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Nathalie Lambert

Showing results (21-30 of 41) with videos related to

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Blood|May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LGStéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Frontiers in Immunology|February 5, 2026
Allergen extract outperforms molecular components in basophil activation test in a pediatric cohortAlexandre Chhing, Simone Choi, Dounia Khelifi-Touhami, et al.
Frontiers in Immunology|December 3, 2019
Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A DeficiencyMarie-Thérèse El-Daher, Julie Lemale, Julie Bruneau, et al.
Cell|November 19, 2003
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.
Pediatric Transplantation|September 3, 2011
Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCIDGrace P Yu, Kari C Nadeau, David R Berk, et al.
Journal of Immunology Research|March 9, 2017
<i>TMEM187-IRAK1</i> Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic OriginOlfa Khalifa, Nathalie Balandraud, Nathalie Lambert, et al.
Human Mutation|June 7, 2017
A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosisVirginie Grandin, Fernando E Sepulveda, Nathalie Lambert, et al.
Clinical Immunology (Orlando, Fla.)|July 19, 2015
SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signalingFabian Hauck, Britta Blumenthal, Sebastian Fuchs, et al.
Journal of Clinical Immunology|September 26, 2022
Lymphoma as an Exclusion Criteria for CVID Diagnosis RevisitedVincent Allain, Virginie Grandin, Véronique Meignin, 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.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Blood|May 6, 2011
Human X-linked variable immunodeficiency caused by a hypomorphic mutation in XIAP in association with a rare polymorphism in CD40LGStéphanie Rigaud, Eduardo Lopez-Granados, Sophie Sibéril, et al.
Frontiers in Immunology|February 5, 2026
Allergen extract outperforms molecular components in basophil activation test in a pediatric cohortAlexandre Chhing, Simone Choi, Dounia Khelifi-Touhami, et al.
Frontiers in Immunology|December 3, 2019
Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A DeficiencyMarie-Thérèse El-Daher, Julie Lemale, Julie Bruneau, et al.
Cell|November 19, 2003
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.
Pediatric Transplantation|September 3, 2011
Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCIDGrace P Yu, Kari C Nadeau, David R Berk, et al.
Journal of Immunology Research|March 9, 2017
<i>TMEM187-IRAK1</i> Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic OriginOlfa Khalifa, Nathalie Balandraud, Nathalie Lambert, et al.
Human Mutation|June 7, 2017
A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosisVirginie Grandin, Fernando E Sepulveda, Nathalie Lambert, et al.
Clinical Immunology (Orlando, Fla.)|July 19, 2015
SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signalingFabian Hauck, Britta Blumenthal, Sebastian Fuchs, et al.
Journal of Clinical Immunology|September 26, 2022
Lymphoma as an Exclusion Criteria for CVID Diagnosis RevisitedVincent Allain, Virginie Grandin, Véronique Meignin, 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.
Pageof 5