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Nathalie Lambert

Showing results (31-40 of 41) with videos related to

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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.
The Journal of Clinical Investigation|September 3, 2024
Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiencyMarta Benavides-Nieto, Frédéric Adam, Emmanuel Martin, et al.
The Journal of Clinical Investigation|December 3, 2013
TTC7A mutations disrupt intestinal epithelial apicobasal polarityAmélie E Bigorgne, Henner F Farin, Roxane Lemoine, et al.
The Journal of Allergy and Clinical Immunology|June 20, 2014
Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriersClaire Aguilar, Christelle Lenoir, Nathalie Lambert, et al.
Journal of Human Immunity|December 15, 2025
Intronic branchpoint-to-acceptor variants underlying inborn errors of immunityNajiba Alioua, Nathalie Lambert, Mathilde Puel, et al.
Blood|December 2, 2010
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.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
Journal of Clinical Immunology|November 22, 2024
2q33 Deletions Underlying Syndromic and Non-syndromic CTLA4 DeficiencyCharlyne Brakta, Anne-Claude Tabet, Mathilde Puel, et al.
Journal of Clinical Immunology|July 12, 2018
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 DeficiencyJérémie Rosain, Carmen Oleaga-Quintas, Caroline Deswarte, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
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.
The Journal of Clinical Investigation|September 3, 2024
Somatic RAP1B gain-of-function variant underlies isolated thrombocytopenia and immunodeficiencyMarta Benavides-Nieto, Frédéric Adam, Emmanuel Martin, et al.
The Journal of Clinical Investigation|December 3, 2013
TTC7A mutations disrupt intestinal epithelial apicobasal polarityAmélie E Bigorgne, Henner F Farin, Roxane Lemoine, et al.
The Journal of Allergy and Clinical Immunology|June 20, 2014
Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriersClaire Aguilar, Christelle Lenoir, Nathalie Lambert, et al.
Journal of Human Immunity|December 15, 2025
Intronic branchpoint-to-acceptor variants underlying inborn errors of immunityNajiba Alioua, Nathalie Lambert, Mathilde Puel, et al.
Blood|December 2, 2010
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.
The Journal of Allergy and Clinical Immunology|July 14, 2016
X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) geneChantal Lagresle-Peyrou, Sonia Luce, Farid Ouchani, et al.
Journal of Clinical Immunology|November 22, 2024
2q33 Deletions Underlying Syndromic and Non-syndromic CTLA4 DeficiencyCharlyne Brakta, Anne-Claude Tabet, Mathilde Puel, et al.
Journal of Clinical Immunology|July 12, 2018
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 DeficiencyJérémie Rosain, Carmen Oleaga-Quintas, Caroline Deswarte, et al.
Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.
Pageof 5