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Palabras clave – provistas por la editorial

human cytomegalovirus; core nuclear egress complex; ORF-UL50 deletion; pUL50 phosphosite mutants; phenotypical changes; differential functional relevance; Epstein–Barr virus; BGLF4 kinase; nuclear egress; BFRF1; nuclear envelope modulation; herpesviruses; primary envelopment; de-envelopment; herpesvirus; pseudorabies virus; PrV; vesicle-associated membrane protein associated protein; VAPA; VAPB; CRISPR/Cas9 genome editing; enveloped virus budding; ESCRT; membrane scission; HSV1; pUL34; pUL31; NEC; targeting integral membrane proteins; TA membrane proteins; inner nuclear membrane (INM); nuclear import; importins; n/a; CMV; peptide therapy; tegument; phosphorylation; nuclear envelopment complex; membrane fusion; hemi-fusion; virus assembly; virus–cell interactions; capsid migration; UL53; UL50; myosin Va; major capsid protein; mass spectrometry; virus genetics; complementing cells; null mutants