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Human Mutation|April 13, 1999
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. OnlineF X Arrendondo-Vega, I Santisteban, L D Notarangelo, et al.The Journal of Clinical Investigation|May 1, 1990
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findingsM E Conley, R H Buckley, R Hong, et al.Bone Marrow Transplantation|May 1, 1996
Cure of X-linked lymphoproliferative disease (XLP) with allogeneic hematopoietic stem cell transplantation (HSCT): report from the XLP registryT G Gross, A H Filipovich, M E Conley, et al.The New England Journal of Medicine|November 14, 1996
Mutations in the mu heavy-chain gene in patients with agammaglobulinemiaL Yel, Y Minegishi, E Coustan-Smith, et al.The Journal of Clinical Investigation|October 1, 1994
Hyper IgM syndrome associated with defective CD40-mediated B cell activationM E Conley, M Larché, V R Bonagura, et al.Journal of Investigational Allergology & Clinical Immunology|September 13, 2011
Membranous glomerulopathy in an adult patient with X-linked agammaglobulinemia receiving intravenous gammaglobulinL M Endo, J V Giannobile, A K Dobbs, et al.The Journal of Clinical Investigation|January 1, 1996
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndromeQ Lin, J Rohrer, R C Allen, et al.Clinical Immunology (Orlando, Fla.)|December 9, 2000
Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndromeY Minegishi, A Lavoie, C Cunningham-Rundles, et al.Genomics|November 1, 1987
Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor gamma chain in mouse and manR F Holcombe, W Strauss, F L Owen, et al.Science (New York, N.Y.)|February 12, 1993
CD40 ligand gene defects responsible for X-linked hyper-IgM syndromeR C Allen, R J Armitage, M E Conley, et al.Pageof 12