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Constitutive and ghrelin-dependent GHSR1a activation impairs CaV2.1 and CaV2.2 currents in hypothalamic neurons
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cne.20823openalex-snapshot
Expression of ghrelin receptor mRNA in the rat and the mouse brain
inferredcites →https://doi.org/10.1002/cne.23627openalex-snapshot
Neuroanatomical characterization of a growth hormone secretagogue receptor‐green fluorescent protein reporter mouse
inferredcites →https://doi.org/10.1007/s00424-014-1476-4openalex-snapshot
CaV2.2 channel cell surface expression is regulated by the light chain 1 (LC1) of the microtubule-associated protein B (MAP1B) via UBE2L3-mediated ubiquitination and degradation
inferredcites →https://doi.org/10.1016/j.bbamem.2012.10.004openalex-snapshot
Regulation of CaV2 calcium channels by G protein coupled receptors
inferredcites →https://doi.org/10.1016/j.cell.2009.04.022openalex-snapshot
Loss of GABAergic Signaling by AgRP Neurons to the Parabrachial Nucleus Leads to Starvation
inferredcites →https://doi.org/10.1016/j.cell.2011.07.039openalex-snapshot
Hunger States Switch a Flip-Flop Memory Circuit via a Synaptic AMPK-Dependent Positive Feedback Loop
inferredcites →https://doi.org/10.1016/j.jsb.2010.06.001openalex-snapshot
Three-dimensional structured illumination microscopy of liver sinusoidal endothelial cell fenestrations
inferredcites →https://doi.org/10.1016/j.neulet.2012.06.074openalex-snapshot
A118G Mu Opioid Receptor polymorphism increases inhibitory effects on CaV2.2 channels
inferredcites →https://doi.org/10.1016/j.neuron.2004.07.014openalex-snapshot
Presynaptic Ca2+ Channels Compete for Channel Type-Preferring Slots in Altered Neurotransmission Arising from Ca2+ Channelopathy
inferredcites →https://doi.org/10.1016/j.neuron.2008.03.002openalex-snapshot
D1 Receptors Physically Interact with N-Type Calcium Channels to Regulate Channel Distribution and Dendritic Calcium Entry
inferredcites →https://doi.org/10.1016/j.neuron.2008.09.005openalex-snapshot
Calcium Channel Regulation and Presynaptic Plasticity
inferredcites →https://doi.org/10.1016/j.neuron.2010.07.001openalex-snapshot
Modulation of High-Voltage Activated Ca2+ Channels by Membrane Phosphatidylinositol 4,5-Bisphosphate
inferredcites →https://doi.org/10.1016/j.neuron.2011.10.038openalex-snapshot
Apo-Ghrelin Receptor Forms Heteromers with DRD2 in Hypothalamic Neurons and Is Essential for Anorexigenic Effects of DRD2 Agonism
inferredcites →https://doi.org/10.1016/j.neuroscience.2011.07.063openalex-snapshot
Investigation of the presence of ghrelin in the central nervous system of the rat and mouse
inferredcites →https://doi.org/10.1016/j.neuroscience.2013.09.008openalex-snapshot
Analysis of brain nuclei accessible to ghrelin present in the cerebrospinal fluid
inferredcites →https://doi.org/10.1016/j.regpep.2009.04.001openalex-snapshot
Characterization of a novel ghrelin cell reporter mouse
inferredcites →https://doi.org/10.1016/j.regpep.2011.08.011openalex-snapshot
Design and characterization of a fluorescent ghrelin analog for imaging the growth hormone secretagogue receptor 1a
inferredcites →https://doi.org/10.1016/j.tins.2013.06.008openalex-snapshot
Control of neuronal voltage-gated calcium ion channels from RNA to protein
inferredcites →https://doi.org/10.1016/s0076-6879(04)89001-3openalex-snapshot
Quantitative Real-Time Polymerase Chain Reaction Measurement of Regulators of G-Protein Signaling mRNA Levels in Mouse Tissues
inferredcites →https://doi.org/10.1016/s0896-6273(00)80740-0openalex-snapshot
Expression of RGS2 Alters the Coupling of Metabotropic Glutamate Receptor 1a to M-Type K+ and N-Type Ca2+ Channels
inferredcites →https://doi.org/10.1016/s0896-6273(03)00063-1openalex-snapshot
The Distribution and Mechanism of Action of Ghrelin in the CNS Demonstrates a Novel Hypothalamic Circuit Regulating Energy Homeostasis
inferredcites →https://doi.org/10.1038/35051587openalex-snapshot
A role for ghrelin in the central regulation of feeding
inferredcites →https://doi.org/10.1038/380255a0openalex-snapshot
Voltage-dependent modulation of N-type calcium channels by G-protein β γsubunits
inferredcites →https://doi.org/10.1038/nature01118openalex-snapshot
Dual regulation of voltage-gated calcium channels by PtdIns(4,5)P2
inferredcites →https://doi.org/10.1038/nature07181openalex-snapshot
UCP2 mediates ghrelin’s action on NPY/AgRP neurons by lowering free radicals
inferredcites →https://doi.org/10.1038/ncomms2439openalex-snapshot
Peptide hormone ghrelin enhances neuronal excitability by inhibition of Kv7/KCNQ channels
inferredcites →https://doi.org/10.1038/nn.2167openalex-snapshot
Synaptic release of GABA by AgRP neurons is required for normal regulation of energy balance
inferredcites →https://doi.org/10.1038/nn.3067openalex-snapshot
VAMP4 directs synaptic vesicles to a pool that selectively maintains asynchronous neurotransmission
inferredcites →https://doi.org/10.1038/nn1180openalex-snapshot
Agonist-independent modulation of N-type calcium channels by ORL1 receptors
inferredcites →https://doi.org/10.1038/nn1605openalex-snapshot
ORL1 receptor–mediated internalization of N-type calcium channels
inferredcites →https://doi.org/10.1038/nn1656openalex-snapshot
Ghrelin controls hippocampal spine synapse density and memory performance
inferredcites →https://doi.org/10.1038/nn1848openalex-snapshot
Alternative splicing controls G protein–dependent inhibition of N-type calcium channels in nociceptors
inferredcites →https://doi.org/10.1038/nprot.2006.86openalex-snapshot
High Ca2+-phosphate transfection efficiency in low-density neuronal cultures
inferredcites →https://doi.org/10.1073/pnas.0136826100openalex-snapshot
Arachidonic acid mediates muscarinic inhibition and enhancement of N-type Ca 2+ current in sympathetic neurons
inferredcites →https://doi.org/10.1073/pnas.0509588102openalex-snapshot
The cannabinoid agonist WIN55,212-2 increases intracellular calcium via CB 1 receptor coupling to G q/11 G proteins
inferredcites →https://doi.org/10.1073/pnas.1121434109openalex-snapshot
Membrane-localized β-subunits alter the PIP 2 regulation of high-voltage activated Ca 2+ channels
inferredcites →https://doi.org/10.1073/pnas.1212137110openalex-snapshot
Rapid sensing of circulating ghrelin by hypothalamic appetite-modifying neurons
inferredcites →https://doi.org/10.1073/pnas.1313798111openalex-snapshot
Ghrelin triggers the synaptic incorporation of AMPA receptors in the hippocampus
inferredcites →https://doi.org/10.1074/jbc.273.46.30183openalex-snapshot
Interaction of the Xanthine Nucleotide Binding Goα Mutant with G Protein-coupled Receptors
inferredcites →https://doi.org/10.1074/jbc.m111.287607openalex-snapshot
Mutually Opposite Signal Modulation by Hypothalamic Heterodimerization of Ghrelin and Melanocortin-3 Receptors
inferredcites →https://doi.org/10.1074/jbc.m112.382473openalex-snapshot
Promiscuous Dimerization of the Growth Hormone Secretagogue Receptor (GHS-R1a) Attenuates Ghrelin-mediated Signaling
inferredcites →https://doi.org/10.1074/jbc.m114.581397openalex-snapshot
G Protein and β-Arrestin Signaling Bias at the Ghrelin Receptor
inferredcites →https://doi.org/10.1074/jbc.m303266200openalex-snapshot
Direct Interaction and Functional Coupling between Metabotropic Glutamate Receptor Subtype 1 and Voltage-sensitive Cav2.1 Ca2+ Channel
inferredcites →https://doi.org/10.1085/jgp.200910203openalex-snapshot
The Ca2+ channel β subunit determines whether stimulation of Gq-coupled receptors enhances or inhibits N current
inferredcites →https://doi.org/10.1085/jgp.201411245openalex-snapshot
Voltage-dependent regulation of CaV2.2 channels by Gq-coupled receptor is facilitated by membrane-localized β subunit
inferredcites →https://doi.org/10.1097/00001756-200307180-00006openalex-snapshot
Changes in ghrelin and ghrelin receptor expression according to feeding status
inferredcites →https://doi.org/10.1111/ejn.12650openalex-snapshot
Melanocortin 4 receptor activation inhibits presynaptic N‐type calcium channels in amygdaloid complex neurons
inferredcites →https://doi.org/10.1111/jne.12168openalex-snapshot
Divergent Neuronal Circuitries Underlying Acute Orexigenic Effects of Peripheral or Central Ghrelin: Critical Role of Brain Accessibility
inferredcites →https://doi.org/10.1124/jpet.107.123141openalex-snapshot
Four Missense Mutations in the Ghrelin Receptor Result in Distinct Pharmacological Abnormalities
inferredcites →https://doi.org/10.1124/mol.109.056101openalex-snapshot
Growth Hormone Secretagogues and Growth Hormone Releasing Peptides Act As Orthosteric Super-Agonists but Not Allosteric Regulators for Activation of the G Protein Gαo1 by the Ghrelin Receptor
inferredcites →https://doi.org/10.1126/science.273.5277.974openalex-snapshot
A Receptor in Pituitary and Hypothalamus That Functions in Growth Hormone Release
inferredcites →https://doi.org/10.1159/000334144openalex-snapshot
Anorexigenic and Orexigenic Hormone Modulation of Mammalian Target of Rapamycin Complex 1 Activity and the Regulation of Hypothalamic Agouti-Related Protein mRNA Expression
inferredcites →https://doi.org/10.1172/jci25303openalex-snapshot
Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature
inferredcites →https://doi.org/10.1172/jci57660openalex-snapshot
Ghrelin mediates stress-induced food-reward behavior in mice
inferredcites →https://doi.org/10.1210/en.2007-0441openalex-snapshot
Evidence that Ghrelin Is as Potent as Growth Hormone (GH)-Releasing Hormone (GHRH) in Releasing GH from Primary Pituitary Cell Cultures of a Nonhuman Primate (Papio anubis), Acting through Intracellular Signaling Pathways Distinct from GHRH
inferredcites →https://doi.org/10.1210/en.2008-1638openalex-snapshot
In Vivo Characterization of High Basal Signaling from the Ghrelin Receptor
inferredcites →https://doi.org/10.1210/me.2003-0069openalex-snapshot
High Constitutive Signaling of the Ghrelin Receptor—Identification of a Potent Inverse Agonist
inferredcites →https://doi.org/10.1210/me.2005-0084openalex-snapshot
Ghrelin Amplifies Dopamine Signaling by Cross Talk Involving Formation of Growth Hormone Secretagogue Receptor/Dopamine Receptor Subtype 1 Heterodimers
inferredcites →https://doi.org/10.1210/me.2011-1001openalex-snapshot
Ghrelin Directly Stimulates Glucagon Secretion from Pancreatic α-Cells
inferredcites →https://doi.org/10.1371/journal.pone.0031462openalex-snapshot
Ghrelin Indirectly Activates Hypophysiotropic CRF Neurons in Rodents
inferredcites →https://doi.org/10.1523/jneurosci.20-15-05623.2000openalex-snapshot
A voltage-independent calcium current inhibitory pathway activated by muscarinic agonists in rat sympathetic neurons requires both Galpha q/11 and Gbeta gamma.
inferredcites →https://doi.org/10.1523/jneurosci.3187-10.2011openalex-snapshot
Ghrelin Inhibits Visceral Afferent Activation of Catecholamine Neurons in the Solitary Tract Nucleus
inferredcites →https://doi.org/10.1523/jneurosci.3869-04.2004openalex-snapshot
Phosphotidylinositol 4,5-Bisphosphate Signals Underlie Receptor-Specific G q/11 -Mediated Modulation of N-Type Ca 2+ Channels
inferredcites →https://doi.org/10.1523/jneurosci.3890-09.2009openalex-snapshot
Ghrelin Promotes and Protects Nigrostriatal Dopamine Function via a UCP2-Dependent Mitochondrial Mechanism
inferredcites →https://doi.org/10.3389/fnins.2013.00121openalex-snapshot
Ghrelin and eating behavior: evidence and insights from genetically-modified mouse models
inferredcites →https://doi.org/10.4161/chan.2.4.6402openalex-snapshot
D2 dopamine receptors interact directly with N-type calcium channels and regulate channel surface expression levels
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3944544openalex-extracted
GHS-R1a Deletion Selectively Reduces Inhibitory Drive of Dca1 Pyramidal Neurons to Improve Memory and Prevent LPS-Induced Memory Impairment
inferred← citeshttps://doi.org/10.1002/cphy.c200007openalex-snapshot
Neuroendocrine Peptides of the Gut and Their Role in the Regulation of Food Intake
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2021.tb00157.xopenalex-snapshot
Neuroendocrine Peptides of the Gut and Their Role in the Regulation of Food Intake
inferred← citeshttps://doi.org/10.1007/978-3-319-89506-2_7openalex-snapshot
Gastrointestinal Hormones Controlling Energy Homeostasis and Their Potential Role in Obesity
inferred← citeshttps://doi.org/10.1007/s00018-022-04302-5openalex-snapshot
GHSR controls food deprivation-induced activation of CRF neurons of the hypothalamic paraventricular nucleus in a LEAP2-dependent manner
inferred← citeshttps://doi.org/10.1007/s12035-019-01738-yopenalex-snapshot
Ghrelin Selectively Inhibits CaV3.3 Subtype of Low-Voltage-Gated Calcium Channels
inferred← citeshttps://doi.org/10.1007/s12035-023-03221-1openalex-snapshot
Chlorpromazine, an Inverse Agonist of D1R-Like, Differentially Targets Voltage-Gated Calcium Channel (CaV) Subtypes in mPFC Neurons
inferred← citeshttps://doi.org/10.1016/b978-0-12-813814-4.00011-0openalex-snapshot
Hormones and the Regulation of Neuronal Voltage-Sensing Ion Channels
inferred← citeshttps://doi.org/10.1016/j.arr.2019.100945openalex-snapshot
Ghrelin in Alzheimer’s disease: Pathologic roles and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101187openalex-snapshot
A new understanding of GHSR1a——independent of ghrelin activation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.03.007openalex-snapshot
GHS-R1a activity suppresses synaptic function of primary cultured hippocampal neurons
inferred← citeshttps://doi.org/10.1016/j.brainres.2017.09.028openalex-snapshot
Ghrelin upregulates the phosphorylation of the GluN2B subunit of the NMDA receptor by activating GHSR1a and Fyn in the rat hippocampus
inferred← citeshttps://doi.org/10.1016/j.brainres.2026.150346openalex-snapshot
Age-related shifts in ghrelin responsiveness of dorsomedial and ventromedial hypothalamic neurons in rats
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2026.111959openalex-snapshot
Neurobiological mechanisms of second-generation antipsychotic-induced obesity: Interactions between ghrelin signaling and neurotransmitter systems
inferred← citeshttps://doi.org/10.1016/j.drudis.2016.09.003openalex-snapshot
Electrophysiological approaches to unravel the neurobiological basis of appetite and satiety: use of the multielectrode array as a screening strategy
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.120284openalex-snapshot
ACE2 internalization induced by a SARS-CoV-2 recombinant protein is modulated by angiotensin II type 1 and bradykinin 2 receptors
inferred← citeshttps://doi.org/10.1016/j.mce.2016.07.016openalex-snapshot
Ghrelin binding to serum albumin and its biological impact
inferred← citeshttps://doi.org/10.1016/j.mce.2019.110573openalex-snapshot
Development of a novel fluorescent ligand of growth hormone secretagogue receptor based on the N-Terminal Leap2 region
inferred← citeshttps://doi.org/10.1016/j.mce.2022.111777openalex-snapshot
Functional alterations of two novel MC4R mutations found in Argentinian pediatric patients with early onset obesity
inferred← citeshttps://doi.org/10.1016/j.molmet.2019.11.014openalex-snapshot
Fasting induces remodeling of the orexigenic projections from the arcuate nucleus to the hypothalamic paraventricular nucleus, in a growth hormone secretagogue receptor–dependent manner
inferred← citeshttps://doi.org/10.1016/j.molmet.2020.101004openalex-snapshot
Metabolic insights from a GHSR-A203E mutant mouse model
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2020.10.017openalex-snapshot
THE INTRIGUING LIGAND-DEPENDENT AND LIGAND-INDEPENDENT ACTIONS OF THE GROWTH HORMONE SECRETAGOGUE RECEPTOR ON REWARD-RELATED BEHAVIORS
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2022.104952openalex-snapshot
Beyond appetite: Acylated ghrelin as a learning, memory and fear behavior-modulating hormone
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2021.108871openalex-snapshot
Ghrelin signaling in dCA1 suppresses neuronal excitability and impairs memory acquisition via PI3K/Akt/GSK-3β cascades
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2017.01.007openalex-snapshot
Melanocortin 4 receptor constitutive activity inhibits L-type voltage-gated calcium channels in neurons
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2016.01.027openalex-snapshot
Ghrelin activates hypophysiotropic corticotropin-releasing factor neurons independently of the arcuate nucleus
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2020.104594openalex-snapshot
Olanzapine increases AMPK-NPY orexigenic signaling by disrupting H1R-GHSR1a interaction in the hypothalamic neurons of mice
inferred← citeshttps://doi.org/10.1016/j.tem.2019.09.006openalex-snapshot
Ghrelin Signaling: GOAT and GHS-R1a Take a LEAP in Complexity
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2016.05.022openalex-snapshot
Ghrelin suppresses the GnRH-induced preovulatory gonadotropin surge in dairy heifers
inferred← citeshttps://doi.org/10.1021/acschemneuro.9b00426openalex-snapshot
Dopamine Receptor Type 2 and Ghrelin Receptor Coexpression Alters CaV2.2 Modulation by G Protein Signaling Cascades
inferred← citeshttps://doi.org/10.1038/s41401-022-00859-wopenalex-snapshot
Ghrelin infusion into the basolateral amygdala suppresses CTA memory formation in rats via the PI3K/Akt/mTOR and PLC/PKC signaling pathways
inferred← citeshttps://doi.org/10.1038/s41598-020-67053-yopenalex-snapshot
Ghrelin inhibits autonomic response to gastric distension in rats by acting on vagal pathway
inferred← citeshttps://doi.org/10.1038/s41598-023-29226-3openalex-snapshot
Ghrelin signaling in the cerebellar cortex enhances GABAergic transmission onto Purkinje cells
inferred← citeshttps://doi.org/10.1042/ns20200095openalex-snapshot
The life cycle of voltage-gated Ca2+ channels in neurons: an update on the trafficking of neuronal calcium channels
inferred← citeshttps://doi.org/10.1085/jgp.201511462openalex-snapshot
All roads lead to presynaptic calcium channel inhibition by the ghrelin receptor: Separate agonist-dependent and -independent signaling pathways
inferred← citeshttps://doi.org/10.1085/jgp.201912492openalex-snapshot
Constitutive activity of dopamine receptor type 1 (D1R) increases CaV2.2 currents in PFC neurons
inferred← citeshttps://doi.org/10.1093/cercor/bhac230openalex-snapshot
GHSR1a deficiency suppresses inhibitory drive on dCA1 pyramidal neurons and contributes to memory reinforcement
inferred← citeshttps://doi.org/10.1096/fj.201901433ropenalex-snapshot
Short‐chain fatty acids and microbiota metabolites attenuate ghrelin receptor signaling
inferred← citeshttps://doi.org/10.1111/bph.16006openalex-snapshot
Constitutive activity of the dopamine (D5) receptor, highly expressed in CA1 hippocampal neurons, selectively reduces CaV3.2 and CaV3.3 currents
inferred← citeshttps://doi.org/10.1111/febs.15718openalex-snapshot
The ups and downs of growth hormone secretagogue receptor signaling
inferred← citeshttps://doi.org/10.1111/jne.12349openalex-snapshot
Des‐Acyl Ghrelin Directly Targets the Arcuate Nucleus in a Ghrelin‐Receptor Independent Manner and Impairs the Orexigenic Effect of Ghrelin
inferred← citeshttps://doi.org/10.1111/nyas.14087openalex-snapshot
The actions of ghrelin in the paraventricular nucleus: energy balance and neuroendocrine implications
inferred← citeshttps://doi.org/10.1113/jp276256openalex-snapshot
Growth hormone secretagogue receptor constitutive activity impairs voltage‐gated calcium channel‐dependent inhibitory neurotransmission in hippocampal neurons
inferred← citeshttps://doi.org/10.1124/molpharm.124.000957openalex-snapshot
Ghrelin Modulates Voltage-Gated Ca2+ Channels through Voltage-Dependent and Voltage-Independent Pathways in Rat Gastric Vagal Afferent Neurons
inferred← citeshttps://doi.org/10.1126/scisignal.abb1953openalex-snapshot
Ligand-independent activity of the ghrelin receptor modulates AMPA receptor trafficking and supports memory formation
inferred← citeshttps://doi.org/10.1177/1536012120952623openalex-snapshot
A Decade’s Progress in the Development of Molecular Imaging Agents Targeting the Growth Hormone Secretagogue Receptor
inferred← citeshttps://doi.org/10.1210/en.2016-1815openalex-snapshot
Circulating Ghrelin Acts on GABA Neurons of the Area Postrema and Mediates Gastric Emptying in Male Mice
inferred← citeshttps://doi.org/10.1210/en.2017-03101openalex-snapshot
Evidence Supporting a Role for Constitutive Ghrelin Receptor Signaling in Fasting-Induced Hyperphagia in Male Mice
inferred← citeshttps://doi.org/10.1210/endocr/bqae160openalex-snapshot
Selective Colocalization of GHSR and GLP-1R in a Subset of Hypothalamic Neurons and Their Functional Interaction
inferred← citeshttps://doi.org/10.1210/endocr/bqaf104openalex-snapshot
Mini-ghrelins: Functional Characterization of N-terminal Peptides Derived From Ghrelin Proteolysis in Male Samples
inferred← citeshttps://doi.org/10.1242/jcs.207886openalex-snapshot
Constitutive activity of the Ghrelin receptor reduces surface expression of voltage-gated Ca2+ channels in a CaVβ-dependent manner
inferred← citeshttps://doi.org/10.1530/joe-21-0427openalex-snapshot
Intrauterine malnutrition disrupts leptin and ghrelin milk hormones, programming rats
inferred← citeshttps://doi.org/10.23889/suthesis.58915openalex-snapshot
Characterisation of the ghrelinergic system in human models of neurodegenerative diseases
inferred← citeshttps://doi.org/10.3389/fcell.2021.595914openalex-snapshot
Ghrelin-Mediated Regeneration and Plasticity After Nervous System Injury
inferred← citeshttps://doi.org/10.3389/fendo.2023.1094458openalex-snapshot
Feeding-induced hepatokines and crosstalk with multi-organ: A novel therapeutic target for Type 2 diabetes
inferred← citeshttps://doi.org/10.3389/fncel.2019.00205openalex-snapshot
The Role of Ghrelin in Regulating Synaptic Function and Plasticity of Feeding-Associated Circuits
inferred← citeshttps://doi.org/10.3389/fphar.2021.712437openalex-snapshot
LEAP2 Impairs the Capability of the Growth Hormone Secretagogue Receptor to Regulate the Dopamine 2 Receptor Signaling
inferred← citeshttps://doi.org/10.3390/biom16060788openalex-snapshot
A Dimer for Dinner: The Impact of GHS-R1a Heterodimerization on Feeding Circuits
inferred← citeshttps://doi.org/10.3390/cimb46070434openalex-snapshot
Ghrelin/GHSR System in Depressive Disorder: Pathologic Roles and Therapeutic Implications
inferred← citeshttps://doi.org/10.3390/ijms18030638openalex-snapshot
Is Ghrelin Synthesized in the Central Nervous System?
inferred← citeshttps://doi.org/10.3390/ijms18040859openalex-snapshot
Clarifying the Ghrelin System’s Ability to Regulate Feeding Behaviours Despite Enigmatic Spatial Separation of the GHSR and Its Endogenous Ligand
inferred← citeshttps://doi.org/10.3390/ijms18112486openalex-snapshot
Alterations in Rat Accumbens Endocannabinoid and GABA Content during Fentanyl Treatment: The Role of Ghrelin
inferred← citeshttps://doi.org/10.3390/ijms22010210openalex-snapshot
Alterations in Rat Accumbens Dopamine, Endocannabinoids and GABA Content During WIN55,212-2 Treatment: The Role of Ghrelin
inferred← citeshttps://doi.org/10.35537/10915/141297openalex-snapshot
Estudio de los efectos de la actividad constitutiva del receptor de dopamina tipo 1 (D1R) sobre los canales de calcio operados por voltaje (CaV) y su rol en neuronas de la corteza prefrontal
inferred← citeshttps://doi.org/10.35537/10915/145078openalex-snapshot
Evaluación del impacto de la coexpresión del receptor de ghrelina (GHSR) y los receptores de dopamina tipo 1 y 2 (D1R y D2R) sobre la modulación de los canales de calcio operados por voltaje presinápticos (CaV2)
inferred← citeshttps://doi.org/10.35537/10915/51031openalex-snapshot
Estudio del efecto de dos modos de activación del receptor de melanocortinas tipo 4 sobre los canales de calcio operados por voltaje y su impacto sobre la actividad neuronal
inferred← citeshttps://doi.org/10.35537/10915/73001openalex-snapshot
Estudio de la inhibición de los canales de calcio presinápticos tipo CaV2 por la actividad constitutiva del receptor de ghrelina (GHSR) y su impacto sobre la actividad sináptica en neuronas hipocampales
inferred← citeshttps://doi.org/10.35537/10915/73341openalex-snapshot
Estudio de los efectos de la ghrelina sobre los circuitos neuronales del tallo encefálico
inferred← citeshttps://doi.org/10.35537/10915/73585openalex-snapshot
Estudio del rol modulador de ghrelina y su receptor sobre los circuitos hipotalámicos que controlan el balance energético
inferred← citeshttps://doi.org/10.35537/10915/88182openalex-snapshot
Estudio del efecto del receptor de ghrelina (GHSR) sobre la densidad en membrana de canales de calcio operados por voltaje (CaV) y sobre las propiedades biofísicas del sub-tipo CaV3
inferred← citeshttps://doi.org/10.3892/ijmm.2018.3490openalex-snapshot
Cav 1.2 and Cav 2.2 expression is regulated by different endogenous ghrelin levels in pancreatic acinar cells during acute pancreatitis
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.