IRIS
NALDINI, LUIGI
 Distribuzione geografica
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Continente #
EU - Europa 75
NA - Nord America 9
AS - Asia 4
SA - Sud America 1
Totale 89
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Nazione #
IT - Italia 42
FR - Francia 17
US - Stati Uniti d'America 9
UA - Ucraina 5
NL - Olanda 3
CZ - Repubblica Ceca 2
DE - Germania 2
GB - Regno Unito 2
JP - Giappone 2
BR - Brasile 1
CH - Svizzera 1
CN - Cina 1
IE - Irlanda 1
LB - Libano 1
Totale 89
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Città #
Milan 30
Ancona 4
Ashburn 3
Torino 3
Amsterdam 2
Council Bluffs 2
Frankfurt am Main 2
Tappahannock 2
Beirut 1
Bergamo 1
Brasília 1
Chiaravalle 1
Dublin 1
Hayes 1
Newcastle upon Tyne 1
Paris 1
Portland 1
Shanghai 1
Totale 58
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Nome #
Dynamics and genomic landscape of CD8+ T cells undergoing hepatic priming, file e0c35a4d-0b7c-5883-e053-d805fe0ac580 29
Gene-Based Immune Reprogramming Overcomes the Immunosuppressive Microenvironment of Liver Metastases and Enables Protective T Cell Responses, file 3d9b77a3-3f40-4da6-9c68-06114dd92459 15
Multiple Integrated Non-clinical Studies Predict the Safety of Lentivirus-Mediated Gene Therapy for β-Thalassemia, file e0c35a4c-756d-5883-e053-d805fe0ac580 9
Lentiviral haemopoietic stem-cell gene therapy in early-onset metachromatic leukodystrophy: an ad-hoc analysis of a non-randomised, open-label, phase 1/2 trial, file e0c35a4b-ec6a-5883-e053-d805fe0ac580 4
The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection, file e0c35a4c-06ec-5883-e053-d805fe0ac580 4
Genotoxic effects of base and prime editing in human hematopoietic stem cells, file 875b53f3-c96f-4a41-bc79-8beab1e66d68 3
In vivo macrophage engineering reshapes the tumor microenvironment leading to eradication of liver metastases, file 2841e4b7-3865-41ec-9363-7fead5d703ed 2
Mesenchymal stromal cells improve the transplantation outcome of CRISPR-Cas9 gene-edited human HSPCs., file 2eddc1f6-8752-4afa-859c-66baed9b536d 2
Integration of Retroviral Vector Induces Minor Changes in the Transcriptional Activity of T Cells from ADA-SCID Patients Treated with Gene Therapy, file e0c35a4c-5a85-5883-e053-d805fe0ac580 2
Lentiviral haematopoietic stem-cell gene therapy for early-onset metachromatic leukodystrophy: long-term results from a non-randomised, open-label, phase 1/2 trial and expanded access, file e0c35a4c-f8c1-5883-e053-d805fe0ac580 2
Ensuring a future for gene therapy for rare diseases, file 18cbbfaf-3faf-4464-9336-2b6d250390e6 1
Hematopoietic stem-and progenitor-cell gene therapy for hurler syndrome, file 5cf84237-3871-4e7a-a50b-2d161a1838d9 1
TIE2-Expressing Macrophages Limit the Therapeutic Efficacy of the Vascular Disrupting Agent, Combretastatin A4 Phosphate, file e0c35a4b-d7b2-5883-e053-d805fe0ac580 1
In Vivo Tracking of Human Hematopoiesis Reveals Patterns of Clonal Dynamics during Early and Steady-State Reconstitution Phases, file e0c35a4b-de5a-5883-e053-d805fe0ac580 1
Lentiviral-mediated gene therapy leads to improvement of B-cell functionality in a murine model of Wiskott-Aldrich syndrome, file e0c35a4b-df49-5883-e053-d805fe0ac580 1
Integration of Retroviral Vector Induces Minor Changes in the Transcriptional Activity of T Cells from ADA-SCID Patients Treated with Gene Therapy, file e0c35a4b-e321-5883-e053-d805fe0ac580 1
Preclinical safety and efficacy of human CD34(+) cells transduced with lentiviral vector for the treatment of Wiskott-Aldrich syndrome., file e0c35a4b-e7a7-5883-e053-d805fe0ac580 1
Editing T cell specificity towards leukemia by zinc finger nucleases and lentiviral gene transfer, file e0c35a4b-ead2-5883-e053-d805fe0ac580 1
Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy, file e0c35a4b-f636-5883-e053-d805fe0ac580 1
Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy, file e0c35a4b-f637-5883-e053-d805fe0ac580 1
Lentiviral haemopoietic stem-cell gene therapy in early-onset metachromatic leukodystrophy: an ad-hoc analysis of a non-randomised, open-label, phase 1/2 trial, file e0c35a4c-05a0-5883-e053-d805fe0ac580 1
Genome editing: a tool for research and therapy: Targeted genome editing hits the clinic, file e0c35a4c-061a-5883-e053-d805fe0ac580 1
Hematopoietic Stem Cell Gene Transfer in a Tumor-Prone Mouse Model Uncovers Low Genotoxicity of Lentiviral Vector Integration, file e0c35a4c-0a06-5883-e053-d805fe0ac580 1
The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy, file e0c35a4c-0d18-5883-e053-d805fe0ac580 1
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next-generation human artificial chromosomes for Duchenne muscular dystrophy, file e0c35a4c-59fd-5883-e053-d805fe0ac580 1
Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemia, file e0c35a4c-6a2b-5883-e053-d805fe0ac580 1
Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study, file e0c35a4d-05c3-5883-e053-d805fe0ac580 1
Totale 89
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Categoria #
all - tutte 288
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 288
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201 0 0 0 0 0 0 0 0 0 1 0 0
2021/20225 0 0 0 0 0 0 0 0 0 0 3 2
2022/202322 0 0 2 3 0 5 2 1 5 0 4 0
2023/202444 1 1 2 6 3 1 6 2 15 7 0 0
Totale 89