IRIS
CANTORE, ALESSIO
 Distribuzione geografica
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Continente #
NA - Nord America 167
EU - Europa 154
AS - Asia 22
SA - Sud America 1
Totale 344
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Nazione #
US - Stati Uniti d'America 167
SE - Svezia 103
IT - Italia 33
CN - Cina 15
DE - Germania 5
IE - Irlanda 5
FI - Finlandia 4
JP - Giappone 4
ES - Italia 3
SG - Singapore 2
AR - Argentina 1
CH - Svizzera 1
HK - Hong Kong 1
Totale 344
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Città #
Ashburn 36
Lawrence 21
Princeton 21
New York 20
Shanghai 15
Los Angeles 8
Milan 6
Dublin 5
Washington 5
Helsinki 4
Ancona 3
Arezzo 2
Barcelona 2
Bologna 2
Clusone 2
Florence 2
Genoa 2
Gunzenhausen 2
Nerviano 2
Rome 2
Borås 1
Brugherio 1
Chiaravalle 1
Fontana 1
Frankfurt am Main 1
Genova 1
Hanover 1
La Plata 1
Molina de Segura 1
Piemonte 1
Redwood City 1
Seattle 1
Segrate 1
Tokyo 1
Viadana 1
Zurich 1
Totale 178
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Nome #
Dynamics and genomic landscape of CD8+ T cells undergoing hepatic priming 28
Laboratory-Scale Lentiviral Vector Production and Purification for Enhanced Ex Vivo and In Vivo Genetic Engineering 25
A microRNA-regulated lentiviral vector mediates stable correction of hemophilia B mice 22
Site-specific integration and tailoring of cassette design for sustainable gene transfer 22
Phagocytosis-shielded lentiviral vectors improve liver gene therapy in nonhuman primates 19
In vivo Gene Therapy to the Liver and Nervous System: Promises and Challenges 16
ENDOGENOUS MICRORNA CAN BE BROADLY EXPLOITED TO REGULATE TRANSGENE EXPRESSION ACCORDING TO TISSUE, LINEAGE AND DIFFERENTIATION STATE 16
In vivo delivery of a microRNA-regulated transgene induces antigen-specific regulatory T cells and promotes immunologic tolerance 15
WFH State-of-the-art paper 2020: In vivo lentiviral vector gene therapy for haemophilia 15
Genome editing for scalable production of alloantigen-free lentiviral vectors for in vivo gene therapy 15
Retrieval of vector integration sites from cell-free DNA 15
Liver-directed lentiviral gene therapy in a dog model of hemophilia B 14
Targeting Integration to Selected Genomic Loci and In Situ Tailoring of Cassette Design Allows Robust Transgene Expression without Perturbing Endogenous Transcription 13
Mouse Models To Assess the Risk of Vector Insertional Mutagenesis upon Systemic Delivery 13
Hyperfunctional coagulation factor IX improves the efficacy of gene therapy in hemophilic mice 13
Insulin B chain 9-23 gene transfer to hepatocytes protects from type 1 diabetes by inducing Ag-specific FoxP3+ Tregs 12
Liver gene therapy by lentiviral vectors reverses anti-factor IX pre-existing immunity in haemophilic mice 12
Modulation of immune responses in lentiviral vector-mediated gene transfer 12
Therapeutic liver repopulation by transient acetaminophen selection of gene-modified hepatocytes 12
Liver-directed lentiviral gene therapy corrects hemophilia A mice and achieves normal-range factor VIII activity in non-human primates 11
In vivo generation of CAR T cells in the presence of human myeloid cells 11
Hepatocyte-targeted expression by integrase-defective lentiviral vectors induces antigen-specific tolerance in mice with low genotoxic risk. 11
Regenerative medicine: the red planet for clinicians 11
In vitro differentiation of human Mesenchymal Stem Cells from various sources 9
In vivo models to assess the risk of insertional mutagenesis in the liver upon vector systemic delivery 8
Isolation and in vitro differentiation of human Mesenchymal Stem Cells from new alternative sources: fetal membranes and placenta 8
LSpECifying transgene expression 3
GP64-pseudotyped lentiviral vectors target liver endothelial cells and correct hemophilia A mice 1
Totale 382
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Categoria #
all - tutte 4.474
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 4.474
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205 1 0 0 2 1 0 0 0 0 1 0 0
2020/202111 0 0 0 2 3 5 1 0 0 0 0 0
2021/202239 0 0 0 18 4 1 4 2 1 0 3 6
2022/2023164 48 38 16 7 2 26 7 8 4 3 5 0
2023/2024154 1 3 35 35 15 29 8 16 3 8 1 0
Totale 382