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Human Mutation|October 23, 2001
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiencyL D Notarangelo, P Mella, A Jones, et al.European Journal of Gastroenterology & Hepatology|September 28, 2000
Gastric adenocarcinoma in a patient with X-linked agammaglobulinaemiaC Bachmeyer, M Monge, A Cazier, et al.Blood|November 15, 1996
Role of interleukin-2 (IL-2), IL-7, and IL-15 in natural killer cell differentiation from cord blood hematopoietic progenitor cells and from gamma c transduced severe combined immunodeficiency X1 bone marrow cellsM Cavazzana-Calvo, S Hacein-Bey, G de Saint Basile, et al.The Journal of Pediatrics|July 1, 1996
Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein geneG de Saint Basile, R D Lagelouse, N Lambert, et al.Immunological Reviews|February 24, 2001
Gene therapy of severe combined immunodeficienciesA Fischer, S Hacein-Bey, F Le Deist, et al.Annals of Hematology|August 1, 1991
X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriersG De Saint-Basile, N Schlegel, M Caniglia, et al.The Journal of Cell Biology|June 12, 1998
Deficient peptide loading and MHC class II endosomal sorting in a human genetic immunodeficiency disease: the Chediak-Higashi syndromeW Faigle, G Raposo, D Tenza, et al.Cancer|May 15, 1991
A familial occurrence of natural killer cell--T-lymphocyte proliferation disease in two childrenF Le Deist, G de Saint Basile, L Coulombel, et al.Human Molecular Genetics|January 1, 1995
DNA-based mutation analysis of Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinaemiaI Vorechovský, M Vihinen, G de Saint Basile, et al.The Journal of Biological Chemistry|June 21, 1996
Tissue-specific activity of the gammac chain gene promoter depends upon an Ets binding site and is regulated by GA-binding proteinS Markiewicz, R Bosselut, F Le Deist, et al.Pageof 9