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Genetic basis of human circadian rhythm disorders
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PubMed
title
Genetic basis of human circadian rhythm disorders
(English)
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PubMed
main subject
nervous system development
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circadian rhythm
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author name string
Christopher R. Jones
series ordinal
1
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Crossref
Angela L. Huang
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Louis J. Ptáček
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Ying-Hui Fu
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language of work or name
English
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PubMed
publication date
May 2013
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published in
Experimental Neurology
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PubMed
volume
243
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PubMed
page(s)
28-33
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PubMed
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A CLOCK polymorphism associated with human diurnal preference
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Polymorphism in the PER3 promoter associates with diurnal preference and delayed sleep phase disorder
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Circadian clock genes and sleep homeostasis.
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Oscillating per-cision
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Two decades of circadian time
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The hypothalamic integrator for circadian rhythms
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A length polymorphism in the circadian clock gene Per3 is linked to delayed sleep phase syndrome and extreme diurnal preference
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Practice Parameters for the Role of Actigraphy in the Study of Sleep and Circadian Rhythms: An Update for 2002
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Life between clocks: daily temporal patterns of human chronotypes
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Familial advanced sleep-phase syndrome: A short-period circadian rhythm variant in humans
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Human Circadian Rhythms in Continuous Darkness: Entrainment by Social Cues
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Circadian pacemaker interferes with sleep onset at specific times each day: role in insomnia
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Adaptation to abrupt time shifts of the oscillator(s) controlling human circadian rhythms
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31 May 2018
The genetics of the human circadian clock
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514403
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Association study of a variable-number tandem repeat polymorphism in the clock gene PERIOD3 and chronotype in Norwegian university students
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PubMed Central
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Constant light housing during nursing causes human DSPS (delayed sleep phase syndrome) behaviour in Clock-mutant mice
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PubMed Central
reference URL
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Deletion of the mammalian circadian clock gene BMAL1/Mop3 alters baseline sleep architecture and the response to sleep deprivation
1 reference
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PubMed Central
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The 3111 Clock gene polymorphism is not associated with sleep and circadian rhythmicity in phenotypically characterized human subjects
1 reference
stated in
PubMed Central
reference URL
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28 November 2018
Association of intrinsic circadian period with morningness-eveningness, usual wake time, and circadian phase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514403
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28 November 2018
Mouse model for morningness/eveningness
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514403
retrieved
28 November 2018
Light suppresses melatonin secretion in humans
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22849821
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.EXPNEUROL.2012.07.012
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4258413
OpenCitations bibliographic resource ID
4258413
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4258413
PMC publication ID
3514403
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4258413
PubMed publication ID
22849821
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4258413
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