Abstract
Human adenoviruses are divided into at least three
subgroups on the basis of their oncogenicity in hamsters:
subgroup A containing highly oncogenic viruses, subgroup B weakly oncogenic viruses, and subgroup C (most of the)
nononcogenic viruses. Despite these clear
distinctions in oncogenic activity among the three sugroups,
all human adenoviruses are capable of transforming cultured
cells
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