Food Intake, Water Intake, and Drinking Spout Side Preference of 28 Mouse Strains

Brown Adipose Tissue: Function and Physiological Significance

CANNON, B., & NEDERGAARD, J. (2004) · Physiological Reviews · doi:10.1152/physrev.00015.2003 · Cited by 6,433

Microglia facilitate repair of demyelinated lesions via post-squalene sterol synthesis

Berghoff, S. A., Spieth, L., Sun, T., Hosang, L., Schlaphoff, L., Depp, C., Düking, T., Winchenbach, J., Neuber, J., Ewers, D., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00757-6 · Cited by 307

Scheduled exercise phase shifts the circadian clock in skeletal muscle

WOLFF, G., & ESSER, K. A. (2012) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e318255cf4c · Cited by 291

NAD Deficiency, Congenital Malformations, and Niacin Supplementation

Shi, H., Enriquez, A., Rapadas, M., Martin, E. M. M. A., Wang, R., Moreau, J., Lim, C. K., Szot, J. O., Ip, E., Hughes, J. N., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1616361 · Cited by 246

7,8-Dihydroxyflavone Prevents Synaptic Loss and Memory Deficits in a Mouse Model of Alzheimer’s Disease

Zhang, Z., Liu, X., Schroeder, J. P., Chan, C.-B., Song, M., Yu, S. P., Weinshenker, D., & Ye, K. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2013.243 · Cited by 242

Distribution and accumulation of dietary ergothioneine and its metabolites in mouse tissues

Tang, R. M. Y., Cheah, I. K.-M., Yew, T. S. K., & Halliwell, B. (2018) · Scientific Reports · doi:10.1038/s41598-018-20021-z · Cited by 163

The regulation of glucose metabolism: implications and considerations for the assessment of glucose homeostasis in rodents

Kowalski, G. M., & Bruce, C. R. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00165.2014 · Cited by 154

Neural Control and Modulation of Thirst, Sodium Appetite, and Hunger

Augustine, V., Lee, S., & Oka, Y. (2020) · Cell · doi:10.1016/j.cell.2019.11.040 · Cited by 135

Candida albicans Inhibits Pseudomonas aeruginosa Virulence through Suppression of Pyochelin and Pyoverdine Biosynthesis

Lopez-Medina, E., Fan, D., Coughlin, L. A., Ho, E. X., Lamont, I. L., Reimmann, C., Hooper, L. V., & Koh, A. Y. (2015) · PLOS Pathogens · doi:10.1371/journal.ppat.1005129 · Cited by 143

Protective role of spermidine in colitis and colon carcinogenesis

Gobert, A. P., Latour, Y. L., Asim, M., Barry, D. P., Allaman, M. M., Finley, J. L., Smith, T. M., McNamara, K. M., Singh, K., Sierra, J. C., et al. (2022) · Gastroenterology · doi:10.1053/j.gastro.2021.11.005 · Cited by 143

Rescuing Over-activated Microglia Restores Cognitive Performance in Juvenile Animals of the Dp(16) Mouse Model of down Syndrome.

Pinto, B., Morelli, G., Rastogi, M., Savardi, A., Fumagalli, A., Petretto, A., Bartolucci, M., Varea, E., Catelani, T., Contestabile, A., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.010 · Cited by 135

N-acetylcysteine normalizes neurochemical changes in the glutathione-deficient schizophrenia mouse model during development

das Neves Duarte, J. M., Kulak, A., Gholam-Razaee, M. M., Cuenod, M., Gruetter, R., & Do, K. Q. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.07.035 · Cited by 124

Reversal of synapse loss in Alzheimer mouse models by targeting mGluR5 to prevent synaptic tagging by C1Q

Spurrier, J., Nicholson, L., Fang, X. T., Stoner, A. J., Toyonaga, T., Holden, D., Siegert, T. R., Laird, W., Allnutt, M. A., Chiasseu, M., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abi8593 · Cited by 114

Food additive carrageenan: Part I: A critical review of carrageenan in vitro studies, potential pitfalls, and implications for human health and safety

McKim, J. M. (2014) · Critical Reviews in Toxicology · doi:10.3109/10408444.2013.861797 · Cited by 108

Comparison of murine steatohepatitis models identifies a dietary intervention with robust fibrosis, ductular reaction, and rapid progression to cirrhosis and cancer

Wei, G., An, P., Vaid, K. A., Nasser, I., Huang, P., Tan, L., Zhao, S., Schuppan, D., & Popov, Y. V. (2020) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00041.2019 · Cited by 84

Hepatocyte sortilin 1 knockout and treatment with a sortilin 1 inhibitor reduced plasma cholesterol in Western diet-fed mice

Chen, C., Li, J., Matye, D. J., Wang, Y., & Li, T. (2019) · Journal of Lipid Research · doi:10.1194/jlr.m089789 · Cited by 37

Cellular and molecular changes in hippocampal glutamate Signaling and alterations in learning, attention, and impulsivity following prenatal nicotine exposure

Polli, F. S., Ipsen, T. H., Caballero-Puntiverio, M., Østerbøg, T. B., Aznar, S., Andreasen, J. T., & Kohlmeier, K. A. (2020) · Molecular Neurobiology · doi:10.1007/s12035-019-01854-9 · Cited by 25

Prenatal nicotine is associated with reduced AMPA and NMDA receptor-mediated rises in calcium within the laterodorsal tegmentum: a pontine nucleus involved in addiction processes

McNair, L. F., & Kohlmeier, K. A. (2015) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174414000439 · Cited by 22

Does eating good-tasting food influence body weight?

Tordoff, M. G., Pearson, J. A., Ellis, H. T., & Poole, R. L. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.12.013 · Cited by 17

Electrophysiological changes in laterodorsal tegmental neurons associated with prenatal nicotine exposure: Implications for heightened susceptibility to addict to drugs of abuse

Christensen, M. H., Nielsen, M. L., & Kohlmeier, K. A. (2015) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s204017441400049x · Cited by 17

Vulnerability to nicotine self-administration in adolescent mice correlates with age-specific expression of α4* nicotinic receptors

Renda, A., Penty, N., Komal, P., & Nashmi, R. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.04.019 · Cited by 17

Effects of dietary aspirin on high-LET radiation-induced prostaglandin E2 levels and gastrointestinal tumorigenesis in Apc mice

Suman, S., Kumar, S., Moon, B.-H., Angdisen, J., Kallakury, B. V. S., Datta, K., & Fornace Jr, A. J. (2021) · Life Sciences in Space Research · doi:10.1016/j.lssr.2021.09.001 · Cited by 11

Reward magnitude determines reinforcement learning efficiency

Gong, S., Martell, A., Dudman, J. T., & Coddington, L. T. (2026) · Science · doi:10.1126/science.aeb0813 · Cited by 2