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Fabien Touzot

Showing results (31-40 of 53) with videos related to

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Human Mutation|November 1, 2012
Primary microcephaly, impaired DNA replication, and genomic instability caused by compound heterozygous ATR mutationsHouda Mokrani-Benhelli, Laetitia Gaillard, Patricia Biasutto, et al.
Journal of Medical Genetics|May 2, 2024
Homozygous variant in <i>TKFC</i> abolishing triokinase activities is associated with isolated immunodeficiencyCamille Tremblay-Laganière, Coralie Michaud, Raphaël Abourjaili-Bilodeau, et al.
Haematologica|September 21, 2019
Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapyAlessandra Magnani, Corinne Pondarré, Naïm Bouazza, et al.
Blood Advances|January 4, 2018
Extended clinical and genetic spectrum associated with biallelic <i>RTEL1</i> mutationsFabien Touzot, Laetitia Kermasson, Laurent Jullien, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 17, 2019
Haploidentical Hematopoietic Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immunodeficiencies and Inherited Disorders in ChildrenBénédicte Neven, Jean-Sébastien Diana, Martin Castelle, et al.
The Journal of Allergy and Clinical Immunology|September 19, 2012
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiencyFabian Hauck, Clotilde Randriamampita, Emmanuel Martin, et al.
The Journal of Allergy and Clinical Immunology|July 30, 2015
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiationTangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, et al.
Blood|January 10, 2022
Inherited human Apollo deficiency causes severe bone marrow failure and developmental defectsLaëtitia Kermasson, Dmitri Churikov, Aya Awad, et al.
Nature Immunology|September 13, 2016
Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
Molecular Therapy. Methods & Clinical Development|March 27, 2019
Safety of CD34<sup>+</sup> Hematopoietic Stem Cells and CD4<sup>+</sup> T Lymphocytes Transduced with LVsh5/C46 in HIV-1 Infected Patients with High-Risk LymphomaMarianne Delville, Fabien Touzot, Chloé Couzin, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Human Mutation|November 1, 2012
Primary microcephaly, impaired DNA replication, and genomic instability caused by compound heterozygous ATR mutationsHouda Mokrani-Benhelli, Laetitia Gaillard, Patricia Biasutto, et al.
Journal of Medical Genetics|May 2, 2024
Homozygous variant in <i>TKFC</i> abolishing triokinase activities is associated with isolated immunodeficiencyCamille Tremblay-Laganière, Coralie Michaud, Raphaël Abourjaili-Bilodeau, et al.
Haematologica|September 21, 2019
Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapyAlessandra Magnani, Corinne Pondarré, Naïm Bouazza, et al.
Blood Advances|January 4, 2018
Extended clinical and genetic spectrum associated with biallelic <i>RTEL1</i> mutationsFabien Touzot, Laetitia Kermasson, Laurent Jullien, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|March 17, 2019
Haploidentical Hematopoietic Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immunodeficiencies and Inherited Disorders in ChildrenBénédicte Neven, Jean-Sébastien Diana, Martin Castelle, et al.
The Journal of Allergy and Clinical Immunology|September 19, 2012
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiencyFabian Hauck, Clotilde Randriamampita, Emmanuel Martin, et al.
The Journal of Allergy and Clinical Immunology|July 30, 2015
An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiationTangui Le Guen, Fabien Touzot, Isabelle André-Schmutz, et al.
Blood|January 10, 2022
Inherited human Apollo deficiency causes severe bone marrow failure and developmental defectsLaëtitia Kermasson, Dmitri Churikov, Aya Awad, et al.
Nature Immunology|September 13, 2016
Evidence of innate lymphoid cell redundancy in humansFrédéric Vély, Vincent Barlogis, Blandine Vallentin, et al.
Molecular Therapy. Methods & Clinical Development|March 27, 2019
Safety of CD34<sup>+</sup> Hematopoietic Stem Cells and CD4<sup>+</sup> T Lymphocytes Transduced with LVsh5/C46 in HIV-1 Infected Patients with High-Risk LymphomaMarianne Delville, Fabien Touzot, Chloé Couzin, et al.
Pageof 6