List of works - Oumeya Adjali

Accurate Titration of Infectious AAV Particles Requires Measurement of Biologically Active Vector Genomes and Suitable Controls

scientific article published on 27 July 2018

Cross-Packaging and Capsid Mosaic Formation in Multiplexed AAV Libraries

scientific article published on 26 November 2019

Different pharmacological profile of two closely related endocannabinoid ester analogs

scientific article published in August 2005

Early interaction of adeno-associated virus serotype 8 vector with the host immune system following intramuscular delivery results in weak but detectable lymphocyte and dendritic cell transduction

scientific article

Efficient intrathymic gene transfer following in situ administration of a rAAV serotype 8 vector in mice and nonhuman primates.

scientific article

Five Years of Successful Inducible Transgene Expression Following Locoregional Adeno-Associated Virus Delivery in Nonhuman Primates with No Detectable Immunity

scientific article published on 16 April 2019

Forelimb treatment in a large cohort of dystrophic dogs supports delivery of a recombinant AAV for exon skipping in Duchenne patients.

scientific article

Generation and in vivo evaluation of IL10-treated dendritic cells in a nonhuman primate model of AAV-based gene transfer

scientific article published on 23 July 2014

Homologous Recombination Offers Advantages Over Transposition-Based Systems to Generate Recombinant Baculovirus for Adeno-Associated Viral Vector Production

scientific article published on 16 October 2020

In vivo and ex vivo gene transfer in thymocytes and thymocyte precursors

scientific article

In vivo correction of ZAP-70 immunodeficiency by intrathymic gene transfer

scientific article

Intra-CSF AAV9 and AAVrh10 Administration in Nonhuman Primates: Promising Routes and Vectors for Which Neurological Diseases?

scientific article published on 11 April 2020

Intrathymic adeno-associated virus gene transfer rapidly restores thymic function and long-term persistence of gene-corrected T cells

scientific article published on 09 September 2019

Intrathymic administration of hematopoietic progenitor cells enhances T cell reconstitution in ZAP-70 severe combined immunodeficiency

scientific article

Intrathymic transplantation of bone marrow-derived progenitors provides long-term thymopoiesis

scientific article

Lack of immunotoxicity after regional intravenous (RI) delivery of rAAV to nonhuman primate skeletal muscle

scientific article published on 3 November 2009

Lentiviral transduction of immune cells

scientific article published on 01 January 2008

Liver-specific transcriptional modules identified by genome-wide in silico analysis enable efficient gene therapy in mice and non-human primates

scientific article

Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy.

scientific article

Measuring Immune Responses to Recombinant AAV Gene Transfer ⬇️

scientific article published on January 1, 2011

Proteomic analysis of astrocytic secretion in the mouse. Comparison with the cerebrospinal fluid proteome

scientific article published on 22 April 2003

Safety and Long-Term Efficacy of AAV4 Gene Therapy in Patients with RPE65 Leber Congenital Amaurosis

scientific article published on 19 September 2017

Stability of the adeno-associated virus 8 reference standard material

scientific article published on 29 March 2019

T-cell receptor-induced phosphorylation of the zeta chain is efficiently promoted by ZAP-70 but not Syk.

scientific article published in April 2004

Tetramer-Based Enrichment of Preexisting Anti-AAV8 CD8+ T Cells in Human Donors Allows the Detection of a TEMRA Subpopulation

scientific article published on 01 January 2019

The SSV-Seq 2.0 PCR-free method improves the sequencing of adeno-associated viral vector genomes containing GC-rich regions and homopolymers

scientific article published on 16 October 2020

The protooncogene Vav1 regulates murine leukemia virus-induced T-cell leukemogenesis.

scientific article

Transgene regulation using the tetracycline-inducible TetR-KRAB system after AAV-mediated gene transfer in rodents and nonhuman primates

scientific article

Unraveling the complex story of immune responses to AAV vectors trial after trial

scientific article

Vascular Delivery of Allogeneic MuStem Cells in Dystrophic Dogs Requires Only Short-Term Immunosuppression to Avoid Host Immunity and Generate Clinical/Tissue Benefits

scientific article published on 05 June 2018

[Gene therapy for retinitis pigmentosa]

scientific article published on 01 June 2020

List of works by Oumeya Adjali

Accurate Titration of Infectious AAV Particles Requires Measurement of Biologically Active Vector Genomes and Suitable Controls

Cross-Packaging and Capsid Mosaic Formation in Multiplexed AAV Libraries

Different pharmacological profile of two closely related endocannabinoid ester analogs

Early interaction of adeno-associated virus serotype 8 vector with the host immune system following intramuscular delivery results in weak but detectable lymphocyte and dendritic cell transduction

Efficient intrathymic gene transfer following in situ administration of a rAAV serotype 8 vector in mice and nonhuman primates.

Five Years of Successful Inducible Transgene Expression Following Locoregional Adeno-Associated Virus Delivery in Nonhuman Primates with No Detectable Immunity

Forelimb treatment in a large cohort of dystrophic dogs supports delivery of a recombinant AAV for exon skipping in Duchenne patients.

Generation and in vivo evaluation of IL10-treated dendritic cells in a nonhuman primate model of AAV-based gene transfer

Homologous Recombination Offers Advantages Over Transposition-Based Systems to Generate Recombinant Baculovirus for Adeno-Associated Viral Vector Production

In vivo and ex vivo gene transfer in thymocytes and thymocyte precursors

In vivo correction of ZAP-70 immunodeficiency by intrathymic gene transfer

Intra-CSF AAV9 and AAVrh10 Administration in Nonhuman Primates: Promising Routes and Vectors for Which Neurological Diseases?

Intrathymic adeno-associated virus gene transfer rapidly restores thymic function and long-term persistence of gene-corrected T cells

Intrathymic administration of hematopoietic progenitor cells enhances T cell reconstitution in ZAP-70 severe combined immunodeficiency

Intrathymic transplantation of bone marrow-derived progenitors provides long-term thymopoiesis

Lack of immunotoxicity after regional intravenous (RI) delivery of rAAV to nonhuman primate skeletal muscle

Lentiviral transduction of immune cells

Liver-specific transcriptional modules identified by genome-wide in silico analysis enable efficient gene therapy in mice and non-human primates

Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy.

Measuring Immune Responses to Recombinant AAV Gene Transfer ⬇️

Proteomic analysis of astrocytic secretion in the mouse. Comparison with the cerebrospinal fluid proteome

Safety and Long-Term Efficacy of AAV4 Gene Therapy in Patients with RPE65 Leber Congenital Amaurosis

Stability of the adeno-associated virus 8 reference standard material

T-cell receptor-induced phosphorylation of the zeta chain is efficiently promoted by ZAP-70 but not Syk.

Tetramer-Based Enrichment of Preexisting Anti-AAV8 CD8+ T Cells in Human Donors Allows the Detection of a TEMRA Subpopulation

The SSV-Seq 2.0 PCR-free method improves the sequencing of adeno-associated viral vector genomes containing GC-rich regions and homopolymers

The protooncogene Vav1 regulates murine leukemia virus-induced T-cell leukemogenesis.

Transgene regulation using the tetracycline-inducible TetR-KRAB system after AAV-mediated gene transfer in rodents and nonhuman primates

Unraveling the complex story of immune responses to AAV vectors trial after trial

Vascular Delivery of Allogeneic MuStem Cells in Dystrophic Dogs Requires Only Short-Term Immunosuppression to Avoid Host Immunity and Generate Clinical/Tissue Benefits

[Gene therapy for retinitis pigmentosa]