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https://doi.org/10.5281/zenodo.23511202

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.cell.2011.07.039zenodo-depositor-declared
Hunger States Switch a Flip-Flop Memory Circuit via a Synaptic AMPK-Dependent Positive Feedback Loop
inferredcites →https://doi.org/10.1016/j.cell.2015.01.033zenodo-depositor-declared
Sensory Detection of Food Rapidly Modulates Arcuate Feeding Circuits
inferredcites →https://doi.org/10.1016/j.celrep.2017.11.036zenodo-depositor-declared
Nutritive, Post-ingestive Signals Are the Primary Regulators of AgRP Neuron Activity
inferredcites →https://doi.org/10.1016/j.neuron.2017.09.043zenodo-depositor-declared
Dynamics of Gut-Brain Communication Underlying Hunger
inferredcites →https://doi.org/10.1016/s0955-0674(02)00314-9zenodo-depositor-declared
Self-perpetuating states in signal transduction: positive feedback, double-negative feedback and bistability
inferredcites →https://doi.org/10.1038/nature11270zenodo-depositor-declared
Deconstruction of a neural circuit for hunger
inferredcites →https://doi.org/10.1038/nature12956zenodo-depositor-declared
An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger
inferredcites →https://doi.org/10.1038/nature14416zenodo-depositor-declared
Neurons for hunger and thirst transmit a negative-valence teaching signal
inferredcites →https://doi.org/10.1038/nn.2739zenodo-depositor-declared
AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training
inferredcites →https://doi.org/10.1038/nrn1845zenodo-depositor-declared
Dendritic peptide release and peptide-dependent behaviours
inferredcites →https://doi.org/10.1038/s41586-021-03729-3zenodo-depositor-declared
Food cue regulation of AGRP hunger neurons guides learning
inferredcites →https://doi.org/10.1038/s42255-024-00987-zzenodo-depositor-declared
Reciprocal activity of AgRP and POMC neurons governs coordinated control of feeding and metabolism
inferredcites →https://doi.org/10.1073/pnas.82.9.3055zenodo-depositor-declared
A mechanism for memory storage insensitive to molecular turnover: a bistable autophosphorylating kinase.
inferredcites →https://doi.org/10.1126/science.1115524zenodo-depositor-declared
NPY/AgRP Neurons Are Essential for Feeding in Adult Mice but Can Be Ablated in Neonates
inferredcites →https://doi.org/10.1210/en.2004-1397zenodo-depositor-declared
Fasting Induces a Large, Leptin-Dependent Increase in the Intrinsic Action Potential Frequency of Orexigenic Arcuate Nucleus Neuropeptide Y/Agouti-Related Protein Neurons
inferredcites →https://doi.org/10.1523/jneurosci.0647-17.2017zenodo-depositor-declared
The Relevance of AgRP Neuron-Derived GABA Inputs to POMC Neurons Differs for Spontaneous and Evoked Release
inferredcites →https://doi.org/10.3389/fncir.2018.00053zenodo-depositor-declared
Eligibility Traces and Plasticity on Behavioral Time Scales: Experimental Support of NeoHebbian Three-Factor Learning Rules
inferredcites →https://doi.org/10.3389/fncom.2016.00027zenodo-depositor-declared
Computational Analysis of the Hypothalamic Control of Food Intake
inferredcites →https://doi.org/10.3934/dcdsb.2021114zenodo-depositor-declared
A short-term food intake model involving glucose, insulin and ghrelin
inferredcites →https://doi.org/10.7554/elife.07122zenodo-depositor-declared
Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
inferredcites →https://doi.org/10.7554/elife.18640zenodo-depositor-declared
Hunger neurons drive feeding through a sustained, positive reinforcement signal
inferredcites →https://doi.org/10.7554/elife.46348zenodo-depositor-declared
Sustained NPY signaling enables AgRP neurons to drive feeding

What points at this work

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inferred← citeshttps://doi.org/10.5281/zenodo.23511291zenodo-depositor-declared
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