Differences in gene copy number carried by different MHC ancestral haplotypes. Quantitation after physical separation of haplotypes by pulsed field gel electrophoresis
暂无分享,去创建一个
[1] F. Christiansen,et al. Some disease-associated ancestral haplotypes carry a polymorphism of TNF. , 1989, Human immunology.
[2] S. Gitelman,et al. Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[3] P. Santamaria,et al. Involvement of class II MHC molecules in the LPS-induction of IL-1/TNF secretions by human monocytes. Quantitative differences at the polymorphic level. , 1989, Journal of immunology.
[4] T. Strachan,et al. Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21‐hydroxylase and complement C4 gene repeats in 21‐hydroxylase deficiency haplotypes. , 1989, The EMBO journal.
[5] B. Uring-Lambert,et al. Molecular basis of complete C4 deficiency. A study of three patients. , 1989, Human immunology.
[6] E. Albert,et al. Myasthenia Gravis: Joint Report , 1989 .
[7] F. Christiansen,et al. The Genomic Structure of Ancestral Haplotypes Revealed by Pulsed Field Gel Electrophoresis (PFGE) , 1989 .
[8] F. Christiansen,et al. Association Between Myasthenia Gravis and HLA Bw46, BfS, C4A4, C4B2, DRw9 in Chinese , 1989 .
[9] D. Wofsy,et al. Chronic therapy with recombinant tumor necrosis factor-alpha in autoimmune NZB/NZW F1 mice. , 1989, Clinical immunology and immunopathology.
[10] N. Morling,et al. Association between HLA‐DR2 and Production of Tumour Necrosis Factor α and Interleukin 1 by Mononuclear Cells Activated by Lipopolysaccharide , 1988, Scandinavian journal of immunology.
[11] F. Christiansen,et al. Coexistence of an MHC chromosomal segment marked by HLA B17,BfS,C4A6,B1,DR7, and DQw9 in different ethnic groups. , 1988, Human immunology.
[12] F. Christiansen,et al. Extensive deletions and insertions in different MHC supratypes detected by pusled field gel electrophoresis , 1988, The Journal of experimental medicine.
[13] J. Nerup,et al. Endotoxin‐Stimulated Human Monocyte Secretion of Interleukin 1, Tumour Necrosis Factor Alpha, and Prostaglandin E2 Shows Stable Interindividual Differences , 1988, Scandinavian journal of immunology.
[14] B. Mevåg,et al. Restriction fragment length polymorphisms of the complement component C4 loci on chromosome 6: studies with emphasis on the determination of gene number , 1988, Annals of human genetics.
[15] L. Flaherty. Major histocompatibility complex polymorphism: a nonimmune theory for selection. , 1988, Human immunology.
[16] V. Sutton,et al. Mapping of a restriction fragment length polymorphism associated with defective DR beta 4 chain expression to the HLA-DRB1 gene. , 1988, Human immunology.
[17] B. Beutler,et al. The role of cachectin/TNF in endotoxic shock and cachexia. , 1988, Immunology today.
[18] H. Mcdevitt,et al. Tumour necrosis factor-alpha in murine autoimmune 'lupus' nephritis. , 1988, Nature.
[19] P. Kay,et al. C4 allotyping on plasma or serum: application to routine laboratories. , 1988, Human immunology.
[20] A. Fauci,et al. Effect of tumor necrosis factor alpha on mitogen-activated human B cells , 1987, The Journal of experimental medicine.
[21] E. Southern,et al. A model for the separation of large DNA molecules by crossed field gel electrophoresis. , 1987, Nucleic acids research.
[22] D. Larhammar,et al. Class II genes of the human major histocompatibility complex. Organization and evolutionary relationship of the DR beta genes. , 1987, The Journal of biological chemistry.
[23] M. Carroll. Molecular genetics of the fourth component of human complement. , 1987, Federation proceedings.
[24] A. Wilton,et al. HETEROGENEITY OF STEROID 21‐HYDROXYLASE GENES IN CLASSICAL CONGENITAL ADRENAL HYPERPLASIA , 1987, Journal of immunogenetics.
[25] E. Sim,et al. Phenotyping of human complement component C4, a class-III HLA antigen. , 1986, The Biochemical journal.
[26] H. Colten,et al. Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants. , 1986, The Journal of clinical investigation.
[27] P. White,et al. Structure of human steroid 21-hydroxylase genes. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[28] J. Bodmer,et al. Gene clusters and the evolution of the major histocompatibility system. , 1986, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[29] M. Tilanus,et al. Reduced complexity of RFLP for HLA-DR typing by the use of a DR beta 3' cDNA probe. , 1986, Tissue antigens.
[30] K. C. Reed,et al. Rapid transfer of DNA from agarose gels to nylon membranes. , 1985, Nucleic acids research.
[31] D. Goeddel,et al. Human lymphotoxin and tumor necrosis factor genes: structure, homology and chromosomal localization. , 1985, Nucleic acids research.
[32] P. A. Peterson,et al. HLA-DR beta genes vary in number between different DR specificities, whereas the number of DQ beta genes is constant. , 1985, Journal of immunology.
[33] Bharat B. Aggarwal,et al. Human tumour necrosis factor: precursor structure, expression and homology to lymphotoxin , 1984, Nature.
[34] D. Bentley,et al. The factor B and C2 genes. , 1984, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[35] K. Belt,et al. The structural basis of the multiple forms of human complement component C4 , 1984, Cell.
[36] R. Campbell,et al. Internal homologies of the Ba fragment from human complement component Factor B, a class III MHC antigen. , 1984, The EMBO journal.
[37] F. Christiansen,et al. Complement allotyping in SLE: association with C4A null. , 1983, Australian and New Zealand journal of medicine.
[38] A. Feinberg,et al. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.
[39] Eric O Long,et al. Complete sequence of an HLA‐dR beta chain deduced from a cDNA clone and identification of multiple non‐allelic DR beta chain genes. , 1983, The EMBO journal.
[40] J. McCluskey,et al. Disease Associations with Complotypes, Supratypes and Haplotypes , 1983, Immunological reviews.
[41] 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.
[42] R. Dawkins. Immunogenetics in rheumatology : musculoskeletal disease and D-penicillamine : including reports from the D-Pen-HLA 82 Workshop held in Perth, Western Australia, 14-22 April 1982 , 1982 .
[43] B. Dupont,et al. CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) , 1977, The Lancet.