B
Blair R. Renshaw
Researcher at Amgen
Publications - 23
Citations - 2727
Blair R. Renshaw is an academic researcher from Amgen. The author has contributed to research in topics: Interleukin & Receptor. The author has an hindex of 14, co-authored 21 publications receiving 2452 citations.
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Journal ArticleDOI
Genomic organization of the interleukin-1 locus.
TL;DR: The order, orientation, and intergenic distance of the nine IL-1 family genes that lie on human chromosome 2 are determined and the order and orientation of the mouse genes have been mapped, and the mouse locus compared with the human locus.
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Binding of interleukin-18 to the interleukin-1 receptor homologous receptor IL-1Rrp1 leads to activation of signaling pathways similar to those used by interleukin-1
TL;DR: From the binding and signaling studies, it is concluded that the IL-18 receptor complex consists of IL- 18, theIL-1Rrp1, and another thus far unidentified receptor molecule.
Journal ArticleDOI
Cloning of a Putative Ligand for the T1/ST2 Receptor
Margit A. Gayle,Jennifer L. Slack,Timothy P. Bonnert,Blair R. Renshaw,Gonosuke Sonoda,Takahiro Taguchi,Joseph R. Testa,Steven K. Dower,John E. Sims +8 more
TL;DR: In searching for a ligand for T1/ST2, this paper cloned a cell surface protein to which it binds, but this protein is unable to initiate signal transduction by the T1-ST2 receptor in several in vitro assays.
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Identification and characterization of two members of a novel class of the interleukin-1 receptor (IL-1R) family. Delineation of a new class of IL-1R-related proteins based on signaling.
Teresa L. Born,Dirk E. Smith,Kirsten E. Garka,Blair R. Renshaw,Jeanette S. Bertles,John E. Sims +5 more
TL;DR: Two novel members of the interleukin-1 receptor (IL-1R) family, identified by homology searches of human genomic sequence data bases, are described, and a functional assay utilizing a panel of chimeric receptors containing the extracellular and transmembrane domains of either type I IL- 1R or IL-1r accessory protein (AcP) coupled to the cytoplasmic domains of all family members.
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A novel mutation of IL1RN in the deficiency of interleukin‐1 receptor antagonist syndrome: Description of two unrelated cases from Brazil
Adriana Almeida de Jesus,Mazen Osman,Clovis A. Silva,Peter W. Kim,T. Pham,Massimo Gadina,Barbara Yang,Débora Romeo Bertola,Magda Carneiro-Sampaio,Polly J. Ferguson,Blair R. Renshaw,Ken Schooley,Michael Brown,Asma Al-Dosari,Jamil Al-Alami,John E. Sims,Raphaela Goldbach-Mansky,Hatem El-Shanti,Hatem El-Shanti +18 more
TL;DR: The presence of the same homozygous novel mutation in IL1RN in 2 unrelated Brazilian patients suggests that this genetic variant may be a founder mutation that has been introduced in the Brazilian population.