The present invention provides methods of treatment of adenoviral mediated disease, improved methods for transducing cells with adenoviral and related vectors, and improved methods of gene therapy utilizing such methods.
申请公布号
WO03070256(A1)
申请公布日期
2003.08.28
申请号
WO2003US04571
申请日期
2003.02.14
申请人
RESEARCH DEVELOPMENT FOUNDATION;CHAUDHURI, SAUMYA, RAY;HURTWITZ, RICHARD, L.;HURWITZ, MARY, Y.;HOLCOMBE, VIEN;MARCUS, KAREN, T.
发明人
CHAUDHURI, SAUMYA, RAY;HURTWITZ, RICHARD, L.;HURWITZ, MARY, Y.;HOLCOMBE, VIEN;MARCUS, KAREN, T.
