Seed M - Search Results

1

Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemia.

Thomas ER, Atanur SS, Norsworthy PJ, Encheva V, Snijders AP, Game L, Vandrovcova J, Siddiq A, Seed M, Soutar AK, Aitman TJ. Thomas ER, et al. Among authors: seed m. Mol Genet Genomic Med. 2013 Sep;1(3):155-61. doi: 10.1002/mgg3.17. Epub 2013 Jun 13. Mol Genet Genomic Med. 2013. PMID: 24498611 Free PMC article.

2

Improved cardiovascular outcomes following temporal advances in lipid-lowering therapy in a genetically-characterised cohort of familial hypercholesterolaemia homozygotes.

Thompson GR, Seed M, Naoumova RP, Neuwirth C, Walji S, Aitman TJ, Scott J, Myant NB, Soutar AK. Thompson GR, et al. Among authors: seed m. Atherosclerosis. 2015 Nov;243(1):328-33. doi: 10.1016/j.atherosclerosis.2015.09.029. Epub 2015 Sep 28. Atherosclerosis. 2015. PMID: 26433113 Free article.

3

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. Among authors: seed m. J Clin Invest. 1991 Aug;88(2):483-92. doi: 10.1172/JCI115329. J Clin Invest. 1991. PMID: 1830890 Free PMC article.

4

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. Among authors: seed m. Clin Genet. 1991 Jul;40(1):17-28. doi: 10.1111/j.1399-0004.1991.tb03064.x. Clin Genet. 1991. PMID: 1884514

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: seed m. Arterioscler Thromb. 1992 Jul;12(7):762-70. doi: 10.1161/01.atv.12.7.762. Arterioscler Thromb. 1992. PMID: 1319734

6

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: seed m. Arterioscler Thromb. 1993 Jan;13(1):56-63. doi: 10.1161/01.atv.13.1.56. Arterioscler Thromb. 1993. PMID: 8093663

7

Catabolism of lipoprotein(a) in familial hypercholesterolaemic subjects.

Knight BL, Perombelon YF, Soutar AK, Wade DP, Seed M. Knight BL, et al. Among authors: seed m. Atherosclerosis. 1991 Apr;87(2-3):227-37. doi: 10.1016/0021-9150(91)90025-x. Atherosclerosis. 1991. PMID: 1830206

8

Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk.

Humphries SE, Whittall RA, Hubbart CS, Maplebeck S, Cooper JA, Soutar AK, Naoumova R, Thompson GR, Seed M, Durrington PN, Miller JP, Betteridge DJ, Neil HA; Simon Broome Familial Hyperlipidaemia Register Group and Scientific Steering Committee. Humphries SE, et al. Among authors: seed m. J Med Genet. 2006 Dec;43(12):943-9. doi: 10.1136/jmg.2006.038356. J Med Genet. 2006. PMID: 17142622 Free PMC article.

9

Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations.

Futema M, Plagnol V, Li K, Whittall RA, Neil HA, Seed M; Simon Broome Consortium; Bertolini S, Calandra S, Descamps OS, Graham CA, Hegele RA, Karpe F, Durst R, Leitersdorf E, Lench N, Nair DR, Soran H, Van Bockxmeer FM; UK10K Consortium; Humphries SE. Futema M, et al. Among authors: seed m. J Med Genet. 2014 Aug;51(8):537-44. doi: 10.1136/jmedgenet-2014-102405. Epub 2014 Jul 1. J Med Genet. 2014. PMID: 24987033 Free PMC article.

10

Four DNA polymorphisms in the LDL receptor gene: their genetic relationship and use in the study of variation at the LDL receptor locus.

Taylor R, Jeenah M, Seed M, Humphries S. Taylor R, et al. Among authors: seed m. J Med Genet. 1988 Oct;25(10):653-9. doi: 10.1136/jmg.25.10.653. J Med Genet. 1988. PMID: 2906372 Free PMC article.

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