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Chemokine receptors are subjected to heterologous desensitization by activation of formyl peptide receptors.
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Activation of formyl peptide receptor (FPR1) on the human astrocytoma cell line U87 promotes cell motility, growth and angiogenesis.
Expression and activation of Formyl Peptide Receptors (FPRs) were shown through flow cytometry/PCR and FURA assay, respectively.
A previous investigation in human peripheral blood monocytes, demonstrated that chemotaxis towards Aβ and APP occurs via the activation of formyl peptide receptor like-1 (FPRL1), a low affinity receptor located on leukocytes and mononuclear phagocytes (Kaneider et al., 2004).
It also has analgesic properties which may be mediated by activation of the central opioid system.
We have investigated the role of two polymorphic sites (R190W and N192K) on the binding and activation of the formyl peptide receptor (FPR) by viral and formyl peptides.
In addition to being antimicrobial, antifungal and antiviral, LL-37 is chemoattractant through activation of the formyl peptide receptor-like 1 (FPreceptorepton on leukocytes, and can induce keratinocyte IL-8 and IL-18 secretion through activation of the epidermal growth factor receptor or the p38 and ERK1/2 MAP kinase pathways, respectively [5].
The recent characterization by SEESR of formyl radicals stabilized by spin traps is commented in the light of previous observations by ir spectroscopic techniques of adsorbed formyl radicals occuring in the course of methanol or formaldehyde electrooxidation at platinum.
Immunotherapy strengthens the immune system by supporting activation of the body's cancer-fighting T-cells.
The product of the first gene of the operon, fhs (TKV_c19930), probably catalyzes the initial ATP-dependent activation of formate to formyl-THF.
However, this does not lead to a net energy conservation, since ATP formed via the glycine reductase reaction is consumed for the activation of formate to form formyl-THF.
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