Zobrazeno 1 - 7 of 7 pro vyhledávání: '"C. M. Milner"'
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The coding sequence of the hemolytically inactive C4A6 allotype of human complement component C4 reveals that a single arginine to tryptophan substitution at beta-chain residue 458 is the likely cause of the defect
Autor: M J Anderson, C M Milner, R G Cotton, R D Campbell
Publikováno v: The Journal of Immunology. 148:2795-2802
The C4A6 allotype of the human complement component C4 is known to be defective in C5 binding within the C5 convertase. To characterize the position and nature of the molecular defect in the C4A6 allotype we have isolated the C4A6 gene from a cosmid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e8eb2120117d943b5fc5c6660424ff56
https://doi.org/10.4049/jimmunol.148.9.2795
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3
A novel variant of the MHC-linked hsp70, hsp70-hom, is associated with rheumatoid arthritis
Autor: S C, Jenkins, R E, March, R D, Campbell, C M, Milner
Publikováno v: Tissue antigens. 56(1)
The three major histocompatibility complex (MHC)-linked hsp70s have been screened for variation in their 28 kDa C-terminal regions by direct nucleotide sequencing of the corresponding DNA fragments. No amino acid variation was detected in the major h
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b65adf184a8bc2006b457f21ca10e7f9
https://pubmed.ncbi.nlm.nih.gov/10958354
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4
Cloning and characterization of a sialidase from the murine histocompatibility-2 complex: low levels of mRNA and a single amino acid mutation are responsible for reduced sialidase activity in mice carrying the Neu1a allele
Autor: M B, Carrillo, C M, Milner, S T, Ball, M, Snoek, R D, Campbell
Publikováno v: Glycobiology. 7(7)
The Neu1 locus, in the S region of the murine histocompatibility-2 complex, regulates the sialic acid content of several liver lysosomal enzymes. Three alleles, Neu1a, Neu1b, and Neu1c, have been described on the basis of differential sialylation of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f6085b73168c93a2c6693e268a3429f8
https://pubmed.ncbi.nlm.nih.gov/9363440
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6
Genes, genes and more genes in the human major histocompatibility complex
Autor: C M, Milner, R D, Campbell
Publikováno v: BioEssays : news and reviews in molecular, cellular and developmental biology. 14(8)
The human major histocompatibility complex (MHC), on the short arm of chromosome 6, represents one of the most extensively characterised regions of the human genome. This approximately 4 Mb segment of DNA contains genes encoding the polymorphic MHC c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2778731674beff2572aed2e39c87efc0
https://pubmed.ncbi.nlm.nih.gov/1365911
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7
The coding sequence of the hemolytically inactive C4A6 allotype of human complement component C4 reveals that a single arginine to tryptophan substitution at beta-chain residue 458 is the likely cause of the defect
Autor: M J, Anderson, C M, Milner, R G, Cotton, R D, Campbell
Publikováno v: Journal of immunology (Baltimore, Md. : 1950). 148(9)
The C4A6 allotype of the human complement component C4 is known to be defective in C5 binding within the C5 convertase. To characterize the position and nature of the molecular defect in the C4A6 allotype we have isolated the C4A6 gene from a cosmid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::859d6007fa611dc58b9521f1e60a75d2
https://pubmed.ncbi.nlm.nih.gov/1573268
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