM ID: 7502536 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5381 (Electronic) Linking ISSN: 00071188 NLM ISO Abbreviation: Br J Pharmacol Subsets: MEDLINE
Database: MEDLINE Ultimate
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Description
ISSN:1476-5381
DOI:10.1111/bph.16018