Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G de Saint-Basile

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

Pageof 9
Sort By:
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.
Pageof 9

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

Sort By:
Pageof 9
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.
Pageof 9