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10.1093/bib/bbab169

http://scihub22266oqcxt.onion/10.1093/bib/bbab169
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33956950!8136014!33956950
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suck abstract from ncbi


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pmid33956950      Brief+Bioinform 2021 ; 22 (6): ä
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  • The peripheral and core regions of virus-host network of COVID-19 #MMPMID33956950
  • Wang B; Dong X; Hu J; Ma X; Han C; Wang Y; Gao L
  • Brief Bioinform 2021[Nov]; 22 (6): ä PMID33956950show ga
  • Two thousand nineteen novel coronavirus SARS-CoV-2, the pathogen of COVID-19, has caused a catastrophic pandemic, which has a profound and widespread impact on human lives and social economy globally. However, the molecular perturbations induced by the SARS-CoV-2 infection remain unknown. In this paper, from the perspective of omnigenic, we analyze the properties of the neighborhood perturbed by SARS-CoV-2 in the human interactome and disclose the peripheral and core regions of virus-host network (VHN). We find that the virus-host proteins (VHPs) form a significantly connected VHN, among which highly perturbed proteins aggregate into an observable core region. The non-core region of VHN forms a large scale but relatively low perturbed periphery. We further validate that the periphery is non-negligible and conducive to identifying comorbidities and detecting drug repurposing candidates for COVID-19. We particularly put forward a flower model for COVID-19, SARS and H1N1 based on their peripheral regions, and the flower model shows more correlations between COVID-19 and other two similar diseases in common functional pathways and candidate drugs. Overall, our periphery-core pattern can not only offer insights into interconnectivity of SARS-CoV-2 VHPs but also facilitate the research on therapeutic drugs.
  • |*Drug Repositioning[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |COVID-19/*genetics/pathology/virology[MESH]
  • |Host-Pathogen Interactions/genetics[MESH]
  • |Humans[MESH]
  • |Influenza A Virus, H1N1 Subtype/drug effects/pathogenicity[MESH]


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