Cardiomyocyte-specific BMAL1 plays critical roles in metabolism, signaling, and maintenance of contractile function of the heart

Journal of Biological Rhythms

Volumn 29, Issue 4, 2014, Pages 257-276

  Young, Martin E ^a   Brewer, Rachel A ^a   Peliciari Garcia, Rodrigo A ^a,b   Collins, Helen E ^c   He, Lan ^d   Birky, Tana L ^a   Peden, Bradley W ^a   Thompson, Emily G ^a   Ammons, Billy Joe ^a   Bray, Molly S ^d   Chatham, John C ^c   Wende, Adam R ^c   Yang, Qinglin ^d   Chow, Chi Wing ^e   Martino, Tami A ^f   Gamble, Karen L ^g  

^a University of Alabama at Birmingham and Birmingham Veterans Affairs Medical Center   (United States)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

^c University of Alabama at Birmingham   (United States)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^e ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^f UNIVERSITY OF GUELPH   (Canada)

^g UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

chronobiology; circadian; metabolism; signaling; transcriptome

Indexed keywords

ARNTL PROTEIN, MOUSE; GLUCOSE; KETONE BODY; TRANSCRIPTION FACTOR ARNTL;

ANIMAL; C57BL MOUSE; CIRCADIAN RHYTHM; HEART; HEART MUSCLE CELL; KNOCKOUT MOUSE; MALE; METABOLISM; MOUSE; PHYSIOLOGY; SIGNAL TRANSDUCTION;

ANIMALS; ARNTL TRANSCRIPTION FACTORS; CIRCADIAN CLOCKS; CIRCADIAN RHYTHM; GLUCOSE; HEART; KETONE BODIES; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MYOCYTES, CARDIAC; SIGNAL TRANSDUCTION;

EID: 84905962204     PISSN: 07487304     EISSN: 15524531     Source Type: Journal    
DOI: 10.1177/0748730414543141     Document Type: Article

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