Metabolism and cancer: the circadian clock connection

On the origin of cancer cells

Warburg, O. (1956) · Science · doi:10.1126/science.123.3191.309 · Cited by 13,425 · see citing works

Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase

Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510 · see citing works

hSIR2SIRT1 Functions as an NAD-Dependent p53 Deacetylase

Vaziri, H., Dessain, S. K., Eaton, E. N., Imai, S., Frye, R. A., Pandita, T. K., Guarente, L., & Weinberg, R. A. (2001) · Cell · doi:10.1016/s0092-8674(01)00527-x · Cited by 2,653 · see citing works

Obesity and Metabolic Syndrome in Circadian <i>Clock</i> Mutant Mice

Turek, F. W., Joshu, C., Kohsaka, A., Lin, E., Ivanova, G., McDearmon, E., Laposky, A., Losee-Olson, S., Easton, A., Jensen, D. R., et al. (2005) · Science · doi:10.1126/science.1108750 · Cited by 2,485 · see citing works

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 &amp; Development · doi:10.1101/gad.183500 · Cited by 2,394 · see citing works

Adverse metabolic and cardiovascular consequences of circadian misalignment

Scheer, F. A. J. L., Hilton, M. F., Mantzoros, C. S., & Shea, S. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808180106 · Cited by 2,351 · see citing works

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 2,272 · see citing works

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 · see citing works

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 · see citing works

Role of the CLOCK Protein in the Mammalian Circadian Mechanism

Gekakis, N., Staknis, D., Nguyen, H. B., Davis, F. C., Wilsbacher, L. D., King, D. P., Takahashi, J. S., & Weitz, C. J. (1998) · Science · doi:10.1126/science.280.5369.1564 · Cited by 1,997 · see citing works

Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-γ

Picard, F., Kurtev, M. V., Chung, N., Topark‐Ngarm, A., Senawong, T., de Oliveira, R. M., Leid, M. E., McBurney, M. W., & Guarente, L. (2004) · Nature · doi:10.1038/nature02583 · Cited by 1,943 · see citing works

Mutagenesis and Mapping of a Mouse Gene, <i>Clock</i> , Essential for Circadian Behavior

Vitaterna, M. H., King, D. P., Chang, A.-M., Kornhauser, J. M., Lowrey, P. L., McDonald, J. D., Dove, W. F., Pinto, L. H., Turek, F. W., & Takahashi, J. S. (1994) · Science · doi:10.1126/science.8171325 · Cited by 1,632 · see citing works

Mop3 is an essential component of the master circadian pacemaker in mammals.

Bunger, M. K., Wilsbacher, L. D., Moran, S. M., Clendenin, C., Radcliffe, L. A., Hogenesch, J. B., Simon, M. C., Takahashi, J. S., & Bradfield, C. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00205-1 · Cited by 1,621 · see citing works

The NAD+-dependent deacetylase SIRT1 modulates CLOCK-mediated chromatin remodeling and circadian control

Nakahata, Y., Kaluzova, M., Grimaldi, B., Sahar, S., Hirayama, J., Chen, D., Guarente, L. P., & Sassone-Corsi, P. (2008) · Cell · doi:10.1016/j.cell.2008.07.002 · Cited by 1,427 · see citing works

Mammalian Cry1 and Cry2 are essential for maintenance of circadian rhythms

Horst, G. T. J. V. D., Muijtjens, M., Kobayashi, K., Takano, R., Kanno, S.-I., Takao, M., Wit, J. D., Verkerk, A., Eker, A. P. M., Leenen, D. V., et al. (1999) · Nature · doi:10.1038/19323 · Cited by 1,402 · see citing works

Positional Cloning of the Mouse Circadian Gene

King, D. P., Zhao, Y., Sangoram, A. M., Wilsbacher, L. D., Tanaka, M., Antoch, M. P., Steeves, T. D. L., Vitaterna, M. H., Kornhauser, J. M., Lowrey, P. L., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80245-7 · Cited by 1,382 · see citing works

SIRT1 regulates circadian clock gene expression through PER2 deacetylation

Asher, G., Gatfield, D., Stratmann, M., Reinke, H., Dibner, C., Kreppel, F., Mostoslavsky, R., Alt, F. W., & Schibler, U. (2008) · Cell · doi:10.1016/j.cell.2008.06.050 · Cited by 1,376 · see citing works

Mammalian sirtuins—emerging roles in physiology, aging, and calorie restriction

Haigis, M. C., & Guarente, L. P. (2006) · Genes &amp; Development · doi:10.1101/gad.1467506 · Cited by 1,295 · see citing works

The Circadian Gene Period2 Plays an Important Role in Tumor Suppression and DNA Damage Response In Vivo

Fu, L., Pelicano, H., Liu, J., Huang, P., & Lee, C. C. (2002) · Cell · doi:10.1016/s0092-8674(02)00961-3 · Cited by 1,256 · see citing works

Circadian Control of the NAD ⁺ Salvage Pathway by CLOCK-SIRT1

Nakahata, Y., Sahar, S., Astarita, G., Kaluzova, M., & Sassone-Corsi, P. (2009) · Science · doi:10.1126/science.1170803 · Cited by 1,198 · see citing works

A clockwork web: circadian timing in brain and periphery, in health and disease

Hastings, M. H., Reddy, A. B., & Maywood, E. S. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1177 · Cited by 1,189 · see citing works

Early aging and age-related pathologies in mice deficient in BMAL1, the core componentof the circadian clock

Kondratov, R. V., Kondratova, A. A., Gorbacheva, V. Y., Vykhovanets, O. V., & Antoch, M. P. (2006) · Genes &amp; Development · doi:10.1101/gad.1432206 · Cited by 1,188 · see citing works

Defects in Adaptive Energy Metabolism with CNS-Linked Hyperactivity in PGC-1α Null Mice

Lin, J., Wu, P.-H., Tarr, P. T., Lindenberg, K. S., St-Pierre, J., Zhang, C.-Y., Mootha, V. K., Jäger, S., Vianna, C. R., Reznick, R. M., et al. (2004) · Cell · doi:10.1016/j.cell.2004.09.013 · Cited by 1,162 · see citing works

Time zones: a comparative genetics of circadian clocks

Young, M. W., & Kay, S. A. (2001) · Nature Reviews Genetics · doi:10.1038/35088576 · Cited by 1,143 · see citing works

Rotating night shifts and risk of breast cancer in women participating in the nurses׳ health study

Schernhammer, E. S., Laden, F., Speizer, F. E., Willett, W. C., Hunter, D. J., Kawachi, I., & Colditz, G. A. (2001) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/93.20.1563 · Cited by 1,142 · see citing works

Control Mechanism of the Circadian Clock for Timing of Cell Division in Vivo

Matsuo, T., Yamaguchi, S., Mitsui, S., Emi, A., Shimoda, F., & Okamura, H. (2003) · Science · doi:10.1126/science.1086271 · Cited by 1,132 · see citing works

Circadian Clock Feedback Cycle Through NAMPT-Mediated NAD ⁺ Biosynthesis

Ramsey, K. M., Yoshino, J., Brace, C. S., Abrassart, D., Kobayashi, Y., Marcheva, B., Hong, H.-K., Chong, J. L., Buhr, E. D., Lee, C., et al. (2009) · Science · doi:10.1126/science.1171641 · Cited by 1,126 · see citing works

A Functional Genomics Strategy Reveals Rora as a Component of the Mammalian Circadian Clock

Sato, T. K., Panda, S., Miraglia, L. J., Reyes, T. M., Rudic, R. D., McNamara, P., Naik, K. A., FitzGerald, G. A., Kay, S. A., & Hogenesch, J. B. (2004) · Neuron · doi:10.1016/j.neuron.2004.07.018 · Cited by 1,115 · see citing works

Tumor suppressors and cell metabolism: a recipe for cancer growth

Jones, R. G., & Thompson, C. B. (2009) · Genes &amp; Development · doi:10.1101/gad.1756509 · Cited by 1,085 · see citing works

SIRT1 deacetylase protects against neurodegeneration in models for Alzheimer's disease and amyotrophic lateral sclerosis

Kim, D., Nguyen, M. D., Dobbin, M. M., Fischer, A., Sananbenesi, F., Rodgers, J. T., Delalle, I., Baur, J. A., Sui, G., Armour, S. M., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601758 · Cited by 1,074 · see citing works

BMAL1 and CLOCK, two essential components of the circadian clock, are involved in glucose homeostasis

Rudic, R. D., McNamara, P., Curtis, A.-M., Boston, R. C., Panda, S., Hogenesch, J. B., & FitzGerald, G. A. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020377 · Cited by 1,059 · see citing works

Physiological significance of a peripheral tissue circadian clock

Lamia, K. A., Storch, K.-F., & Weitz, C. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806717105 · Cited by 1,048 · see citing works

The age of cancer

DePinho, R. A. (2000) · Nature · doi:10.1038/35041694 · Cited by 951 · see citing works

PGC-1α Deficiency Causes Multi-System Energy Metabolic Derangements: Muscle Dysfunction, Abnormal Weight Control and Hepatic Steatosis

Leone, T. C., Lehman, J. J., Finck, B. N., Schaeffer, P. J., Wende, A. R., Boudina, S., Courtois, M., Wozniak, D. F., Sambandam, N., Bernal-Mizrachi, C., et al. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030101 · Cited by 951 · see citing works

Nuclear Receptor Expression Links the Circadian Clock to Metabolism

Yang, X., Downes, M., Yu, R. T., Bookout, A. L., He, W., Straume, M., Mangelsdorf, D. J., & Evans, R. M. (2006) · Cell · doi:10.1016/j.cell.2006.06.050 · Cited by 934 · see citing works

The Meter of Metabolism

Green, C. B., Takahashi, J. S., & Bass, J. (2008) · Cell · doi:10.1016/j.cell.2008.08.022 · Cited by 902 · cited 1× · see citing works

Nonredundant roles of the mPer1 and mPer2 genes in the mammalian circadian clock.

Zheng, B., Albrecht, U., Kaasik, K., Sage, M., Lu, W., Vaishnav, S., Li, Q., Sun, Z. S., Eichele, G., Bradley, A., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00380-4 · Cited by 900 · see citing works

Differential Functions of mPer1, mPer2, and mPer3 in the SCN Circadian Clock

Bae, K., Jin, X., Maywood, E. S., Hastings, M. H., Reppert, S. M., & Weaver, D. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00302-6 · Cited by 900 · see citing works

Circadian Regulator CLOCK Is a Histone Acetyltransferase

Doi, M., Hirayama, J., & Sassone‐Corsi, P. (2006) · Cell · doi:10.1016/j.cell.2006.03.033 · Cited by 890 · see citing works

A Differential Response of Two Putative Mammalian Circadian Regulators, mper1and mper2, to Light

Albrecht, U., Sun, Z. S., Eichele, G., & Lee, C. C. (1997) · Cell · doi:10.1016/s0092-8674(00)80495-x · Cited by 879 · see citing works

Post-translational modifications regulate the ticking of the circadian clock

Gallego, M., & Virshup, D. M. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2106 · Cited by 863 · see citing works

Positional Syntenic Cloning and Functional Characterization of the Mammalian Circadian Mutation tau

Lowrey, P. L., Shimomura, K., Antoch, M. P., Yamazaki, S., Zemenides, P. D., Ralph, M. R., Menaker, M., & Takahashi, J. S. (2000) · Science · doi:10.1126/science.288.5465.483 · Cited by 860 · see citing works

SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging

Oberdoerffer, P., Michan, S., McVay, M., Mostoslavsky, R., Vann, J., Park, S.-K., Hartlerode, A., Stegmuller, J., Hafner, A., Loerch, P., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.025 · Cited by 852 · see citing works

Statins and cancer prevention

Demierre, M., Higgins, P., Gruber, S. B., Hawk, E. T., & Lippman, S. M. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1751 · Cited by 822 · see citing works

Two period Homologs: Circadian Expression and Photic Regulation in the Suprachiasmatic Nuclei

Shearman, L. P., Zylka, M. J., Weaver, D. R., Kolakowski, L. F., & Reppert, S. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80417-1 · Cited by 781 · see citing works

Impaired DNA Damage Response, Genome Instability, and Tumorigenesis in SIRT1 Mutant Mice

Wang, R.-H., Sengupta, K., Li, C., Kim, H., Cao, L., Xiao, C., Kim, S., Xu, X., Yin, Z., Chilton, B. S., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.09.001 · Cited by 769 · see citing works

A Web of Circadian Pacemakers

Schibler, U., & Sassone‐Corsi, P. (2002) · Cell · doi:10.1016/s0092-8674(02)01225-4 · Cited by 752 · see citing works

The mPer2 gene encodes a functional component of the mammalian circadian clock

Zheng, B., Larkin, D. W., Albrecht, U., Sun, Z. S., Sage, M., Eichele, G., Lee, C. C., & Bradley, A. (1999) · Nature · doi:10.1038/22118 · Cited by 718 · see citing works

Differential regulation of mammalian <i>Period</i> genes and circadian rhythmicity by cryptochromes 1 and 2

Vitaterna, M. H., Selby, C. P., Todo, T., Niwa, H., Thompson, C., Fruechte, E. M., Hitomi, K., Thresher, R. J., Ishikawa, T., Miyazaki, J., et al. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12114 · Cited by 690 · see citing works

Rhythmic histone acetylation underlies transcription in the mammalian circadian clock

Etchegaray, J.-P., Lee, C., Wade, P. A., & Reppert, S. M. (2003) · Nature · doi:10.1038/nature01314 · Cited by 679 · see citing works

Tumor Suppressor HIC1 Directly Regulates SIRT1 to Modulate p53-Dependent DNA-Damage Responses

Chen, W., Wang, D. H., Yen, R.-W. C., Luo, J., Gu, W. J., & Baylin, S. B. (2005) · Cell · doi:10.1016/j.cell.2005.08.011 · Cited by 649 · see citing works

Transcriptional coactivator PGC-1α integrates the mammalian clock and energy metabolism

Liu, C., Li, S., Liu, T., Borjigin, J., & Lin, J. D. (2007) · Nature · doi:10.1038/nature05767 · Cited by 643 · see citing works

SIRT1 Deacetylates and Positively Regulates the Nuclear Receptor LXR

Li, X., Zhang, S., Blander, G., Tse, J. G., Krieger, M., & Guarente, L. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.07.032 · Cited by 631 · see citing works

The circadian gene per1 plays an important role in cell growth and DNA damage control in human cancer cells

Gery, S., Komatsu, N., Baldjyan, L., Yu, A., Koo, D., & Koeffler, H. P. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.03.038 · Cited by 630 · see citing works

FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis.

Hasmann, M., & Schemainda, I. (2003) · PubMed · Cited by 618 · see citing works

Rhythmic CLOCK-BMAL1 binding to multiple E-box motifs drives circadian Dbp transcription and chromatin transitions

Ripperger, J. A., & Schibler, U. (2006) · Nature Genetics · doi:10.1038/ng1738 · Cited by 593 · see citing works

The SIRT1 deacetylase suppresses intestinal tumorigenesis and colon cancer growth.

Firestein, R., Blander, G., Michan, S., Oberdoerffer, P., Ogino, S., Campbell, J., Bhimavarapu, A., Luikenhuis, S., de Cabo, R., Fuchs, C., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002020 · Cited by 588 · see citing works

Acetylation of the C Terminus of Ku70 by CBP and PCAF Controls Bax-Mediated Apoptosis

Cohen, H. Y., Lavu, S., Bitterman, K. J., Hekking, B., Imahiyerobo, T. A., Miller, C. M., Frye, R. A., Ploegh, H. L., Kessler, B. M., & Sinclair, D. A. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00094-2 · Cited by 574 · see citing works

NPAS2: an analog of clock operative in the mammalian forebrain

Reick, M., Garcia, J. A., Dudley, C., & McKnight, S. L. (2001) · Science · doi:10.1126/science.1060699 · Cited by 572 · see citing works

Circadian Mutant Overtime Reveals F-box Protein FBXL3 Regulation of Cryptochrome and Period Gene Expression

Siepka, S. M., Yoo, S. H., Park, J., Song, W., Kumar, V., Hu, Y., Lee, C., & Takahashi, J. S. (2007) · Cell · doi:10.1016/j.cell.2007.04.030 · Cited by 536 · see citing works

Decoding the Epigenetic Language of Neuronal Plasticity

Borrelli, E., Nestler, E. J., Allis, C. D., & Sassone‐Corsi, P. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.012 · Cited by 529 · see citing works

CLOCK-mediated acetylation of BMAL1 controls circadian function

Hirayama, J., Sahar, S., Grimaldi, B., Tamaru, T., Takamatsu, K., Nakahata, Y., & Sassone‐Corsi, P. (2007) · Nature · doi:10.1038/nature06394 · Cited by 525 · see citing works

SCF Fbxl3 Controls the Oscillation of the Circadian Clock by Directing the Degradation of Cryptochrome Proteins

Busino, L., Bassermann, F. C., Maiolica, A., Lee, C., Nolan, P. M., Godinho, S. I. H., Draetta, G. F., & Pagano, M. (2007) · Science · doi:10.1126/science.1141194 · Cited by 509 · see citing works

Circadian and CLOCK-controlled regulation of the mouse transcriptome and cell proliferation

Miller, B. H., McDearmon, E. L., Panda, S., Hayes, K. R., Zhang, J., Andrews, J. L., Antoch, M. P., Walker, J. R., Esser, K. A., Hogenesch, J. B., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611724104 · Cited by 509 · see citing works

Increased breast cancer risk among women who work predominantly at night

Hansen, J. (2001) · Epidemiology · doi:10.1097/00001648-200101000-00013 · Cited by 503 · see citing works

CLOCK and NPAS2 have overlapping roles in the suprachiasmatic circadian clock

DeBruyne, J. P., Weaver, D. R., & Reppert, S. M. (2007) · Nature Neuroscience · doi:10.1038/nn1884 · Cited by 484 · see citing works

The After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period

Godinho, S. I. H., Maywood, E. S., Shaw, L. E., Tucci, V., Barnard, A. R., Busino, L., Pagano, M., Kendall, R., Quwailid, M. M., Romero, M. R., et al. (2007) · Science · doi:10.1126/science.1141138 · Cited by 468 · see citing works

A clock shock: mouse CLOCK is not required for circadian oscillator function

DeBruyne, J. P., Noton, E., Lambert, C. M., Maywood, E. S., Weaver, D. R., & Reppert, S. M. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.041 · Cited by 430 · see citing works

How does SIRT1 affect metabolism, senescence and cancer?

Brooks, C. L., & Gu, W. J. (2008) · Nature reviews. Cancer · doi:10.1038/nrc2562 · Cited by 426 · see citing works

Deregulated expression of the PER1 , PER2 and PER3 genes in breast cancers

Chen, S., Choo, K., Hou, M., Yeh, K., Kuo, S., & Chang, J. (2005) · Carcinogenesis · doi:10.1093/carcin/bgi075 · Cited by 419 · see citing works

Conserved Metabolic Regulatory Functions of Sirtuins

Schwer, B., & Verdin, E. M. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.006 · Cited by 415 · see citing works

Altered patterns of sleep and behavioral adaptability in NPAS2-deficient mice

Dudley, C. A., Erbel-Sieler, C., Estill, S. J., Reick, M., Franken, P., Pitts, S., & McKnight, S. L. (2003) · Science · doi:10.1126/science.1082795 · Cited by 415 · see citing works

Role of Mouse Cryptochrome Blue-Light Photoreceptor in Circadian Photoresponses

Thresher, R., Vitaterna, M. H., Miyamoto, Y., Kazantsev, A. G., Hsu, D. S., Petit, C. R., Selby, C. P., Dawut, L., Smithies, O., Takahashi, J. S., et al. (1998) · Science · doi:10.1126/science.282.5393.1490 · Cited by 401 · see citing works

Nampt: linking NAD biology, metabolism and cancer

Garten, A., Petzold-Quinque, S., Körner, A., Imai, S., & Kieß, W. (2008) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2008.10.004 · Cited by 399 · see citing works

Poly(ADP-ribose) Polymerase-1-dependent Cardiac Myocyte Cell Death during Heart Failure Is Mediated by NAD+ Depletion and Reduced Sir2α Deacetylase Activity

Pillai, J. B., Isbatan, A., Imai, S., & Gupta, M. P. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m506162200 · Cited by 391 · see citing works

Setting Clock Speed in Mammals: The CK1ɛ tau Mutation in Mice Accelerates Circadian Pacemakers by Selectively Destabilizing PERIOD Proteins

Meng, Q., Logunova, L., Maywood, E. S., Gallego, M., Lebiecki, J., Brown, T. M., Sládek, M., Semikhodskii, A. G., Glossop, N. R. J., Piggins, H. D., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.019 · Cited by 372 · see citing works

Reciprocal regulation of haem biosynthesis and the circadian clock in mammals

Kaasik, K., & Lee, C. C. (2004) · Nature · doi:10.1038/nature02724 · Cited by 341 · see citing works

Genome-wide Expression Analysis of Mouse Liver Reveals CLOCK-regulated Circadian Output Genes

Oishi, K., Miyazaki, K., Kadota, K., Kikuno, R. F., Nagase, T., Atsumi, G.-I., Ohkura, N., Azama, T., Mesaki, M., Yukimasa, S., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304564200 · Cited by 341 · see citing works

Living by the clock: The circadian pacemaker in older people

Hofman, M. A., & Swaab, D. F. (2005) · Ageing Research Reviews · doi:10.1016/j.arr.2005.07.001 · Cited by 335 · see citing works

Circadian Clock Control by SUMOylation of BMAL1

Cardone, L., Hirayama, J., Giordano, F., Tamaru, T., Palvimo, J. J., & Sassone‐Corsi, P. (2005) · Science · doi:10.1126/science.1110689 · Cited by 329 · see citing works

A genomewide oscillation in transcription gates DNA replication and cell cycle

Klevecz, R. R., Bolen, J., Forrest, G., & Murray, D. B. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0306490101 · Cited by 321 · see citing works

Coupling of Human Circadian and Cell Cycles by the Timeless Protein

Ünsal-Kaçmaz, K., Mullen, T. E., Kaufmann, W. K., & Sancar, A. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.8.3109-3116.2005 · Cited by 310 · see citing works

Active and inactive forms of 3-hydroxy-3-methylglutaryl coenzyme A reductase in the liver of the rat. Comparison with the rate of cholesterol synthesis in different physiological states.

Brown, M. S., Goldstein, J. L., & Dietschy, J. (1979) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)50571-8 · Cited by 308 · see citing works

Circadian Disruption and Breast Cancer

Stevens, R. G. (2005) · Epidemiology · doi:10.1097/01.ede.0000152525.21924.54 · Cited by 295 · see citing works

Nuclear receptor corepressor and histone deacetylase 3 govern circadian metabolic physiology

Alenghat, T., Meyers, K. C., Mullican, S. E., Leitner, K., Adeniji‐Adele, A., Avila, J. L., Bućan, M., Ahima, R. S., Kaestner, K. H., & Lazar, M. A. (2008) · Nature · doi:10.1038/nature07541 · Cited by 293 · see citing works

SCFβ-TRCP Controls Clock-dependent Transcription via Casein Kinase 1-dependent Degradation of the Mammalian Period-1 (Per1) Proteinm

Shirogane, T., Jin, J., Cambronne, X. A., & Harper, J. W. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502862200 · Cited by 293 · see citing works

Control of Intracellular Dynamics of Mammalian Period Proteins by Casein Kinase I ε (CKIε) and CKIδ in Cultured Cells

Akashi, M., Tsuchiya, Y., Yoshino, T., & Nishida, E. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.6.1693-1703.2002 · Cited by 292 · see citing works

Circadian sensitivity to the chemotherapeutic agent cyclophosphamide depends on the functional status of the CLOCK/BMAL1 transactivation complex

Gorbacheva, V., Kondratov, R. V., Zhang, R., Cherukuri, S., Gudkov, A. V., Takahashi, J. S., & Antoch, M. P. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409897102 · Cited by 270 · see citing works

Involvement of the MAP kinase cascade in resetting of the mammalian circadian clockPreprint

Akashi, M., & Nishida, E. (2000) · Genes & Development · doi:10.1101/gad.14.6.645 · Cited by 269 · see citing works

Light induces chromatin modification in cells of the mammalian circadian clock

Crosio, C., Cermakian, N., Allis, C. D., & Sassone‐Corsi, P. (2000) · Nature Neuroscience · doi:10.1038/81767 · Cited by 264 · see citing works

Altered behavioral rhythms and clock gene expression in mice with a targeted mutation in the Period1 gene

Cermakian, N., Monaco, L., Pando, M. P., Dierich, A., & Sassone‐Corsi, P. (2001) · The EMBO Journal · doi:10.1093/emboj/20.15.3967 · Cited by 252 · see citing works

Casein Kinase 1 Delta Regulates the Pace of the Mammalian Circadian Clock

Etchegaray, J., Machida, K., Noton, E., Constance, C. M., Dallmann, R., Napoli, M. N. D., DeBruyne, J. P., Lambert, C. M., Yu, E. A., Reppert, S. M., et al. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00338-09 · Cited by 237 · see citing works

Oestrogen-receptor-mediated transcription and the influence of co-factors and chromatin state

Green, K., & Carroll, J. (2007) · Nature Reviews. Cancer · doi:10.1038/nrc2211 · Cited by 235 · see citing works

Restriction of DNA Replication to the Reductive Phase of the Metabolic Cycle Protects Genome Integrity

Chen, Z., Odstrcil, E. A., Tu, B. P., & McKnight, S. L. (2007) · Science · doi:10.1126/science.1140958 · Cited by 234 · see citing works

The clock gene Per2 links the circadian system to the estrogen receptor

Gery, S., Virk, R. K., Chumakov, K., Yu, A., & Koeffler, H. P. (2007) · Oncogene · doi:10.1038/sj.onc.1210585 · Cited by 218 · see citing works

The circadian clock protein Period 1 regulates expression of the renal epithelial sodium channel in mice

Gumz, M. L., Stow, L. R., Lynch, I. J., Greenlee, M. M., Rudin, A., Cain, B. D., Weaver, D. R., & Wingo, C. S. (2009) · Journal of Clinical Investigation · doi:10.1172/jci36908 · Cited by 216 · see citing works

Loss of Nocturnin, a circadian deadenylase, confers resistance to hepatic steatosis and diet-induced obesity

Green, C. B., Douris, N., Kojima, S., Strayer, C. A., Fogerty, J., Lourim, D., Keller, S. R., & Besharse, J. C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0702448104 · Cited by 215 · see citing works

Cyclin D1 and breast cancer

Roy, P. G., & Thompson, A. M. (2006) · The Breast · doi:10.1016/j.breast.2006.02.005 · Cited by 212 · see citing works

Riding Tandem: Circadian Clocks and the Cell Cycle

Hunt, T., & Sassone‐Corsi, P. (2007) · Cell · doi:10.1016/j.cell.2007.04.015 · Cited by 211 · see citing works

Requirement of Mammalian Timeless for Circadian Rhythmicity

Barnes, J. W., Tischkau, S. A., Barnes, J. A., Mitchell, J. W., Burgoon, P. W., Hickok, J. R., & Gillette, M. U. (2003) · Science · doi:10.1126/science.1086593 · Cited by 207 · see citing works

Circadian oscillation of nucleotide excision repair in mammalian brain

Kang, T., Reardon, J. T., Kemp, M. G., & Sancar, A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812638106 · Cited by 205 · see citing works

Control of AIF-mediated Cell Death by the Functional Interplay of SIRT1 and PARP-1 in Response to DNA Damage

Kolthur‐Seetharam, U., Dantzer, F., McBurney, M. W., de MURCIA, G., & Sassone‐Corsi, P. (2006) · Cell Cycle · doi:10.4161/cc.5.8.2690 · Cited by 203 · see citing works

Implications of circadian clocks for the rhythmic delivery of cancer therapeutics

Lévi, F., Focan, C., Karaboué, A., de la Valette, V., Focan-Henrard, D., Baron, B., Kreutz, F., & Giacchetti, S. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2006.11.001 · Cited by 199 · see citing works

Loss of cryptochrome reduces cancer risk in p53 mutant mice

Öztürk, N., Lee, J. H., Gaddameedhi, S., & Sancar, A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813028106 · Cited by 192 · see citing works

Identification of Rev-erbα as a physiological repressor of apoC-III gene transcription

Raspé, E., Duez, H., Mansén, A., Fontaine, C., Fiévet, C., Fruchart, J.-C., Vennström, B., & Staels, B. (2002) · Journal of Lipid Research · doi:10.1194/jlr.m200386-jlr200 · Cited by 183 · see citing works

The circadian cycle: daily rhythms from behaviour to genes

Merrow, M. W., Spoelstra, K., & Roenneberg, T. (2005) · EMBO Reports · doi:10.1038/sj.embor.7400541 · Cited by 183 · see citing works

Cryptochrome, Circadian Cycle, Cell Cycle Checkpoints, and Cancer

Gauger, M. A., & Sancar, A. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1119 · Cited by 181 · see citing works

DNA repair deficiency as a therapeutic target in cancer

Martin, S. A., Lord, C. J., & Ashworth, A. (2008) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2008.01.016 · Cited by 174 · see citing works

Severe Atherosclerosis and Hypoalphalipoproteinemia in the Staggerer Mouse, a Mutant of the Nuclear Receptor RORα

Mamontova, A., Séguret-Macé, S., Esposito, B., Chaniale, C., Bouly, M., Delhaye-Bouchaud, N., Luc, G., Staels, B., Duverger, N., Mariani, J., et al. (1998) · Circulation · doi:10.1161/01.cir.98.24.2738 · Cited by 172 · see citing works

Molecular Analysis of Mammalian Timeless

Zylka, M. J., Shearman, L. P., Levine, J. D., Jin, X., Weaver, D. R., & Reppert, S. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80628-5 · Cited by 169 · see citing works

Transcription profiling of C/EBP targets identifies Per2 as a gene implicated in myeloid leukemia

Gery, S., Gombart, A. F., Yi, W. S., Koeffler, C., Hofmann, W., & Koeffler, H. P. (2005) · Blood · doi:10.1182/blood-2005-01-0358 · Cited by 169 · see citing works

Poly(ADP‐ribose) Polymerase–1 Activation During DNA Damage and Repair

Dantzer, F., Amé, J., Schreiber, V., Nakamura, J., Murcia, J. M., & de MURCIA, G. (2006) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)09029-4 · Cited by 167 · see citing works

Peripheral circadian oscillators require CLOCK

DeBruyne, J. P., Weaver, D. R., & Reppert, S. M. (2007) · Current Biology · doi:10.1016/j.cub.2007.05.067 · Cited by 160 · see citing works

Mitogen-activated Protein Kinase Phosphorylates and Negatively Regulates Basic Helix-Loop-Helix-PAS Transcription Factor BMAL1

Sanada, K., Okano, T., & Fukada, Y. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m107850200 · Cited by 151 · see citing works

A role of the circadian system and circadian proteins in aging

KONDRATOV, R. (2007) · Ageing Research Reviews · doi:10.1016/j.arr.2007.02.003 · Cited by 149 · see citing works

Melatonin and Breast Cancer: A Prospective Study

Travis, R. C., Allen, D. S., Fentiman, I. S., & Key, T. J. (2004) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djh077 · Cited by 149 · see citing works

Metabolism control by the circadian clock and vice versa

Eckel‐Mahan, K. L., & Sassone‐Corsi, P. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1595 · Cited by 146 · see citing works

Disruption of the circadian clock due to theClockmutation has discrete effects on aging and carcinogenesis

Antoch, M. P., Gorbacheva, V., Vykhovanets, O. V., Toshkov, I. A., Kondratov, R. V., Kondratova, A. A., Lee, C., & Nikitin, A. Y. (2008) · Cell Cycle · doi:10.4161/cc.7.9.5886 · Cited by 144 · see citing works

The Neurospora Checkpoint Kinase 2: A Regulatory Link Between the Circadian and Cell Cycles

Pregueiro, A. M., Liu, Q., Baker, C. L., Dunlap, J., & Loros, J. (2006) · Science · doi:10.1126/science.1121716 · Cited by 142 · see citing works

Phase Resetting of the Mammalian Circadian Clock by DNA Damage

Oklejewicz, M., Destici, E., Tamanini, F., Hut, R. A., Janssens, R. C., & van der Horst, G. T. J. (2008) · Current Biology · doi:10.1016/j.cub.2008.01.047 · Cited by 132 · see citing works

Central and peripheral circadian oscillator mechanisms in flies and mammals

Glossop, N. R. J., & Hardin, P. E. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.17.3369 · Cited by 120 · see citing works

Recent advances in research on multistage tumorigenesis

Compagni, A., & Christofori, G. (2000) · British Journal of Cancer · doi:10.1054/bjoc.2000.1309 · Cited by 110 · see citing works

Circadian chemotherapy for gynecological and genitourinary cancers

Kobayashi, M., Wood, P. A., & Hrushesky, W. J. M. (2002) · Chronobiology International · doi:10.1081/cbi-120002600 · Cited by 110 · see citing works

The days and nights of cancer cells.

Canaple, L., Kakizawa, T., & Laudet, V. (2003) · PubMed · Cited by 110 · see citing works

Circadian Clock and Breast Cancer: A Molecular Link

Saha, S., & Sassone‐Corsi, P. (2007) · Cell Cycle · doi:10.4161/cc.6.11.4295 · Cited by 106 · see citing works

Common pathways in circadian and cell cycle clocks: Light-dependent activation of Fos/AP-1 in zebrafish controls CRY-1a and WEE-1

Hirayama, J., Cardone, L., Doi, M., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502610102 · Cited by 104 · see citing works

The Circadian Gene NPAS2, a Putative Tumor Suppressor, Is Involved in DNA Damage Response

Hoffman, A. E., Zheng, T., Ba, Y., & Zhu, Y. L. (2008) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-07-2094 · Cited by 102 · see citing works

Structural and functional features of transcription factors controlling the circadian clock

Hirayama, J., & Sassone‐Corsi, P. (2005) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2005.07.003 · Cited by 101 · see citing works

Circadian gating of S phase in human ovarian cancer.

Klevecz, R. R., Shymko, R. M., Blumenfeld, D., & Braly, P. S. (1987) · PubMed · Cited by 101 · see citing works

Urinary 6-Sulfatoxymelatonin Levels and Risk of Breast Cancer in Postmenopausal Women

Schernhammer, E. S., Berrino, F., Krogh, V., Secreto, G., Micheli, A., Venturelli, E., Sieri, S., Sempos, C. T., Cavalleri, A., Schünemann, H. J., et al. (2008) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djn171 · Cited by 101 · see citing works

Inhibition of casein kinase 1-epsilon induces cancer-cell-selective, PERIOD2-dependent growth arrest

Yang, W. S., & Stockwell, B. R. (2008) · Genome biology · doi:10.1186/gb-2008-9-6-r92 · Cited by 95 · see citing works

Cryptochromes impair phosphorylation of transcriptional activators in the clock: a general mechanism for circadian repression

Dardente, H., Fortier, E. E., Martineau, V., & Cermakian, N. (2007) · Biochemical Journal · doi:10.1042/bj20060827 · Cited by 92 · see citing works

Posttranslational Regulation of Circadian Transcriptional Clock (NPAS2)/BMAL1 Complex by Cryptochromes

Kondratov, R. V., Kondratova, A. A., Lee, C., Gorbacheva, V., Chernov, M. V., & Antoch, M. P. (2006) · Cell Cycle · doi:10.4161/cc.5.8.2684 · Cited by 88 · see citing works

Rapid activation of CLOCK by Ca2+‐dependent protein kinase C mediates resetting of the mammalian circadian clock

Shim, H. S., Kim, H. J., Lee, J., Son, G. H., Cho, S., Oh, T. H., Kang, S. H., Seen, D., Lee, K. H., & Kim, K. (2007) · EMBO Reports · doi:10.1038/sj.embor.7400920 · Cited by 80 · see citing works

DNA synthesis and ploidy in non-Hodgkin's lymphomas demonstrate intrapatient variation depending on circadian stage of cell sampling.

Smaaland, R., Lote, K., Sothern, R. B., & Lærum, O. D. (1993) · PubMed · Cited by 66 · see citing works

Circadian timing in cancer treatment: the biological foundation for an integrative approach

Lis, C. G., Grutsch, J. F., Wood, P., You, M., Rich, I., & Hrushesky, W. J. M. (2003) · Integrative Cancer Therapies · doi:10.1177/1534735403002002002 · Cited by 48 · see citing works

A Phylogenetically Conserved DNA Damage Response Resets the Circadian Clock

Gamsby, J. J., Loros, J., & Dunlap, J. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730409334748 · Cited by 44 · see citing works

Circadian Disruption and Breast Cancer

Stevens, R. G. (2001) · Springer eBooks · doi:10.1007/978-3-642-59512-7_28 · Cited by 40 · see citing works

Circadian rhythm and cell cycle: possible entraining mechanisms.

Rensing, L., & Goedeke, K. (1976) · PubMed · Cited by 19 · see citing works

Hepatic gluconeogenic key enzymes in patients with hepatic cancer

Tsubouchi, H., Kamibeppu, A., Fujisaki, K., et al. (1980) · Gastroenterologia Japonica · doi:10.1007/bf02773759 · Cited by 4 · see citing works

Metabolic Flexibility as an Adaptation to Energy Resources and Requirements in Health and Disease

Smith, R. L., Soeters, M. R., Wüst, R. C. I., & Houtkooper, R. H. (2018) · Endocrine Reviews · doi:10.1210/er.2017-00211 · Cited by 787 · see citing works

SIRT1 Mediates Central Circadian Control in the SCN by a Mechanism that Decays with Aging

Chang, H.-C., & Guarente, L. (2013) · Cell · doi:10.1016/j.cell.2013.05.027 · Cited by 615 · see citing works

Circadian Rhythm Disruption Promotes Lung Tumorigenesis

Papagiannakopoulos, T., Bauer, M. R., Davidson, S. M., Heimann, M., Subbaraj, L., Bhutkar, A., Bartlebaugh, J., Vander Heiden, M. G., & Jacks, T. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.07.001 · Cited by 557 · see citing works

PER2 controls lipid metabolism by direct regulation of PPARγ

Grimaldi, B., Bellet, M. M., Katada, S., Astarita, G., Hirayama, J., Amin, R. H., Granneman, J. G., Piomelli, D., Leff, T., & Sassone-Corsi, P. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.10.005 · Cited by 489 · see citing works

Cellular Metabolic Stress: Considering How Cells Respond to Nutrient Excess

Wellen, K. E., & Thompson, C. B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.10.004 · Cited by 486 · see citing works

bHLH-PAS proteins in cancer

Bersten, D. C., Sullivan, A. E., Peet, D. J., & Whitelaw, M. L. (2013) · Nature Reviews Cancer · doi:10.1038/nrc3621 · Cited by 267 · see citing works

The circadian clock in cancer development and therapy

Fu, L., & Kettner, N. M. (2013) · Progress in Molecular Biology and Translational Science · doi:10.1016/b978-0-12-396971-2.00009-9 · Cited by 251 · see citing works

Lung adenocarcinoma distally rewires hepatic circadian homeostasis

Masri, S., Papagiannakopoulos, T., Kinouchi, K., Liu, Y., Cervantes, M., Baldi, P., Jacks, T., & Sassone-Corsi, P. (2016) · Cell · doi:10.1016/j.cell.2016.04.039 · Cited by 234 · see citing works

Regulation of metabolism: the circadian clock dictates the time

Sahar, S., & Sassone-Corsi, P. (2012) · Trends in Endocrinology &amp; Metabolism · doi:10.1016/j.tem.2011.10.005 · Cited by 222 · see citing works

Circadian disruption and metabolic disease: Findings from animal models

Arble, D. M., Ramsey, K. M., Bass, J., & Turek, F. W. (2010) · Best Practice &amp; Research Clinical Endocrinology &amp; Metabolism · doi:10.1016/j.beem.2010.08.003 · Cited by 192 · see citing works

Endocrine Effects of Circadian Disruption

Bedrosian, T. A., Fonken, L. K., & Nelson, R. J. (2016) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021115-105102 · Cited by 170 · see citing works

Circadian Clock, Cancer, and Chemotherapy

Sancar, A., Lindsey-Boltz, L. A., Gaddameedhi, S., Selby, C. P., Ye, R., Chiou, Y.-Y., Kemp, M. G., Hu, J., Lee, J. H., & Ozturk, N. (2015) · Biochemistry · doi:10.1021/bi5007354 · Cited by 170 · see citing works

Tipping the metabolic scales towards increased longevity in mammals

Riera, C. E., & Dillin, A. (2015) · Nature Cell Biology · doi:10.1038/ncb3107 · Cited by 153 · see citing works

Cancer and stress: NextGen strategies

Cui, B., Peng, F., Lu, J., He, B., Su, Q., Luo, H., Deng, Z., Jiang, T., Su, K., Huang, Y., et al. (2021) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2020.11.005 · Cited by 152 · see citing works

The neuroendocrine control of the circadian system: Adolescent chronotype

Hagenauer, M. H., & Lee, T. M. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2012.04.003 · Cited by 143 · see citing works

The adrenal peripheral clock: Glucocorticoid and the circadian timing system

Son, G. H., Chung, S., & Kim, K. (2011) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2011.07.003 · Cited by 136 · see citing works

Dietary intake is associated with human chronotype as assessed by both morningness-eveningness score and preferred midpoint of sleep in young Japanese women

Sato-Mito, N., Shibata, S., Sasaki, S., & Sato, K. (2011) · International Journal of Food Sciences and Nutrition · doi:10.3109/09637486.2011.560563 · Cited by 117 · see citing works

The E3 ubiquitin ligase UBE3A is an integral component of the molecular circadian clock through regulating the BMAL1 transcription factor

Gossan, N. C., Zhang, F., Guo, B., Jin, D., Yoshitane, H., Yao, A., Glossop, N., Zhang, Y. Q., Fukada, Y., & Meng, Q.-J. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku225 · Cited by 106 · see citing works

Epigenetic control and the circadian clock: Linking metabolism to neuronal responses

Orozco-Solis, R., & Sassone-Corsi, P. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.043 · Cited by 94 · see citing works

Altered behavioral and metabolic circadian rhythms in mice with disrupted NAD+ oscillation

Sahar, S., Nin, V., Barbosa, M. T., Chini, E. N., & Sassone-Corsi, P. (2011) · Aging · doi:10.18632/aging.100368 · Cited by 79 · see citing works

Minireview: NAD+, a Circadian Metabolite with an Epigenetic Twist

Sassone-Corsi, P. (2012) · Endocrinology · doi:10.1210/en.2011-1535 · Cited by 71 · see citing works

The Molecular Clock and Neurodegenerative Disease: A Stressful Time

Carter, B., Justin, H. S., Gulick, D., & Gamsby, J. J. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.644747 · Cited by 42 · see citing works

A "Timed" Kiss Is Essential for Reproduction: Lessons from Mammalian Studies

Putteeraj, M., Soga, T., Ubuka, T., & Parhar, I. S. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00121 · Cited by 28 · see citing works

Circadian Rhythms

Lear, B. C., & Allada, R. (2012) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0000040.pub2 · Cited by 1 · see citing works

Plant Circadian Rhythms: An Overview

Tripathi, M. (2016) · International Journal of Photochemistry

Circadian rhythms and physical activity

Racinais, S. (2008) · Cited by 2 · see citing works

Keeping time in the dark: Potato diel and circadian rhythmic gene expression reveals tissue‐specific circadian clocks

Hoopes, G. M., Zarka, D. G., Feke, A., Acheson, K., Hamilton, J. P., Douches, D. S., Buell, C. R., & Farré, E. M. (2022) · Plant Direct · doi:10.1002/pld3.425 · Cited by 19 · see citing works

Pharmacological and Genetic Approaches for the Study of Circadian Rhythms in Mammals

Turek, F. W., Pinto, L. H., Vitaterna, M. H., et al. (1995) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1995.1007 · Cited by 26 · see citing works