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Isolation of timeless by PER Protein Interaction: Defective Interaction Between timeless Protein and Long-Period Mutant PER L

Gekakis, N., Sáez, L., Delahaye-Brown, A.-M., Myers, M. P., Sehgal, A., Young, M. W., & Weitz, C. J. (1995) · Science · doi:10.1126/science.270.5237.811 · Cited by 370

The Circadian Clock Mutation Alters Sleep Homeostasis in the Mouse

Naylor, E., Bergmann, B. M., Krauski, K., Zee, P. C., Takahashi, J. S., Vitaterna, M. H., & Turek, F. W. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-21-08138.2000 · Cited by 367

Light and circadian rhythmicity regulate MAP kinase activation in the suprachiasmatic nuclei

Obrietan, K. H., Impey, S., & Storm, D. R. (1998) · Nature Neuroscience · doi:10.1038/3695 · Cited by 369

Identification of the circadian transcriptome in adult mouse skeletal muscle

McCarthy, J. J., Andrews, J. L., McDearmon, E. L., Campbell, K. S., Barber, B. K., Miller, B. H., Walker, J. R., Hogenesch, J. B., Takahashi, J. S., & Esser, K. A. (2007) · Physiological Genomics · doi:10.1152/physiolgenomics.00066.2007 · Cited by 368

Zebrafish Clock rhythmic expression reveals independent peripheral circadian oscillators

Whitmore, D., Foulkes, N. S., Strähle, U., & Sassone‐Corsi, P. (1998) · Nature Neuroscience · doi:10.1038/3703 · Cited by 357

Mammalian Circadian Autoregulatory Loop

Sangoram, A. M., Sáez, L., Antoch, M. P., Gekakis, N., Staknis, D., Whiteley, A. R., Fruechte, E. M., Vitaterna, M. H., Shimomura, K., King, D. P., et al. (1998) · Neuron · doi:10.1016/s0896-6273(00)80627-3 · Cited by 355

Light-induced resetting of a circadian clock is mediated by a rapid increase in frequency transcript

Crosthwaite, S. K., Loros, J., & Dunlap, J. (1995) · Cell · doi:10.1016/s0092-8674(05)80005-4 · Cited by 358

Mammalian Per-Arnt-Sim Proteins in Environmental Adaptation

McIntosh, B. E., Hogenesch, J. B., & Bradfield, C. A. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135922 · Cited by 352

Sleep and circadian rhythms: key components in the regulation of energy metabolism

Laposky, A. D., Bass, J., Kohsaka, A., & Turek, F. W. (2008) · FEBS Letters · doi:10.1016/j.febslet.2007.06.079 · Cited by 351

Deficient of a Clock Gene, Brain and Muscle Arnt-Like Protein-1 (BMAL1), Induces Dyslipidemia and Ectopic Fat Formation

Shimba, S., Ogawa, T., Hitosugi, S., Ichihashi, Y., Nakadaira, Y., Kobayashi, M., Tezuka, M., Kosuge, Y., Ishige, K., Ito, Y., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025231 · Cited by 353

Challenging the omnipotence of the suprachiasmatic timekeeper: are circadian oscillators present throughout the mammalian brain?

Guilding, C., & Piggins, H. D. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05581.x · Cited by 356

Mutagenesis and mapping of a mouse gene, Clock, essential for circadian …

Vitaterna, M. H. (1994) · Science · Cited by 144

Mutagenesis and behavioral screening for altered circadian activity identifies the mouse mutant, Wheels

Pickard, G. E., Sollars, P. J., Rinchik, E. M., Nolan, P. M., & Bućan, M. (1995) · Brain Research · doi:10.1016/0006-8993(95)01171-4 · Cited by 36

The Mouse Clock Mutation Behaves as an Antimorph and Maps Within the W19H Deletion, Distal of Kit

King, D. P., Vitaterna, M. H., Chang, A., Dove, W. F., Pinto, L. H., Turek, F. W., & Takahashi, J. S. (1997) · Genetics · doi:10.1093/genetics/146.3.1049 · Cited by 162

Generation of mouse mutants as tools in dissecting the molecular clock

Anand, S. N., Edwards, J. K., & Nolan, P. M. (2012) · Progress in brain research · doi:10.1016/b978-0-444-59427-3.00015-0 · Cited by 2

Chemical Mutagenesis and Screening for Mouse Mutations with an Altered Rest–Activity Pattern

Nolan, P. M., Houpt, T. A., & Bućan, M. (2019) · CRC Press eBooks · doi:10.1201/9780429186844-12