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Development of a genetically-encoded oxytocin sensor
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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.24116openalex-snapshot
Oxytocin receptors are expressed on dopamine and glutamate neurons in the mouse ventral tegmental area that project to nucleus accumbens and other mesolimbic targets
inferredcites →https://doi.org/10.1016/j.bbr.2008.12.021openalex-snapshot
The main olfactory system and social learning in mammals
inferredcites →https://doi.org/10.1016/j.biopsych.2015.08.008openalex-snapshot
Oxytocin Pathway Genes: Evolutionary Ancient System Impacting on Human Affiliation, Sociality, and Psychopathology
inferredcites →https://doi.org/10.1016/j.cell.2014.05.017openalex-snapshot
Natural Neural Projection Dynamics Underlying Social Behavior
inferredcites →https://doi.org/10.1016/j.cell.2016.06.001openalex-snapshot
Microbial Reconstitution Reverses Maternal Diet-Induced Social and Synaptic Deficits in Offspring
inferredcites →https://doi.org/10.1016/j.cell.2018.06.042openalex-snapshot
A Genetically Encoded Fluorescent Sensor Enables Rapid and Specific Detection of Dopamine in Flies, Fish, and Mice
inferredcites →https://doi.org/10.1016/j.copsyc.2017.02.011openalex-snapshot
Oxytocin: a parenting hormone
inferredcites →https://doi.org/10.1016/j.neuron.2012.09.012openalex-snapshot
Neuromodulation of Brain States
inferredcites →https://doi.org/10.1016/j.neuron.2017.06.003openalex-snapshot
Biased Oxytocinergic Modulation of Midbrain Dopamine Systems
inferredcites →https://doi.org/10.1016/j.neuron.2017.07.002openalex-snapshot
Oxytocin Mobilizes Midbrain Dopamine toward Sociality
inferredcites →https://doi.org/10.1016/j.neuron.2019.02.037openalex-snapshot
A Genetically Encoded Fluorescent Sensor for Rapid and Specific In Vivo Detection of Norepinephrine
inferredcites →https://doi.org/10.1016/j.neuropharm.2013.10.004openalex-snapshot
Oxytocin activation of neurons in ventral tegmental area and interfascicular nucleus of mouse midbrain
inferredcites →https://doi.org/10.1016/j.pbb.2013.06.011openalex-snapshot
Oxytocin, motivation and the role of dopamine
inferredcites →https://doi.org/10.1016/j.peptides.2004.05.019openalex-snapshot
Oxytocin, vasopressin, and social recognition in mammals
inferredcites →https://doi.org/10.1016/j.yhbeh.2015.05.015openalex-snapshot
Neural mechanisms of mother–infant bonding and pair bonding: Similarities, differences, and broader implications
inferredcites →https://doi.org/10.1021/cn4000605openalex-snapshot
A Comparison of the Subsecond Dynamics of Neurotransmission of Dopamine and Serotonin
inferredcites →https://doi.org/10.1038/nature12475openalex-snapshot
Prolonged dopamine signalling in striatum signals proximity and value of distant rewards
inferredcites →https://doi.org/10.1038/nature12518openalex-snapshot
Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin
inferredcites →https://doi.org/10.1038/nbt.4184openalex-snapshot
A genetically encoded fluorescent acetylcholine indicator for in vitro and in vivo studies
inferredcites →https://doi.org/10.1038/nmeth.4234openalex-snapshot
Temporally precise labeling and control of neuromodulatory circuits in the mammalian brain
inferredcites →https://doi.org/10.1038/npp.2008.154openalex-snapshot
The CRF System Mediates Increased Passive Stress-Coping Behavior Following the Loss of a Bonded Partner in a Monogamous Rodent
inferredcites →https://doi.org/10.1038/nrn3044openalex-snapshot
Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine
inferredcites →https://doi.org/10.1073/pnas.1417910112openalex-snapshot
Engineering an improved light-induced dimer (iLID) for controlling the localization and activity of signaling proteins
inferredcites →https://doi.org/10.1073/pnas.1705521114openalex-snapshot
Intranasal oxytocin treatment for social deficits and biomarkers of response in children with autism
inferredcites →https://doi.org/10.1074/jbc.m112.344101openalex-snapshot
Inositol 1,4,5-Trisphosphate 3-Kinase A Is a Novel Microtubule-associated Protein
inferredcites →https://doi.org/10.1111/j.1749-6632.1992.tb34342.xopenalex-snapshot
Oxytocin and Vasopressin
inferredcites →https://doi.org/10.1126/science.1255514openalex-snapshot
A critical time window for dopamine actions on the structural plasticity of dendritic spines
inferredcites →https://doi.org/10.1126/science.aan4994openalex-snapshot
Gating of social reward by oxytocin in the ventral tegmental area
inferredcites →https://doi.org/10.1126/science.aat4422openalex-snapshot
Ultrafast neuronal imaging of dopamine dynamics with designed genetically encoded sensors
inferredcites →https://doi.org/10.1210/en.2009-1271openalex-snapshot
Oxytocin-Dopamine Interactions Mediate Variations in Maternal Behavior in the Rat
inferredcites →https://doi.org/10.1515/revneuro-2017-0068openalex-snapshot
Role of central oxytocin and dopamine systems in nociception and their possible interactions: suggested hypotheses
inferredcites →https://doi.org/10.3389/fnbeh.2015.00001openalex-snapshot
Shining light on motivation, emotion, and memory processes
inferredcites →https://doi.org/10.3389/fnbeh.2015.00251openalex-snapshot
Marmosets treated with oxytocin are more socially attractive to their long-term mate
inferredcites →https://doi.org/10.3389/fnins.2017.00010openalex-snapshot
MEG Signatures of a Perceived Match or Mismatch between Individual and Group Opinions
inferredcites →https://doi.org/10.3389/fnins.2017.00567openalex-snapshot
Social Context, Stress, Neuropsychiatric Disorders, and the Vasopressin 1b Receptor
inferredcites →https://doi.org/10.3389/fnins.2018.00001openalex-snapshot
Peripheral Neuron Survival and Outgrowth on Graphene
inferredcites →https://doi.org/10.3389/fnins.2018.00461openalex-snapshot
Neuroimaging Studies Reveal the Subtle Difference Among Social Network Size Measurements and Shed Light on New Directions
inferredcites →https://doi.org/10.7554/elife.33892openalex-snapshot
Oxytocin functions as a spatiotemporal filter for excitatory synaptic inputs to VTA dopamine neurons
inferredcites →https://doi.org/10.7554/elife.34110openalex-snapshot
A novel source of arterial valve cells linked to bicuspid aortic valve without raphe in mice
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/anie.202206122openalex-snapshot
Probing Neuropeptide Volume Transmission In Vivo by Simultaneous Near‐Infrared Light‐Triggered Release and Optical Sensing**
inferred← citeshttps://doi.org/10.1002/ctm2.1124openalex-snapshot
Genetically encoded tools for in vivo G‐protein‐coupled receptor agonist detection at cellular resolution
inferred← citeshttps://doi.org/10.1016/j.conb.2023.102751openalex-snapshot
Current and emerging methods for probing neuropeptide transmission
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2021.109407openalex-snapshot
Current and future techniques for detecting oxytocin: Focusing on genetically-encoded GPCR sensors
inferred← citeshttps://doi.org/10.1016/j.matt.2021.02.012openalex-snapshot
Nanotransducers for wireless neuromodulation
inferred← citeshttps://doi.org/10.1016/j.peptides.2020.170456openalex-snapshot
Detection of neuropeptides in vivo and open questions for current and upcoming fluorescent sensors for neuropeptides
inferred← citeshttps://doi.org/10.1021/acschemneuro.2c00394openalex-snapshot
New Technologies to Investigate Neuropeptides at Scale
inferred← citeshttps://doi.org/10.1038/d41586-023-02545-1openalex-snapshot
The neural circuit that makes maternal mice respond to pups’ cries
inferred← citeshttps://doi.org/10.1038/s41586-023-06540-4openalex-snapshot
Neural circuitry for maternal oxytocin release induced by infant cries
inferred← citeshttps://doi.org/10.1038/s41587-022-01561-2openalex-snapshot
A genetically encoded sensor measures temporal oxytocin release from different neuronal compartments
inferred← citeshttps://doi.org/10.1038/s41589-023-01480-6openalex-snapshot
A single-component, light-assisted uncaging switch for endoproteolytic release
inferred← citeshttps://doi.org/10.1038/s41592-022-01597-xopenalex-snapshot
A fluorescent sensor for real-time measurement of extracellular oxytocin dynamics in the brain
inferred← citeshttps://doi.org/10.1038/s42003-025-09442-5openalex-snapshot
SNAP-47 mediates somatic oxytocin dynamics in hypothalamic neurons
inferred← citeshttps://doi.org/10.1073/pnas.2314795121openalex-snapshot
Near-infrared nanosensors enable optical imaging of oxytocin with selectivity over vasopressin in acute mouse brain slices
inferred← citeshttps://doi.org/10.1101/2021.07.30.454450openalex-snapshot
A fluorescent sensor for the real-time measurement of extracellular oxytocin dynamics in the brain
inferred← citeshttps://doi.org/10.1101/2022.10.05.511026openalex-snapshot
Near Infrared Nanosensors Enable Optical Imaging of Oxytocin with Selectivity over Vasopressin in Acute Mouse Brain Slices
inferred← citeshttps://doi.org/10.1111/jne.13049openalex-snapshot
The oxytocin system and early‐life experience‐dependent plastic changes
inferred← citeshttps://doi.org/10.1111/jne.13333openalex-snapshot
Heralding a new era of oxytocinergic research: New tools, new problems?
inferred← citeshttps://doi.org/10.1126/science.abq8173openalex-snapshot
A tool kit of highly selective and sensitive genetically encoded neuropeptide sensors
inferred← citeshttps://doi.org/10.1126/science.adn6671openalex-snapshot
Neuromodulator and neuropeptide sensors and probes for precise circuit interrogation in vivo
inferred← citeshttps://doi.org/10.1146/annurev-neuro-102320-102847openalex-snapshot
Oxytocin, Neural Plasticity, and Social Behavior
inferred← citeshttps://doi.org/10.1186/s13041-021-00885-5openalex-snapshot
The emergence of molecular systems neuroscience
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