Publications and ressources

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene.

Marina Cavazzana, Chantal LAGRESLE-PEYROU, Aude Magerus, Frédéric Rieux-Laucat, Anne DURANDY, Sven KRACKER, Geneviève de Saint Basile, Alain Fischer, Marina Cavazzana, Isabelle André

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

Sven KRACKER, Marina Cavazzana, Alain Fischer

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Reticular dysgenesis: international survey on clinical presentation, transplantation, and outcome.

Chantal LAGRESLE-PEYROU, Despina Moshous, Alain Fischer, Marina Cavazzana

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Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study.

Frédéric Rieux-Laucat, Sylvain Latour, Alain Fischer, Jean-Laurent CASANOVA , Anne DURANDY, Despina Moshous, Sven KRACKER

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

Marina Cavazzana, Chantal LAGRESLE-PEYROU

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

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

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Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study

Sven KRACKER, Anne DURANDY

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AK2 deficiency compromises the mitochondrial energy metabolism required for differentiation of human neutrophil and lymphoid lineages.

Emmanuelle SIX, Chantal LAGRESLE-PEYROU, Corinne de Chappedelaine, Alain Fischer, Isabelle André, Marina Cavazzana

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An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation.

Chantal LAGRESLE-PEYROU, Laëtitia Kermasson, Patrick Nitschké, Marina Cavazzana, Alain Fischer, Jean-Pierre De Villartay, Patrick Revy

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A human immunodeficiency caused by mutations in the PIK3R1 gene.

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

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

Emmanuelle SIX, Alain Fischer, Marina Cavazzana

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The BLNK adaptor protein has a nonredundant role in human B-cell differentiation.

Chantal LAGRESLE-PEYROU, Hanem SADEK, Marina Cavazzana

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Successful RAG1-SCID gene therapy depends on the level of RAG1 expression.

Marina Cavazzana, Chantal LAGRESLE-PEYROU

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Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome.

Chantal LAGRESLE-PEYROU, Marina Cavazzana

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Human T-lymphoid progenitors generated in a feeder-cell-free Delta-like-4 culture system promote T-cell reconstitution in NOD/SCID/γc(-/-) mice.

Emmanuelle SIX, Chantal LAGRESLE-PEYROU, Corinne de Chappedelaine, Marina Cavazzana, Isabelle André

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