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10.1128/JVI.00684-10

http://scihub22266oqcxt.onion/10.1128/JVI.00684-10
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20631151!2937825!20631151
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suck abstract from ncbi


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pmid20631151      J+Virol 2010 ; 84 (19): 9658-65
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  • Advances in human B19 erythrovirus biology #MMPMID20631151
  • Servant-Delmas A; Lefrere JJ; Morinet F; Pillet S
  • J Virol 2010[Oct]; 84 (19): 9658-65 PMID20631151show ga
  • Since its discovery, human parvovirus B19 (B19V), now termed erythrovirus, has been associated with many clinical situations (neurological and myocardium infections, persistent B19V DNAemia) in addition to the prototype clinical manifestations, i.e., erythema infectiosum and erythroblastopenia crisis. In 2002, the use of new molecular tools led to the characterization of three different genotypes of human B19 erythrovirus. Although the genomic organization is conserved, the geographic distribution of the different genotypes varies worldwide, and the nucleotidic divergences can impact the molecular diagnosis of B19 virus infection. The cell cycle of the virus remains partially unresolved; however, recent studies have shed light on the mechanism of cell entry and the interactions of B19V proteins with apoptosis pathways.
  • |Apoptosis[MESH]
  • |Genetic Variation[MESH]
  • |Host-Pathogen Interactions[MESH]
  • |Humans[MESH]
  • |Molecular Epidemiology[MESH]
  • |Parvoviridae Infections/epidemiology/*etiology/immunology/virology[MESH]
  • |Parvovirus B19, Human/*genetics/*pathogenicity/physiology/ultrastructure[MESH]
  • |Phylogeny[MESH]
  • |Virus Internalization[MESH]


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