Nathalie Lambert

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

Jérôme Feldmann, Isabelle Callebaut, Graça Raposo et al. · Cell · 2003 · 916 citations · Full text

Is Mutated, Lymphoid Neoplasia, Hematological Malignancy +8

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

Stéphanie Rigaud, Marie‐Claude Fondanèche, Nathalie Lambert et al. · Nature · 2006 · 696 citations

Primary Immunodeficiency, Autoimmune Disease, Immunology +5

Long-Term Fetal Microchimerism in Peripheral Blood Mononuclear Cell Subsets in Healthy Women and Women With Scleroderma

Paul C. Evans, Nathalie Lambert, Sean Maloney et al. · Blood · 1999 · 396 citations

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous et al. · Blood · 2010 · 364 citations · Full text

Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product

Benoit Pasquier, Yin Luo, Marie‐Claude Fondanèche et al. · The Journal of Experimental Medicine · 2005 · 336 citations · Full text

Lymphocyte Development, Immunology, Immunologic Mechanism +16