HLA B44 is associated with decreased severity of autoimmune lymphoproliferative syndrome in patients with CD95 defects (ALPS type Ia)
- 31 January 2006
- journal article
- Published by Elsevier in Clinical Immunology
- Vol. 118 (1) , 59-65
- https://doi.org/10.1016/j.clim.2005.09.006
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Influence of Human Leukocyte Antigen in the Pathogenesis of Me´nie`re's Disease in the South Korean PopulationActa Oto-Laryngologica, 2002
- The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosisBlood, 2001
- The family based association test method: strategies for studying general genotype–phenotype associationsEuropean Journal of Human Genetics, 2001
- Invited anniversary review: HLA associated diseasesHuman Immunology, 1997
- Mutations in Fas Associated with Human Lymphoproliferative Syndrome and AutoimmunityScience, 1995
- Dominant interfering fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndromeCell, 1995
- A novel lymphoproliferative/autoimmune syndrome resembling murine lpr/gld disease.Journal of Clinical Investigation, 1992
- Refined structure of the human histocompatibility antigen HLA-A2 at 2.6 Å resolutionJournal of Molecular Biology, 1991
- The two major subtypes of HLA‐B44 differ for a single amino acid in codon 156Tissue Antigens, 1991
- The foreign antigen binding site and T cell recognition regions of class I histocompatibility antigensNature, 1987