Comparing Viral Vectors for Gene Therapy Delivery: AAV and lentivirus both have pros and cons in their use for specific gene therapy applications.

Detalles Bibliográficos
Publicado en:BioPharm International Vol. 37; no. 7; pp. 10 - 13
Autor principal: MIRASOL, FELIZA
Formato: pictorial Journal Article
Publicado: MJH Life Sciences Jul/Aug2024
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=179074685&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 179074685
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        1542166X
        5NE
      jtl: BioPharm International
      issn: 1542166X
      maglogo: N
    pubinfo:
      dt: Jul/Aug2024
      vid: 37
      iid: 7
      pid: 54670
      pub: MJH Life Sciences
      place: Cranbury, New Jersey
    artinfo:
      ui:
        179074685
        179074685
        179074685
        179074685
      ppf: 10
      ppct: 3
      formats:
        fmt:
          @attributes:
            type: P
      tig:
        atl: Comparing Viral Vectors for Gene Therapy Delivery: AAV and lentivirus both have pros and cons in their use for specific gene therapy applications.
      aug:
        au: MIRASOL, FELIZA
      sug:
        subj:
          Gene Therapy Methods
          DNA Viruses
          Retroviruses
          Treatment Outcomes
          Genetic Engineering Methods
          Immunogenicity, Vaccine
          Carrier Proteins Physiology
          Genomics
          Gene Expression
      pubtype: Trade Publication
      doctype:
        pictorial
        Journal Article
      ougenre: Article
      ab:
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N