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- W3119143802 abstract "Abstract Background: Our aim is to compute NCAPH and RFC4 subnetworks containing CDKN3 (feedback) for the novel molecular and cellular mechanisms of HCC (HBV or HCV) related cancer development from high UNG-activated upstream network. Methods: Non-SMC condensin I complex subunit H (NCAPH) and replication factor C subunit 4 (RFC4) common molecular and knowledge subnetworks containing cyclin-dependent kinase inhibitor 3-CDKN3 (feedback) related to cancer by references were identified in HCC (HBV or HCV), based on our established significant high expression uracil DNA glycosylase (UNG)-activated upstream Gene (protein) reconstruction network inference (GRNInfer) and Database for Annotation, Visualization and Integrated Discovery (DAVID). Results: Our results show the common molecules MAPT interaction with CDKN3 with RRM2 with HIST1H3H from UNG-activated upstream GRNInfer database; The common biological process and molecular function of MAPT as microtubule binding; HIST1H3H as cellular protein metabolic process from UNG-activated upstream DAVID database; The common cellular component of UNG, NCAPH, CDKN3, RRM2, HIST1H3H at nucleus; NCAPH, HIST1H3H at membrane; The common tissue distributions of NCAPH and RFC4 in Leukemiapromyelocytic(hl60), leukemialymphoblastic(molt4), etc. Conclusions: We propose and mutual positively verify membrane protein metabolism in UNG-activated NCAPH and RFC4 subnetworks for viral HCC|blood cancer development via inside-out microtubule binding." @default.
- W3119143802 created "2021-01-18" @default.
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- W3119143802 date "2020-08-28" @default.
- W3119143802 modified "2023-09-26" @default.
- W3119143802 title "Membrane Protein Metabolism in UNG-Activated NCAPH and RFC4 Subnetworks for Viral HCC|blood Cancer Development Via Inside-Out Microtubule Binding" @default.
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- W3119143802 doi "https://doi.org/10.21203/rs.3.rs-66105/v1" @default.
- W3119143802 hasPublicationYear "2020" @default.
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