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Results: 1-12 |
Results: 12

Authors: O'Neill, FH Patel, DD Knight, BL Neuwirth, CKY Bourbon, M Soutar, AK Taylor, GW Thompson, GR Naoumova, RP
Citation: Fh. O'Neill et al., Determinants of variable response to statin treatment in patients with refractory familial hypercholesterolemia, ART THROM V, 21(5), 2001, pp. 832-837

Authors: Riddell, DR Sun, XM Stannard, AK Soutar, AK Owen, JS
Citation: Dr. Riddell et al., Localization of apolipoprotein E receptor 2 to caveolae in the plasma membrane, J LIPID RES, 42(6), 2001, pp. 998-1002

Authors: Slimane, MN Lestavel, S Sun, XM Maatouk, F Soutar, AK Ben Farhat, MH Clavey, V Benlian, P Hammami, M
Citation: Mn. Slimane et al., Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian families, ATHEROSCLER, 154(3), 2001, pp. 557-565

Authors: Eden, ER Naoumova, RP Burden, JJ McCarthy, MI Soutar, AK
Citation: Er. Eden et al., Use of homozygosity mapping to identify a region on chromosome 1 bearing adefective gene that causes autosomal recessive homozygous hypercholesterolemia in two unrelated families, AM J HU GEN, 68(3), 2001, pp. 653-660

Authors: Ekstrom, U Abrahamson, M Sveger, T Sun, XM Soutar, AK Nilsson-Ehle, P
Citation: U. Ekstrom et al., Expression of an LDL receptor allele with two different mutations (E256K and I402T), J CL PATH-M, 53(1), 2000, pp. 31-36

Authors: Patel, DD Knight, BL Soutar, AK Gibbons, GF Wade, DP
Citation: Dd. Patel et al., The effect of peroxisome-proliferator-activated receptor-alpha on the activity of the cholesterol 7 alpha-hydroxylase gene, BIOCHEM J, 351, 2000, pp. 747-753

Authors: Kreuter, R Soutar, AK Wade, DP
Citation: R. Kreuter et al., Transcription factors CCAAT/enhancer-binding protein beta and nuclear factor-Y bind to discrete regulatory elements in the very low density lipoprotein receptor promoter, J LIPID RES, 40(3), 1999, pp. 376-386

Authors: Norman, D Sun, XM Bourbon, M Knight, BL Naoumova, RP Soutar, AK
Citation: D. Norman et al., Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia, J CLIN INV, 104(5), 1999, pp. 619-628

Authors: Sun, XM Soutar, AK
Citation: Xm. Sun et Ak. Soutar, Expression in vitro of alternatively spliced variants of the messenger RNAfor human apolipoprotein E receptor-2 identified in human tissues by ribonuclease protection assays, EUR J BIOCH, 262(1), 1999, pp. 230-239

Authors: Bourbon, M Fowler, AM Sun, XM Soutar, AK
Citation: M. Bourbon et al., Inheritance of two different alleles of the low-density lipoprotein (LDL)-receptor gene carrying the recurrent Pro664Leu mutation in a patient with homozygous familial hypercholesterolaemia, CLIN GENET, 56(3), 1999, pp. 225-231

Authors: Ekstrom, U Abrahamson, M Floren, CH Tollig, H Wettrell, G Nilsson, E Sun, XM Soutar, AK Nilsson-Ehle, P
Citation: U. Ekstrom et al., An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F), CLIN GENET, 55(5), 1999, pp. 332-339

Authors: Soutar, AK
Citation: Ak. Soutar, Low-density lipoprotein receptors, LIPOPROTEINS IN HEALTH AND DISEASE, 1999, pp. 303-322
Risultati: 1-12 |