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About:
SARS‐CoV‐2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells
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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
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Attributes
Values
type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
SARS‐CoV‐2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells
Creator
Boots, Agnes
Kreuter, Michael
Schneider, Marc
Conrad, Christian
Eils, Roland
Hennig, Bianca
Kahn, Nicolas
Lukassen, Soeren
Meister, Michael
Muley, Thomas
Trefzer, Timo
Veith, Carmen
Winter, Hauke
Lorenz Chua, Robert
topic
covid:78c7ab1626fb6f72c09c280f8587f64ae7763d61#this
Source
Medline; PMC; WHO
abstract
The SARS‐CoV‐2 pandemic affecting the human respiratory system severely challenges public health and urgently demands for increasing our understanding of COVID‐19 pathogenesis, especially host factors facilitating virus infection and replication. SARS‐CoV‐2 was reported to enter cells via binding to ACE2, followed by its priming by TMPRSS2. Here, we investigate ACE2 and TMPRSS2 expression levels and their distribution across cell types in lung tissue (twelve donors, 39,778 cells) and in cells derived from subsegmental bronchial branches (four donors, 17,521 cells) by single nuclei and single cell RNA sequencing, respectively. While TMPRSS2 is strongly expressed in both tissues, in the subsegmental bronchial branches ACE2 is predominantly expressed in a transient secretory cell type. Interestingly, these transiently differentiating cells show an enrichment for pathways related to RHO GTPase function and viral processes suggesting increased vulnerability for SARS‐CoV‐2 infection. Our data provide a rich resource for future investigations of COVID‐19 infection and pathogenesis.
has issue date
2020-04-14
(
xsd:dateTime
)
bibo:doi
10.15252/embj.20105114
bibo:pmid
32246845
has license
cc-by
sha1sum (hex)
78c7ab1626fb6f72c09c280f8587f64ae7763d61
schema:url
https://doi.org/10.15252/embj.20105114
resource representing a document's title
SARS‐CoV‐2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells
has PubMed Central identifier
PMC7232010
has PubMed identifier
32246845
schema:publication
EMBO J
resource representing a document's body
covid:78c7ab1626fb6f72c09c280f8587f64ae7763d61#body_text
is
http://vocab.deri.ie/void#inDataset
of
https://covidontheweb.inria.fr:4443/about/id/http/ns.inria.fr/covid19/78c7ab1626fb6f72c09c280f8587f64ae7763d61
is
schema:about
of
named entity 'cells'
named entity 'cell types'
named entity 'facilitating'
named entity 'cells'
named entity 'respiratory system'
named entity 'PRIMING'
named entity 'RESOURCE'
named entity 'TRANSIENT'
named entity 'SINGLE'
named entity 'REPORTED'
named entity 'BINDING'
named entity 'REPLICATION'
named entity 'RESPIRATORY SYSTEM'
named entity 'VULNERABILITY'
named entity 'RHO GTPASE'
named entity 'HUMAN'
named entity 'LEVELS'
named entity 'PUBLIC HEALTH'
named entity 'INCREASING'
named entity 'DEMANDS'
covid:arg/78c7ab1626fb6f72c09c280f8587f64ae7763d61
named entity 'pandemic'
named entity 'expressed'
named entity 'vulnerability'
named entity 'TMPRSS2'
named entity 'enter'
named entity 'rich'
named entity 'function'
named entity 'SARS-CoV-2'
named entity 'expression'
named entity 'branches'
named entity 'infection'
named entity 'COVID'
named entity 'ACE2'
named entity 'infection'
named entity 'single cell RNA sequencing'
named entity 'TMPRSS2'
named entity 'SARS-CoV-2 pandemic'
named entity 'virus infection'
named entity 'infection'
named entity 'pathogenesis'
named entity 'TMPRSS2'
named entity 'infection'
named entity 'liquid nitrogen'
named entity 'epithelia'
named entity 'FURIN'
named entity 'ethics committee'
named entity 'protein'
named entity 'DTT'
named entity 'SARS-CoV-2'
named entity 'FURIN'
named entity 'Wilcoxon rank sum test'
named entity 'smokers'
named entity 'SARS-CoV-2'
named entity 'ACE2'
named entity 'single cell sequencing'
named entity 'ACE2'
named entity 'MTA'
named entity 'pseudostratified'
named entity 'infection'
named entity 'expression levels'
named entity '39,778'
named entity 'SARS-CoV-2'
named entity 'FURIN'
named entity 'SARS'
named entity 'cell types'
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