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Anne K. Soutar

Imperial College London

52H指数
214论文数
9.2K被引数
收录论文 39
发表时间
Improved cardiovascular outcomes following temporal advances in lipid-lowering therapy in a genetically-characterised cohort of familial hypercholesterolaemia homozygotes
err2015-11-01
err39
errOAAI
errThompson, Gilbert R.; Seed, Mary; Naoumova, Rossi P.; Neuwirth, Clare; Walji, Shahenaz; Aitman, Timothy J.; Scott, James; Myant, Nicolas B.; Soutar, Anne K.
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In Memoriam: Nick Myant (1917-2015)
err2015-06-01
err1
errOAAI
errGibbons, Geoffrey; Soutar, Anne; Thompson, Gilbert
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The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia
err2013-12-01
err60
errOAAI
errVandrovcova, Jana; Thomas, Ellen R. A.; Atanur, Santosh S.; Norsworthy, Penny J.; Neuwirth, Clare; Tan, Yvonne; Kasperaviciute, Dalia; Biggs, Jennifer; Game, Laurence; Mueller, Michael; Soutar, Anne K.; Aitman, Timothy J.
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Novel functional APOB mutations outside LDL-binding region causing familial hypercholesterolaemia
err2013-11-13
err70
errOAAI
errAlves, Ana Catarina; Etxebarria, Aitor; Soutar, Anne Katherine; Martin, Cesar; Bourbon, Mafalda
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In vitro functional characterization of missense mutations in the LDLR gene
err2012-11-01
err24
PREAI
errSilva, S.; Alves, A. C.; Patel, D.; Malho, R.; Soutar, A. K.; Bourbon, M.
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Increased Secretion of Lipoproteins in Transgenic Mice Expressing Human D374Y PCSK9 Under Physiological Genetic Control
err2010-07-01
err72
errOAAI
errHerbert, Bronwen; Patel, Dilipkumar; Waddington, Simon N.; Eden, Emily R.; McAleenan, Alexandra; Sun, Xi-Ming; Soutar, Anne K.
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Genetic diagnosis of familial hypercholesterolaemia: the importance of functional analysis of potential splice-site mutations
err2009-05-01
err42
errOAAI
errBourbon, M.; Duarte, M. A.; Alves, A. C.; Medeiros, A. M.; Marques, L.; Soutar, A. K.
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Degradation of LDLR protein mediated by 'gain of function' PCSK9 mutants in normal and ARH cells
err2009-03-01
err72
PREAI
errFasano, Tommaso; Sun, Xi-Ming; Patel, Dilipkumar D.; Soutar, Anne K.
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Effects of ezetimibe and/or simvastatin on LDL receptor protein expression and on LDL receptor and HMG-CoA reductase gene expression: A randomized trial in healthy men依泽替米贝和/或辛伐他汀对LDL受体蛋白表达以及LDL受体和hmg-coa还原酶基因表达的影响: 健康男性的随机试验
err2008-05-01
err67
PREAI
errGouni-Berthold, Ioanna; Berthold, Heiner K.; Gylling, Helena; Hallikainen, Maarit; Giannakidou, Eleni; Stier, Sebastian; Ko, Yon; Patel, Dilip; Soutar, Anne K.; Seedorf, Udo; Mantzoros, Christos S.; Plat, Jogchum; Krone, Wilhelm
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Familial hypercholesterolaemia in Portugal葡萄牙中的家族性高胆固醇血症
err2008-02-01
err91
errOAAI
errBourbon, M.; Alves, A. C.; Medeiros, A. M.; Silva, S.; Soutar, A. K.
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Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk
err2006-07-06
err238
errOAAI
errHumphries, S. E.; Whittall, R. A.; Hubbart, C. S.; Maplebeck, S.; Cooper, J. A.; Soutar, A. K.; Naoumova, R.; Thompson, G. R.; Seed, M.; Durrington, P. N.; Miller, J. P.; Betteridge, D. J. B.; Neil, H. A. W.
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A single point mutation in the low-density lipoprotein receptor switches the degradation of its mature protein from the proteasome to the lysosome
err2006-01-01
err12
PREAI
errMartin de Llano, Jose Javier; Fuertes, Graciela; Andreu, Enrique Jose; Puig, Oscar; Chaves, F. Javier; Soutar, Anne K.; Armengod, Maria-Eugenia; Knecht, Erwin
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Autosomal recessive hypercholesterolaemia: long-term follow up and response to treatment
err2004-05-01
err35
PREAI
errNaoumova, RP; Neuwirth, C; Lee, P; Miller, JP; Taylor, KG; Soutar, AK
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Genetic diagnosis of familial hypercholesterolaemia: a mutation and a rare non-pathogenic amino acid variant in the same family
err2004-05-01
err15
PREAI
errNaoumova, RP; Neuwirth, C; Pottinger, B; Whittal, R; Humphries, SE; Soutar, AK
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