Corpus overview


MeSH Disease

HGNC Genes

SARS-CoV-2 proteins

There are no SARS-CoV-2 protein terms in the subcorpus


SARS-CoV-2 Proteins
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    Remdesivir but not famotidine inhibits SARS-CoV-2 replication in human pluripotent stem cell-derived intestinal organoids

    Authors: Jan Krueger; Ruediger Gross; Carina Conzelmann; Janis A Mueller; Lennart Koepke; Konstantin Sparrer; Desiree Schuetz; Thomas Seufferlein; Thomas F.E. Barth; Steffen Stenger; Sandra Heller; Alexander Kleger; Jan Muench

    doi:10.1101/2020.06.10.144816 Date: 2020-06-11 Source: bioRxiv

    Gastrointestinal symptoms in COVID-19 MESHD are associated with prolonged symptoms and increased severity. We employed human intestinal organoids derived from pluripotent stem cells ( PSC-HIOs MESHD) to analyze SARS-CoV-2 pathogenesis and to validate efficacy of specific drugs in the gut. Certain, but not all cell types in PSC-HIOs MESHD express SARS-CoV-2 entry factors ACE2 HGNC and TMPRSS2 HGNC, rendering them susceptible to SARS-CoV-2 infection MESHD. Remdesivir, a promising drug to treat COVID-19 MESHD, effectively suppressed SARS-CoV-2 infection of PSC-HIOs MESHD. In contrast, the histamine-2-blocker famotidine showed no effect. Thus, PSC-HIOs MESHD provide an interesting platform to study SARS-CoV-2 infection MESHD and to identify or validate drugs.

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MeSH Disease
HGNC Genes
SARS-CoV-2 Proteins

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