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Nature, ISSN 0028-0836, 05/2012, Volume 485, Issue 7396, pp. 123 - 127
Journal Article
Nature, ISSN 0028-0836, 07/2010, Volume 466, Issue 7306, pp. 627 - 631
Journal Article
Cell Metabolism, ISSN 1550-4131, 12/2015, Volume 22, Issue 6, pp. 1009 - 1019
The oncogene encodes MYC, a transcription factor that binds the genome through sites termed E-boxes (5′-CACGTG-3′), which are identical to the binding sites of... 
GENE | COPY NUMBER | TRANSCRIPTION | ENDOCRINOLOGY & METABOLISM | N-MYC | C-MYC | REV-ERB-ALPHA | NEUROBLASTOMA | OVARIAN-CANCER | DIFFERENTIATION | EXPRESSION | CELL BIOLOGY | Humans | CLOCK Proteins - chemistry | Glutamine - metabolism | CLOCK Proteins - genetics | RNA, Messenger - metabolism | Nuclear Receptor Subfamily 1, Group D, Member 1 - antagonists & inhibitors | Repressor Proteins - antagonists & inhibitors | CLOCK Proteins - metabolism | Period Circadian Proteins - genetics | RNA Interference | Base Sequence | Binding Sites | Dimerization | Nuclear Receptor Subfamily 1, Group D, Member 1 - metabolism | Genes, Reporter | Repressor Proteins - metabolism | Promoter Regions, Genetic | ARNTL Transcription Factors - genetics | Nuclear Receptor Subfamily 1, Group D, Member 1 - genetics | ARNTL Transcription Factors - metabolism | Repressor Proteins - genetics | Receptors, Cytoplasmic and Nuclear - genetics | Circadian Rhythm | Proto-Oncogene Proteins c-myc - metabolism | Period Circadian Proteins - metabolism | Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors | ARNTL Transcription Factors - chemistry | Cell Line, Tumor | Glucose - metabolism | Proto-Oncogene Proteins c-myc - genetics | RNA, Small Interfering - metabolism | Receptors, Cytoplasmic and Nuclear - metabolism | Glucose metabolism | Medical colleges | Genomics | Cancer cells | Physiological aspects | Glucose | Dextrose | Cancer | Resveratrol
Journal Article
Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2013, Volume 110, Issue 5, pp. 1592 - 1599
Mammalian circadian clocks restrict cell proliferation to defined time windows, but the mechanism and consequences of this interrelationship are not fully... 
Wound healing | RNA | Cell cycle | Cellular senescence | Stem cells | Cell lines | Fibroblasts | Cell division | Cell cycle proteins | Cells | P54nrb | Keratinocyte | RNA-binding protein | Paraspeckle protein | PSF | DNA-DAMAGE RESPONSE | MULTIDISCIPLINARY SCIENCES | paraspeckle protein | PROLIFERATION | NUCLEAR-PROTEIN | p54nrb | CANCER | MAMMALIAN TIMELESS | keratinocyte | IN-VIVO | GENE-EXPRESSION | P54(NRB) | TRANSCRIPTION FACTOR | Cell Cycle - genetics | Cell Proliferation | Male | Circadian Clocks - genetics | Promoter Regions, Genetic - genetics | DNA-Binding Proteins - metabolism | Period Circadian Proteins - genetics | RNA Interference | Trans-Activators - genetics | Female | Wound Healing - genetics | Fibroblasts - metabolism | Cellular Senescence - genetics | Dermis - metabolism | Mice, Inbred C57BL | Cells, Cultured | Cellular Senescence - physiology | Cyclin-Dependent Kinase Inhibitor p16 - genetics | DNA-Binding Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mice, Knockout | Animals | Period Circadian Proteins - metabolism | Cell Cycle - physiology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Protein Binding | Dermis - pathology | Trans-Activators - metabolism | Fibroblasts - cytology | Mice | Wound Healing - physiology | Mutation | Circadian Clocks - physiology | Circadian rhythms | Physiological aspects | Cytogenetics | Genetic aspects | Research | Gene expression | Health aspects | Index Medicus | Biological Sciences
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 02/2011, Volume 20, Issue 4, pp. 731 - 751
Mammalian circadian rhythms are synchronized to the external time by daily resetting of the suprachiasmatic nucleus (SCN) in response to light. As the master... 
RESPONSE ELEMENT | POLY(A) BINDING-PROTEIN | MESSENGER-RNA | RETT-SYNDROME | SUPRACHIASMATIC NUCLEUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SLEEP PHASE SYNDROME | GENETICS & HEREDITY | GENE-EXPRESSION | POLY(A)-BINDING PROTEIN | HISTONE ACETYLTRANSFERASE | ACTIVE GENES | NIH 3T3 Cells | Humans | Methyl-CpG-Binding Protein 2 - metabolism | Chromatin Assembly and Disassembly - genetics | MicroRNAs - metabolism | E1A-Associated p300 Protein - metabolism | Chromatin Assembly and Disassembly - drug effects | Retinoblastoma-Binding Protein 2 - metabolism | Immediate-Early Proteins - metabolism | Period Circadian Proteins - genetics | Light | HEK293 Cells | Suprachiasmatic Nucleus - metabolism | DNA-Binding Proteins | Tumor Suppressor Proteins - metabolism | Signal Transduction | Mice, Inbred C57BL | Circadian Rhythm - genetics | Computational Biology | Gene Expression Regulation | Mice, Transgenic | RNA Stability | Animals | Period Circadian Proteins - metabolism | Mice | MicroRNAs - genetics | Jumonji Domain-Containing Histone Demethylases | Suprachiasmatic nucleus | Calcium | Transcription | CLOCK protein | BTG2 protein | Period 1 protein | Methyl-CpG binding protein | Entrainment | miRNA | Period 2 protein | Circadian rhythms | Obesity | Translation | mRNA turnover | Cyclic AMP | Light effects | Oscillators | Promoters | Chromatin remodeling | Neurological diseases | Period protein | Sleep | MeCP2 protein | Workers | Pacemakers | Cardiovascular diseases | Cancer
Journal Article