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The role of microsomal Prostaglandin E syntase-1(mPGES-1)/PGE<sub>2</sub> axis facilitates granulation tissueformation

Abstract

Discussion(0)

Related publications

The microsomal prostaglandin E synthase-1/PGE<sub>2</sub> /EP4 axis induces blood flow recovery via recruitment of regulatory T cells

mPGES-1/PGE<sub>2</sub>/EP4 axis induces blood flow recovery via accumulation of regulatory T cells to ischemic muscle

Microglia‐specific expression of microsomal prostaglandin E<sub>2</sub> synthase‐1 contributes to lipopolysaccharide‐induced prostaglandin E<sub>2</sub> production

Microsomal prostaglandin E synthase‐1 contributes to ischaemic excitotoxicity through prostaglandin E<sub>2</sub> EP<sub>3</sub> receptors

Inhibition of microsomal prostaglandin E synthase-1 facilitates liver repair after hepatic injury in mice

The role of microsomal Prostaglandin E syntase-1(mPGES-1)/PGE&lt;sub&gt;2&lt;/sub&gt; axis facilitates granulation tissueformation

Abstract

Discussion(0)

Related publications

The microsomal prostaglandin E synthase-1/PGE&lt;sub&gt;2&lt;/sub&gt; /EP4 axis induces blood flow recovery via recruitment of regulatory T cells

mPGES-1/PGE&lt;sub&gt;2&lt;/sub&gt;/EP4 axis induces blood flow recovery via accumulation of regulatory T cells to ischemic muscle

Microglia‐specific expression of microsomal prostaglandin E<sub>2</sub> synthase‐1 contributes to lipopolysaccharide‐induced prostaglandin E<sub>2</sub> production

Microsomal prostaglandin E synthase‐1 contributes to ischaemic excitotoxicity through prostaglandin E<sub>2</sub> EP<sub>3</sub> receptors

Inhibition of microsomal prostaglandin E synthase-1 facilitates liver repair after hepatic injury in mice

The role of microsomal Prostaglandin E syntase-1(mPGES-1)/PGE<sub>2</sub> axis facilitates granulation tissueformation

The microsomal prostaglandin E synthase-1/PGE<sub>2</sub> /EP4 axis induces blood flow recovery via recruitment of regulatory T cells

mPGES-1/PGE<sub>2</sub>/EP4 axis induces blood flow recovery via accumulation of regulatory T cells to ischemic muscle