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J. Richard Brewer

Researcher at Icahn School of Medicine at Mount Sinai

Publications -  9
Citations -  726

J. Richard Brewer is an academic researcher from Icahn School of Medicine at Mount Sinai. The author has contributed to research in topics: Fibroblast growth factor & Receptor tyrosine kinase. The author has an hindex of 3, co-authored 6 publications receiving 272 citations.

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Inflammasome activation in infected macrophages drives COVID-19 pathology

TL;DR: In this article , the authors showed that SARS-CoV-2 infection and replication in lung resident human macrophages is a critical driver of lung pathology, as inhibition of the NLRP3 inflammasome pathway reversed chronic lung pathology.
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Genetic insights into the mechanisms of Fgf signaling

TL;DR: These studies support an important role for Erk1/2 as a mediator of FgF signaling in many biological processes but have also provided strong evidence for additional signaling pathways in transmitting Fgf signaling in vivo.
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Inflammasome activation in infected macrophages drives COVID-19 pathology

TL;DR: In this paper , the authors showed that SARS-CoV-2 infection and replication in lung resident human macrophages is a critical driver of lung pathology, as inhibition of the NLRP3 inflammasome pathway reversed chronic lung pathology.
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Distinct Requirements for FGFR1 and FGFR2 in Primitive Endoderm Development and Exit from Pluripotency.

TL;DR: Mechanisms through which FGF signaling regulates inner cell mass lineage restriction and cell commitment during preimplantation development are identified.
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Fgfr1 regulates development through the combinatorial use of signaling proteins

TL;DR: Analysis of each mutant indicates that Frs2 binding to Fgfr1 has the most pleiotropic functions in development but also that the receptor uses multiple proteins additively in vivo, suggesting that Erk1/2-independent signaling pathways are functionally important for Fgf signaling in vivo.