Omenn Syndrome: A Disorder of Rag1 and Rag2 Genes
- 1 January 1999
- journal article
- review article
- Published by Springer Nature in Journal of Clinical Immunology
- Vol. 19 (2) , 87-97
- https://doi.org/10.1023/a:1020550432126
Abstract
No abstract availableKeywords
This publication has 69 references indexed in Scilit:
- Neoteny in Lymphocytes: Rag1 and Rag2 Expression in Germinal Center B CellsScience, 1996
- Reexpression of RAG-1 and RAG-2 Genes in Activated Mature Mouse B cellsScience, 1996
- Identification of a nonsense mutation in the carboxyl-terminal region of DNA-dependent protein kinase catalytic subunit in the scid mouse.Proceedings of the National Academy of Sciences, 1996
- Mechanism of V(D)J recombinationCurrent Opinion in Immunology, 1996
- Treatment of Omenn syndrome by bone marrow transplantationThe Journal of Pediatrics, 1995
- Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency.Journal of Clinical Investigation, 1993
- RAG-1 and RAG-2, Adjacent Genes That Synergistically Activate V(D)J RecombinationScience, 1990
- Novel T-Lymphocyte Population in Combined Immunodeficiency with Features of Graft-versus-Host DiseaseNew England Journal of Medicine, 1989
- Identification by HLA Typing of Intrauterine-Derived Maternal T Cells in Four Patients with Severe Combined ImmunodeficiencyNew England Journal of Medicine, 1982
- Combined immunodeficiency and reticuloendotheliosis with eosinophiliaThe Journal of Pediatrics, 1974