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10.1038/s41598-021-90556-1

http://scihub22266oqcxt.onion/10.1038/s41598-021-90556-1
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34045524!8160150!34045524
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suck abstract from ncbi


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pmid34045524      Sci+Rep 2021 ; 11 (1): 11241
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  • Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection #MMPMID34045524
  • Tanaka Y; Higashihara K; Nakazawa MA; Yamashita F; Tamada Y; Okuno Y
  • Sci Rep 2021[May]; 11 (1): 11241 PMID34045524show ga
  • The current pandemic of SARS-CoV-2 has caused extensive damage to society. The characterization of SARS-CoV-2 profiles has been addressed by researchers globally with the aim of resolving this disruptive crisis. This investigation process is indispensable to understand how SARS-CoV-2 behaves in human host cells. However, little is known about the systematic molecular mechanisms involved in the effects of SARS-CoV-2 infection on human host cells. Here, we present gene-to-gene regulatory networks in response to SARS-CoV-2 using a Bayesian network. We examined the dynamic changes in the SARS-CoV-2-purturbated networks established by our proposed framework for gene network analysis, thus revealing that interferon signaling gradually switched to the subsequent inflammatory cytokine signaling cascades. Furthermore, we succeeded in capturing a COVID-19 patient-specific network in which transduction of these signals was concurrently induced. This enabled us to explore the local regulatory systems influenced by SARS-CoV-2 in host cells more precisely at an individual level. Our panel of network analyses has provided new insights into SARS-CoV-2 research from the perspective of cellular systems.
  • |*Gene Regulatory Networks[MESH]
  • |Bayes Theorem[MESH]
  • |COVID-19/genetics/*metabolism/virology[MESH]
  • |Cell Line[MESH]
  • |Computational Biology[MESH]
  • |Databases, Genetic[MESH]
  • |Humans[MESH]
  • |RNA-Seq[MESH]
  • |SARS-CoV-2/genetics/*metabolism[MESH]
  • |Signal Transduction/*genetics[MESH]


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