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SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor

Hoffmann M.

Дата публикации: 2021-04-27

Дата публикации в реестре: 2021-10-05T18:37:02Z

Аннотация:
Ключевые слова:
angiotensin converting enzyme 2, camostat mesilate, neutralizing antibody, serine protease TMPRSS2, serine proteinase, unclassified drug, virus spike protein, (3-ethoxycarbonyloxirane-2-carbonyl)leucine (3-methylbutyl) amide, ammonium chloride, angiotensin converting enzyme 2, camostat, coronavirus spike glycoprotein, dipeptidyl carboxypeptidase, gabexate, leucine, neutralizing antibody, proteinase inhibitor, serine proteinase, spike glycoprotein, SARS-CoV, TMPRSS2 protein, human, virus antibody, virus receptor, animal cell, antibody response, Article, controlled study, coronavirus disease 2019, coronavirus disease 2019, Coronavirus infection, human, human cell, mouse, nonhuman, priority journal, protein degradation, SARS coronavirus, SARS-related coronavirus, severe acute respiratory syndrome, Severe acute respiratory syndrome coronavirus 2, virus entry, virus neutralization, virus spike, animal, Betacoronavirus, cell line, chemistry, Coronavirinae, Coronavirus infection, drug development, drug effect, genetics, immunology, metabolism, pandemic, passive immunization, physiology, Vesiculovirus, virus entry, virus pneumonia, Ammonium Chloride, Animals, Antibodies, Neutralizing, Antibodies, Viral, Betacoronavirus, Cell Line, Coronavirus, Coronavirus Infections, Drug Development, Gabexate, Humans, Immunization, Passive, Leucine, Pandemics, Peptidyl-Dipeptidase A, Pneumonia, Viral, Protease Inhibitors, Receptors, Virus, SARS Virus, Serine Endopeptidases, Spike Glycoprotein, Coronavirus, Vesiculovirus, Virus Internalization

Тип: info:eu-repo/semantics/journal-article

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