Search Results
137 items found for "Bryan L Roth"
- Immunomodulatory Role of Neuropeptides in the Cornea
The cornea is the most densely innervated tissue of the body and possesses both immune and vascular privilege
- TM5-TM6: structural switches that modulate the coupling of serotonin receptors to Gs or Gi
, in the case of promiscuous receptors they found that these receptors shared conserved residues of both G protein families, suggesting that receptors that activate both Gs and Gi/o do so by combining the
- N-Acyl Amides from Neisseria meningitidis and Their Role in Sphingosine Receptor Signaling
Both groups of metabolites suppress anti-inflammatory interleukin-10 signaling in human macrophage cell
- Keratinocyte-derived defensins activate neutrophil-specific receptors Mrgpra2a/b to prevent skin...
Def and Mrgpra2 mutant animals both exhibited skin dysbiosis, with reduced microbial diversity and expansion
- GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for...
In contrast to A2AAR agonists, which simultaneously interact with both Ser2777.42 and His2787.43, 2 only
- Structural perspectives on the mechanism of signal activation, ligand selectivity and allosteric...
Recently, X-ray structures of both AngII receptors (AT1 and AT2 receptors) bound to peptide and non-peptide
- Functional modulation of PTH1R activation and signaling by RAMP2
Additionally, RAMP2 increases both PTH- and PTHrP-triggered β-arrestin2 recruitment to PTH1R.
- Targeting mGluR2/3 for treatment of neurodegenerative and neuropsychiatric diseases
use of various drugs including orthosteric and allosteric ligands acting on either mGluR2, mGluR3 or both
- Professor Charlotte Deane Joins Exscientia as Chief Scientist of Biologics AI
She will maintain both of these roles, in addition to her role at Exscientia .
- The Bile Acid Membrane Receptor TGR5 in Cancer: Friend or Foe?
In this review, we discuss both the ‘friend’ and ‘foe’ features of TGR5 by summarizing its tumor-suppressing
- A NanoBRET-Based H 3 R Conformational Biosensor to Study Real-Time H 3 Receptor Pharmacology in...
a NanoBRET-based conformational histamine H3 receptor (H3R) biosensor that allowed the detection of both
- Discovery of 3(2-aminoethyl)-thiazolidine-2,4-diones as a novel chemotype of sigma-1 receptor ligand
We have explored hydrophobic groups of different sizes on both sides of the five-membered ring scaffold
- GPR84 signaling promotes intestinal mucosal inflammation via enhancing NLRP3 inflammasome activation
Infiltrating GPR84+ macrophages are significantly increased in the colonic mucosa of both the UC patients
- To probe the activation mechanism of the Delta opioid receptor by an agonist ADL5859 started from...
Although the high-resolution crystal structures of the DOR with both agonist and antagonist have recently
- Neuropeptide S Encodes Stimulus Salience in the Paraventricular Thalamus
Taking advantage of a striking deficit of both NPS receptor (NPSR1) and NPS precursor knockout mice in
- TeachOpenCADD - A teaching platform for computer-aided drug design
Since we cover both the theoretical as well as practical aspect of these topics, the platform addresses
- Bell-Evans model and steered molecular dynamics in uncovering the dissociation kinetics of ligands..
In the experiment, similar sets of residues were found to be in significant contact with both ligands
- Structural basis of adhesion GPCR GPR110 activation by stalk peptide and G-proteins coupling
This is also where Gq/Gs bind the receptor through both hydrophobic and polar interaction, while Gi/G12
- Anosmin 1 N-terminal domains modulate prokineticin receptor 2 activation by prokineticin 2
domain 1 (FnIII.1) suggest the cysteine-rich (CR) and the FnIII.1 domains could assist the WAP domain both
- In vitro assays for the functional characterization of (psychedelic) substances at the serotonin...
discussed that one should consider when attempting to compare functional outcomes from different studies, both
- PAR-Induced Harnessing of EZH2 to β-Catenin: Implications for Colorectal Cancer
Both PAR4 and PAR2 are able to drive the association of methyltransferase EZH2 with β-catenin, culminating
- Combined docking and machine learning identify key molecular determinants of ligand pharmacological
Meanwhile, the antagonist ligands made interactions with W2866.48×48 and Y3167.43×42, both residues considered
- Glyco-sulfo hotspots in the chemokine receptor system
sites of N-acetyl galactosamine (GalNAc)-type O-glycosylation in their N-termini as well as sulfation, both Both PTMs were shown to contribute to the binding of CCL5 and CCL8 and to a minor extend CCL3. The combined effects of both PTMs as well as the relevance of specific acceptor sites and glycan composition
- Pharmacological targeting of cGAS/STING-YAP axis suppresses pathological angiogenesis and...
Pharmacological targeting of cGAS/STING-YAP signaling by both a small-molecule STING agonist, SR-717,
- Adrenal G Protein-Coupled Receptors and the Failing Heart: A Long-distance, Yet Intimate Affair
Chronic human HF is characterized by several important neurohormonal perturbations, emanating from both
- Engineered synaptic tools reveal localized cAMP signaling in synapse assembly
In vivo, suppression of postsynaptic cAMP signaling in CA1 neurons prevented formation of both Schaffer-collateral
- GRK2 in cardiovascular disease and its potential as a therapeutic target
interactome includes numerous proteins which interact with differential domains of GRK2 to modulate both
- Signaling pathways activated by sea bass gonadotropin-inhibitory hormone peptides in COS-7 cells...
evident increase in SRE-luc activity was noticed when COS-7 cells expressing GnIHR were challenged with both