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126 results
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Current management of severe homozygous hypercholesterolaemias.
Naoumova RP, Thompson GR, Soutar AK. Naoumova RP, et al. Among authors: soutar ak. Curr Opin Lipidol. 2004 Aug;15(4):413-22. doi: 10.1097/01.mol.0000137222.23784.2a. Curr Opin Lipidol. 2004. PMID: 15243214 Review.
Identification of a point mutation in growth factor repeat C of the low density lipoprotein-receptor gene in a patient with homozygous familial hypercholesterolemia that affects ligand binding and intracellular movement of receptors.
Soutar AK, Knight BL, Patel DD. Soutar AK, et al. Proc Natl Acad Sci U S A. 1989 Jun;86(11):4166-70. doi: 10.1073/pnas.86.11.4166. Proc Natl Acad Sci U S A. 1989. PMID: 2726768 Free PMC article.
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: soutar ak. 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.
Degradation of LDLR protein mediated by 'gain of function' PCSK9 mutants in normal and ARH cells.
Fasano T, Sun XM, Patel DD, Soutar AK. Fasano T, et al. Among authors: soutar ak. Atherosclerosis. 2009 Mar;203(1):166-71. doi: 10.1016/j.atherosclerosis.2008.10.027. Epub 2008 Nov 6. Atherosclerosis. 2009. PMID: 19081568
Adaptor protein disabled-2 modulates low density lipoprotein receptor synthesis in fibroblasts from patients with autosomal recessive hypercholesterolaemia.
Eden ER, Sun XM, Patel DD, Soutar AK. Eden ER, et al. Among authors: soutar ak. Hum Mol Genet. 2007 Nov 15;16(22):2751-9. doi: 10.1093/hmg/ddm232. Epub 2007 Aug 29. Hum Mol Genet. 2007. PMID: 17761685
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia.
Vandrovcova J, Thomas ER, Atanur SS, Norsworthy PJ, Neuwirth C, Tan Y, Kasperaviciute D, Biggs J, Game L, Mueller M, Soutar AK, Aitman TJ. Vandrovcova J, et al. Among authors: soutar ak. Genet Med. 2013 Dec;15(12):948-57. doi: 10.1038/gim.2013.55. Epub 2013 May 16. Genet Med. 2013. PMID: 23680767
Premature senescence in cells from patients with autosomal recessive hypercholesterolemia (ARH): evidence for a role for ARH in mitosis.
Sun XM, Patel DD, Acosta JC, Gil J, Soutar AK. Sun XM, et al. Among authors: soutar ak. Arterioscler Thromb Vasc Biol. 2011 Oct;31(10):2270-7. doi: 10.1161/ATVBAHA.111.232223. Epub 2011 Jul 21. Arterioscler Thromb Vasc Biol. 2011. PMID: 21778424
Unexpected roles for PCSK9 in lipid metabolism.
Soutar AK. Soutar AK. Curr Opin Lipidol. 2011 Jun;22(3):192-6. doi: 10.1097/MOL.0b013e32834622b5. Curr Opin Lipidol. 2011. PMID: 21494143 Review.
Increased secretion of lipoproteins in transgenic mice expressing human D374Y PCSK9 under physiological genetic control.
Herbert B, Patel D, Waddington SN, Eden ER, McAleenan A, Sun XM, Soutar AK. Herbert B, et al. Among authors: soutar ak. Arterioscler Thromb Vasc Biol. 2010 Jul;30(7):1333-9. doi: 10.1161/ATVBAHA.110.204040. Epub 2010 May 6. Arterioscler Thromb Vasc Biol. 2010. PMID: 20448210
Rare genetic causes of autosomal dominant or recessive hypercholesterolaemia.
Soutar AK. Soutar AK. IUBMB Life. 2010 Feb;62(2):125-31. doi: 10.1002/iub.299. IUBMB Life. 2010. PMID: 20073037 Free article. Review.
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