Search Results - "Olavesen, M G"

Human protectin (CD59), an 18,000-20,000 MW complement lysis restricting factor, inhibits C5b-8 catalysed insertion of C9 into lipid bilayers by MERI, P, MORGAN, B. P, DAVIES, A, DANIELS, R. H, OLAVESEN, M. G, WALDMANN, H, LACHMANN, P. J

“…Human cells are relatively resistant to lysis by the homologous complement system. Here we describe the mechanism of action of a recently discovered and widely…”
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High-Resolution YAC Fragmentation Map of 1q21 by Lioumi, Maria, Olavesen, M.G., Nizetic, Dean, Ragoussis, Jiannis

“…Chromosomal band 1q21 contains a number of genes, constituting the Epidermal differentiation complex (EDC), most of which are involved in the process of…”
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Fine Mapping of 39 ESTs on Human Chromosome 6p23–p25 by Olavesen, M.G., Bentley, E., Mason, R.V.F., Stephens, R.J., Ragoussis, J.

“…Loci conferring susceptibility to schizophrenia, coeliac disease, and orofacial clefting have been assigned to the 6p23–p25 region of human chromosome 6. To…”
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Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region by Davies, A F, Stephens, R J, Olavesen, M G, Heather, L, Dixon, M J, Magee, A, Flinter, F, Ragoussis, J

“…Orofacial clefting is genetically complex, no single gene being responsible for all forms. It can, however, result from a single gene defect either as part of…”
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Localization of Eight Additional Genes in the Human Major Histocompatibility Complex, Including the Gene Encoding the Casein Kinase II β Subunit (CSNK2B) by Albertella, Mark R., Jones, Helene, Thomson, Wendy, Olavesen, Mark G., Campbell, R.Duncan

“…A wide range of autoimmune and other diseases are known to be associated with the major histocompatibility complex. Many of these diseases are linked to the…”
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Up-regulation of type 1 plasminogen activator inhibitor messenger RNA with thrombotic changes in renal grafts by WANG, Y, PRATT, J. R, TAM, F. W. K, HARTLEY, B, WOLFF, J. A, OLAVESEN, M. G, SACKS, S. H

“…Small vessel thrombosis is a prominent feature in kidneys undergoing vascular rejection. Type I and type 2 plasminogen activator inhibitors (PAI-1 and PAI-2,…”
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Localization of a new gene adjacent to the HSP70 genes in human and mouse MHCs by OLAVESEN, M. G, SNOEK, M, CAMPBELL, R. D

“…A large number of genes have now been defined in the 1100 kilobases (kb) of DNA which separates the MHC class I and class II multigene families. These encode a…”
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Coding sequences and levels of expression of Hsc70t are identical in mice with different orch-1 alleles by SNOEK, M, OLAVESEN, M. G, VAN VUGT, H, MILNER, C. M, TEUSCHER, C, CAMPBELL, R. D

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Three Hsp70 genes are located in the C4-H-2D region: possible candidates for the Orch-1 locus by Snoek, M, Jansen, M, Olavesen, M G, Campbell, R D, Teuscher, C, van Vugt, H

“…The central region of the mouse MHC harbors a recombinational hot spot area. Most recombinations in this part of the complex take place between the Hsp70.1…”
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Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease by Olavesen, M G, Hampe, J, Mirza, M M, Saiz, R, Lewis, C M, Bridger, S, Teare, D, Easton, D F, Herrmann, T, Scott, G, Hirst, J, Sanderson, J, Hodgson, S V, Lee, J, MacPherson, A, Schreiber, S, Lennard-Jones, J E, Curran, M E, Mathew, C G

“…Genetic linkage analysis in families with multiple cases of inflammatory bowel disease (IBD) has mapped a gene which confers susceptibility to IBD to the…”
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A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome by Davies, A F, Olavesen, M G, Stephens, R J, Davidson, R, Delneste, D, Van Regemorter, N, Vamos, E, Flinter, F, Abusaad, I, Ragoussis, J

“…Deletions of the short arm of chromosome 6 are relatively rare, only 16 cases having been described in the literature so far. Here we present a detailed…”
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An integrated map of human chromosome 6p23 by Olavesen, M G, Davies, A F, Broxholme, S J, Wixon, J L, Senger, G, Nizetic, D, Campbell, R D, Ragoussis, J

“…The human chromosomal band 6p23 is a Giemsa-negative (light) band that may be expected to be relatively gene rich. The genes for spinocerebellar ataxia type 1…”
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Presence of a membrane attack complex inhibiting protein on the human epithelial cell line HeLa by Morgan, B P, Olavesen, M G, Watts, M J

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Localisation of eight additional genes in the human major histocompatibility complex, including the gene encoding the casein kinase II beta subunit, and DNA sequence analysis of the class III region by Albertella, M R, Jones, H, Thomson, W, Olavesen, M G, Neville, M, Campbell, R D

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A detailed investigation of two cases exibiting characteristics of the 6p deletion syndrome by DAVIES, A. F, OLAVESEN, M. G, STEPHENS, R. J, DAVIDSON, R, DELNESTE, D, VAN REGEMORTER, N, VAMOS, E, FLINTER, F, ABUSAAD, I, RAGOUSSIS, J

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