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Dietary and sex-specific factors regulate hypothalamic neurogenesis in young adult mice

https://doi.org/10.3389/fnins.2014.00157
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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/(sici)1097-4695(19980215)34:3<242::aid-neu4>3.0.co;2-2openalex-snapshot
Cell death in the sexually dimorphic dorsal preoptic area/anterior hypothalamus of perinatal male and female ferrets
inferredcites →https://doi.org/10.1002/cne.21492openalex-snapshot
Evidence for constitutive neural cell proliferation in the adult murine hypothalamus
inferredcites →https://doi.org/10.1002/cne.22273openalex-snapshot
Differential distribution of tight junction proteins suggests a role for tanycytes in blood‐hypothalamus barrier regulation in the adult mouse brain
inferredcites →https://doi.org/10.1002/cne.23355openalex-snapshot
Tanycyte‐like cells form a blood–cerebrospinal fluid barrier in the circumventricular organs of the mouse brain
inferredcites →https://doi.org/10.1002/cne.23514openalex-snapshot
DCX‐expressing cells in the vicinity of the hypothalamic neurogenic niche: A comparative study between mouse, sheep, and human tissues
inferredcites →https://doi.org/10.1002/jnr.23206openalex-snapshot
Neurogenesis in the circumventricular organs of adult mouse brains
inferredcites →https://doi.org/10.1016/0031-9384(78)90162-2openalex-snapshot
Estrogen modification of feeding behavior in the female rat: Influence of metabolic state
inferredcites →https://doi.org/10.1016/j.cmet.2013.03.004openalex-snapshot
Tanycytic VEGF-A Boosts Blood-Hypothalamus Barrier Plasticity and Access of Metabolic Signals to the Arcuate Nucleus in Response to Fasting
inferredcites →https://doi.org/10.1016/j.devcel.2012.07.012openalex-snapshot
Wnt Signaling Regulates Postembryonic Hypothalamic Progenitor Differentiation
inferredcites →https://doi.org/10.1016/j.expneurol.2004.12.021openalex-snapshot
Neurogenesis in the ependymal layer of the adult rat 3rd ventricle
inferredcites →https://doi.org/10.1016/j.ijdevneu.2012.07.003openalex-snapshot
Functional implications of hypothalamic neurogenesis in the adult mammalian brain
inferredcites →https://doi.org/10.1016/j.mcn.2009.04.007openalex-snapshot
Circumventricular organs: A novel site of neural stem cells in the adult brain
inferredcites →https://doi.org/10.1016/j.molmet.2013.09.005openalex-snapshot
Neuroinflammatory basis of metabolic syndrome
inferredcites →https://doi.org/10.1016/j.tem.2012.11.003openalex-snapshot
Neuroinflammation and neurodegeneration in overnutrition-induced diseases
inferredcites →https://doi.org/10.1016/j.tem.2013.10.005openalex-snapshot
Role of hypothalamic neurogenesis in feeding regulation
inferredcites →https://doi.org/10.1016/j.tins.2012.12.008openalex-snapshot
Hypothalamic tanycytes: potential roles in the control of feeding and energy balance
inferredcites →https://doi.org/10.1016/j.yfrne.2012.06.001openalex-snapshot
Organizational and activational effects of sex steroids on kisspeptin neuron development
inferredcites →https://doi.org/10.1016/j.yfrne.2013.05.001openalex-snapshot
Hypothalamic neurogenesis in the adult brain
inferredcites →https://doi.org/10.1023/a:1022529918810openalex-snapshot
Ontogeny of Sex Differences in the Mammalian Hypothalamus and Preoptic Area
inferredcites →https://doi.org/10.1038/nature05453openalex-snapshot
Genome-wide atlas of gene expression in the adult mouse brain
inferredcites →https://doi.org/10.1038/ncb2562openalex-snapshot
IKKβ/NF-κB disrupts adult hypothalamic neural stem cells to mediate a neurodegenerative mechanism of dietary obesity and pre-diabetes
inferredcites →https://doi.org/10.1038/ncomms3049openalex-snapshot
α-Tanycytes of the adult hypothalamic third ventricle include distinct populations of FGF-responsive neural progenitors
inferredcites →https://doi.org/10.1038/nm749openalex-snapshot
Irradiation induces neural precursor-cell dysfunction
inferredcites →https://doi.org/10.1038/nn.2178openalex-snapshot
Pubertal hormones modulate the addition of new cells to sexually dimorphic brain regions
inferredcites →https://doi.org/10.1038/nn.2545openalex-snapshot
A genomic atlas of mouse hypothalamic development
inferredcites →https://doi.org/10.1038/nn.3079openalex-snapshot
Tanycytes of the hypothalamic median eminence form a diet-responsive neurogenic niche
inferredcites →https://doi.org/10.1073/pnas.0404644101openalex-snapshot
Deletion of Bax eliminates sex differences in the mouse forebrain
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.1219443110openalex-snapshot
Pubertally born neurons and glia are functionally integrated into limbic and hypothalamic circuits of the male Syrian hamster
inferredcites →https://doi.org/10.1097/nen.0b013e31822200aaopenalex-snapshot
Comparative Characterization of the Human and Mouse Third Ventricle Germinal Zones
inferredcites →https://doi.org/10.1111/j.1460-9568.2010.07220.xopenalex-snapshot
IGF‐I stimulates neurogenesis in the hypothalamus of adult rats
inferredcites →https://doi.org/10.1111/j.1460-9568.2010.07521.xopenalex-snapshot
Emerging new sites for adult neurogenesis in the mammalian brain: a comparative study between the hypothalamus and the classical neurogenic zones
inferredcites →https://doi.org/10.1126/science.1115360openalex-snapshot
Neurogenesis in the Hypothalamus of Adult Mice: Potential Role in Energy Balance
inferredcites →https://doi.org/10.1146/annurev-physiol-021113-170347openalex-snapshot
Feed Your Head: Neurodevelopmental Control of Feeding and Metabolism
inferredcites →https://doi.org/10.1172/jci43134openalex-snapshot
Remodeling of the arcuate nucleus energy-balance circuit is inhibited in obese mice
inferredcites →https://doi.org/10.1172/jci59660openalex-snapshot
Obesity is associated with hypothalamic injury in rodents and humans
inferredcites →https://doi.org/10.1210/en.2009-0870openalex-snapshot
Role of Estradiol in the Dynamic Control of Tanycyte Plasticity Mediated by Vascular Endothelial Cells in the Median Eminence
inferredcites →https://doi.org/10.1371/journal.pgen.1003217openalex-snapshot
Sex-Specific Signaling in the Blood–Brain Barrier Is Required for Male Courtship in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0072029openalex-snapshot
Cerebral Cell Renewal in Adult Mice Controls the Onset of Obesity
inferredcites →https://doi.org/10.1371/journal.pone.0078236openalex-snapshot
Evidence for NG2-glia Derived, Adult-Born Functional Neurons in the Hypothalamus
inferredcites →https://doi.org/10.1371/journal.pone.0090381openalex-snapshot
Rax-CreERT2 Knock-In Mice: A Tool for Selective and Conditional Gene Deletion in Progenitor Cells and Radial Glia of the Retina and Hypothalamus
inferredcites →https://doi.org/10.1371/journal.pone.0102875openalex-snapshot
Correction: Rax-CreERT2 Knock-In Mice: A Tool for Selective and Conditional Gene Deletion in Progenitor Cells and Radial Glia of the Retina and Hypothalamus
inferredcites →https://doi.org/10.1523/jneurosci.0135-09.2009openalex-snapshot
Estrogen Induces Caspase-Dependent Cell Death during Hypothalamic Development
inferredcites →https://doi.org/10.1523/jneurosci.21-17-06706.2001openalex-snapshot
Infusion of Brain-Derived Neurotrophic Factor into the Lateral Ventricle of the Adult Rat Leads to New Neurons in the Parenchyma of the Striatum, Septum, Thalamus, and Hypothalamus
inferredcites →https://doi.org/10.1523/jneurosci.2437-12.2013openalex-snapshot
Fgf10-Expressing Tanycytes Add New Neurons to the Appetite/Energy-Balance Regulating Centers of the Postnatal and Adult Hypothalamus
inferredcites →https://doi.org/10.1523/jneurosci.2479-09.2010openalex-snapshot
De Novo Neurogenesis in Adult Hypothalamus as a Compensatory Mechanism to Regulate Energy Balance
inferredcites →https://doi.org/10.1667/rr2214.1openalex-snapshot
Localized CT-Guided Irradiation Inhibits Neurogenesis in Specific Regions of the Adult Mouse Brain
inferredcites →https://doi.org/10.2337/db12-1605openalex-snapshot
Hypothalamic Inflammation: Marker or Mechanism of Obesity Pathogenesis?
inferredcites →https://doi.org/10.3389/fnins.2013.00263openalex-snapshot
Opposite effects of a high-fat diet and calorie restriction on ciliary neurotrophic factor signaling in the mouse hypothalamus
inferredcites →https://doi.org/10.3791/50716openalex-snapshot
Functional Interrogation of Adult Hypothalamic Neurogenesis with Focal Radiological Inhibition

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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GFAP-Expressing Progenitors are the Main Source of Adult Neural Stem Cells in the Hypothalamus
inferred← citeshttps://doi.org/10.1002/cne.24376openalex-snapshot
A comparative study of the neural stem cell niche in the adult hypothalamus of human, mouse, rat and gray mouse lemur (Microcebus murinus)
inferred← citeshttps://doi.org/10.1002/glia.23817openalex-snapshot
Tanycyte ablation in the arcuate nucleus and median eminence increases obesity susceptibility by increasing body fat content in male mice
inferred← citeshttps://doi.org/10.1002/jbmr.3967openalex-snapshot
Both NPY-Expressing and CART-Expressing Neurons Increase Energy Expenditure and Trabecular Bone Mass in Response to AP1 Antagonism, But Have Opposite Effects on Bone Resorption
inferred← citeshttps://doi.org/10.1007/978-3-319-41603-8openalex-snapshot
Stem Cells in Neuroendocrinology
inferred← citeshttps://doi.org/10.1007/978-3-319-41603-8_11openalex-snapshot
Perspective on Stem Cells in Developmental Biology, with Special Reference to Neuroendocrine Systems
inferred← citeshttps://doi.org/10.1007/s00394-018-1715-0openalex-snapshot
Switching from high-fat diet to foods containing resveratrol as a calorie restriction mimetic changes the architecture of arcuate nucleus to produce more newborn anorexigenic neurons
inferred← citeshttps://doi.org/10.1007/s11515-015-1351-5openalex-snapshot
Metabolic regulation of adult stem cell-derived neurons
inferred← citeshttps://doi.org/10.1007/s11920-015-0639-0openalex-snapshot
Hypocretins, Neural Systems, Physiology, and Psychiatric Disorders
inferred← citeshttps://doi.org/10.1007/s12015-025-10995-5openalex-snapshot
Region-Specific Adult Neural Stem Cell Niches of the Mediobasal Hypothalamus and Medulla Oblongata
inferred← citeshttps://doi.org/10.1007/s12640-020-00298-7openalex-snapshot
Adult Endogenous Dopaminergic Neuroregeneration Against Parkinson’s Disease: Ideal Animal Models?
inferred← citeshttps://doi.org/10.1016/b978-0-12-819975-6.00006-6openalex-snapshot
Neurogenesis in the adult hypothalamus: A distinct form of structural plasticity involved in metabolic and circadian regulation, with potential relevance for human pathophysiology
inferred← citeshttps://doi.org/10.1016/j.biochi.2022.08.012openalex-snapshot
Fatty acid sensing in the brain: The role of glial-neuronal metabolic crosstalk and horizontal lipid flux
inferred← citeshttps://doi.org/10.1016/j.brainres.2015.04.029openalex-snapshot
Classic and novel stem cell niches in brain homeostasis and repair
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117685openalex-snapshot
Tanycyte BMAL1 regulates high-fat diet weight gain and shapes arcuate neurogenesis in female mice
inferred← citeshttps://doi.org/10.1016/j.dcn.2022.101141openalex-snapshot
Sex differences in proliferation and attrition of pubertally born cells in the rat posterior dorsal medial amygdala
inferred← citeshttps://doi.org/10.1016/j.engreg.2023.10.002openalex-snapshot
Fabrication and characterisation of random and aligned electrospun scaffolds to investigate hypothalamic stem/progenitor cell behaviour
inferred← citeshttps://doi.org/10.1016/j.jchemneu.2021.101920openalex-snapshot
Seasonal changes in adenosine kinase in tanycytes of the Arctic ground squirrel (Urocitellus parryii)
inferred← citeshttps://doi.org/10.1016/j.mce.2016.08.020openalex-snapshot
Pivotal role of median eminence tanycytes for hypothalamic function and neurogenesis
inferred← citeshttps://doi.org/10.1016/j.metabol.2021.154837openalex-snapshot
Bone morphogenetic proteins (BMPs) in the central regulation of energy balance and adult neural plasticity
inferred← citeshttps://doi.org/10.1016/j.molmet.2017.08.015openalex-snapshot
Amino acid sensing in hypothalamic tanycytes via umami taste receptors
inferred← citeshttps://doi.org/10.1016/j.molmet.2018.04.007openalex-snapshot
Sex and gender differences in developmental programming of metabolism
inferred← citeshttps://doi.org/10.1016/j.molmet.2021.101312openalex-snapshot
Adult-born proopiomelanocortin neurons derived from Rax-expressing precursors mitigate the metabolic effects of congenital hypothalamic proopiomelanocortin deficiency
inferred← citeshttps://doi.org/10.1016/j.nbd.2018.03.013openalex-snapshot
Stepwise impairment of neural stem cell proliferation and neurogenesis concomitant with disruption of blood-brain barrier in recurrent ischemic stroke
inferred← citeshttps://doi.org/10.1016/j.neulet.2024.137674openalex-snapshot
GFAP-expressing cells in the adult hypothalamus can generate multiple neural cell lineages in vitro
inferred← citeshttps://doi.org/10.1016/j.neures.2021.05.012openalex-snapshot
Effects of leptin on proliferation of astrocyte- and tanycyte-like neural stem cells in the adult mouse medulla oblongata
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.12.037openalex-snapshot
High-fat Diet and Physical Exercise Differentially Modulate Adult Neurogenesis in the Mouse Hypothalamus
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.04.001openalex-snapshot
Regulation and function of neurogenesis in the adult mammalian hypothalamus
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.09.001openalex-snapshot
Neurobiological characteristics underlying metabolic differences between males and females
inferred← citeshttps://doi.org/10.1016/j.stemcr.2026.102953openalex-snapshot
Effects of voluntary exercise, diet, and selenium on hypothalamic adult neurogenesis
inferred← citeshttps://doi.org/10.1016/j.yfrne.2014.11.004openalex-snapshot
Seasonal regulation of structural plasticity and neurogenesis in the adult mammalian brain: Focus on the sheep hypothalamus
inferred← citeshttps://doi.org/10.1016/j.yfrne.2017.07.009openalex-snapshot
Differential vulnerability to adverse nutritional conditions in male and female rats: Modulatory role of estradiol during development
inferred← citeshttps://doi.org/10.1016/j.yfrne.2020.100871openalex-snapshot
Hypothalamic neurogenesis and its implications for obesity-induced anxiety disorders
inferred← citeshttps://doi.org/10.1016/j.yfrne.2024.101154openalex-snapshot
Astrogenesis in the hypothalamus: A life-long process contributing to the development and plasticity of neuroendocrine networks
inferred← citeshttps://doi.org/10.1017/s0029665118002665openalex-snapshot
Role of hypothalamic tanycytes in nutrient sensing and energy balance
inferred← citeshttps://doi.org/10.1017/s0954422416000081openalex-snapshot
Modulating adult neurogenesis through dietary interventions
inferred← citeshttps://doi.org/10.1038/s41467-024-46589-xopenalex-snapshot
Maternal dietary fat during lactation shapes single nucleus transcriptomic profile of postnatal offspring hypothalamus in a sexually dimorphic manner in mice
inferred← citeshttps://doi.org/10.1038/s41574-024-01036-1openalex-snapshot
Control of tuberal hypothalamic development and its implications in metabolic disorders
inferred← citeshttps://doi.org/10.1038/s41598-018-24381-4openalex-snapshot
Pineal-dependent increase of hypothalamic neurogenesis contributes to the timing of seasonal reproduction in sheep
inferred← citeshttps://doi.org/10.1038/s41598-020-68110-2openalex-snapshot
Activation of GPR40 induces hypothalamic neurogenesis through p38- and BDNF-dependent mechanisms
inferred← citeshttps://doi.org/10.1038/s41598-024-66726-2openalex-snapshot
Gestational bisphenol A exposure alters energy homeostasis and adult hypothalamic neurogenesis in female mice
inferred← citeshttps://doi.org/10.1038/s42255-022-00610-zopenalex-snapshot
Glial cells as integrators of peripheral and central signals in the regulation of energy homeostasis
inferred← citeshttps://doi.org/10.1038/s44319-023-00016-2openalex-snapshot
An analogue of the Prolactin Releasing Peptide reduces obesity and promotes adult neurogenesis
inferred← citeshttps://doi.org/10.1093/med/9780197519233.003.0008openalex-snapshot
Neurogenic and Non-Neurogenic Regions
inferred← citeshttps://doi.org/10.1101/2021.12.15.472761openalex-snapshot
The neural cell adhesion molecule NrCAM regulates development of hypothalamic tanycytes
inferred← citeshttps://doi.org/10.1101/2023.02.09.527879openalex-snapshot
Telomerase reverse transcriptase (TERT)-expressing cells mark a novel stem cell population in the adult mouse brain
inferred← citeshttps://doi.org/10.1101/2023.12.22.573029openalex-snapshot
High fat diet promotes obesity by driving miRNA dependent neurogenesis and integration of orexigenic neurons in the feeding circuitry
inferred← citeshttps://doi.org/10.1101/2025.04.21.649851openalex-snapshot
Tanycyte Bmal1 sex-specifically regulates weight gain and hypothalamic neurogenesis in female mice
inferred← citeshttps://doi.org/10.1101/637587openalex-snapshot
Ablation of tanycytes of the arcuate nucleus and median eminence increases visceral adiposity and decreases insulin sensitivity in male mice
inferred← citeshttps://doi.org/10.1111/jnc.15188openalex-snapshot
The FGF2‐induced tanycyte proliferation involves a connexin 43 hemichannel/purinergic‐dependent pathway
inferred← citeshttps://doi.org/10.1126/sciadv.abg3777openalex-snapshot
Control of neurogenic competence in mammalian hypothalamic tanycytes
inferred← citeshttps://doi.org/10.1152/ajpregu.00296.2020openalex-snapshot
What is the physiological role of hypothalamic tanycytes in metabolism?
inferred← citeshttps://doi.org/10.1155/2016/3276383openalex-snapshot
The Role of Hypothalamic Neuropeptides in Neurogenesis and Neuritogenesis
inferred← citeshttps://doi.org/10.1186/s13041-016-0224-4openalex-snapshot
Control of adult neurogenesis by programmed cell death in the mammalian brain
inferred← citeshttps://doi.org/10.1210/er.2017-00235openalex-snapshot
The Versatile Tanycyte: A Hypothalamic Integrator of Reproduction and Energy Metabolism
inferred← citeshttps://doi.org/10.1242/jeb.173377openalex-snapshot
Food consumption increases cell proliferation in the python brain
inferred← citeshttps://doi.org/10.1523/eneuro.0027-16.2016openalex-snapshot
Adult Neurogenesis in the Female Mouse Hypothalamus: Estradiol and High-Fat Diet Alter the Generation of Newborn Neurons Expressing Estrogen Receptor α
inferred← citeshttps://doi.org/10.1523/jneurosci.1711-14.2014openalex-snapshot
The LIM Homeodomain Factor Lhx2 Is Required for Hypothalamic Tanycyte Specification and Differentiation
inferred← citeshttps://doi.org/10.1523/jneurosci.3222-16.2017openalex-snapshot
Circadian Kinetics of Cell Cycle Progression in Adult Neurogenic Niches of a Diurnal Vertebrate
inferred← citeshttps://doi.org/10.1530/jme-16-0182openalex-snapshot
Glial cells and energy balance
inferred← citeshttps://doi.org/10.15368/theses.2017.86openalex-snapshot
Effects of Food Consumption on Cell Proliferation in the Brain of Python regius
inferred← citeshttps://doi.org/10.18794/aams/207316openalex-snapshot
Orexin receptor-1 expression in edult rodent neurogenic regions: evidence from the subgranular zone and the median eminence
inferred← citeshttps://doi.org/10.21860/medflum2017_12openalex-snapshot
inferred← citeshttps://doi.org/10.21860/medflum2017_179749openalex-snapshot
Adult neurogenesis – accent on subgranular and subventricular zone in mammals
inferred← citeshttps://doi.org/10.2337/db16-0586openalex-snapshot
Inhibiting Microglia Expansion Prevents Diet-Induced Hypothalamic and Peripheral Inflammation
inferred← citeshttps://doi.org/10.3233/bpl-160035openalex-snapshot
The Role of Lipid Metabolism for Neural Stem Cell Regulation
inferred← citeshttps://doi.org/10.32657/10220/48326openalex-snapshot
Mechanisms regulating adult neurogenesis in the hypothalamus using a genetic inducible-approach to label and optogenetically stimulate hypothalamic neural progenitors
inferred← citeshttps://doi.org/10.3389/978-2-88963-988-5openalex-snapshot
Generation of Neurons and Their Integration in Pre-Existing Circuits in the Postnatal Brain: Signalling in Physiological and Regenerative Contexts
inferred← citeshttps://doi.org/10.3389/fcell.2019.00065openalex-snapshot
Lack of Brain Serotonin Affects Feeding and Differentiation of Newborn Cells in the Adult Hypothalamus
inferred← citeshttps://doi.org/10.3389/fendo.2015.00042openalex-snapshot
Role of Non-Neuronal Cells in Body Weight and Appetite Control
inferred← citeshttps://doi.org/10.3389/fendo.2017.00051openalex-snapshot
Non-Neuronal Cells in the Hypothalamic Adaptation to Metabolic Signals
inferred← citeshttps://doi.org/10.3389/fendo.2017.00275openalex-snapshot
Advances in Understanding of Structural Reorganization in the Hypothalamic Neurosecretory System
inferred← citeshttps://doi.org/10.3389/fendo.2019.00286openalex-snapshot
Tanycyte Gene Expression Dynamics in the Regulation of Energy Homeostasis
inferred← citeshttps://doi.org/10.3389/fendo.2022.953995openalex-snapshot
The Properties and Functions of Glial Cell Types of the Hypothalamic Median Eminence
inferred← citeshttps://doi.org/10.3389/fncel.2014.00440openalex-snapshot
Neurodevelopmental origin and adult neurogenesis of the neuroendocrine hypothalamus
inferred← citeshttps://doi.org/10.3389/fncel.2020.576444openalex-snapshot
Beyond the Hippocampus and the SVZ: Adult Neurogenesis Throughout the Brain
inferred← citeshttps://doi.org/10.3389/fnins.2017.00190openalex-snapshot
Hypothalamic Neurogenesis as an Adaptive Metabolic Mechanism
inferred← citeshttps://doi.org/10.3389/fnins.2017.00570openalex-snapshot
Adult Neurogenesis in Sheep: Characterization and Contribution to Reproduction and Behavior
inferred← citeshttps://doi.org/10.3389/fnins.2021.763856openalex-snapshot
Irx3 and Irx5 - Novel Regulatory Factors of Postnatal Hypothalamic Neurogenesis
inferred← citeshttps://doi.org/10.3389/fnins.2022.832961openalex-snapshot
Loss of Function of the Neural Cell Adhesion Molecule NrCAM Regulates Differentiation, Proliferation and Neurogenesis in Early Postnatal Hypothalamic Tanycytes
inferred← citeshttps://doi.org/10.3390/biom14030335openalex-snapshot
Exploring the Intricacies of Neurogenic Niches: Unraveling the Anatomy and Neural Microenvironments
inferred← citeshttps://doi.org/10.3390/cells12091285openalex-snapshot
The Effects of Extrinsic and Intrinsic Factors on Neurogenesis
inferred← citeshttps://doi.org/10.3390/cells12131801openalex-snapshot
Neurochemical Basis of Inter-Organ Crosstalk in Health and Obesity: Focus on the Hypothalamus and the Brainstem
inferred← citeshttps://doi.org/10.3390/ijms222011010openalex-snapshot
Female Mice with Selenocysteine tRNA Deletion in Agrp Neurons Maintain Leptin Sensitivity and Resist Weight Gain While on a High-Fat Diet
inferred← citeshttps://doi.org/10.3390/ijms262210914openalex-snapshot
Perspective for Modulation of Hypothalamic Neurogenesis: Integrating Anatomical Insights with Exercise and Dietary Interventions
inferred← citeshttps://doi.org/10.3390/nu14132564openalex-snapshot
A Short-Term Sucrose Diet Impacts Cell Proliferation of Neural Precursors in the Adult Hypothalamus
inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-23-01865openalex-snapshot
Potential role of tanycyte-derived neurogenesis in Alzheimer’s disease
inferred← citeshttps://doi.org/10.64898/2025.12.31.697168openalex-snapshot
Ciliary sensing in tanycytes couples nutrient availability to metabolic regulation
inferred← citeshttps://doi.org/10.70675/49c584f3z87f6z4320z924bz64015ded1e39openalex-snapshot
Cell neogenesis in the postnatal hypothalamus as a new mechanism of control of the reproductive function
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