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    Browsing by Author "Yandle, Tim G."

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        Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin b12 levels in post-acute coronary syndromes patients 

        Whalley, Gillian; Palmer, Barry R.; Slow, Sandy; Ellis, Katrina L.; Pilbrow, Anna P.; Skelton, Lorraine; Frampton, Chris M.; Palmer, Suetonia C.; Troughton, R.W.; Yandle, Tim G.; Doughty, Robert N.; Lever, Michael; George, Peter M.; Chambers, Stephen T.; Ellis, Chris J.; Richards, A.M.; Cameron, Vicky A. (Public Library of Science, 2014-03-11)
        Background and Aims: The methylene-tetrahydrofolate dehydrogenase (NADP+ dependent) 1-like (MTHFD1L) gene is involved in mitochondrial tetrahydrofolate metabolism. Polymorphisms in MTHFD1L, including rs6922269, have been ...
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        Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients 

        Palmer, Barry R.; Slow, Sandy; Ellis, Katrina L.; Pilbrow, Anna P.; Skelton, Lorraine; Frampton, Chris M.; Palmer, Suetonia C.; Troughton, R.W.; Yandle, Tim G.; Doughty, Robert N.; Whalley, Gillian; Lever, Michael; George, Peter M.; Chambers, Stephen T.; Ellis, Chris J.; Richards, A.M.; Cameron, Vicky A. (Plos One, 2014-03-11)
        Background and Aims: The methylene-tetrahydrofolate dehydrogenase (NADP+ dependent) 1-like (MTHFD1L) gene is involved in mitochondrial tetrahydrofolate metabolism. Polymorphisms in MTHFD1L, including rs6922269, have been ...
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        Genetic variation in the renin–angiotensin–aldosterone system is associated with cardiovascular risk factors and early mortality in established coronary heart disease 

        Whalley, Gillian; Ellis, Katrina L.; Palmer, Barry R.; Frampton, Chris M.; Troughton, R.W.; Doughty, Robert N.; Ellis, Chris J.; Pilbrow, Anna P.; Skelton, Lorraine; Yandle, Tim G.; Richards, A.M.; Cameron, Vicky A. (2012)
        This study examined renin–angiotensin–aldosterone (RAAS) system gene variants for associations with cardiovascular risk factors and outcomes in coronary heart disease. Coronary disease patients (n¼1186) were genotyped for ...
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        Genomic Risk Variants at 1p13.3, 1q41, and 3q22.3 Are Associated With Subsequent Cardiovascular Outcomes in Healthy Controls and in Established Coronary Artery Genomic Risk Variants at 1p13.3, 1q41, and 3q22.3 Are Associated With Subsequent Cardiovascular Outcomes in Healthy Controls and in Established Coronary Artery Disease 

        Whalley, Gillian; Ellis, Katrina L.; Frampton, Chris M.; Pilbrow, Anna P.; Troughton, R.W.; Doughty, Robert N.; Ellis, Chris J.; Skelton, Lorraine; Thomson, Judith; Yandle, Tim G.; Richards, A.M.; Cameron, Vicky A. (2011)
        Coronary artery disease (CAD) has multifactorial origins, and although some families are particularly affected, no precise mode of inheritance has been identified. It is likely that this reflects the contribution of numerous ...

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