Related references
Note: Only part of the references are listed.Hypocretin (orexin) is critical in sustaining theta/gamma-rich waking behaviors that drive sleep need
Anne Vassalli et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Suprachiasmatic Nucleus and Subparaventricular Zone Lesions Disrupt Circadian Rhythmicity but Not Light-Induced Masking Behavior in Nile Grass Rats
Andrew J. Gall et al.
JOURNAL OF BIOLOGICAL RHYTHMS (2016)
Beta EEG reflects sensory processing in active wakefulness and homeostatic sleep drive in quiet wakefulness
Janne Gronli et al.
JOURNAL OF SLEEP RESEARCH (2016)
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome
Wei-Hsiang Huang et al.
NEURON (2016)
The relationship between gamma frequency and running speed differs for slow and fast gamma rhythms in freely behaving rats
Chenguang Zheng et al.
HIPPOCAMPUS (2015)
Reentrainment Impairs Spatial Working Memory until Both Activity Onset and Offset Reentrain
Norman F. Ruby et al.
JOURNAL OF BIOLOGICAL RHYTHMS (2015)
Expression in the human brain of retinoic acid induced 1, a protein associated with neurobehavioural disorders
Yara Dadalti Fragoso et al.
BRAIN STRUCTURE & FUNCTION (2015)
Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions
C. Dubourg et al.
MOLECULAR SYNDROMOLOGY (2014)
Circadian abnormalities in mouse models of smith-magenis syndrome: Evidence for involvement of RAI1
Melanie Lacaria et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2013)
Smith-Magenis Syndrome Results in Disruption of CLOCK Gene Transcription and Reveals an Integral Role for RAI1 in the Maintenance of Circadian Rhythmicity
Stephen R. Williams et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Distinct Retinohypothalamic Innervation Patterns Predict the Developmental Emergence of Species-Typical Circadian Phase Preference in Nocturnal Norway Rats and Diurnal Nile Grass Rats
William D. Todd et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2012)
Complex interaction of circadian and non-circadian effects of light on mood: Shedding new light on an old story
Kathryn M. Stephenson et al.
SLEEP MEDICINE REVIEWS (2012)
Linking neural activity and molecular oscillations in the SCN
Christopher S. Colwell
NATURE REVIEWS NEUROSCIENCE (2011)
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Chuong B. Do et al.
PLOS GENETICS (2011)
Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome
Paulina Carmona-Mora et al.
BMC MOLECULAR BIOLOGY (2010)
Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome
Brooke Burns et al.
HUMAN MOLECULAR GENETICS (2010)
Retinoic acid signaling in mammalian eye development
Ales Cvekl et al.
EXPERIMENTAL EYE RESEARCH (2009)
Increased Gamma Oscillatory Activity in the Subthalamic Nucleus During Tremor in Parkinson's Disease Patients
M. Weinberger et al.
JOURNAL OF NEUROPHYSIOLOGY (2009)
Effects of VPAC2 Receptor Activation on Membrane Excitability and GABAergic Transmission in Subparaventricular Zone Neurons Targeted by Suprachiasmatic Nucleus
M. L. H. J. Hermes et al.
JOURNAL OF NEUROPHYSIOLOGY (2009)
Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism
Bert van der Zwaag et al.
PLOS ONE (2009)
Smith-Magenis syndrome
Sarah H. Elsea et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Parkinsonian Beta Oscillations in the External Globus Pallidus and Their Relationship with Subthalamic Nucleus Activity
Nicolas Mallet et al.
JOURNAL OF NEUROSCIENCE (2008)
Retinal TrkB receptors regulate neural development in the inner, but not outer, retina
Ruslan N. Grishanin et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2008)
Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes
Weimin Bi et al.
HUMAN MOLECULAR GENETICS (2007)
Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases
E. A. Edelman et al.
CLINICAL GENETICS (2007)
Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype
Lorraine Potocki et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Expression of Tgfα in the suprachiasiviatic nuclei of nocturnal and diurnal rodents
B. B. Tournier et al.
NEUROSCIENCE (2007)
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data
Jan Hellemans et al.
GENOME BIOLOGY (2007)
Lentiviral gene transfer of Rpe65 rescues survival and function of cones in a mouse model of Leber congenital amaurosis
Alexis-Pierre Bemelmans et al.
PLOS MEDICINE (2006)
A role for cardiotrophin-like cytokine in the circadian control of mammalian locomotor activity
S Kraves et al.
NATURE NEUROSCIENCE (2006)
Inverted rhythm of melatonin secretion in Smith-Magenis syndrome: from symptoms to treatment
Helene De Leersnyder
TRENDS IN ENDOCRINOLOGY AND METABOLISM (2006)
Photons, clocks, and consciousness
GC Brainard et al.
JOURNAL OF BIOLOGICAL RHYTHMS (2005)
Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome
WM Bi et al.
HUMAN MOLECULAR GENETICS (2005)
Light and diurnal cycle affect autonomic cardiac balance in human; poss ible role for the biological clock
FAJL Scheer et al.
AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL (2004)
Differences in the suprachiasmatic nucleus and lower subparaventricular zone of diurnal and nocturnal rodents
MD Schwartz et al.
NEUROSCIENCE (2004)
Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia
A Toulouse et al.
GENOMICS (2003)
Mutations in RAI1 associated with Smith-Magenis syndrome
RE Slager et al.
NATURE GENETICS (2003)
Hyperactivity and reduced energy cost of physical activity in serotonin 5-HT2c receptor mutant mice
K Nonogaki et al.
DIABETES (2003)
beta(1)-adrenergic antagonists and melatonin reset the clock and restore sleep in a circadian disorder, Smith-Magenis syndrome
H De Leersnyder et al.
JOURNAL OF MEDICAL GENETICS (2003)
Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del (17) (p11.2p11.2)]
L Potocki et al.
GENETICS IN MEDICINE (2003)
Role of melanopsin in circadian responses to light
NF Ruby et al.
SCIENCE (2002)
Separation of circadian and wake duration-dependent modulation of EEG activation during wakefulness
C Cajochen et al.
NEUROSCIENCE (2002)
Regulation of daily locomotor activity and sleep by hypothalamic EGF receptor signaling
A Kramer et al.
SCIENCE (2001)
Transition from dim to bright light in the morning induces an immediate elevation of cortisol levels
R Leproult et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2001)
Dose-response relationship for light intensity and ocular and electroencephalographic correlates of human alertness
C Cajochen et al.
BEHAVIOURAL BRAIN RESEARCH (2000)
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)
S Hayes et al.
HUMAN MOLECULAR GENETICS (2000)
Circadian rhythm abnormalities of melatonin in Smith-Magenis syndrome
L Potocki et al.
JOURNAL OF MEDICAL GENETICS (2000)
BDNF regulates eating behavior and locomotor activity in mice
SG Kernie et al.
EMBO JOURNAL (2000)
Share Paper
