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Subject Areas on Research
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Activation of protein kinase C inhibits human keratinocyte migration.
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Adhesion properties of catechol-based biodegradable amino acid-based poly(ester urea) copolymers inspired from mussel proteins.
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Alterations in calcium metabolism in murine macrophages by the benzene metabolite 1,4-benzoquinone.
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Bioactive surface modification of metal oxides via catechol-bearing modular peptides: multivalent-binding, surface retention, and peptide bioactivity.
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Biomass and toxicity responses of poison ivy (Toxicodendron radicans) to elevated atmospheric CO2.
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Catechol-O-methyltransferase inhibition alters pain and anxiety-related volitional behaviors through activation of β-adrenergic receptors in the rat.
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Catechol-O-methyltransferase inhibition increases pain sensitivity through activation of both beta2- and beta3-adrenergic receptors.
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Compounds from Sichuan and Melegueta peppers activate, covalently and non-covalently, TRPA1 and TRPV1 channels.
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Endotoxin (LPS) stimulates in vitro migration of macrophages from LPS-resistant mice but not from LPS-sensitive mice.
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Fe(III) coordination properties of two new saccharide-based enterobactin analogues: methyl 2,3,4-tris-O-[N-[2,3-di(hydroxy)benzoyl-glycyl]-aminopropyl]-alpha-D-glucopyranoside and methyl 2,3,4-tris-O-[N-[2,3-di-(hydroxy)-benzoyl]-aminopropyl]-alpha-D-glucopyranoside.
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IL-33/ST2 signaling excites sensory neurons and mediates itch response in a mouse model of poison ivy contact allergy.
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In vitro inhibition of collagen cross links by catechol analogs.
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In vivo monitoring of cardiomyocyte proliferation to identify chemical modifiers of heart regeneration.
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Inhibition of lysyl hydroxylase by catechol analogs.
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Low catechol-O-methyltransferase and stress potentiate functional pain and depressive behavior, especially in female mice.
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Modification of Poly(propylene fumarate)-Bioglass Composites with Peptide Conjugates to Enhance Bioactivity.
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Near-real-time determination of hydrogen peroxide generated from cigarette smoke.
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On eating poison ivy.
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Persistent Catechol-O-methyltransferase-dependent Pain Is Initiated by Peripheral β-Adrenergic Receptors.
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Sustained stimulation of β2- and β3-adrenergic receptors leads to persistent functional pain and neuroinflammation.
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The selection and evaluation of new chelating agents for the treatment of iron overload.
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Transcriptome profiling reveals Th2 bias and identifies endogenous itch mediators in poison ivy contact dermatitis.