About: Renin–angiotensin system in human coronavirus pathogenesis

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About: Renin–angiotensin system in human coronavirus pathogenesis Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Renin–angiotensin system in human coronavirus pathogenesis
Creator	Van Der Hoek, Lia Wevers, Brigitte
Source	Medline; PMC
abstract	Although initially considered relatively harmless pathogens, human coronaviruses (HCoVs) are nowadays known to be associated with more severe clinical complications. Still, their precise pathogenic potential is largely unknown, particularly regarding the most recently identified species HCoV-NL63 and HCoV-HKU1. HCoVs need host cell proteins to successively establish infections. Proteases of the renin–angiotensin system serve as receptors needed for entry into target cells; this article describes the current knowledge on the involvement of this system in HCoV pathogenesis.
has issue date	2010-03-01(xsd:dateTime)
bibo:doi	10.2217/fvl.10.4
bibo:pmid	32201502
has license	cc-by
sha1sum (hex)	74eab3a3e909673c339bd66babb0ad77b9a2903a
schema:url	https://doi.org/10.2217/fvl.10.4
resource representing a document's title	Renin–angiotensin system in human coronavirus pathogenesis
has PubMed Central identifier	PMC7079966
has PubMed identifier	32201502
schema:publication	Future Virol
resource representing a document's body	covid:74eab3a3e909673c339bd66babb0ad77b9a2903a#body_text
is schema:about of	named entity 'RENIN' named entity 'PROTEASES' named entity 'HUMAN CORONAVIRUS' named entity 'INTERACTIONS' named entity 'ANGIOTENSIN' named entity 'RENIN-ANGIOTENSIN SYSTEM' named entity 'pathogenesis' named entity 'RAS' named entity 'angiotensin' named entity 'mice' named entity 'ace2' named entity 'cell proliferation' named entity 'homologous' named entity 'infection' named entity 'phenotype' named entity 'ACE2' named entity 'alveolar' named entity 'lung failure' named entity 'lung failure' named entity 'negative regulator' named entity 'membrane-bound' named entity 'vasodilatation' named entity 'control individuals' named entity '3, 4' named entity 'SARS-CoV' named entity 'N-terminal' named entity 'cathepsin' named entity 'synaptic junctions' named entity 'genotype' named entity 'phagocytosis' named entity 'HCoV-NL63' named entity 'RAS' named entity 'immunocompromised patients' named entity 'Prolyl carboxypeptidase' named entity 'ACE' named entity 'proteases' named entity 'HCoV-HKU1' named entity 'cell surface' named entity 'self-limiting' named entity 'hypercytokinemia' named entity 'ACE' named entity 'enzyme' named entity 'RAS' named entity 'cell culture' named entity 'HCoV-NL63' named entity 'CoV' named entity 'RAS' named entity 'amino acid residues' named entity 'protein' named entity 'sarcoidosis, pulmonary' named entity 'human pathogen' named entity 'host cells' named entity 'SARS-CoV' named entity 'host cell' named entity 'Ang II' named entity 'Ang II' named entity 'cell entry' named entity 'platelet' named entity 'monocytes' named entity 'vasodilatation' named entity 'cytokines' named entity 'clinical symptoms' named entity 'SARS-CoV' named entity 'peptides' named entity 'vascular endothelial cells' named entity 'HCoV-229E' named entity 'liver' named entity 'ARDS' named entity 'Cell surface' named entity 'measles virus' named entity 'influenza C virus' named entity 'normal physiological processes' named entity 'chemokine' named entity 'pathophysiological' named entity 'antidiuretic hormone' named entity 'signaling pathways' named entity 'aminopeptidase' named entity 'proteases' named entity 'downregulation' named entity 'NF-kB'

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