Mitofusins 1 and 2 are essential for postnatal metabolic remodeling in heart

Circulation Research

Volumn 111, Issue 8, 2012, Pages 1012-1026

  Papanicolaou, Kyriakos N ^a   Kikuchi, Ryosuke ^a   Ngoh, Gladys A ^a   Coughlan, Kimberly A ^a   Dominguez, Isabel ^a   Stanley, William C ^b   Walsh, Kenneth ^a  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

Author keywords

biogenesis; cardiac growth cardiomyopathy; mitochondrial DNA; mitochondrial fusion; p62

Indexed keywords

MITOCHONDRIAL DNA; MITOFUSIN 1; MITOFUSIN 2;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BIOGENESIS; CARDIOMYOPATHY; CONTROLLED STUDY; DENSITY; DOWN REGULATION; ELECTRON; GENE EXPRESSION; GENETIC ANALYSIS; HEART DEVELOPMENT; HEART MUSCLE CELL; HEART VENTRICLE REMODELING; LOXP SITE; MEMBRANE STRUCTURE; MITOCHONDRION; MITOPHAGY; MOUSE; NONHUMAN; PERINATAL PERIOD; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN METABOLISM; SURVIVAL;

ANIMALS; ANIMALS, NEWBORN; DNA, MITOCHONDRIAL; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GTP PHOSPHOHYDROLASES; HEART; HEART FAILURE; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MICROSCOPY, ELECTRON; MITOCHONDRIA; MYOCARDIUM; MYOCYTES, CARDIAC; MYOFIBRILS; SURVIVAL RATE;

EID: 84866894493     PISSN: 00097330     EISSN: 15244571     Source Type: Journal    
DOI: 10.1161/CIRCRESAHA.112.274142     Document Type: Article

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