Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector.
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Gene therapy for hemophiliaAdeno-associated viral vectors engineered for macrolide-adjustable transgene expression in mammalian cells and miceAnalysis of the role of von Willebrand factor, platelet glycoprotein VI-, and α2β1-mediated collagen binding in thrombus formation.Regulatable gutless adenovirus vectors sustain inducible transgene expression in the brain in the presence of an immune response against adenoviruses.Graded or threshold response of the tet-controlled gene expression: all depends on the concentration of the transactivator.Pathologic mechanisms of type 1 VWD mutations R1205H and Y1584C through in vitro and in vivo mouse models.Lentiviral vector-based insertional mutagenesis identifies genes associated with liver cancer.Hepcidin and Hfe in iron overload in beta-thalassemia.Phenotype reversion in fetal human liver epithelial cells identifies the role of an intermediate meso-endodermal stage before hepatic maturation.The antiproliferative ELF2 isoform, ELF2B, induces apoptosis in vitro and perturbs early lymphocytic development in vivoCancer gene discovery: exploiting insertional mutagenesis.A long term, non-tumorigenic rat hepatocyte cell line and its malignant counterpart, as tools to study hepatocarcinogenesis.Adeno-Associated Virus Gene Therapy for Liver Disease.The cancer-testis antigen BORIS phenocopies the tumor suppressor CTCF in normal and neoplastic cells.Overexpression of the lens epithelium-derived growth factor/p75 integrase binding domain inhibits human immunodeficiency virus replication.Regulated and multiple miRNA and siRNA delivery into primary cells by a lentiviral platform.The retroviral vector family: something for everyone.Tightly regulated 'all-in-one' lentiviral vectors for protection of human hematopoietic cells from anticancer chemotherapy.Gene transfer engineering for astrocyte-specific silencing in the CNS.Liver-directed lentiviral gene therapy in a dog model of hemophilia B.A microRNA-regulated and GP64-pseudotyped lentiviral vector mediates stable expression of FVIII in a murine model of Hemophilia A.Autoregulatory lentiviral vectors allow multiple cycles of doxycycline-inducible gene expression in human hematopoietic cells in vivo.
P2860
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P2860
Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
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2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
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2005年學術文章
@zh-hant
name
Efficient Tet-dependent expres ...... -regulating lentiviral vector.
@en
type
label
Efficient Tet-dependent expres ...... -regulating lentiviral vector.
@en
prefLabel
Efficient Tet-dependent expres ...... -regulating lentiviral vector.
@en
P2093
P50
P1433
P1476
Efficient Tet-dependent expres ...... -regulating lentiviral vector.
@en
P2093
Andrew D Simmons
Elisa Vigna
Fabrizio Benedicenti
P304
P356
10.1016/J.YMTHE.2004.11.017
P577
2005-05-01T00:00:00Z