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	Pour les 83 documents Envoyer sur ORCID RSS ATOM Exporter BibTeX XML-TEI CSV RTF EndNote PDF HTML Export avancé	Page : Page précédente 1 2 3 Page suivante	triés par Pertinence Auteur A→Z Auteur Z→A Titre A→Z Titre Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante

		Evaluation of diversity indices to estimate clonal dominance in gene therapy studies Guillaume Corre , Anne Galy Molecular Therapy - Methods and Clinical Development, 2023, 29, pp.418-425. ⟨10.1016/j.omtm.2023.05.003⟩ Article dans une revue hal-04324363v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		464. RCL-Pooling Assay: A Simplified Method for the Detection of Replication Competent Lentiviruses in Vector Batches Using Sequential Pooling Guillaume Corre , Corre Guillaume , Michel Dessainte , Jean-Brice Marteau , Bruno Dalle , et al. ASGCT, 2019, washington, DC, United States. pp.S184, ⟨10.1016/S1525-0016(16)33273-7⟩ Communication dans un congrès hal-02178331v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Quantitative proteomic analysis of lentiviral vectors using 2‐DE Jérôme Denard , Stéphanie Rundwasser , Nicolas Laroudie , Florence Gonnet , Luigi Naldini , et al. Proteomics, 2009, 9 (14), pp.3666-3676. ⟨10.1002/pmic.200800747⟩ Article dans une revue hal-04381121v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Temporary Reduction of Membrane CD4 with the Antioxidant MnTBAP Is Sufficient to Prevent Immune Responses Induced by Gene Transfer S. da Rocha , J. Bigot , F. Onodi , Jérémie Cosette , Guillaume Corre , et al. Mol Ther Methods Clin Dev, 2019, 14, pp.285-299. ⟨10.1016/j.omtm.2019.06.011⟩ Article dans une revue hal-02880792v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Gene therapy on the move K. B. Kaufmann , H. Buning , A. Galy , A. Schambach , M. Grez EMBO Mol Med, 2013, ⟨10.1002/emmm.201202287⟩ Article dans une revue hal-02881127v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Human syncytins can pseudotype lentiviral vectors, enabling gene transfer into B cells M. Ferrand , Y. Coquin , A. Seye , S. Frin , E. Renaud , et al. Human Gene Therapy, 2021, 32 (19-20), pp.A88-A89 Article dans une revue hal-03789526v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome A. Aiuti , L. Biasco , S. Scaramuzza , F. Ferrua , M. P. Cicalese , et al. Science, 2013, 341 (6148), pp.1233151. ⟨10.1126/science.1233151⟩ Article dans une revue hal-02881198v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		MyD88 signaling in B cells regulates the production of Th1-dependent antibodies to AAV M. Sudres , S. Cire , V. Vasseur , L. Brault , S. da Rocha , et al. Molecular Therapy, 2012, 20 (8), pp.1571-81. ⟨10.1038/mt.2012.101⟩ Article dans une revue hal-02881210v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		The Wiskott-Aldrich syndrome protein permits assembly of a focused immunological synapse enabling sustained T-cell receptor signaling R. Calvez , F. Lafouresse , J. de Meester , A. Galy , S. Valitutti , et al. Haematologica, 2011, 96 (10), pp.1415-1423. ⟨10.3324/haematol.2011.040204⟩ Article dans une revue hal-03765488v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCID S. Charrier , C. Lagresle-Peyrou , V. Poletti , M. Rothe , G. Cedrone , et al. Mol Ther Methods Clin Dev, 2019, 15, pp.232-245. ⟨10.1016/j.omtm.2019.08.014⟩ Article dans une revue hal-02880790v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Gene therapy for Wiskott-Aldrich syndrome in a severely affected adult E. C. Morris , T. Fox , R. Chakraverty , R. Tendeiro , K. Snell , et al. Blood, 2017, 130 (11), pp.1327-1335. ⟨10.1182/blood-2017-04-777136⟩ Article dans une revue hal-02881008v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome Alessandro Aiuti , Luca Biasco , Samantha Scaramuzza , Francesca Ferrua , Maria Pia Cicalese , et al. Science, 2013, 341 (6148), ⟨10.1126/science.1233151⟩ Article dans une revue hal-03765427v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Wiskott-Aldrich syndrome protein-deficient hematopoietic cells can be efficiently mobilized by granulocyte colony-stimulating factor S. Charrier , M. Blundell , G. Cedrone , F. Louache , W. Vainchenker , et al. Haematologica, 2013, 98 (8), pp.1300-8. ⟨10.3324/haematol.2012.077040⟩ Article dans une revue hal-02881150v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia Paula Río , Susana Navarro , Wei Wang , Rebeca Sánchez-Domínguez , Roser M. Pujol , et al. Nature Medicine, 2019, 25, pp.1396-1401. ⟨10.1038/s41591-019-0550-z⟩ Article dans une revue hal-02880813v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Recent advances using genetic therapies against infectious diseases and for vaccination Anne Galy , Ben Berkhout , Karine Breckpot , Chantal Pichon , Kristie Bloom , et al. Human Gene Therapy, 2023, ⟨10.1089/hum.2023.123⟩ Article dans une revue hal-04197730v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Increased production of pro-inflammatory cytokines and enhanced T cell responses after activation of human dendritic cells with IL-1 and CD40 ligand. Amy Wesa , Anne Galy BMC Immunology, 2002, 3, pp.14 Article dans une revue inserm-00123511v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Efficacité et sécurité du traitement par thérapie génique des patients atteints du syndrome de Wiskott-Aldrich Anne Galy , Guillaume Corre , Marina Cavazzana , Salima Hacein-Bey-Abina Médecine/Sciences, 2015, 31 (12), pp.1066-1069. ⟨10.1051/medsci/20153112006⟩ Article dans une revue hal-02178298v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Gene therapy for the Wiskott-Aldrich syndrome A. Galy , A. J. Thrasher Curr Opin Allergy Clin Immunol, 2011, 11 (6), pp.545-50. ⟨10.1097/ACI.0b013e32834c230c⟩ Article dans une revue hal-02881154v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Twelfth Annual Meeting of the French Society of Cell and Gene Therapy Els Verhoeyen , Sophie Gomez , Anne Galy , Eduard Ayuso , Patrick Midoux , et al. Human Gene Therapy, 2016, 27 (7), pp.555-558. ⟨10.1089/hum.2016.29031.eve⟩ Article dans une revue hal-01469045v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Like Angler Fish, CAARs Lure Their Prey A. Galy Molecular Therapy, 2016, 24 (8), pp.1339-41. ⟨10.1038/mt.2016.165⟩ Article dans une revue hal-02880980v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Major Advances in the Development of Vectors for Clinical Gene Therapy of Hematopoietic Stem Cells from European Groups over the Last 25 Years A. Galy Human Gene Therapy, 2017, 28 (11), pp.964-971. ⟨10.1089/hum.2017.152⟩ Article dans une revue hal-02880981v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Vectofusin-1 Improves Transduction of Primary Human Cells with Diverse Retroviral and Lentiviral Pseudotypes, Enabling Robust, Automated Closed-System Manufacturing C. Radek , O. Bernadin , K. Drechsel , N. Cordes , R. Pfeifer , et al. Human Gene Therapy, 2019, 30, pp.1477-1493. ⟨10.1089/hum.2019.157⟩ Article dans une revue hal-02880812v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Toward a Scalable Purification Protocol of GaLV-TR-Pseudotyped Lentiviral Vectors D. Boudeffa , B. Bertin , A. Biek , M. Mormin , F. Leseigneur , et al. Hum Gene Ther Methods, 2019, 30, pp.153-171. ⟨10.1089/hgtb.2019.076⟩ Article dans une revue hal-02880786v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Vectofusin-1 Promotes RD114-TR-Pseudotyped Lentiviral Vector Transduction of Human HSPCs and T Lymphocytes C. Piovan , V. Marin , C. Scavullo , S. Corna , E. Giuliani , et al. Mol Ther Methods Clin Dev, 2017, 5, pp.22-30. ⟨10.1016/j.omtm.2017.02.003⟩ Article dans une revue hal-02881009v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome Salima Hacein-Bey Abina , H Bobby Gaspar , Johanna Blondeau , Laure Caccavelli , Sabine Charrier , et al. Journal of the American Medical Association, 2015, 313 (15), pp.1550-63. ⟨10.1001/jama.2015.3253⟩ Article dans une revue hal-02880982v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Non-Clinical Efficacy and Safety Studies on G1XCGD, a Lentiviral Vector for Ex Vivo Gene Therapy of X-Linked Chronic Granulomatous Disease Christian Brendel , Michael Rothe , Giorgia Santilli , Sabine Charrier , Stefan Stein , et al. Human gene therapy. Clinical development, 2018, 29 (2), pp.69-79. ⟨10.1089/humc.2017.245⟩ Article dans une revue hal-03765483v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Stem cell gene therapy for fanconi anemia: report from the 1st international Fanconi anemia gene therapy working group meeting J. Tolar , J. E. Adair , M. Antoniou , C. C. Bartholomae , P. S. Becker , et al. Molecular Therapy, 2011, 19 (7), pp.1193-8. ⟨10.1038/mt.2011.78⟩ Article dans une revue hal-02881136v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients S Charrier , L Dupré , S Scaramuzza , L Jeanson-Leh , M Blundell , et al. Gene Therapy, 2007, 14 (5), pp.415-428. ⟨10.1038/sj.gt.3302863⟩ Article dans une revue hal-03765501v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Quantification of lentiviral vector copy numbers in individual hematopoietic colony-forming cells shows vector dose-dependent effects on the frequency and level of transduction S. Charrier , M. Ferrand , M. Zerbato , G. Precigout , A. Viornery , et al. Gene Ther, 2011, 18 (5), pp.479-87. ⟨10.1038/gt.2010.163⟩ Article dans une revue hal-02881185v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene Céline Bouquet , Catherine Vignal Clermont , Anne Galy , Serge Fitoussi , Laure Blouin , et al. JAMA Ophthalmology, 2019, 137 (4), pp.399. ⟨10.1001/jamaophthalmol.2018.6902⟩ Article dans une revue hal-02131584v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More

Filtrer vos résultats

Evaluation of diversity indices to estimate clonal dominance in gene therapy studies

464. RCL-Pooling Assay: A Simplified Method for the Detection of Replication Competent Lentiviruses in Vector Batches Using Sequential Pooling

Quantitative proteomic analysis of lentiviral vectors using 2‐DE

Temporary Reduction of Membrane CD4 with the Antioxidant MnTBAP Is Sufficient to Prevent Immune Responses Induced by Gene Transfer

Gene therapy on the move

Human syncytins can pseudotype lentiviral vectors, enabling gene transfer into B cells

Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome

MyD88 signaling in B cells regulates the production of Th1-dependent antibodies to AAV

The Wiskott-Aldrich syndrome protein permits assembly of a focused immunological synapse enabling sustained T-cell receptor signaling

Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCID

Gene therapy for Wiskott-Aldrich syndrome in a severely affected adult

Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome

Wiskott-Aldrich syndrome protein-deficient hematopoietic cells can be efficiently mobilized by granulocyte colony-stimulating factor

Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia

Recent advances using genetic therapies against infectious diseases and for vaccination

Increased production of pro-inflammatory cytokines and enhanced T cell responses after activation of human dendritic cells with IL-1 and CD40 ligand.

Efficacité et sécurité du traitement par thérapie génique des patients atteints du syndrome de Wiskott-Aldrich

Gene therapy for the Wiskott-Aldrich syndrome

Twelfth Annual Meeting of the French Society of Cell and Gene Therapy

Like Angler Fish, CAARs Lure Their Prey

Major Advances in the Development of Vectors for Clinical Gene Therapy of Hematopoietic Stem Cells from European Groups over the Last 25 Years

Vectofusin-1 Improves Transduction of Primary Human Cells with Diverse Retroviral and Lentiviral Pseudotypes, Enabling Robust, Automated Closed-System Manufacturing

Toward a Scalable Purification Protocol of GaLV-TR-Pseudotyped Lentiviral Vectors

Vectofusin-1 Promotes RD114-TR-Pseudotyped Lentiviral Vector Transduction of Human HSPCs and T Lymphocytes

Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome

Non-Clinical Efficacy and Safety Studies on G1XCGD, a Lentiviral Vector for Ex Vivo Gene Therapy of X-Linked Chronic Granulomatous Disease

Stem cell gene therapy for fanconi anemia: report from the 1st international Fanconi anemia gene therapy working group meeting

Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients

Quantification of lentiviral vector copy numbers in individual hematopoietic colony-forming cells shows vector dose-dependent effects on the frequency and level of transduction

Immune Response and Intraocular Inflammation in Patients With Leber Hereditary Optic Neuropathy Treated With Intravitreal Injection of Recombinant Adeno-Associated Virus 2 Carrying the ND4 Gene