Résultat de recherche

1789 results found for your search

  • PAICS deficiency, a new defect of de novo purine synthesis resulting in multiple congenital anomalies and fatal outcome.

    Stanislas Lyonnet, Anna Pelet

    Source :

    Hum. Mol. Genet.

    2019 Dec 29

    Pmid / DOI:

    31600779

  • A Nontoxic Transduction Enhancer Enables Highly Efficient Lentiviral Transduction of Primary Murine T Cells and Hematopoietic Stem Cells.

    Marianne DELVILLE, Adeline DENIS, Chantal LAGRESLE-PEYROU, Marina Cavazzana, Isabelle André, Emmanuelle SIX

    Source :

    Mol Ther Methods Clin Dev

    2019 Nov 20

    Pmid / DOI:

    30191160

  • Plerixafor enables safe, rapid, efficient mobilization of hematopoietic stem cells in sickle cell disease patients after exchange transfusion.

    Chantal LAGRESLE-PEYROU, Oriana Romano, Tristan Felix, Marianne DELVILLE, Isabelle André, Marina Cavazzana, Annarita Miccio , Tristan Felix

    Source :

    Haematologica

    2019 Jul 8

    Pmid / DOI:

    29472357

  • Generation of adult human T-cell progenitors for immunotherapeutic applications.

    Corinne de Chappedelaine, Ranjita MOIRANGTHEM, Chantal LAGRESLE-PEYROU, Antonio Rausell, Marina Cavazzana, Isabelle André

    Source :

    J. Allergy Clin. Immunol.

    2019 Jul 31

    Pmid / DOI:

    29208547

  • Gene Therapy for X-Linked Severe Combined Immunodeficiency: Where Do We Stand?

    Marina Cavazzana, Emmanuelle SIX, Chantal LAGRESLE-PEYROU, Isabelle André

    Source :

    Hum. Gene Ther.

    2016 Nov 4

    Pmid / DOI:

    26790362

  • Gene Therapy with Hematopoietic Stem Cells: The Diseased Bone Marrow's Point of View.

    Marina Cavazzana, Chantal LAGRESLE-PEYROU, Isabelle André

    Source :

    Stem Cells Dev.

    2017 Sep 11

    Pmid / DOI:

    27750026

  • Gene-corrected human Munc13-4-deficient CD8+ T cells can efficiently restrict EBV-driven lymphoproliferation in immunodeficient mice.

    Chantal LAGRESLE-PEYROU, Geneviève de Saint Basile, Isabelle André, Marina Cavazzana

    Source :

    Blood

    2018 Jan 17

    Pmid / DOI:

    27799161

  • Loss of ARHGEF1 causes a human primary antibody deficiency.

    Marina Cavazzana, Isabelle André, Anne DURANDY, Alain Fischer, Sven KRACKER

    Source :

    J. Clin. Invest.

    2019 Nov 20

    Pmid / DOI:

    30521495

  • Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1).

    Sven KRACKER, Marina Cavazzana, Alain Fischer

    Source :

    Haematologica

    2018 Sep 7

    Pmid / DOI:

    28428270

  • Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study.

    Sven KRACKER, Marina Cavazzana, Alain Fischer

    Source :

    J. Allergy Clin. Immunol. 2017

    2017 Jun 15

    Pmid / DOI:

    27221134

  • A human immunodeficiency caused by mutations in the PIK3R1 gene.

    Sven KRACKER, Marina Cavazzana, Alain Fischer, Christine Bole, Patrick Nitschké

    Source :

    J. Clin. Invest.

    2015 May 29

    Pmid / DOI:

    25831445