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In our predictions, there are 39 genes that were predicted to be potential pathogenic genes.
Epitope or similarity analysis through Algpred (see materials and methods), revealed that 12 488%) of these presumably non-allergenic proteins were predicted to be potential allergens.
Several sites on YY1 were predicted to be potential phosphorylation sites for Plk1, and resembled previously reported Plk1 phosphorylation sites on other proteins [59], [66].
There are additional multiple 15 mer fragments that were predicted to be potential epitopes for HLA-DR.B1 molecule by SYFPEITHI algorithm as well (data not shown).
Many mRNAs have been predicted to be potential targets of miR-122, but only a few genes such as cationic amino acid transporter1 (cyclinG1yclinG1, or Smarcd1/Baf60a have been demonstrated to be bona fide targets [15], [22], [23], [24], [25].
In contrast, only a few genes were predicted to be potential targets of sRNA- Xcc2.
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MMP-13 has been predicted to be a potential target of miR-127-5p miR-127-5p miR-127-5p
As such, graphene has been widely predicted to be a potential material for post-complimentary metal-oxide semiconductor technology, particularly for use as ballistic transistors or interconnects [8 12].
Additionally, during latency, M. tuberculosis continues to be under oxidative stress; thus, the accumulation of mutations caused by oxidative DNA damage was predicted to be a potential risk for drug resistance (Ford et al., 2011).
Junctional adhesion molecule A (JAM-A) was predicted to be a potential target of miR-495 by bioinformatics analysis and was subsequently verified by luciferase assay and Western blotting.
Meanwhile, Ser 184 is predicted to be a potential site for MAP kinase kinase kinase, protein kinase A, and various protein kinase C isoforms.
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CEO of Professional Science Editing for Scientists @ prosciediting.com