Absence of central circadian pacemaker abnormalities in humans with loss of function mutation in prokineticin 2

Journal of Clinical Endocrinology and Metabolism

Volumn 99, Issue 3, 2014, Pages

  Balasubramanian, Ravikumar ^a   Cohen, Daniel A ^b,e   Klerman, Elizabeth B ^b   Pignatelli, Duarte ^c,d   Hall, Janet E ^a   Dwyer, Andrew A ^a,f   Czeisler, Charles A ^b   Pitteloud, Nelly ^a,f   Crowley Jr , William F ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c UNIVERSITY OF PORTO   (Portugal)

^d University of Porto   (Portugal)

^e Sentara Medical Group   (United States)

^f LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CIRCADIAN RHYTHM SIGNALING PROTEIN; HYDROCORTISONE; MELATONIN; PROKINETICIN 2; UNCLASSIFIED DRUG;

ADULT; AGED; ALERTNESS; ARTICLE; CENTRAL CIRCADIAN PACEMAKER; CIRCADIAN RHYTHM; CONTROLLED STUDY; CORE TEMPERATURE; FEMALE; FRAMESHIFT MUTATION; GENE LOSS; GENE MUTATION; HUMAN; HUMAN EXPERIMENT; HYDROCORTISONE BLOOD LEVEL; LOSS OF FUNCTION MUTATION; MALE; MIDDLE AGED; NORMAL HUMAN; PRIORITY JOURNAL; PSYCHOMOTOR PERFORMANCE; SIGNAL TRANSDUCTION; SLEEP TIME;

AGED; AGED, 80 AND OVER; BIOLOGICAL CLOCKS; CASE-CONTROL STUDIES; CHRONOBIOLOGY DISORDERS; CODON, NONSENSE; FEMALE; GASTROINTESTINAL HORMONES; GONADOTROPIN-RELEASING HORMONE; HUMANS; HYPOGONADISM; MALE; MIDDLE AGED; NEUROPEPTIDES; SIBLINGS; SLEEP;

EID: 84895788405     PISSN: 0021972X     EISSN: 19457197     Source Type: Journal    
DOI: 10.1210/jc.2013-2096     Document Type: Article

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