Lista de obras - Antonia Follenzi - Dominio Público Uruguay

'Advanced' generation lentiviruses as efficient vectors for cardiomyocyte gene transduction in vitro and in vivo.

artículo científico publicado en 2003

A human immunodeficiency virus type 1 pol gene-derived sequence (cPPT/CTS) increases the efficiency of transduction of human nondividing monocytes and T lymphocytes by lentiviral vectors

artículo científico publicado en 2002

A sustainable one-pot method to transform seashell waste calcium carbonate to osteoinductive hydroxyapatite micro-nanoparticles

artículo científico publicado en 2023

Annexin A2 binds to endosomes following organelle destabilization by particulate wear debris.

artículo científico publicado en 2012

Author Correction: Insulin-producing organoids engineered from islet and amniotic epithelial cells to treat diabetes

scientific article published on 09 October 2020

Axons mediate the distribution of arylsulfatase A within the mouse hippocampus upon gene delivery.

artículo científico publicado en 2005

Biological Activation of pro-HGF (Hepatocyte Growth Factor) by Urokinase Is Controlled by a Stoichiometric Reaction

artículo científico publicado en 1995

Cardiomyocytes induce endothelial cells to trans-differentiate into cardiac muscle: implications for myocardium regeneration

artículo científico publicado en 2001

Correction of mucopolysaccharidosis type IIIb fibroblasts by lentiviral vector-mediated gene transfer

artículo científico publicado en 2002

Deletion in a (T)8 microsatellite abrogates expression regulation by 3'-UTR.

artículo científico publicado en 2003

Deletion of the ectodomain unleashes the transforming, invasive, and tumorigenic potential of the MET oncogene

artículo científico publicado en 2009

Dendritic cell-mediated in vivo bone resorption.

artículo científico publicado en 2010

Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia

artículo científico publicado en 2014

Dopamine-modified alpha-synuclein blocks chaperone-mediated autophagy

artículo científico publicado en 2008

Efficiency of onco-retroviral and lentiviral gene transfer into primary mouse and human B-lymphocytes is pseudotype dependent

artículo científico publicado en 2003

Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector

artículo científico publicado en 2005

Efficient gene delivery and targeted expression to hepatocytes in vivo by improved lentiviral vectors

artículo científico publicado en 2002

EphrinB reverse signaling contributes to endothelial and mural cell assembly into vascular structures.

artículo científico publicado en 2009

Ex vivo gene therapy with lentiviral vectors rescues adenosine deaminase (ADA)-deficient mice and corrects their immune and metabolic defects

artículo científico publicado en 2006

Extrahepatic sources of factor VIII potentially contribute to the coagulation cascade correcting the bleeding phenotype of mice with hemophilia A.

artículo científico publicado en 2015

Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

artículo científico publicado en 2000

Generation of β cell-specific human cytotoxic T cells by lentiviral transduction and their survival in immunodeficient human leucocyte antigen-transgenic mice

artículo científico publicado en 2015

Hepatic targeting of transplanted liver sinusoidal endothelial cells in intact mice

artículo científico publicado en 2005

Hepatocyte growth factor induces proliferation and differentiation of multipotent and erythroid hemopoietic progenitors.

artículo científico publicado en 1994

Hepatocyte transplantation-induced liver inflammation is driven by cytokines-chemokines associated with neutrophils and Kupffer cells.

artículo científico publicado en 2009

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice

artículo científico publicado en 2010

Immune responses to lentiviral vectors.

artículo científico publicado en 2007

In vitro gene therapy of mucopolysaccharidosis type I by lentiviral vectors

artículo científico publicado en 2002

Insulin-producing organoids engineered from islet and amniotic epithelial cells to treat diabetes

artículo científico publicado en 2019

Isolation and characterization of a spontaneously immortalized multipotent mesenchymal cell line derived from mouse subcutaneous adipose tissue

artículo científico publicado en 2013

Lentivectors encoding immunosuppressive proteins genetically engineer pancreatic beta-cells to correct diabetes in allogeneic mice.

artículo científico publicado en 2008

Lentiviral transduction of primary myeloma cells with CD80 and CD154 generates antimyeloma effector T cells

artículo científico publicado en 2005

Lentiviral vector interactions with the host cell

artículo científico publicado en 2016

Lentiviral vector-mediated gene transfer in T cells from Wiskott-Aldrich syndrome patients leads to functional correction.

artículo científico publicado en 2004

Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivo

artículo científico publicado en 2002

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 act

artículo científico publicado en 2008

Lentivirus-mediated superoxide dismutase1 gene delivery protects against oxidative stress-induced liver injury in mice

artículo científico publicado en 2007

Mechanism of anion selectivity and stoichiometry of the Na+/I- symporter (NIS).

artículo científico publicado en 2011

Microautophagy of Cytosolic Proteins by Late Endosomes

Microautophagy of cytosolic proteins by late endosomes

scientific journal article

Monophasic and biphasic electrical stimulation induces a precardiac differentiation in progenitor cells isolated from human heart.

artículo científico publicado en 2014

Mouse hepatocytes and LSEC proteome reveal novel mechanisms of ischemia/reperfusion damage and protection by A2aR stimulation.

artículo científico publicado en 2014

Multiparameter flow cytometric detection and quantification of senescent cells in vitro

artículo científico publicado en 2020

Nrf2, but not β-catenin, mutation represents an early event in rat hepatocarcinogenesis.

artículo científico publicado en 2015

Pharmacological postconditioning protects against hepatic ischemia/reperfusion injury

artículo científico publicado en 2011

RNAi technology and lentiviral delivery as a powerful tool to suppress Tpr-Met-mediated tumorigenesis.

artículo científico publicado en 2005

Repressor element-1 silencing transcription factor (REST)-dependent epigenetic remodeling is critical to ischemia-induced neuronal death

artículo científico publicado en 2012

Role of MAPK phosphatase-1 in sustained activation of JNK during ethanol-induced apoptosis in hepatocyte-like VL-17A cells

artículo científico publicado en 2007

Role of bone marrow transplantation for correcting hemophilia A in mice

artículo científico publicado en 2012

Secretion of the adipocyte-specific secretory protein adiponectin critically depends on thiol-mediated protein retention.

artículo científico publicado en 2007

Stability of lentiviral vector-mediated transgene expression in the brain in the presence of systemic antivector immune responses

artículo científico publicado en 2005

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.

artículo científico publicado en 2009

Targeting lentiviral vector expression to hepatocytes limits transgene-specific immune response and establishes long-term expression of human antihemophilic factor IX in mice

artículo científico publicado en 2003

The MET oncogene drives a genetic programme linking cancer to haemostasis

artículo científico publicado en 2005

The endogenous inhibitor of Akt, CTMP, is critical to ischemia-induced neuronal death

artículo científico publicado en 2009

The immune response to lentiviral-delivered transgene is modulated in vivo by transgene-expressing antigen-presenting cells but not by CD4+CD25+ regulatory T cells.

artículo científico publicado en 2007

The promise of lentiviral gene therapy for liver cancer

artículo científico publicado en 2004

Transplantation of endothelial cells corrects the phenotype in hemophilia A mice

artículo científico publicado en 2005

Transplanted endothelial cells repopulate the liver endothelium and correct the phenotype of hemophilia A mice

artículo científico publicado en 2008

Treatment of the mouse model of mucopolysaccharidosis type IIIB with lentiviral-NAGLU vector

artículo científico publicado en 2005

[26] Generation of HIV-1 derived lentiviral vectors

article

Lista de obras de Antonia Follenzi

'Advanced' generation lentiviruses as efficient vectors for cardiomyocyte gene transduction in vitro and in vivo.

A human immunodeficiency virus type 1 pol gene-derived sequence (cPPT/CTS) increases the efficiency of transduction of human nondividing monocytes and T lymphocytes by lentiviral vectors

A sustainable one-pot method to transform seashell waste calcium carbonate to osteoinductive hydroxyapatite micro-nanoparticles

Annexin A2 binds to endosomes following organelle destabilization by particulate wear debris.

Author Correction: Insulin-producing organoids engineered from islet and amniotic epithelial cells to treat diabetes

Axons mediate the distribution of arylsulfatase A within the mouse hippocampus upon gene delivery.

Biological Activation of pro-HGF (Hepatocyte Growth Factor) by Urokinase Is Controlled by a Stoichiometric Reaction

Cardiomyocytes induce endothelial cells to trans-differentiate into cardiac muscle: implications for myocardium regeneration

Correction of mucopolysaccharidosis type IIIb fibroblasts by lentiviral vector-mediated gene transfer

Deletion in a (T)8 microsatellite abrogates expression regulation by 3'-UTR.

Deletion of the ectodomain unleashes the transforming, invasive, and tumorigenic potential of the MET oncogene

Dendritic cell-mediated in vivo bone resorption.

Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia

Dopamine-modified alpha-synuclein blocks chaperone-mediated autophagy

Efficiency of onco-retroviral and lentiviral gene transfer into primary mouse and human B-lymphocytes is pseudotype dependent

Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector

Efficient gene delivery and targeted expression to hepatocytes in vivo by improved lentiviral vectors

EphrinB reverse signaling contributes to endothelial and mural cell assembly into vascular structures.

Ex vivo gene therapy with lentiviral vectors rescues adenosine deaminase (ADA)-deficient mice and corrects their immune and metabolic defects

Extrahepatic sources of factor VIII potentially contribute to the coagulation cascade correcting the bleeding phenotype of mice with hemophilia A.

Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

Generation of β cell-specific human cytotoxic T cells by lentiviral transduction and their survival in immunodeficient human leucocyte antigen-transgenic mice

Hepatic targeting of transplanted liver sinusoidal endothelial cells in intact mice

Hepatocyte growth factor induces proliferation and differentiation of multipotent and erythroid hemopoietic progenitors.

Hepatocyte transplantation-induced liver inflammation is driven by cytokines-chemokines associated with neutrophils and Kupffer cells.

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice

Immune responses to lentiviral vectors.

In vitro gene therapy of mucopolysaccharidosis type I by lentiviral vectors

Insulin-producing organoids engineered from islet and amniotic epithelial cells to treat diabetes

Isolation and characterization of a spontaneously immortalized multipotent mesenchymal cell line derived from mouse subcutaneous adipose tissue

Lentivectors encoding immunosuppressive proteins genetically engineer pancreatic beta-cells to correct diabetes in allogeneic mice.

Lentiviral transduction of primary myeloma cells with CD80 and CD154 generates antimyeloma effector T cells

Lentiviral vector interactions with the host cell

Lentiviral vector-mediated gene transfer in T cells from Wiskott-Aldrich syndrome patients leads to functional correction.

Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivo

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 act

Lentivirus-mediated superoxide dismutase1 gene delivery protects against oxidative stress-induced liver injury in mice

Mechanism of anion selectivity and stoichiometry of the Na+/I- symporter (NIS).

Microautophagy of Cytosolic Proteins by Late Endosomes

Microautophagy of cytosolic proteins by late endosomes

Monophasic and biphasic electrical stimulation induces a precardiac differentiation in progenitor cells isolated from human heart.

Mouse hepatocytes and LSEC proteome reveal novel mechanisms of ischemia/reperfusion damage and protection by A2aR stimulation.

Multiparameter flow cytometric detection and quantification of senescent cells in vitro

Nrf2, but not β-catenin, mutation represents an early event in rat hepatocarcinogenesis.

Pharmacological postconditioning protects against hepatic ischemia/reperfusion injury

RNAi technology and lentiviral delivery as a powerful tool to suppress Tpr-Met-mediated tumorigenesis.

Repressor element-1 silencing transcription factor (REST)-dependent epigenetic remodeling is critical to ischemia-induced neuronal death

Role of MAPK phosphatase-1 in sustained activation of JNK during ethanol-induced apoptosis in hepatocyte-like VL-17A cells

Role of bone marrow transplantation for correcting hemophilia A in mice

Secretion of the adipocyte-specific secretory protein adiponectin critically depends on thiol-mediated protein retention.

Stability of lentiviral vector-mediated transgene expression in the brain in the presence of systemic antivector immune responses

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.

Targeting lentiviral vector expression to hepatocytes limits transgene-specific immune response and establishes long-term expression of human antihemophilic factor IX in mice

The MET oncogene drives a genetic programme linking cancer to haemostasis

The endogenous inhibitor of Akt, CTMP, is critical to ischemia-induced neuronal death

The immune response to lentiviral-delivered transgene is modulated in vivo by transgene-expressing antigen-presenting cells but not by CD4+CD25+ regulatory T cells.

The promise of lentiviral gene therapy for liver cancer

Transplantation of endothelial cells corrects the phenotype in hemophilia A mice

Transplanted endothelial cells repopulate the liver endothelium and correct the phenotype of hemophilia A mice

Treatment of the mouse model of mucopolysaccharidosis type IIIB with lentiviral-NAGLU vector

[26] Generation of HIV-1 derived lentiviral vectors