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About:
The dual impact of ACE2 in COVID-19 and ironical actions in geriatrics and pediatrics with possible therapeutic solutions
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
Values
type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
The dual impact of ACE2 in COVID-19 and ironical actions in geriatrics and pediatrics with possible therapeutic solutions
Creator
Kumar, Arun
Arora,
Bungau, Simona
Behl, Tapan
Gokhan, Zengin
Kaur, Ishnoor
Kumar, Chanchal
Pal, Giridhari
Sahil, Kamal
Shrivastava, Gokhan
Shrivastava, Kamal
Uddin, Sahab
Zengin, Sandeep
Source
Elsevier; Medline; PMC
abstract
The novel corona virus disease has shaken the entire world with its deadly effects and rapid transmission rates, posing a significant challenge to the healthcare authorities to develop suitable therapeutic solution to save lives on earth. The review aims to grab the attention of the researchers all over the globe, towards the role of ACE2 in COVID-19 disease. ACE2 serves as a molecular target for the SARS-CoV-2, to enter the target cell, by interacting with the viral glycoprotein spikes. However, the complexity began when numerous studies identified the protective response of ACE2 in abbreviating the harmful effects of vasoconstrictor, anti-inflammatory peptide, angiotensin 2, by mediating its conversion to angiotensin-(1–7), which exercised antagonistic actions to angiotensin 2. Furthermore, certain investigations revealed greater resistance among children as compared to the geriatrics, towards COVID-19 infection, despite the elevated expression of ACE2 in pediatric population. Based upon such evidences, the review demonstrated possible therapeutic interventions, targeting both the protective and deleterious effects of ACE2 in COVID-19 disease, primarily inhibiting ACE2-virus interactions or administering soluble ACE2. Thus, the authors aim to provide an opportunity for the researchers to consider RAAS system to be a significant element in development of suitable treatment regime for COVID-19 pandemic.
has issue date
2020-09-15
(
xsd:dateTime
)
bibo:doi
10.1016/j.lfs.2020.118075
bibo:pmid
32653522
has license
no-cc
sha1sum (hex)
616d7806d2d68ec12bb67cad062988f3d69a3ffb
schema:url
https://doi.org/10.1016/j.lfs.2020.118075
resource representing a document's title
The dual impact of ACE2 in COVID-19 and ironical actions in geriatrics and pediatrics with possible therapeutic solutions
has PubMed Central identifier
PMC7347488
has PubMed identifier
32653522
schema:publication
Life Sci
resource representing a document's body
covid:616d7806d2d68ec12bb67cad062988f3d69a3ffb#body_text
is
schema:about
of
named entity 'AIMS'
named entity 'TRANSMISSION'
named entity 'VASOCONSTRICTOR'
named entity 'HARMFUL'
named entity 'GRAB'
named entity 'RAPID'
named entity 'N A'
named entity 'IDENTIFIED'
named entity 'ADMINISTERING'
named entity 'LIVES'
named entity 'MOLECULAR TARGET'
named entity 'ANTIINFLAMMATORY'
named entity 'GLOBE'
named entity 'SPIKES'
covid:arg/616d7806d2d68ec12bb67cad062988f3d69a3ffb
named entity 'pediatric'
named entity 'geriatrics'
named entity 'COVID-19 disease'
named entity 'corona virus disease'
named entity 'virus'
named entity 'glycoprotein'
named entity 'antiinflammatory'
named entity 'vasoconstrictor'
named entity 'angiotensin 2'
named entity 'geriatrics'
named entity 'pediatrics'
named entity 'ACE2'
named entity 'coughing'
named entity 'ACE2'
named entity 'lung'
named entity 'anti-inflammatory'
named entity 'ACE2'
named entity 'innate response'
named entity 'hypertensive'
named entity 'ACE2'
named entity 'transmembrane'
named entity 'antioxidant'
named entity 'lymphocyte count'
named entity 'adaptive immunity'
named entity 'COVID'
named entity 'infection'
named entity 'RAAS'
named entity 'metalloproteinase'
named entity 'organ'
named entity 'cytoplasm'
named entity 'ACE inhibitors'
named entity 'China'
named entity 'angiotensin 2'
named entity 'cytokines'
named entity 'cluster of differentiation'
named entity 'angiotensin'
named entity 'ACE2'
named entity 'AT1 receptors'
named entity 'ACE2'
named entity 'open reading frames'
named entity 'Russia'
named entity 'ACE'
named entity 'SARS-CoV'
named entity 'angiotensin'
named entity 'renin'
named entity 'cardiovascular'
named entity 'endothelial cells'
named entity 'ACE2'
named entity 'plasma'
named entity 'RAAS'
named entity 'glycoprotein'
named entity 'renal disorders'
named entity 'diabetic nephropathy'
named entity 'wild type'
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