GPIHBP1 VARIANTS CONTRIBUTE TO LIPID LEVELS IN FAMILIAL COMBINED HYPERLIPIDEMIA von Ringham, H.E, Town, M.M, Horswell, S.D, Shoulders, C.C

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Genetics of familial combined hyperlipidemia and risk of coronary heart disease von Shoulders, C.C., Jones, E.L., Naoumova, R.P.

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Choline containing metabolites during cell transfection: an insight into magnetic resonance spectroscopy detectable changes von Griffin, J.L, Mann, C.J, Scott, J, Shoulders, C.C, Nicholson, J.K

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Microsomal triglyceride transfer protein, the abetalipoproteinemia gene product, mediates the secretion of apolipoprotein B-containing lipoproteins from heterologous cells von Leiper, J M, Bayliss, J D, Pease, R J, Brett, D J, Scott, J, Shoulders, C C

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Myeloid tribbles 1 induces early atherosclerosis via enhanced foam cell expansion von Johnston, J.M, Angyal, A, Bauer, R.C, Hamby, S, Suvarna, S.K, Baidžajevas, K, Hegedus, Z, Dear, T.N, Turner, M, Wilson, H.L, Goodall, A.H, Rader, D.J, Shoulders, C.C, Francis, S.E, Kiss-Toth, E

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Variation at the apo AI/CIII/A1V gene complex is associated with elevated plasma levels of apo CIII von Shoulders, C.C., Harry, P.J., Lagrost, L., White, S.E., Shah, N.F., North, J.D., Gilligan, M., Gambert, P., Ball, M.J.

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Human apoHpoprotetas AI, AII, CII and CIII. cDNA sequences and mRNA abundance von Sharpe, C.R., Sidoli, A., Shelley, C.S., Lucero, M.A., Shoulders, C.C., Baralle, F.E.

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Characterization of genetic markers in the 5' flanking region of the apo A1 gene von SHOULDERS, C. C, NARCISI, T. M. E, JARMUZ, A, BRETT, D. J, BAYLISS, J. D, SCOTT, J

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Molecular cloning of human LDL apolipoprotein B cDNA: Evidence for more than one gene per haploid genome von Shoulders, C.C., Myant, N.B., Sidoli, A., Rodriguez, J.C., Cortese, C., Baralle, F.E., Cortese, R.

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Mo-P6:383 Fine mapping a region on chromosome 11P for familial combined hyperlipidemia von Plaisier, C.L., Lusis, A.J., Naoumova, R.P., Shoulders, C.C., Taskinen, M.-R., De Bruin, T.W., Pajukanta, P.

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Dinucleotide repeat polymorphisms at the lipoprotein lipase (LPL) locus von NARCISI, T. M, SCHOTZ, M. C, SCOTT, J, SHOULDERS, C. C

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DNA POLYMORPHISM ADJACENT TO HUMAN APOPROTEIN A-1 GENE: RELATION TO HYPERTRIGLYCERIDAEMIA von Rees, A., Stocks, J., Shoulders, C.C., Galton, D.J., Baralle, F.E.

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Mo-W6:3 Genetics of intracellular lipid transport and familial combined hyperlipidemia von Shoulders, C.C., Jones, B., Jones, E.L., Bonney, S.A., Williams, P.A., Mensenkamp, A.R., Towney, A.K., Horswell, S.D., Stephens, D.J., Naoumova, R.P.

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GENETIC MARKER IN APOLIPOPROTEIN AI/CIII GENE COMPLEX ASSOCIATED WITH HYPERCHOLESTEROLAEMIA von Shoulders, C.C., Ball, M.J., Mann, J.I., Baralle, F.E., Ferns, G.A.A., Stocks, J., Galton, D.J.

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Molecular cloning of human LDL apolipoprotein B cDNA von Shoulders, C.C., Myant, N.B., Sidoli, A., Rodriguez, J.C., Cortese, C., Baralle, F.E., Cortese, R.

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Selective in vitro transcription of one of the two Alu family repeats present in the 5′ flanking region of the human ε-globin gene von Segni, G.Di, Carrara, G., Tocchini-Valentini, G.R., Shoulders, C.C., Baralle, F.E.

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