Soutar AK - Search Results

1

Identification of recurrent and novel mutations in exon 4 of the LDL receptor gene in patients with familial hypercholesterolemia in the United Kingdom.

Gudnason V, King-Underwood L, Seed M, Sun XM, Soutar AK, Humphries SE. Gudnason V, et al. Among authors: soutar ak. Arterioscler Thromb. 1993 Jan;13(1):56-63. doi: 10.1161/01.atv.13.1.56. Arterioscler Thromb. 1993. PMID: 8093663

2

Identification of the 664 proline to leucine mutation in the low density lipoprotein receptor in four unrelated patients with familial hypercholesterolaemia in the UK.

King-Underwood L, Gudnason V, Humphries S, Seed M, Patel D, Knight B, Soutar A. King-Underwood L, et al. Clin Genet. 1991 Jul;40(1):17-28. doi: 10.1111/j.1399-0004.1991.tb03064.x. Clin Genet. 1991. PMID: 1884514

3

Comparison of the genetic defect with LDL-receptor activity in cultured cells from patients with a clinical diagnosis of heterozygous familial hypercholesterolemia. The Familial Hypercholesterolaemia Regression Study Group.

Sun XM, Patel DD, Knight BL, Soutar AK. Sun XM, et al. Among authors: soutar ak. Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):3092-101. doi: 10.1161/01.atv.17.11.3092. Arterioscler Thromb Vasc Biol. 1997. PMID: 9409298

4

Phenotypic variation in heterozygous familial hypercholesterolemia: a comparison of Chinese patients with the same or similar mutations in the LDL receptor gene in China or Canada.

Pimstone SN, Sun XM, du Souich C, Frohlich JJ, Hayden MR, Soutar AK. Pimstone SN, et al. Among authors: soutar ak. Arterioscler Thromb Vasc Biol. 1998 Feb;18(2):309-15. doi: 10.1161/01.atv.18.2.309. Arterioscler Thromb Vasc Biol. 1998. PMID: 9484998

5

Characterization of deletions in the LDL receptor gene in patients with familial hypercholesterolemia in the United Kingdom.

Sun XM, Webb JC, Gudnason V, Humphries S, Seed M, Thompson GR, Knight BL, Soutar AK. Sun XM, et al. Among authors: soutar ak. Arterioscler Thromb. 1992 Jul;12(7):762-70. doi: 10.1161/01.atv.12.7.762. Arterioscler Thromb. 1992. PMID: 1319734

6

Relationship between apolipoprotein(a) phenotype, lipoprotein(a) concentration in plasma, and low density lipoprotein receptor function in a large kindred with familial hypercholesterolemia due to the pro664----leu mutation in the LDL receptor gene.

Soutar AK, McCarthy SN, Seed M, Knight BL. Soutar AK, et al. J Clin Invest. 1991 Aug;88(2):483-92. doi: 10.1172/JCI115329. J Clin Invest. 1991. PMID: 1830890 Free PMC article.

7

Effect of the StuI polymorphism in the LDL receptor gene (Ala 370 to Thr) on lipid levels in healthy individuals.

Gudnason V, Patel D, Sun XM, Humphries S, Soutar AK, Knight BL. Gudnason V, et al. Among authors: soutar ak. Clin Genet. 1995 Feb;47(2):68-74. doi: 10.1111/j.1399-0004.1995.tb03926.x. Clin Genet. 1995. PMID: 7606846

8

Characterization of a splice-site mutation in the gene for the LDL receptor associated with an unpredictably severe clinical phenotype in English patients with heterozygous FH.

Sun XM, Patel DD, Bhatnagar D, Knight BL, Soutar AK. Sun XM, et al. Among authors: soutar ak. Arterioscler Thromb Vasc Biol. 1995 Feb;15(2):219-27. doi: 10.1161/01.atv.15.2.219. Arterioscler Thromb Vasc Biol. 1995. PMID: 7749829

9

Familial hypercholesterolemia in China. Identification of mutations in the LDL-receptor gene that result in a receptor-negative phenotype.

Sun XM, Patel DD, Webb JC, Knight BL, Fan LM, Cai HJ, Soutar AK. Sun XM, et al. Among authors: soutar ak. Arterioscler Thromb. 1994 Jan;14(1):85-94. doi: 10.1161/01.atv.14.1.85. Arterioscler Thromb. 1994. PMID: 7903864

10

The 15th annual meeting of the European Lipoprotein Club.

Aggerbeck LP, Angelin B, Armstrong V, Franceschini G, Humphries S, Rosseneu M, Soutar A, Zechner R. Aggerbeck LP, et al. Arterioscler Thromb. 1993 Apr;13(4):618-27. doi: 10.1161/01.atv.13.4.618. Arterioscler Thromb. 1993. PMID: 8385481 No abstract available.

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