G De Saint Basile - JoVE Visualize

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European Journal of Immunology|February 1, 1994

Interleukin-2 (IL-2) receptor gamma chain mutations in X-linked severe combined immunodeficiency disease result in the loss of high-affinity IL-2 receptor bindingJ P DiSanto, A Dautry-Varsat, S Certain, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 27, 1994

Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cellsJ P DiSanto, F Rieux-Laucat, A Dautry-Varsat, et al.

Journal of the Neurological Sciences|July 22, 2014

Motor neuronopathy in Chediak-Higashi syndromeS Mathis, P Cintas, G de Saint-Basile, et al.

Nature|February 11, 1993

CD40 ligand mutations in x-linked immunodeficiency with hyper-IgMJ P DiSanto, J Y Bonnefoy, J F Gauchat, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 5, 2016

Familial haemophagocytosis lymphohisticytosis type 3: A case reportF Kamoun, M Hsairi, V Grandin, et al.

The Journal of Clinical Investigation|March 1, 1992

Genetic study of a new X-linked recessive immunodeficiency syndromeG de Saint-Basile, F Le Deist, M Caniglia, et al.

The Journal of Clinical Investigation|September 1, 1992

Control of human B cell tumor growth in severe combined immunodeficiency mice by monoclonal anti-B cell antibodiesA Durandy, N Brousse, F Rozenberg, et al.

The Journal of Clinical Investigation|April 1, 1993

Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoireM Milili, F Le Deist, G de Saint-Basile, et al.

Immunology Letters|June 1, 1997

A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA caseE Meffre, F LeDeist, G de Saint-Basile, et al.

Human Mutation|October 23, 2001

Eleven novel JAK3 mutations in patients with severe combined immunodeficiency-including the first patients with mutations in the kinase domainP Mella, R F Schumacher, T Cranston, et al.

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Showing results (11-20 of 83) with videos related to

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European Journal of Immunology|February 1, 1994

Interleukin-2 (IL-2) receptor gamma chain mutations in X-linked severe combined immunodeficiency disease result in the loss of high-affinity IL-2 receptor bindingJ P DiSanto, A Dautry-Varsat, S Certain, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 27, 1994

Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cellsJ P DiSanto, F Rieux-Laucat, A Dautry-Varsat, et al.

Journal of the Neurological Sciences|July 22, 2014

Motor neuronopathy in Chediak-Higashi syndromeS Mathis, P Cintas, G de Saint-Basile, et al.

Nature|February 11, 1993

CD40 ligand mutations in x-linked immunodeficiency with hyper-IgMJ P DiSanto, J Y Bonnefoy, J F Gauchat, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 5, 2016

Familial haemophagocytosis lymphohisticytosis type 3: A case reportF Kamoun, M Hsairi, V Grandin, et al.

The Journal of Clinical Investigation|March 1, 1992

Genetic study of a new X-linked recessive immunodeficiency syndromeG de Saint-Basile, F Le Deist, M Caniglia, et al.

The Journal of Clinical Investigation|September 1, 1992

Control of human B cell tumor growth in severe combined immunodeficiency mice by monoclonal anti-B cell antibodiesA Durandy, N Brousse, F Rozenberg, et al.

The Journal of Clinical Investigation|April 1, 1993

Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoireM Milili, F Le Deist, G de Saint-Basile, et al.

Immunology Letters|June 1, 1997

A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA caseE Meffre, F LeDeist, G de Saint-Basile, et al.

Human Mutation|October 23, 2001

Eleven novel JAK3 mutations in patients with severe combined immunodeficiency-including the first patients with mutations in the kinase domainP Mella, R F Schumacher, T Cranston, et al.

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