The immunological detection of a 21-OH deficiency mutation HLA supratype.
暂无分享,去创建一个
[1] J. McCluskey,et al. The Coexistence of IgA Deficiency and 21‐Hydroxylase Deficiency Marked by Specific MHC Supratypes , 1985, Annals of the New York Academy of Sciences.
[2] J. Hanke,et al. Class II determinants recognized by TNP-specific cloned human T cell lines. , 1985, Human immunology.
[3] E. Albert,et al. Genetic differences between the salt-wasting, simple virilizing, and nonclassical types of congenital adrenal hyperplasia. , 1985, The Journal of clinical endocrinology and metabolism.
[4] S. Libber,et al. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype. , 1985, The Journal of clinical endocrinology and metabolism.
[5] R. Campbell,et al. Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[6] P. White,et al. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation. , 1984 .
[7] M. Breuning,et al. A cloned cytotoxic T-lymphocyte (CTL) line recognizing a subtype of HLA B27. , 1984, Human immunology.
[8] F. Christiansen,et al. Complement allotyping in SLE: association with C4A null. , 1983, Australian and New Zealand journal of medicine.
[9] F. Bach,et al. Genetic and molecular analyses of lymphocyte-defined HLA-D region specificities. , 1983, Human immunology.
[10] B. Kohn,et al. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data. , 1983, The Journal of clinical endocrinology and metabolism.
[11] J. McCluskey,et al. Disease Associations with Complotypes, Supratypes and Haplotypes , 1983, Immunological reviews.
[12] E. Yunis,et al. Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[13] B. Kohn,et al. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia. , 1982, The Journal of clinical endocrinology and metabolism.
[14] J. Feingold,et al. HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population. , 1982, Tissue antigens.
[15] B. Kohn,et al. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency. , 1981, The Journal of clinical endocrinology and metabolism.
[16] J. Dausset. The major histocompatibility complex in man. , 1981, Science.
[17] B. Kohn,et al. HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency. , 1981, American journal of human genetics.
[18] J. Strominger,et al. Virus-immune cytotoxic T cells recognize structural differences between serologically indistinguishable HLA-A2 molecules. , 1980, Human immunology.
[19] Z. Laron,et al. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus. , 1980, Human immunology.
[20] C. Alper,et al. Inherited structural polymorphism of the fourth component of human complement. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[21] J. Winter,et al. Adult-onset familial adrenal 21-hydroxylase deficiency. , 1980, The American journal of medicine.