Crosstalk between Components of Circadian and Metabolic Cycles in Mammals

Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase

Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., Tran, H., Ross, S. E., Mostoslavsky, R., Cohen, H. Y., et al. (2004) · Science · doi:10.1126/science.1094637 · Cited by 3,239

Nutrient control of glucose homeostasis through a complex of PGC-1α and SIRT1

Rodgers, J. T., Lerin, C., Haas, W., Gygi, S. P., Spiegelman, B. M., & Puigserver, P. (2005) · Nature · doi:10.1038/nature03354 · Cited by 3,160

The mammalian circadian timing system: organization and coordination of central and peripheral clocks

Dibner, C., Schibler, U., & Albrecht, U. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135821 · Cited by 2,421

Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus

Damiola, F., Le Minh, N., Preitner, N., Kornmann, B., Fleury-Olela, F., & Schibler, U. (2000) · Genes & Development · doi:10.1101/gad.183500 · Cited by 2,394

PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues

Yoo, S.-H., Yamazaki, S., Lowrey, P. L., Shimomura, K., Ko, C. H., Buhr, E. D., Siepka, S. M., Hong, H.-K., Oh, W. J., Yoo, O. J., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308709101 · Cited by 2,329

Coordinated Transcription of Key Pathways in the Mouse by the Circadian Clock

Panda, S., Antoch, M. P., Miller, B. H., Su, A. I., Schook, A. C., Straume, M., Schultz, P. G., Kay, S. A., Takahashi, J. S., & Hogenesch, J. B. (2002) · Cell · doi:10.1016/s0092-8674(02)00722-5 · Cited by 2,310

The Orphan Nuclear Receptor REV-ERBα Controls Circadian Transcription within the Positive Limb of the Mammalian Circadian Oscillator

Preitner, N., Damiola, F., Luis-Lopez-Molina, Zakany, J., Duboule, D., Albrecht, U., & Schibler, U. (2002) · Cell · doi:10.1016/s0092-8674(02)00825-5 · Cited by 2,198

A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells

Balsalobre, A., Damiola, F., & Schibler, U. (1998) · Cell · doi:10.1016/s0092-8674(00)81199-x · Cited by 2,001

Resetting central and peripheral circadian oscillators in transgenic rats

Yamazaki, S., Numano, R., Abe, M., Hida, A., Takahashi, R.-I., Ueda, M., Block, G. D., Sakaki, Y., Menaker, M., & Tei, H. (2000) · Science · doi:10.1126/science.288.5466.682 · Cited by 1,907

Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis

Inagaki, T., Choi, M., Moschetta, A., Peng, L., Cummins, C. L., McDonald, J. G., Luo, G., Jones, S. A., Goodwin, B., Richardson, J. A., et al. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.09.001 · Cited by 1,865

Daily patterns of mRNA expression of two core circadian regulatory proteins, Clock2 and Per1, and two appetite-regulating peptides, OX and NPY, in goldfish (Carassius auratus)

Hoskins, L. J., & Volkoff, H. (2012) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2012.05.197 · Cited by 30

Circadian Variation in the Response to the Glucose Challenge Test in Pregnancy

Goldberg, R. J., Ye, C., Sermer, M., Connelly, P. W., Hanley, A. J., Zinman, B., & Retnakaran, R. R. (2012) · Diabetes Care · doi:10.2337/dc11-2217 · Cited by 29

Combination of 5‐aminolevulinic acid and ferrous ion reduces plasma glucose and hemoglobin A1c levels in Zucker diabetic fatty rats

Hara, T., Koda, A., Nozawa, N., Ota, U., Kondo, H., Nakagawa, H., Kamiya, A., Miyashita, K., Itoh, H., Nakajima, M., et al. (2016) · FEBS Open Bio · doi:10.1002/2211-5463.12048 · Cited by 29

Interplay between Microbes and the Circadian ClockPreprint

Tognini, P., Murakami, M., & Sassone‐Corsi, P. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028365 · Cited by 29

Preservation of ∼12-h ultradian rhythms of gene expression of mRNA and protein metabolism in the absence of canonical circadian clock

Zhu, B., & Liu, S. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1195001 · Cited by 24

Glucose Alters Per2 Rhythmicity Independent of AMPK, Whereas AMPK Inhibitor Compound C Causes Profound Repression of Clock Genes and AgRP in mHypoE-37 Hypothalamic Neurons

Oosterman, J. E., & Belsham, D. D. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146969 · Cited by 31

Circadian rhythms in white adipose tissue

van der Spek, R., Kreier, F., Fliers, E., & Kalsbeek, A. (2012) · Progress in brain research · doi:10.1016/b978-0-444-59427-3.00011-3 · Cited by 30

Diet and Our Genetic Legacy in the Recent Anthropocene

Lucock, M. D., Martin, C. E., Yates, Z. R., & Veysey, M. J. (2013) · Journal of Evidence-Based Complementary & Alternative Medicine · doi:10.1177/2156587213503345 · Cited by 30

Adipose circadian rhythms: Translating cellular and animal studies to human physiology

Johnston, J. D. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.05.008 · Cited by 29

Clock regulation of dietary lipid absorption

Hussain, M. M., & Pan, X. (2012) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e3283548629 · Cited by 28

Cross-species physiological interactions of endocrine disrupting chemicals with the circadian clock

Bottalico, L. N., & Weljie, A. M. (2020) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2020.113650 · Cited by 30

Time‐limited diets and the gut microbiota in cardiometabolic disease

Ratiner, K., Shapiro, H., Goldenberg, K., & Elinav, E. (2022) · Journal of Diabetes · doi:10.1111/1753-0407.13288 · Cited by 27

CUL4-DDB1-CDT2 E3 Ligase Regulates the Molecular Clock Activity by Promoting Ubiquitination-Dependent Degradation of the Mammalian CRY1

Tong, X., Zhang, D., Guha, A., Arthurs, B., Cazares, V. A., Gupta, N., & Yin, L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0139725 · Cited by 27

Circadian coordination: understanding interplay between circadian clock and mitochondria

Kim, J., & Sun, W. (2024) · Animal Cells and Systems · doi:10.1080/19768354.2024.2347503 · Cited by 26

Quantitative Systems Pharmacology: A Framework for Context

Androulakis, I. P. (2016) · Current Pharmacology Reports · doi:10.1007/s40495-016-0058-x · Cited by 28

NR1D1 Deletion Induces Rupture‐Prone Vulnerable Plaques by Regulating Macrophage Pyroptosis via the NF‐κB/NLRP3 Inflammasome Pathway

Wu, Z., Liao, F., Luo, G., Qian, Y., He, X., Xu, W., Ding, S. Z., & Pu, J. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/5217572 · Cited by 27

Peroxisomal Localization and Circadian Regulation of Ubiquitin-Specific Protease 2

Molusky, M. M., Ma, D., Buelow, K. L., Yin, L., & Lin, J. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0047970 · Cited by 26

Diurnal Rhythmicity Programs of Microbiota and Transcriptional Oscillation of Circadian Regulator, NFIL3

Kubo, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.552188 · Cited by 26

Shift work sleep disorder is closely associated with an increased risk for periodontal disease

Park, J. S., Jeong, Y., Jung, J., Ryu, J., Lim, H., Jung, S., & Song, I. (2021) · Journal Of Clinical Periodontology · doi:10.1111/jcpe.13508 · Cited by 29

Circadian clocks' interactions with oxygen sensing and signalling

Adamovich, Y., Dandavate, V., & Asher, G. (2022) · Acta Physiologica · doi:10.1111/apha.13770 · Cited by 27

Sirtuins and redox signaling interplay in neurogenesis, neurodegenerative diseases, and neural cell reprogramming

Mormone, E., Iorio, E. L., Abate, L., & Rodolfo, C. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1073689 · Cited by 31

Post‐translational timing mechanisms of the Drosophila circadian clock

Weber, F., Zorn, D., Rademacher, C., & Hung, H. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.04.008 · Cited by 25

Maternal obesity disrupts circadian rhythms of clock and metabolic genes in the offspring heart and liver

Wang, D., Chen, S., Liu, M., & Liu, C. (2015) · Chronobiology International · doi:10.3109/07420528.2015.1025958 · Cited by 25

Circadian Disruptions in the Myshkin Mouse Model of Mania Are Independent of Deficits in Suprachiasmatic Molecular Clock Function

Timothy, J. W. S., Klas, N., Sanghani, H., Al-Mansouri, T., Hughes, A. T. L., Kirshenbaum, G. S., Brienza, V., Belle, M. D. C., Ralph, M. R., Clapcote, S. J., et al. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.04.018 · Cited by 25

Disruption of circadian rhythm as a potential pathogenesis of nocturia

Song, Q., Suadicani, S. O., Negoro, H., Jiang, H., Jabr, R. I., Fry, C. H., Xue, W., & Damaser, M. S. (2024) · Nature Reviews Urology · doi:10.1038/s41585-024-00961-0 · Cited by 28

Circadian disruption of feeding-fasting rhythm and its consequences for metabolic, immune, cancer, and cognitive processes

Crespo, M. T., Trebucq, L. L., Senna, C. A., Hokama, G., Paladino, N., Agostino, P. V., & Chiesa, J. J. (2025) · Biomedical Journal · doi:10.1016/j.bj.2025.100827 · Cited by 24

Epigenetic methylations and their connections with metabolism

Chiacchiera, F., Piunti, A., & Pasini, D. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1293-5 · Cited by 25

Tissue-Dependent Alterations of the Clock Gene Expression Rhythms in Leptin-Resistant Zucker Diabetic Fatty Rats

Motosugi, Y., Ando, H., Ushijima, K., Maekawa, T., Ishikawa, E., Kumazaki, M., & Fujimura, A. (2011) · Chronobiology International · doi:10.3109/07420528.2011.613325 · Cited by 24

Metabolic Syndrome, Insulin Resistance, Circadian Disruption, Antioxidants and Pancreatic Carcinoma: an Overview

Giudice, A., Crispo, A., Massimiliano, G., D'Arena, G. F., Tecce, M. F., Grimaldi, M., Amore, A., Esposito, E., & Montella, M. (2014) · Journal of Gastrointestinal and Liver Diseases · doi:10.15403/jgld-1282 · Cited by 24

Night eating model shows time-specific depression-like behavior in the forced swimming test

Haraguchi, A., Fukuzawa, M., Iwami, S., Nishimura, Y., Motohashi, H., Tahara, Y., & Shibata, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-19433-8 · Cited by 24

Physical activity, and not fat mass is a primary predictor of circadian parameters in young men

Tranel, H. R., Schroder, E. A., England, J., Black, W. S., Bush, H., Hughes, M. E., Esser, K. A., & Clasey, J. L. (2015) · Chronobiology International · doi:10.3109/07420528.2015.1043011 · Cited by 22

Spatially and temporally resolved metabolome of the human oral cavity

Ciurli, A., Mohammed, Y., Ammon, C., Derks, R. J. E., Olivier‐Jimenez, D., Ducarmon, Q. R., Slingerland, M., Neefjes, J., & Giera, M. A. (2024) · iScience · doi:10.1016/j.isci.2024.108884 · Cited by 23

Multifunctional CeO2 nanozymes for mitigating high-glucose induced senescence and enhancing bone regeneration in type 2 diabetes mellitus

Wang, Z., Zhang, Y., Chen, S., Qu, Y., Tang, M., Wang, W., Li, W., & Gu, L. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.149842 · Cited by 23

Clock at the Core of Cancer Development

Patel, S. A., & Kondratov, R. V. (2021) · Biology · doi:10.3390/biology10020150 · Cited by 23

Molecular clocks, satellite cells, and skeletal muscle regeneration

Kahn, R. E., Dayanidhi, S., Lacham‐Kaplan, O., & Hawley, J. A. (2023) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00073.2023 · Cited by 26

Circadian Rhythm, Health and Nutrition Relationship: Review

Sözlü, S., & Şanlıer, N. (2016) · Turkiye Klinikleri Journal of Health Sciences · doi:10.5336/healthsci.2015-48902 · Cited by 26

Circadian rhythms and the liver

Costa, R., Mangini, C., Domenie, E. D., Zarantonello, L., & Montagnese, S. (2023) · Liver International · doi:10.1111/liv.15501 · Cited by 23

Effect of Urolithin A on the Improvement of Circadian Rhythm Dysregulation in Intestinal Barrier Induced by Inflammation

Du, Y., Chen, X., Kajiwara, S., & Orihara, K. (2024) · Nutrients · doi:10.3390/nu16142263 · Cited by 22

Mitochondrial H2O2 signaling is controlled by the concerted action of peroxiredoxin III and sulfiredoxin: Linking mitochondrial function to circadian rhythm

Rhee, S. G., & Kil, I. S. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.07.029 · Cited by 22

Delirium clinical motor subtypes: a narrative review of the literature and insights from neurobiology

Fitzgerald, J. (2017) · Aging & Mental Health · doi:10.1080/13607863.2017.1310802 · Cited by 22

Daytime restricted feeding modifies 24 h rhythmicity and subcellular distribution of liver glucocorticoid receptor and the urea cycle in rat liver

Luna-Moreno, D., Ayala-García, B., & Díaz‐Muñoz, M. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512000268 · Cited by 22

Cyclic uniaxial mechanical load enhances chondrogenesis through entraining the molecular circadian clock

Vágó, J., Katona, É., Takács, R., Dócs, K., Hajdú, T., Kovács, P., Zákány, R., van der Veen, D. R., & Matta, C. (2022) · Journal of Pineal Research · doi:10.1111/jpi.12827 · Cited by 21

Transcription Factor Interactions in Genomic Nuclear Receptor Function

George, C. L., Lightman, S. L., & Biddie, S. C. (2011) · Epigenomics · doi:10.2217/epi.11.66 · Cited by 21

Chronic inhibition of endoplasmic reticulum calcium-release channels and calcium-ATPase lengthens the period of hepatic clock gene Per1

Báez‐Ruíz, A., & Díaz‐Muñoz, M. (2011) · Journal of Circadian Rhythms · doi:10.1186/1740-3391-9-6 · Cited by 22

Exploration of tissue-specific gene expression patterns underlying timing of breeding in contrasting temperature environments in a song bird

Laine, V. N., Verhagen, I., Mateman, A. C., Pijl, A. S., Williams, T. D., Gienapp, P., van Oers, K., & Visser, M. E. (2019) · BMC Genomics · doi:10.1186/s12864-019-6043-0 · Cited by 21

Interactions between the circadian clock and metabolism: there are good times and bad times

Shi, M., & Zheng, X. (2012) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gms110 · Cited by 22

KSRP is critical in governing hepatic lipid metabolism through controlling Per2 expression

Chou, C.-F., Zhu, X., Lin, Y.-Y., Gamble, K. L., Garvey, W. T., & Chen, C.-Y. (2015) · Journal of Lipid Research · doi:10.1194/jlr.m050724 · Cited by 20

Metabolomics reveal circadian control of cellular metabolism

Ch, R., Chevallier, O. P., & Elliott, C. T. (2020) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2020.115986 · Cited by 22

Chronobiology Meets Quantum Biology: A New Paradigm Overlooking the Horizon?

Mazzoccoli, G. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.892582 · Cited by 23

DNA polymerase beta connects tumorigenicity with the circadian clock in liver cancer through the epigenetic demethylation of Per1

Chen, S., Zhang, W., Li, X., Cao, Z., & Liu, C. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06462-7 · Cited by 21

Photoperiodic and Diurnal Regulation of WNT Signaling in the Arcuate Nucleus of the Female Djungarian Hamster, Phodopus sungorus

Boucsein, A., Benzler, J., Hempp, C., Stöhr, S., Helfer, G., & Tups, A. (2015) · Endocrinology · doi:10.1210/en.2015-1708 · Cited by 20

Hypothalamic leptin sensitivity and health benefits of time‐restricted feeding are dependent on the time of day in male mice

Boucsein, A., Rizwan, M. Z., & Tups, A. (2019) · The FASEB Journal · doi:10.1096/fj.201901004r · Cited by 20

Exploring the newer oxadiazoles as real inhibitors of human SIRT2 in hepatocellular cancer cells

Dukanya, Shanmugam, M. K., Rangappa, S., Metri, P. K., Mohan, S., Basappa, B., & Rangappa, K. S. (2020) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2020.127330 · Cited by 20

Daily rhythms of glycerophospholipid synthesis in fibroblast cultures involve differential enzyme contributions

Acosta-Rodríguez, V. A., Márquez, S., Salvador, G. A., Pasquaré, S. J., Gorné, L. D., Garbarino‐Pico, E., Giusto, N. M., & Guido, M. E. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m034264 · Cited by 19

Loss of Coiled-Coil Domain Containing 80 Negatively Modulates Glucose Homeostasis in Diet-Induced Obese Mice

Tremblay, F., Huard, C., Dow, J., Gareski, T., Will, S., Richard, A.-M. T., Syed, J., Bailey, S. A., Brenneman, K. A., Martinez, R. V. P., et al. (2012) · Endocrinology · doi:10.1210/en.2012-1242 · Cited by 23

Circadian Metabolic Regulation through Crosstalk between Casein Kinase 1δ and Transcriptional Coactivator PGC-1α

Li, S., Chen, X., Yu, L., Saltiel, A. R., & Lin, J. D. (2011) · Molecular Endocrinology · doi:10.1210/me.2011-1227 · Cited by 19

A-to-I RNA editing enzyme ADAR2 regulates light-induced circadian phase-shift

Terajima, H., Yoshitane, H., Yoshikawa, T., Shigeyoshi, Y., & Fukada, Y. (2018) · Scientific Reports · doi:10.1038/s41598-018-33114-6 · Cited by 19

Association between metabolic risk, oxidative stress and rotating shift work in a tertiary health care facility

Gowda, R., Sukumar, G. M., & Gowda, S. H. (2019) · Clinical Epidemiology and Global Health · doi:10.1016/j.cegh.2019.01.002 · Cited by 19

Phenotypic proteomic profiling identifies a landscape of targets for circadian clock–modulating compounds

Ray, S., Lach, R., Heesom, K. J., Valekunja, U. K., Encheva, V., Snijders, A. P., & Reddy, A. B. (2019) · Life Science Alliance · doi:10.26508/lsa.201900603 · Cited by 18

The importance of chronobiology to drug discovery

Farrow, S. N., Solari, R. C. E., & Willson, T. M. (2012) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2012.689283 · Cited by 19

Dissecting the Rev-erbα Cistrome and the Mechanisms Controlling Circadian Transcription in LiverPreprint

Fang, B., & Lazar, M. A. (2015) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2015.80.027508 · Cited by 20

Dietary Conjugated Linoleic Acid Modulates the Hepatic Circadian Clock Program via PPARα/REV-ERBα-Mediated Chromatin Modification in Mice

Liu, H., Gu, H., Li, Y., Hu, P., Yang, Y., Li, K., Li, H., Zhang, K., Zhou, B., Wu, H., et al. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.711398 · Cited by 18

BMAL1 plays a crucial role in immune homeostasis during sepsis-induced acute lung injury

Zeng, T., Liang, L., Deng, W., Xie, M., Zhao, M.-Y., Wang, S., Liu, J., & Yang, M. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116379 · Cited by 19

Liraglutide Activates AMPK Signaling and Partially Restores Normal Circadian Rhythm and Insulin Secretion in Pancreatic Islets in Diabetic Mice

Wang, K., Sun, Y., Lin, P., Song, J., Zhao, R., Li, W., Hou, X., Wang, C., Wang, L., Zhu, P., et al. (2015) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b15-00024 · Cited by 18

The p75 neurotrophin receptor in AgRP neurons is necessary for homeostatic feeding and food anticipation

Podyma, B., Johnson, D.-A., Sipe, L. M., Remcho, T. P., Battin, K., Liu, Y., Yoon, S. O., Deppmann, C. D., & Güler, A. D. (2020) · eLife · doi:10.7554/elife.52623 · Cited by 18

Saliva Samples as A Tool to Study the Effect of Meal Timing on Metabolic And Inflammatory Biomarkers

Kessler, K., Hornemann, S., Rudovich, N. N., Weber, D., Grune, T., Kramer, A., Pfeiffer, A. F. H., & Pivovarova‐Ramich, O. (2020) · Nutrients · doi:10.3390/nu12020340 · Cited by 22

Electrochemical Detection of Circadian Redox Rhythm in Cyanobacterial Cells via Extracellular Electron Transfer

Nishio, K., Pornpitra, T., Izawa, S., Nishiwaki‐Ohkawa, T., Kato, S., Hashimoto, K., & Nakanishi, S. (2015) · Plant and Cell Physiology · doi:10.1093/pcp/pcv066 · Cited by 18

Resetting the Aging Clock: Implications for Managing Age-Related Diseases

Nobrega, A. K. D., Luz, K. V., & Lyons, L. C. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-42667-5_9 · Cited by 20

Retinoid X Receptors Intersect the Molecular Clockwork in the Regulation of Liver Metabolism

Cosmo, S. D., & Mazzoccoli, G. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00024 · Cited by 19

How Sugar Tunes Your Clock

Hart, G. W. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.01.008 · Cited by 17

Modelling and Analysis of the Feeding Regimen Induced Entrainment of Hepatocyte Circadian Oscillators Using Petri Nets

Tareen, S. H. K., & Ahmad, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117519 · Cited by 17

Circadian transcriptome analysis in human fibroblasts from Hunter syndrome and impact of iduronate-2-sulfatase treatment

Mazzoccoli, G., Tomanin, R., Mazza, T., D’Avanzo, F., Salvalaio, M., Rigon, L., Zanetti, A., Pazienza, V., Francavilla, M., Giuliani, F., et al. (2013) · BMC Medical Genomics · doi:10.1186/1755-8794-6-37 · Cited by 18

Sobriety and Satiety: Is NAD+ the Answer?

Braidy, N., Villalva, M. D., & van Eeden, S. (2020) · Antioxidants · doi:10.3390/antiox9050425 · Cited by 17

Restricted feeding modulates peripheral clocks and nutrient sensing pathways in rats

Rodrigues, L. G. F., de Araújo, L. D., Roa, S. L. R., Bueno, A. C., Uchôa, E. T., Antunes‐Rodrigues, J., Moreira, A. C., Elias, L. L. K., de Castro, M., & Martins, C. S. (2021) · Archives of Endocrinology and Metabolism · doi:10.20945/2359-3997000000407 · Cited by 17

Is Neuronal Histamine Signaling Involved in Cancer Cachexia? Implications and Perspectives

Zwickl, H., Zwickl-Traxler, E., & Pecherstorfer, M. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01409 · Cited by 18

Purine Catabolism Shows a Dampened Circadian Rhythmicity in a High-fat Diet-Induced Mouse Model of Obesity

Sun, R., Huang, J., Yang, N., He, J. B., Yu, X., Feng, S., Xie, Y., Wang, G., Ye, H., & Aa, J. (2019) · Molecules · doi:10.3390/molecules24244524 · Cited by 17

Current perspective on circadian function of the kidney

Benjamin, J. I., & Pollock, D. M. (2023) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00247.2023 · Cited by 18

Japanese flounder (Paralichthys olivaceus) Bmal1 is involved in the regulation of inflammatory response and bacterial infection

Zhang, P., Yu, C., & Sun, L. (2020) · Aquaculture · doi:10.1016/j.aquaculture.2020.735330 · Cited by 14

Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver

Hurni, C., Weger, B. D., Gobet, C., & Naef, F. (2022) · PLOS Genetics · doi:10.1371/journal.pgen.1009903 · Cited by 14

REGγ regulates circadian clock by modulating BMAL1 protein stability

Kubra, S., Zhang, H., Si, Y., Gao, X. C., Wang, T., Pan, L., Li, L., Zhong, N., Fu, J., Zhang, B., et al. (2021) · Cell Death Discovery · doi:10.1038/s41420-021-00704-9 · Cited by 15

Shumian Capsule Improves the Sleep Disorder and Mental Symptoms Through Melatonin Receptors in Sleep-Deprived Mice

Li, W., Cheng, Y., Zhang, Y., Qian, Y., Wu, M., Huang, W., Yang, N., & Liu, Y. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.925828 · Cited by 17

Blind Spot for Sedentarism: Redefining the Diseasome of Physical Inactivity in View of Circadian System and the Irisin/BDNF Axis

Zsuga, J., Móré, C. E., Erdei, T., Papp, C., Harsányi, S., & Gesztelyi, R. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00818 · Cited by 16

CDK9 modulates circadian clock by attenuating REV-ERBα activity

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The mouse liver displays daily rhythms in the metabolism of phospholipids and in the activity of lipid synthesizing enzymes

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