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S. Courtney Frasch

Researcher at National Jewish Health

Publications -  26
Citations -  4453

S. Courtney Frasch is an academic researcher from National Jewish Health. The author has contributed to research in topics: Efferocytosis & Inflammation. The author has an hindex of 21, co-authored 26 publications receiving 4047 citations.

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Cell-Surface Calreticulin Initiates Clearance of Viable or Apoptotic Cells through trans-Activation of LRP on the Phagocyte

TL;DR: It is demonstrated here that calreticulin acts as a second general recognition ligand by binding and activating LDL-receptor-related protein (LRP) on the engulfing cell, which creates an environment where "don't eat me" signals are rendered inactive and "eat me" signalling signals congregate together and signal for removal.
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The role of phosphatidylserine in recognition of apoptotic cells by phagocytes.

TL;DR: It is still not clear which receptors mediate PS recognition on apoptotic cells; however, several interesting candidates have been proposed and a novel activity expressed on macrophages stimulated with digestible particles such as β-glucan is proposed.
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Phosphorylation of Bax Ser184 by Akt regulates its activity and apoptosis in neutrophils

TL;DR: It is suggested that Bax is regulated by phosphorylation of Ser184 in an Akt-dependent manner and thatosphorylation inhibits Bax effects on the mitochondria by maintaining the protein in the cytoplasm, heterodimerized with antiapoptotic Bcl-2 family members.
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Selective activation and functional significance of p38α mitogen-activated protein kinase in lipopolysaccharide-stimulated neutrophils

TL;DR: Findings support a pathway by which LPS stimulation of neutrophils results in activation of MKK3, which in turn activates p38alpha MAPk, ultimately regulating adhesion, NF-kappaB activation, enhanced gene expression of TNF-alpha, and regulation of T NF-alpha synthesis.
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Modulation of macrophage efferocytosis in inflammation.

TL;DR: This review summarizes the current knowledge of the multiple factors that modulate macrophage efferocytic ability and highlights emerging therapeutic targets with significant potential for limiting chronic inflammation.