SARS-CoV-2 Infects Human Engineered Heart Tissues and Models COVID-19 Myocarditis is a research paper published in JACC Basic to Translational Science (2021). On theSindex it has a DataRank of 0. It has been cited 202 times.
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National Institutes of Health
Grant: 75N93019C00062
National Institutes of Health
Grant: R01 AI127828
National Institutes of Health
Grant: R01 HL138466
National Institutes of Health
Grant: R01 HL139714
National Institutes of Health
Grant: R01 HL141086
St. Louis Children's Hospital
Grant: CDI-CORE-2015-505
St. Louis Children's Hospital
Grant: CDI-CORE-2019-813
Defense Advanced Research Projects Agency
Grant: HR001117S0019
Burroughs Wellcome Fund
Grant: 1014782
March of Dimes Foundation
Grant: FY18-BOC-430198
NIAID NIH HHS
Grant: R21 AI148877
NIAID NIH HHS
Grant: T32 AI007163
NIAID NIH HHS
Grant: F30 AI152327
NIGMS NIH HHS
Grant: T32 GM007200
NIAID NIH HHS
Grant: R01 AI157155
National Institutes of Health
Grant: 5R01AI127828-05
Human neutralizing antibodies for Zika virus
National Institutes of Health
Grant: 5R01HL141086-02
Regulation of cardiac power output in health and disease
National Institutes of Health
Grant: 5R01HL138466-04
MACROPHAGE HETEROGENEITY IN HEART FAILURE PROGRESSION AND CARDIAC RECOVERY
National Institutes of Health
Grant: 1R01HL139714-01
MACROPHAGE ONTOGENY SHIFTS IN ISCHEMIC HEART DISEASE
Center for Cellular Imaging, Washington University
Foundation for Barnes-Jewish Hospital
Fields of Study
Keywords
Sustainable Development Goals
Additional file 1 of Major adverse cardiovascular events are associated with necroptosis during severe COVID-19
Additional file 1 of Major adverse cardiovascular events are associated with necroptosis during severe COVID-19
Additional file 2 of Major adverse cardiovascular events are associated with necroptosis during severe COVID-19
Additional file 2 of Major adverse cardiovascular events are associated with necroptosis during severe COVID-19
Additional file 1 of SARS-CoV-2 viral genes Nsp6, Nsp8, and M compromise cellular ATP levels to impair survival and function of human pluripotent stem cell-derived cardiomyocytes
Additional file 1 of SARS-CoV-2 viral genes Nsp6, Nsp8, and M compromise cellular ATP levels to impair survival and function of human pluripotent stem cell-derived cardiomyocytes
Additional file 1 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 1 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 2 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 2 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 3 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 3 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 4 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 4 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 5 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 5 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 6 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 6 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 7 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo
Additional file 7 of SARS-CoV-2 variants divergently infect and damage cardiomyocytes in vitro and in vivo