> top > docs > PMC:7712180 > spans > 25938-27023 > annotations

PMC:7712180 / 25938-27023 JSONTXT

Annnotations TAB JSON ListView MergeView

LitCovid-PubTator

Id Subject Object Predicate Lexical cue tao:has_database_id
909 570-577 Gene denotes α2,3Sia Gene:170589
910 582-589 Gene denotes α2,6Sia Gene:170589
911 737-744 Gene denotes α2,3Sia Gene:170589
912 749-756 Gene denotes α2,6Sia Gene:170589
913 706-708 Gene denotes α2 Gene:170589
914 247-249 Gene denotes α2 Gene:170589
915 236-241 Species denotes human Tax:9606
916 512-519 Gene denotes α2,6Sia Gene:170589
917 449-456 Gene denotes α2,6Sia Gene:170589
918 500-502 Gene denotes α2 Gene:170589
919 52-67 Disease denotes virus infection MESH:D001102
920 810-826 Disease denotes bronchopneumonia MESH:D001996
921 831-856 Disease denotes gastrointestinal symptoms MESH:D012817

LitCovid-sentences

Id Subject Object Predicate Lexical cue
T153 0-68 Sentence denotes Receptor binding specificity determines the site of virus infection.
T154 69-268 Sentence denotes It appears that wild-type influenza B/Victoria HAs possessing G141, R162 and D196 [67] and B/Yamagata HAs with F95 and N194 [68] clearly exhibit binding preference to human-type α2,6Neu5Ac receptors.
T155 269-714 Sentence denotes Investigation of receptor binding preference of IBV clinical isolates in Taiwan during the period from 2001 to 2007 (Table 1) revealed that (i) 83% of Yamagata-like strains prefer α2,6Sia receptors, whereas 17% of them prefer both α2,3Sia and α2,6Sia and (ii) 54% of Victoria-like strains prefer both α2,3Sia and α2,6Sia, whereas 25% of them prefer sulfated glycan, either β-Gal-3-sulfate or 6-HSO3-Galβ1,4GlcNAc, and 21% of them prefer α2,6Sia.
T156 715-862 Sentence denotes The viruses with dual α2,3Sia and α2,6Sia-binding preferences were shown to be associated with bronchopneumonia and gastrointestinal symptoms [66].
T157 863-1085 Sentence denotes These findings indicate that the evolution of receptor binding specificity in IBVs in circulation is different from that in IAVs and indicate tissue tropism and pathogenicity of IBVs, possibly affecting virus transmission.