Cellular radiosensitivity in human severe-combined-immunodeficiency (SCID) syndromes

This publication has 13 references indexed in Scilit:

• Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation
  Cell, 1995
• Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency.
  Journal of Clinical Investigation, 1993
• Severe combined immunodeficiency (SCID) in man: B cell-negative (B-) SCID patients exhibit an irregular recombination pattern at the JH locus.
  The Journal of Experimental Medicine, 1991
• Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).
  Journal of Clinical Investigation, 1991
• The scid mutation in mice causes a general defect in DNA repair
  Nature, 1990
• DRFIT: A Program for Fitting Radiation Survival Models
  International Journal of Radiation Biology, 1990
• Novel T-Lymphocyte Population in Combined Immunodeficiency with Features of Graft-versus-Host Disease
  New England Journal of Medicine, 1989
• Evidence of functional lymphocytes in some (leaky) scid mice.
  The Journal of Experimental Medicine, 1988
• Comparative Human Cellular Radiosensitivity: I. The Effect of SV40 Transformation and Immortalisation on the Gamma-irradiation Survival of Skin Derived Fibroblasts from Normal Individuals and from Ataxia-telangiectasia Patients and Heterozygotes
  International Journal of Radiation Biology, 1988
• Radiosensitivity in Cultured Human Fibroblasts
  International Journal of Radiation Biology and Related Studies in Physics, Chemistry and Medicine, 1980