Mutations in Activation-Induced Cytidine Deaminase in Patients with Hyper IgM Syndrome
- 1 December 2000
- journal article
- Published by Elsevier in Clinical Immunology
- Vol. 97 (3) , 203-210
- https://doi.org/10.1006/clim.2000.4956
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.Journal of Clinical Investigation, 1996
- CD40 ligation induces Apo-1/Fas expression on human B lymphocytes and facilitates apoptosis through the Apo-1/Fas pathway.The Journal of Experimental Medicine, 1995
- Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinaseHuman Molecular Genetics, 1994
- The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndromeCell, 1993
- Molecular and biological characterization of a murine ligand for CD40Nature, 1992
- Molecular Approaches to Analysis of X-Linked ImmunodeficienciesAnnual Review of Immunology, 1992
- Immunodeficiency with hyper IgM after systemic lupus erythematosusJournal of Allergy and Clinical Immunology, 1984
- Persistent Polyclonal Lymphocytosis of B LymphocytesNew England Journal of Medicine, 1982
- IgM cryoprecipitation and anti-immunoglobulin activity in dysgammaglobulinemia type IClinical Immunology and Immunopathology, 1982
- Familial variable immunodeficiency: Autosomal dominant pattern of inheritance with variable expression of the defect(s)The Journal of Pediatrics, 1975