Hypothalamic sensing of fatty acids

Positional cloning of the mouse obese gene and its human homologue

Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419

Central nervous system control of food intake

Schwartz, M. W., Woods, S. C., Porte, D., Seeley, R. J., & Baskin, D. G. (2000) · Nature · doi:10.1038/35007534 · Cited by 6,451

Role of leptin in the neuroendocrine response to fasting

Ahima, R. S., Prabakaran, D., Mantzoros, C., Qu, D., Lowell, B., Maratos-Flier, E., & Flier, J. S. (1996) · Nature · doi:10.1038/382250a0 · Cited by 3,117

Environmental Contributions to the Obesity Epidemic

Hill, J. O., & Peters, J. C. (1998) · Science · doi:10.1126/science.280.5368.1371 · Cited by 2,258

Role of Brain Insulin Receptor in Control of Body Weight and Reproduction

Brüning, J. C., Gautam, D., Burks, D. J., Gillette, J., Schubert, M., Orban, P. C., Klein, R., Krone, W., Müller-Wieland, D., & Kahn, C. R. (2000) · Science · doi:10.1126/science.289.5487.2122 · Cited by 2,235

Leptin levels reflect body lipid content in mice: Evidence for diet-induced resistance to leptin action

Frederich, R. C., Hamann, A., Anderson, S., Löllmann, B., Lowell, B. B., & Flier, J. S. (1995) · Nature Medicine · doi:10.1038/nm1295-1311 · Cited by 1,660

AMP-kinase regulates food intake by responding to hormonal and nutrient signals in the hypothalamus

Minokoshi, Y., Alquier, T., Furukawa, N., Kim, Y.-B., Lee, A., Xue, B., Mu, J., Foufelle, F., Ferré, P., Birnbaum, M. J., et al. (2004) · Nature · doi:10.1038/nature02440 · Cited by 1,637

Cholecystokinin decreases food intake in rats.

Gibbs, J., Young, R. C., & Smith, G. P. (1973) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0034870 · Cited by 1,502

Identification of targets of leptin action in rat hypothalamus.

Schwartz, M. W., Seeley, R. J., Campfield, L. A., Burn, P., & Baskin, D. G. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118891 · Cited by 1,499

The role of depot fat in the hypothalamic control of food intake in the rat

Gc, K. (1953) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1953.0009 · Cited by 1,432

A Fall in Plasma Free Fatty Acid (FFA) Level Activates the Hypothalamic-Pituitary-Adrenal Axis Independent of Plasma Glucose: Evidence for Brain Sensing of Circulating FFA

Oh, Y. T., Oh, K.-S., Kang, I., & Youn, J. H. (2012) · Endocrinology · doi:10.1210/en.2012-1330 · Cited by 16

Dietary triglycerides as signaling molecules that influence reward and motivation

Berland, C., Cansell, C., Hnasko, T. S., Magnan, C., & Luquet, S. H. (2016) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2016.03.005 · Cited by 16

Long Chain Fatty Acids Differentially Regulate Sub-populations of Arcuate POMC and NPY Neurons

Michael, N. J., & Watt, M. J. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.09.045 · Cited by 16

Metabolic Therapy in Heart Failure

Lopatin, Y. (2015) · Cardiac failure review · doi:10.15420/cfr.2015.1.2.112 · Cited by 16

Mapping Brain c‐Fos Immunoreactivity after Insulin‐Induced Voluntary Lard Intake: Insulin‐ and Lard‐Associated Patterns

Warne, J. P., Horneman, H. F., Ginsberg, A. B., Pecoraro, N. C., Foster, M. T., Akana, S. F., & Dallman, M. F. (2007) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2007.01593.x · Cited by 16

Deregulation of Hepatic Insulin Sensitivity Induced by Central Lipid Infusion in Rats Is Mediated by Nitric Oxide

Marsollier, N., Kassis, N., Mezghenna, K., Soty, M., Fioramonti, X., Lacombe, A., Joly‐Amado, A., Pillot, B., Zitoun, C., Vilar, J., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006649 · Cited by 16

Sexually Dimorphic Effects of a Western Diet on Brain Mitochondrial Bioenergetics and Neurocognitive Function

Lord, M. N., Heo, J., Schifino, A. G., Hoffman, J. R., Donohue, K. N., Call, J. A., & Noble, E. E. (2021) · Nutrients · doi:10.3390/nu13124222 · Cited by 16

Maternal obesity increases hypothalamic miR-505-5p expression in mouse offspring leading to altered fatty acid sensing and increased intake of high-fat food

Dearden, L., Furigo, I. C., Pantaleão, L. C., Wong, L. W. P., Fernandez‐Twinn, D. S., de Almeida-Faria, J., Kentistou, K. A., Carreira, M. V., Bidault, G., Vidal‐Puig, A., et al. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002641 · Cited by 18

The response to prolonged fasting in hypothalamic serotonin transporter availability is blunted in obesity

van Galen, K. A., Booij, J., Schrantee, A., Adriaanse, S. M., Unmehopa, U. A., Fliers, E., Schwartz, G. J., Dileone, R., ter Horst, K. W., la Fleur, S. E., et al. (2021) · Metabolism · doi:10.1016/j.metabol.2021.154839 · Cited by 16

Central Control of Glucose Homeostasis

Puglianiello, A., & Cianfarani, S. (2006) · The Review of Diabetic Studies · doi:10.1900/rds.2006.3.54 · Cited by 14

Metabolomic profiles of 38 acylcarnitines in major depressive episodes before and after treatment

Tayeb, A. E. K. A., Colle, R., Chappell, K., El‐Asmar, K., Acquaviva, C., David, D. J. P., Trabado, S., Chanson, P., Fève, B., Becquemont, L., et al. (2023) · Psychological Medicine · doi:10.1017/s003329172300140x · Cited by 14

Gender differences in the relationship between blood pressure and body mass index during adolescence

Kawada, N., Nakanishi, K., Ohama, T., Nishida, M., Yamauchi‐Takihara, K., & Moriyama, T. (2014) · Obesity Research & Clinical Practice · doi:10.1016/j.orcp.2014.07.001 · Cited by 14

Effect of central and peripheral leucine on energy metabolism in the Djungarian hamster (Phodopus sungorus)

Koch, C. E., Göddeke, S., Krüger, M., & Tups, A. (2012) · Journal of Comparative Physiology B · doi:10.1007/s00360-012-0699-y · Cited by 14

Energy status determines hindbrain signal transduction pathway transcriptional reactivity to AMPK in the estradiol-treated ovariectomized female rat

Ibrahim, B. A., Alenazi, F., & Briski, K. P. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.10.068 · Cited by 14

Adult food choices depend on sex and exposure to early-life stress: Underlying brain circuitry, adipose tissue adaptations and metabolic responses

Ruigrok, S. R., Kotah, J. M., Kuindersma, J. E., Speijer, E., van Irsen, A. A. S., la Fleur, S. E., & Kőrösi, A. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100360 · Cited by 15

Paraventricular Nucleus Sim1 Neuron Ablation Mediated Obesity Is Resistant to High Fat Diet

Dong, X., Roizen, J. D., Lai, M., Gandhi, N. M., & Kublaoui, B. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081087 · Cited by 14

Oleic acid stimulates monoamine efflux through PPAR-α: Differential effects in diet-induced obesity

Jagannathan, L., Socks, E., Balasubramanian, P., McGowan, R., Herdt, T. M., Kianian, R., MohanKumar, S. M. J., & MohanKumar, P. S. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117867 · Cited by 13

Oleate induces K ATP channel-dependent hyperpolarization in mouse hypothalamic glucose-excited neurons without altering cellular energy charge

Dadak, S., Beall, C., Walker, J. M. V., Soutar, M. P. M., McCrimmon, R. J., & Ashford, M. L. J. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2016.12.053 · Cited by 14

Neuroendocrine regulation of hunger, satiety and maintenance of energy balance

González-Hita, M. E., Macias, K. G. A., & Enríquez, S. S. (2006) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 14

PPAR-γ action: it's all in your head

Myers, M. G., & Burant, C. (2011) · Nature Medicine · doi:10.1038/nm0511-544 · Cited by 13

Metabolic and humoral mechanisms of feeding and genesis of the ATP/ADP/AMP concept

Nicolaı̈dis, S. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.04.058 · Cited by 13

Feasibility of in vivo measurement of glucose metabolism in the mouse hypothalamus by 1H‐[13C] MRS at 14.1T

Lizarbe, B., Lei, H., Duarte, J. M. N., Lanz, B., Cherix, A., & Rolf Gruetter, A. (2018) · Magnetic Resonance in Medicine · doi:10.1002/mrm.27129 · Cited by 13

Association between plasma metabolites and gene expression profiles in five porcine endocrine tissues

Yang, B., Bassols, A., Saco, Y., & Miguel Pérez-enciso, A. (2011) · Genetics Selection Evolution · doi:10.1186/1297-9686-43-28 · Cited by 16

Editorial: Neuroendocrine Control of Feeding Behavior

Luquet, S. H., Vaudry, H., & Granata, R. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00399 · Cited by 13

Framework Based on Relationship to Describe Non-Hierarchical, Boundaryless and Multi-Perspective Phenomena

Maeshiro, T. (2018) · SICE Journal of Control Measurement and System Integration · doi:10.9746/jcmsi.11.381 · Cited by 12

Outcomes associated with timing of maintenance treatment for COPD exacerbation.

Dalal, A. A., Shah, M. B., D’Souza, A. O., Dhamane, A. D., & Crater, G. (2012) · PubMed · Cited by 10

Beyond Hunger: The Structure, Signaling, and Systemic Roles of Ghrelin

Polishchuk, H., Guzik, K., & Kantyka, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262210996 · Cited by 16

Limited cheese intake reduces HPA axis and behavioral stress responses in male rats

Fourman, S. M., Buesing, D. R., Girvin, S., Nashawi, H., & Ulrich‐Lai, Y. M. (2021) · Physiology & Behavior · doi:10.1016/j.physbeh.2021.113614 · Cited by 11

Role of hypothalamic autophagy in the control of whole body energy balance

Kim, M.-S., Quan, W., & Lee, M. (2013) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-013-9257-5 · Cited by 12

Hormonal and nutritional regulation of muscle carnitine palmitoyltransferase I gene expression in vivo

Liu, H. Y., Zheng, G., Zhu, H., & Woldegiorgis, G. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2007.06.026 · Cited by 11

Brain lipid sensing and the neural control of energy balance

Cruciani‐Guglielmacci, C., Stunff, H. L., & Magnan, C. (2024) · Biochimie · doi:10.1016/j.biochi.2024.05.020 · Cited by 13

[Macronutrients, food intake and body weight; the role of fat].

Carrillo, J. A.-B., Torregrosa, M. D., Almendros, M. M., López‐Millán, B., Burgos, M. A., & Muñoz, E. M. D. V. (2014) · PubMed · doi:10.3305/nh.2015.31.1.8439 · Cited by 10

Control of Fatty Acid Intake and the Role of Essential Fatty Acids in Cognitive Function and Neurological Disorders

Panickar, K. S., & Bhathena, S. J. (2009) · Frontiers in neuroscience · doi:10.1201/9781420067767-c18 · Cited by 10

Lipid-Induced Peroxidation in the Intestine Is Involved in Glucose Homeostasis Imbalance in Mice

Sérino, M., Waget, A., Marsollier, N., Masseboeuf, M., Payros, G., Gallou‐Kabani, C., Denom, J., Lacombe, A., Thiers, J., Nègre‐Salvayre, A., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021184 · Cited by 10

Rethinking Dietary Guidelines

Marantz, P. R. (2010) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2010.526846 · Cited by 9

Glucocorticoids induced high fat diet preference via activating hypothalamic AMPK signaling in chicks

Liu, L., Wang, X., Jiao, H., & Lin, H. (2017) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2017.02.018 · Cited by 10

Central NUCB2/nesfatin-1 signaling ameliorates liver steatosis through suppression of endoplasmic reticulum stress in the hypothalamus

He, Y., Zhang, C., Wu, S., Li, K., Zhang, S., Tian, M., Chen, C., Liu, D., Yang, G., Li, L., et al. (2024) · Metabolism · doi:10.1016/j.metabol.2024.156046 · Cited by 10

Filbertone Protects Obesity-induced Hypothalamic Inflammation by Reduction of Microglia-mediated Inflammatory Responses

Mutsnaini, L., Yang, J., Kim, J., Kim, C.-S., Lee, C.-H., Kim, M., Park, T., Goto, T., & Yu, R. (2021) · Biotechnology and Bioprocess Engineering · doi:10.1007/s12257-020-0220-5 · Cited by 8

Saliva cortisol responses to altered plasma PUFA patterns in guinea pigs

Nemeth, M., Millesi, E., Wagner, K., & Wallner, B. (2018) · British Journal Of Nutrition · doi:10.1017/s0007114518002660 · Cited by 8

Your brain on fat: dietary-induced obesity impairs central nutrient sensing

Schwartz, G. J. (2009) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00177.2009 · Cited by 8

Evaluation of Phenotypic Changes of Acyl-CoA Binding Protein / Diazepam Binding Inhibitor Overexpression in Transgenic Mice and Rats

Oikari, S. (2008) · Cited by 8

Role of saturated fatty acid metabolism in posttranslational modifications of the Tau protein

García-Cruz, V. M., Coria, R., & Arias, C. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05275-2 · Cited by 7

trans -Palmitoleic acid promotes adipose thermogenesis to reduce obesity via hypothalamic FFAR1 signaling

Zhan, H., Wang, W., Ge, Y., Liang, Y., Wang, J., Xu, Y., Wu, S., Peng, L., & He, Z. (2024) · Food & Function · doi:10.1039/d4fo00452c · Cited by 8

Sleep, Circadian Rhythms and Metabolism

Maury, E., Ramsey, K. M., & Bass, J. T. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1607-5_13 · Cited by 12

A System Description Model with Fuzzy Boundaries

Maeshiro, T., Ozawa, Y., & Maeshiro, M. (2017) · Lecture notes in computer science · doi:10.1007/978-3-319-58524-6_31 · Cited by 7

Fatty acids as a tool to compare cachara (Pseudoplatystoma reticulatum) (Siluriformes: Pimelodidae) and hybrid (Pseudoplatystoma corruscans × Pseudoplatystoma reticulatum) larvae during early development

de Mello, P. H., Araújo, B. C., Venturieri, R. L. L., & Moreira, R. G. (2011) · Aquaculture International · doi:10.1007/s10499-011-9466-4 · Cited by 7

Does elevated bilirubin aid weight control by preventing development of hypothalamic leptin resistance?

DiNicolantonio, J. J., McCarty, M. F., & O’Keefe, J. H. (2019) · Open Heart · doi:10.1136/openhrt-2018-000897 · Cited by 7

Regulation of Peripheral Metabolism by Substrate Partitioning in the Brain

Moreno, C. L., Yang, L. C., Dacks, P. A., Isoda, F., Poplawski, M. M., & Mobbs, C. V. (2013) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2012.11.007 · Cited by 8

Giant Island Mice Exhibit Widespread Gene Expression Changes in Key Metabolic Organs

Nolte, M. J., Jing, P., Dewey, C. N., & Payseur, B. A. (2020) · Genome Biology and Evolution · doi:10.1093/gbe/evaa118 · Cited by 6

Diet-Induced Metabolic Dysfunction of Hypothalamic Nutrient Sensing in Rodents

Arrieta‐Cruz, I., Torres-Ávila, B. S., Martínez‐Coria, H., López-Valdés, H. E., & Juárez, R. G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073958 · Cited by 6

Endocannabinoids in Energy Homeostasis and Metabolic Disorders

Matias, I., Marzo, V. D., & Köfalvi, A. (2007) · Springer eBooks · doi:10.1007/978-0-387-74349-3_14 · Cited by 6

Caloric restriction diminishes the pressor response to static exercise

Florian, J. P., Baisch, F. J., Heer, M. A., & Pawelczyk, J. A. (2016) · Extreme Physiology & Medicine · doi:10.1186/s13728-016-0043-3 · Cited by 6

Metabolic inflammation at the adipose-brain axis

Mateus-Gomes, S., Al-Sayyar, A., Lobey, B., Nadjar, A., Rua, R., & Ahmad, R. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2026.1795058 · Cited by 5

Glutaredoxin1 knockout promotes high-fat diet-induced obesity in male mice but not in female ones

Zou, X., Ahmad, M. I., Zhao, D., Zhang, M., & Li, C. (2021) · Food & Function · doi:10.1039/d1fo01241j · Cited by 5

Neuroendocrine Regulation of Food Intake

Watts, A. G. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-375097-6.10014-9 · Cited by 6

Autophagy as a therapeutic linchpin in metabolic diseases and obesity-associated diabetes

Vakili, O., Klionsky, D. J., Reiter, R. J., Ren, J., Deshpande, A., Ahn, K. S., Cho, W., Hushmandi, K., & Kumar, A. P. (2026) · Autophagy · doi:10.1080/15548627.2026.2636096 · Cited by 7

Taste receptor type 1 member 3 enables western diet-induced anxiety in mice

Song, J. W., Lee, K.-H., Seong, H., Shin, D., & Shon, W.-J. (2023) · BMC Biology · doi:10.1186/s12915-023-01723-x · Cited by 4

Fat Metabolism in Insulin Resistance and Type 2 Diabetes

Duez, H., & Lewis, G. F. (2008) · Humana Press eBooks · doi:10.1007/978-1-60327-043-4_4 · Cited by 4

Energy Balance Regulation

Richard, D., & Timofeeva, E. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374387-9.00024-6 · Cited by 4

Portal Glucose Infusion, Afferent Nerve Fibers, and Glucose and Insulin Tolerance of Insulin-Resistant Rats

Joly‐Amado, A., Soty, M., Philippe, E., Lacombe, A., Castel, J., Pillot, B., Vily‐Petit, J., Zitoun, C., Mithieux, G., & Magnan, C. (2022) · Journal of Nutrition · doi:10.1093/jn/nxac097 · Cited by 4

Endocannabinoid system and its role in energy regulation

Matias, I., & Marzo, V. D. (2006) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.1.4.557 · Cited by 4

Co-Administration of Cabergoline and Gliclazide Improve Glycemic Parameters and Lipid Profile in T2DM

Morcos, J. A., Ebeid, A. M., Khodeir, S. A., & El-Azab, G. A. (2017) · Journal of Diabetes & Metabolism · doi:10.4172/2155-6156.1000759 · Cited by 3

O papel dos lipídios na reorganização metabólica associada à dormência sazonal no lagarto teiú Tupinambis merianae (Sauria, Teidae)

Haddad, L. S. (2007) · doi:10.11606/t.41.2007.tde-13022008-170743 · Cited by 4

Sleep disorders contribute to the development of dementia and Alzheimer’s disease

Błaszczyk, J. W. (2023) · Exploration of neuroscience · doi:10.37349/en.2023.00022 · Cited by 4

Association between sleep behaviors and adiposity indices among U.S. adults: a cross-sectional study

Xu, S., Lin, J. M., Xu, Q., Zhao, K., & Xiao, J. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1526422 · Cited by 3

C75, a Fatty Acid Synthase (FAS) Inhibitor

López, M., & Diéguez, C. (2007) · Recent Patents on Endocrine Metabolic & Immune Drug Discovery · doi:10.2174/187221407779814615 · Cited by 3

Salubrinal abrogates palmitate-induced leptin resistance and endoplasmic reticulum stress via nuclear factor kappa-light-chain-enhancer of activated B cell pathway in mHypoE-44 hypothalamic neurons

Zhang, M., Jiang, X., Qu, M., Gu, H., Sha, Q., & Hua, F. (2018) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s179346 · Cited by 3

Glucose and fat sensing in the human hypothalamus

van Opstal, A. M. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-820683-6.00024-5 · Cited by 3

Dis-moi ce que tu manges...

Arboix-Calas, F. (2014) · Éducation et socialisation · doi:10.4000/edso.1002 · Cited by 3

Chronically Elevated Triglycerides as a Result of High Fat Palatable Diet Resulting in a Vicious Cycle on Reinforcing Reward and Dopamine Signaling: A Possible Cause for the Obesity Epidemic Worldwide in the Food Environment Available-A Comprehensive Review

Kul, K. (2019) · Open Access Journal of Endocrinology · doi:10.23880/oaje-16000143 · Cited by 3

The Unrestrained Overeating Behavior and Clinical Perspective

Engin, A. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-63657-8_6 · Cited by 3

Neuron stress-related genes serve as new biomarkers in hypothalamic tissue following high fat diet

Liang, C., 王雪芹, 苏建彬, Qi, F., Chen, T., Shang, Y., Li, Y., Li, Y., Su, S., Zhang, D., et al. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1443880 · Cited by 3

mTORC1 and mTORC2 in Energy Homeostasis

Cornu, M., & Hall, M. N. (2010) · The Enzymes · doi:10.1016/s1874-6047(10)28013-7 · Cited by 3

The hypothalamus and energy balance

Benedini, S. (2009) · Sport Sciences for Health · doi:10.1007/s11332-009-0079-5 · Cited by 3

Hypothalamic mitochondria in energy homeostasis and obesity

Guo, X., Wu, L., Wang, W., Medeiros, D. M., Clarke, S. L., Lucas, E. A., Smith, B. J., Chowanadisai, W., & Lin, D. (2016) · Integrative Molecular Medicine · doi:10.15761/imm.1000209 · Cited by 3

Body Weight and Appetite Regulation)

Machado, M. V., & Ulate-Montero, G. (2010) · Acta Médica Costarricense · Cited by 3

Hypothalamic AgRP neurons and the regulation of appetite and body weight: A review

Wang, P., & Zhang, G. (2018) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/n972018-00413 · Cited by 2

Hypothalamic Microinflammation: New Paradigm In Obesity And Metabolic Disease

Meiliana, A., Dewi, N. M., & Wijaya, A. (2020) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v12i3.1235 · Cited by 2

Non-alcoholic fatty liver disease and metabolic syndrome in childhood

Vlasov, N. N., & Корниенко, Е. А. (2020) · Экспериментальная и клиническая гастроэнтерология · doi:10.31146/1682-8658-ecg-183-11-51-61 · Cited by 4

Blood Level of 2-arachidonoyl Glycerol (2-AG), Neuropeptide Y and Omentin and Their Correlation with Food Habits in Obese Women

Rahmanian, M., Yagin, N. L., & Alizadeh, M. (2020) · Galen Medical Journal · doi:10.31661/gmj.v9i0.1721 · Cited by 3

Neuroendocrine Regulation

Barrios, V., Martos‐Moreno, G. Á., Frago, L. M., Chowen, J. A., & Argente, J. (2010) · Springer eBooks · doi:10.1007/978-1-4419-6039-9_16 · Cited by 3

L-diabetes – causes, pathogenesis and therapy

Liebel, F.-P., & Zimmermann, E. (2006) · Medical Hypotheses · doi:10.1016/j.mehy.2006.02.048 · Cited by 3

Intestinal Lipids as Signaling Molecules

Ahima, R. S. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.05.030 · Cited by 3

Correction: Paraventricular Nucleus Sim1 Neuron Ablation Mediated Obesity Is Resistant to High Fat Diet

Xi, D., Roizen, J. D., Lai, M., Gandhi, N. M., & Kublaoui, B. M. (2014) · PLoS ONE · doi:10.1371/annotation/9239a129-5677-43b0-8fe1-0c1e75e988df · Cited by 3

Seasonal and comparative evidence of adaptive gene expression in mammalian brain size plasticityPreprint

Thomas, W. R., Richter, T. A., O’Neil, E. T., Baldoni, C., Corthals, A., von Elverfeldt, D., Nieland, J. D., Dechmann, D. K. N., Hunter, R. G., & Dávalos, L. M. (2024) · eLife · doi:10.7554/elife.100788 · Cited by 3

Seasonal and comparative evidence of adaptive gene expression in mammalian brain size plasticityPreprint

Thomas, W. R., Richter, T. A., O’Neil, E. T., Baldoni, C., Corthals, A., von Elverfeldt, D., Nieland, J. D., Dechmann, D. K. N., Hunter, R. G., & Dávalos, L. M. (2024) · eLife · doi:10.7554/elife.100788.1 · Cited by 3

Seasonal and comparative evidence of adaptive gene expression in mammalian brain size plasticity

Thomas, W. R., Richter, T. A., O’Neil, E. T., Baldoni, C., Corthals, A., von Elverfeldt, D., Nieland, J. D., Dechmann, D. K. N., Hunter, R. G., & Dávalos, L. M. (2025) · eLife · doi:10.7554/elife.100788.3 · Cited by 2

Review: Keystone issues in ruminant science I. Feed intake control in ruminants

Pittroff, W., & Kothmann, M. M. (2025) · animal · doi:10.1016/j.animal.2025.101553 · Cited by 2

Dysfonctions du système nerveux sympathique et de la signalisation catécholaminergique chez l’obèse

Lafontan, M. (2013) · Obésité · doi:10.1007/s11690-013-0409-2 · Cited by 2

Les acides gras : molécules informatives du contrôle nerveux de l’homéostasie énergétique

Migrenne, S., Cruciani‐Guglielmacci, C., & Magnan, C. (2007) · Cahiers de Nutrition et de Diététique · doi:10.1016/s0007-9960(07)88756-6 · Cited by 2

A novel Transcript is Up‐Regulated by Fasting in the Hypothalamus and Enhances Insulin Signalling

Chai, B., Li, J., Fritze, D. M., Zhang, W., Xia, Z., & Mulholland, M. W. (2012) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2012.02378.x · Cited by 2

Détection centrale des acides gras et contrôle du bilan d’énergie

Migrenne, S., Cruciani‐Guglielmacci, C., & Magnan, C. (2011) · Cahiers de Nutrition et de Diététique · doi:10.1016/j.cnd.2011.06.006 · Cited by 2

An Old Dog Learns a New Trick: Regulation of Peripheral Glucose Homeostasis by the Serotonin (5-HT)2C Receptor

Miller, K. J., & Azzara, A. V. (2008) · Molecular Interventions · doi:10.1124/mi.8.2.4 · Cited by 2

Loss of Autophagy in Hypothalamic Neurons May Be Involved in the Pathogenesis of Obesity

Ávalos, Y., Hernández‐Cáceres, M. P., Toledo, L., & Morselli, E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00013-5 · Cited by 2

Role of bioactive lipids in obesity

Salsinha, A. S., Rodríguez-Alcalá, L. M., Pimentel, L. L., & Pintado, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-824043-4.00012-9 · Cited by 2

Insights into the mechanisms of body weight control

Pereira, S. (2025) · AJP Advances in Physiology Education · doi:10.1152/advan.00091.2025 · Cited by 1

Targeting Gβγ subunits in hypothalamic AgRP neurons to treat obesity

Ye, X., Xiong, X., Wang, X., Wang, Y., Shen, Y. H., Zhang, H., Zhang, R., Chen, L., Zhang, P., Zhang, Y., et al. (2026) · Metabolism · doi:10.1016/j.metabol.2026.156569 · Cited by 1

Influencing energy expenditure and substrate utilisation

Clapham, J. C., & Arch, J. R. S. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-7425-9_8 · Cited by 1

A System Description Model Without Hierarchical Structure

Maeshiro, T., & Maeshiro, M. (2016) · Lecture notes in computer science · doi:10.1007/978-3-319-40349-6_6 · Cited by 1

Central Downregulation of S-Resistin Alleviates Inflammation in EWAT and Liver and Prevents Adipocyte Hypertrophy

Rodríguez-Pérez, M., Moltó, E., Serrano, R., Díaz-Rullo, J., Parralejo, I., Muñoz, D., Andreu, R. M., Seco, J., Gallardo, N., Andrés, A., et al. (2025) · Journal of the Endocrine Society · doi:10.1210/jendso/bvae224 · Cited by 1

MONITORING ENERGY BALANCE: Metabolites of Fatty Acid Synthesis as Hypothalamic Sensors

Dowell, P., Hu, Z., & Lane, M. D. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.074027 · Cited by 81

Hypothalamic nutrient sensing in the control of energy homeostasis

Blouet, C., & Schwartz, G. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.12.024 · Cited by 343

Hypothalamic fatty acid metabolism: A housekeeping pathway that regulates food intake

López, M., Lelliott, C. J., & Vidal‐Puig, A. (2007) · BioEssays · doi:10.1002/bies.20539 · Cited by 150

[Hypothalamic nuclei sense metabolic signals and regulate feeding].

Kohno, D., Toriya, M., Yada, T., Kurita, H., & Kuramochi, M. (2006) · PubMed · Cited by 1

Hypothalamic Lipid Nutritional Sensing and Mechanisms in Appetite Regulation

Jiang, Q. (2013) · Dongwu yingyang xuebao