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David R. Greaves
Researcher at University of Oxford
Publications - 209
Citations - 19184
David R. Greaves is an academic researcher from University of Oxford. The author has contributed to research in topics: Inflammation & Chemokine. The author has an hindex of 67, co-authored 204 publications receiving 17639 citations. Previous affiliations of David R. Greaves include University of Cambridge & Netherlands Cancer Institute.
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Journal ArticleDOI
A new class of membrane-bound chemokine with a CX3C motif
J F Bazan,Kevin B. Bacon,Gary Hardiman,W Wang,K Soo,Devora L. Rossi,David R. Greaves,Albert Zlotnik,T J Schall +8 more
TL;DR: The structure, biochemical features, tissue distribution and chromosomal localization of CX3C chemokine all indicate that it represents a unique class of chemokines that may constitute part of the molecular control of leukocyte traffic at the endothelium.
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Position-independent, high-level expression of the human β-globin gene in transgenic mice
TL;DR: The results indicate that the DNA regions flanking the human beta-globin locus contain dominant regulatory sequences that specify position-independent expression and normally activate the complete human multigene beta- globin loci.
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Oxidative metabolism and PGC-1β attenuate macrophage-mediated inflammation
Divya Vats,Lata Mukundan,Justin I. Odegaard,Lina Zhang,Kristi L. Smith,Christine R. Morel,Roger A. Wagner,David R. Greaves,Peter J. Murray,Ajay Chawla +9 more
TL;DR: In this paper, the authors show that in response to interleukin-4 (IL-4), signal transducer and activator of transcription 6 (STAT6) and PPARgamma-coactivator-1beta (PGC-1β) induce macrophage programs for fatty acid oxidation and mitochondrial biogenesis, suggesting a potential role for metabolic therapies in treating atherogenic inflammation.
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Tumor necrosis factor-alpha-converting enzyme (ADAM17) mediates the cleavage and shedding of fractalkine (CX3CL1).
Kyle J. Garton,Peter J. Gough,Carl P. Blobel,Gillian Murphy,David R. Greaves,Peter J. Dempsey,Elaine W. Raines +6 more
TL;DR: The identification of TACE as a major protease responsible for the conversion of fractalkine from a membrane-bound adhesion molecule to a soluble chemoattractant will provide new information for understanding the physiological function of this chemokine.
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Genetic programs expressed in resting and IL-4 alternatively activated mouse and human macrophages: similarities and differences
Fernando O. Martinez,Laura Helming,Ronny Milde,Audrey Varin,Barbro N. Melgert,Barbro N. Melgert,Christina Draijer,Christina Draijer,Benjamin Thomas,Marco Fabbri,Anjali Crawshaw,Ling-Pei Ho,Nick H. T. ten Hacken,Viviana Cobos Jiménez,Neeltje A. Kootstra,Jörg Hamann,David R. Greaves,Massimo Locati,Alberto Mantovani,Siamon Gordon +19 more
TL;DR: This work analyzes and compares the transcriptome and proteome of human and murine macrophages under resting conditions (M0) and after IL-4 activation (M2) and provides a resource for tools enabling macrophage detection in human tissues by identifying a set of 87 Macrophage-related genes.