Modification of the genetic program of human alveolar macrophages by adenovirus vectors in vitro is feasible but inefficient, limited in part by the low level of expression of the coxsackie/adenovirus receptor

American Journal of Respiratory Cell and Molecular Biology

Volumn 20, Issue 3, 1999, Pages 361-370

  Kaner, Robert J ^a   Worgall, Stefan ^b   Leopold, Philip L ^b   Stolze, Eric ^b   Milano, Eric ^b   Hidaka, Chisa ^b   Ramalingam, Ramu ^b   Hackett, Neil R ^b   Singh, Ravi ^b   Bergelson, Jeffrey ^b   Finberg, Robert ^b   Falck Pedersen, Erik ^b   Crystal, Ronald G ^b  

^a WEILL CORNELL MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADENOVIRIDAE; COXSACKIEVIRUS; HUMAN IMMUNODEFICIENCY VIRUS; MIRIDAE;

BETA GALACTOSIDASE; CAR RECEPTOR; GAMMA INTERFERON; GREEN FLUORESCENT PROTEIN; MESSENGER RNA; PHOTOPROTEIN; VIRUS RECEPTOR;

ADENOVIRUS; ARTICLE; BIOSYNTHESIS; ENTEROVIRUS; GENE TRANSFER; GENE VECTOR; GENETICS; HUMAN; LUNG ALVEOLUS MACROPHAGE; VIROLOGY;

ADENOVIRIDAE; BETA-GALACTOSIDASE; ENTEROVIRUS; GENE TRANSFER TECHNIQUES; GENETIC VECTORS; GREEN FLUORESCENT PROTEINS; HUMANS; INTERFERON TYPE II; LUMINESCENT PROTEINS; MACROPHAGES, ALVEOLAR; RECEPTORS, VIRUS; RNA, MESSENGER;

EID: 0033094833     PISSN: 10441549     EISSN: None     Source Type: Journal    
DOI: 10.1165/ajrcmb.20.3.3398     Document Type: Article

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