about
Correction of mucopolysaccharidosis type IIIb fibroblasts by lentiviral vector-mediated gene transferHepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic miceDopamine-modified alpha-synuclein blocks chaperone-mediated autophagyRepressor element-1 silencing transcription factor (REST)-dependent epigenetic remodeling is critical to ischemia-induced neuronal deathMicroautophagy of cytosolic proteins by late endosomesTransplanted endothelial cells repopulate the liver endothelium and correct the phenotype of hemophilia A miceCardiomyocytes induce endothelial cells to trans-differentiate into cardiac muscle: implications for myocardium regeneration.Lentivectors encoding immunosuppressive proteins genetically engineer pancreatic beta-cells to correct diabetes in allogeneic mice.Mechanism of anion selectivity and stoichiometry of the Na+/I- symporter (NIS).Lentiviral vector-mediated gene transfer in T cells from Wiskott-Aldrich syndrome patients leads to functional correction.Immune responses to lentiviral vectors.Secretion of the adipocyte-specific secretory protein adiponectin critically depends on thiol-mediated protein retention.Role of bone marrow transplantation for correcting hemophilia A in mice.Hepatocyte growth factor induces proliferation and differentiation of multipotent and erythroid hemopoietic progenitors.Lentiviral vectors encoding human immunodeficiency virus type 1 (HIV-1)-specific T-cell receptor genes efficiently convert peripheral blood CD8 T lymphocytes into cytotoxic T lymphocytes with potent in vitro and in vivo HIV-1-specific inhibitory actDendritic cell-mediated in vivo bone resorption.Isolation and characterization of a spontaneously immortalized multipotent mesenchymal cell line derived from mouse subcutaneous adipose tissueEphrinB reverse signaling contributes to endothelial and mural cell assembly into vascular structures.Hepatocyte transplantation-induced liver inflammation is driven by cytokines-chemokines associated with neutrophils and Kupffer cells.Deletion in a (T)8 microsatellite abrogates expression regulation by 3'-UTR.Monophasic and biphasic electrical stimulation induces a precardiac differentiation in progenitor cells isolated from human heart.Lentiviral vector interactions with the host cell.Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia.Annexin A2 binds to endosomes following organelle destabilization by particulate wear debris.T cell receptor (TCR) gene transfer with lentiviral vectors allows efficient redirection of tumor specificity in naive and memory T cells without prior stimulation of endogenous TCR.Deletion of the ectodomain unleashes the transforming, invasive, and tumorigenic potential of the MET oncogene.Lentivirus-mediated superoxide dismutase1 gene delivery protects against oxidative stress-induced liver injury in mice.Role of MAPK phosphatase-1 in sustained activation of JNK during ethanol-induced apoptosis in hepatocyte-like VL-17A cells.Ex vivo gene therapy with lentiviral vectors rescues adenosine deaminase (ADA)-deficient mice and corrects their immune and metabolic defects.Stability of lentiviral vector-mediated transgene expression in the brain in the presence of systemic antivector immune responses.Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector.RNAi technology and lentiviral delivery as a powerful tool to suppress Tpr-Met-mediated tumorigenesis.'Advanced' generation lentiviruses as efficient vectors for cardiomyocyte gene transduction in vitro and in vivo.Extrahepatic sources of factor VIII potentially contribute to the coagulation cascade correcting the bleeding phenotype of mice with hemophilia A.The endogenous inhibitor of Akt, CTMP, is critical to ischemia-induced neuronal death.Generation of β cell-specific human cytotoxic T cells by lentiviral transduction and their survival in immunodeficient human leucocyte antigen-transgenic mice.Treatment of the mouse model of mucopolysaccharidosis type IIIB with lentiviral-NAGLU vector.Lentiviral transduction of primary myeloma cells with CD80 and CD154 generates antimyeloma effector T cells.Targeting lentiviral vector expression to hepatocytes limits transgene-specific immune response and establishes long-term expression of human antihemophilic factor IX in mice.Efficient gene delivery and targeted expression to hepatocytes in vivo by improved lentiviral vectors.
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description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
@hy
name
Antonia Follenzi
@ast
Antonia Follenzi
@en
Antonia Follenzi
@es
Antonia Follenzi
@nl
Antonia Follenzi
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type
label
Antonia Follenzi
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Antonia Follenzi
@en
Antonia Follenzi
@es
Antonia Follenzi
@nl
Antonia Follenzi
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prefLabel
Antonia Follenzi
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Antonia Follenzi
@en
Antonia Follenzi
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Antonia Follenzi
@nl
Antonia Follenzi
@sl
P106
P1153
6601914918
P21
P31
P496
0000-0001-9780-300X