Search Results - "Randy A. Hall"
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Adhesion G protein-coupled receptors: structure, signaling, physiology, and pathophysiology
Published in Physiological reviews (01-10-2022)“…Adhesion G protein-coupled receptors (AGPCRs) are a family of 33 receptors in humans exhibiting a conserved general structure but diverse expression patterns…”
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Adhesion G Protein-Coupled Receptors as Drug Targets
Published in Annual review of pharmacology and toxicology (06-01-2018)“…The adhesion G protein-coupled receptors (aGPCRs) are an evolutionarily ancient family of receptors that play key roles in many different physiological…”
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Fine-tuning of GPCR activity by receptor-interacting proteins
Published in Nature reviews. Molecular cell biology (01-12-2009)“…Key Points G protein-coupled receptors (GPCRs) are a large family of seven-transmembrane proteins that can be activated by a diverse array of ligands,…”
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Adhesion G protein-coupled receptors: signaling, pharmacology, and mechanisms of activation
Published in Molecular pharmacology (01-11-2012)“…The adhesion G protein-coupled receptors (GPCRs) are a distinct family of more than 30 receptors in vertebrate genomes. These receptors have been shown to play…”
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GPR37 and GPR37L1 are receptors for the neuroprotective and glioprotective factors prosaptide and prosaposin
Published in Proceedings of the National Academy of Sciences - PNAS (04-06-2013)“…GPR37 (also known as Pael-R) and GPR37L1 are orphan G protein-coupled receptors that are almost exclusively expressed in the nervous system. We screened these…”
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International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors
Published in Pharmacological reviews (01-04-2015)“…The Adhesion family forms a large branch of the pharmacologically important superfamily of G protein-coupled receptors (GPCRs). As Adhesion GPCRs increasingly…”
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The protective role of prosaposin and its receptors in the nervous system
Published in Brain research (17-10-2014)“…Abstract Prosaposin (also known as SGP-1) is an intriguing multifunctional protein that plays roles both intracellularly, as a regulator of lysosomal enzyme…”
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Disease-associated extracellular loop mutations in the adhesion G protein-coupled receptor G1 (ADGRG1; GPR56) differentially regulate downstream signaling
Published in The Journal of biological chemistry (09-06-2017)“…Mutations to the adhesion G protein-coupled receptor ADGRG1 (G1; also known as GPR56) underlie the neurological disorder bilateral frontoparietal…”
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Mice lacking full length Adgrb1 (Bai1) exhibit social deficits, increased seizure susceptibility, and altered brain development
Published in Experimental neurology (01-05-2022)“…The adhesion G protein-coupled receptor BAI1/ADGRB1 plays an important role in suppressing angiogenesis, mediating phagocytosis, and acting as a brain tumor…”
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The BAI subfamily of adhesion GPCRs: synaptic regulation and beyond
Published in Trends in pharmacological sciences (Regular ed.) (01-04-2014)“…Highlights • BAI1, BAI2, and BAI3 are receptors that can regulate neuronal function and synaptogenesis. • BAI1 has been shown to signal via both G protein and…”
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The N Terminus of the Adhesion G Protein-coupled Receptor GPR56 Controls Receptor Signaling Activity
Published in The Journal of biological chemistry (19-08-2011)“…GPR56 is an adhesion G protein-coupled receptor that plays a key role in cortical development. Mutations to GPR56 in humans cause malformations of the cerebral…”
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Brain-specific Angiogenesis Inhibitor-1 Signaling, Regulation, and Enrichment in the Postsynaptic Density
Published in The Journal of biological chemistry (02-08-2013)“…Brain-specific angiogenesis inhibitor-1 (BAI1) is an adhesion G protein-coupled receptor that has been studied primarily for its anti-angiogenic and…”
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A disease‐associated mutation in the adhesion GPCR BAI2 (ADGRB2) increases receptor signaling activity
Published in Human mutation (01-12-2017)“…Mutations in G protein‐coupled receptors (GPCRs) that increase constitutive signaling activity can cause human disease. A de novo C‐terminal mutation (R1465W)…”
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Heterodimerization of G Protein-Coupled Receptors: Specificity and Functional Significance
Published in Pharmacological reviews (01-09-2005)“…G protein-coupled receptors (GPCRs) are cell surface receptors that mediate physiological responses to a diverse array of stimuli. GPCRs have traditionally…”
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Genome-wide Functional Annotation of Dual-Specificity Protein- and Lipid-Binding Modules that Regulate Protein Interactions
Published in Molecular cell (27-04-2012)“…Emerging evidence indicates that membrane lipids regulate protein networking by directly interacting with protein-interaction domains (PIDs). As a pilot study…”
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Mice lacking Gpr37 exhibit decreased expression of the myelin-associated glycoprotein MAG and increased susceptibility to demyelination
Published in Neuroscience (01-09-2017)“…Highlights • Myelin-associated glycoprotein expression is lower in brains of mice lacking GPR37. • Loss of GPR37 results in increased susceptibility to…”
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The tyrosine phosphatase PTPN13/FAP-1 links calpain-2, TBI and tau tyrosine phosphorylation
Published in Scientific reports (18-09-2017)“…Traumatic brain injury (TBI) increases the risk of Alzheimer’s disease (AD). Calpain activation and tau hyperphosphorylation have been implicated in both TBI…”
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GPR37L1 modulates seizure susceptibility: Evidence from mouse studies and analyses of a human GPR37L1 variant
Published in Neurobiology of disease (01-10-2017)“…Progressive myoclonus epilepsies (PMEs) are disorders characterized by myoclonic and generalized seizures with progressive neurological deterioration. While…”
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Autonomic modulation of olfactory signaling
Published in Science signaling (11-01-2011)“…The olfactory epithelium is extensively innervated by sympathetic nerve endings, which release norepinephrine, and parasympathetic nerve endings, which release…”
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A new human NHERF1 mutation decreases renal phosphate transporter NPT2a expression by a PTH-independent mechanism
Published in PloS one (10-04-2012)“…The sodium-hydrogen exchanger regulatory factor 1 (NHERF1) binds to the main renal phosphate transporter NPT2a and to the parathyroid hormone (PTH) receptor…”
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