Neonatal heart-enriched miR-708 promotes proliferation and stress resistance of cardiomyocytes in rodents

Theranostics

Volumn 7, Issue 7, 2017, Pages 1953-1965

  Deng, Shengqiong ^a,b   Zhao, Qian ^a   Zhang, Chuyi ^a   Zhen, Lixiao ^a   Liu, Cuicui ^a   Wang, Guangxue ^a   Zhang, Lin ^a   Bao, Luer ^a   Lu, Ying ^a   Meng, Lingyu ^a,c   Lü, Jinhui ^a   Yu, Ping ^a   Lin, Xin ^a   Zhang, Yuzhen ^a   Chen, Yi Han ^a   Fan, Huimin ^a   Cho, William C ^d   Liu, Zhongmin ^a   Yu, Zuoren ^a,c  

^a TONGJI UNIVERSITY SCHOOL OF MEDICINE   (China)

^b SECOND MILITARY MEDICAL UNIVERSITY   (China)

^c DALIAN MEDICAL UNIVERSITY   (China)

^d QUEEN ELIZABETH HOSPITAL   (Hong Kong)

Author keywords

Cardiomyocytes; Heart regeneration; MAPK14; miR 708

Indexed keywords

ALPHA ACTIN; ALPHA ACTIN 1; FIBROBLAST GROWTH FACTOR RECEPTOR 1; ISOPRENALINE; MICRORNA; MICRORNA 15B; MICRORNA 17; MICRORNA 18A; MICRORNA 19A; MICRORNA 708; MITOGEN ACTIVATED PROTEIN KINASE 14; SMALL INTERFERING RNA; TROPONIN I; TROPONIN T; TROPONIN T2; UNCLASSIFIED DRUG; VIMENTIN; CARDIOVASCULAR AGENT; MIRN708 MICRORNA, MOUSE;

3' UNTRANSLATED REGION; ADULT; ANIMAL CELL; APOPTOSIS; ARTICLE; BIOINFORMATICS; CARDIAC MUSCLE CELL; CELL CYCLE ARREST; CELL HYPOXIA; CELL LINE; CELL PROLIFERATION; CELL PROTECTION; CELL STRESS; CONTROLLED STUDY; DOWN REGULATION; EMBRYO; GENE DELIVERY SYSTEM; GENE EXPRESSION REGULATION; GENE OVEREXPRESSION; GENE SILENCING; GENETIC ASSOCIATION; H9C2 CELL LINE; HEART FUNCTION; IN VITRO STUDY; IN VIVO STUDY; LIPID NANOPARTICLE DELIVERY; MOUSE; MTT ASSAY; MYOCARDIAL REGENERATION; NEWBORN; NONHUMAN; PROTEIN EXPRESSION; RAT; STRESS INDUCED APOPTOSIS; TISSUE REGENERATION; UPREGULATION; ANIMAL; CELL CULTURE; EMBRYOLOGY; HEART; HEART INFARCTION; METABOLISM; PHYSIOLOGICAL STRESS; PHYSIOLOGY; TREATMENT OUTCOME;

ANIMALS; CARDIOVASCULAR AGENTS; CELL PROLIFERATION; CELLS, CULTURED; HEART; MICE; MICRORNAS; MITOGEN-ACTIVATED PROTEIN KINASE 14; MYOCARDIAL INFARCTION; MYOCYTES, CARDIAC; RATS; STRESS, PHYSIOLOGICAL; TREATMENT OUTCOME;

EID: 85019882094     PISSN: None     EISSN: 18387640     Source Type: Journal    
DOI: 10.7150/thno.16478     Document Type: Article

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