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Nature|September 3, 2013
A statin-dependent QTL for GATM expression is associated with statin-induced myopathyLara M Mangravite, Barbara E Engelhardt, Marisa W Medina, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport SyndromeOliver Gross, Clifford E Kashtan, Michelle N Rheault, et al.
Science Advances|November 16, 2022
Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetesAbhishek Nag, Ryan S Dhindsa, Jonathan Mitchell, et al.
European Heart Journal|October 8, 2022
CODE-EHR best practice framework for the use of structured electronic healthcare records in clinical researchDipak Kotecha, Folkert W Asselbergs, Stephan Achenbach, et al.
Plos Medicine|February 25, 2012
Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication biasRobert Clarke, Derrick A Bennett, Sarah Parish, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 casesJonathan Mitchell, Niedzica Camacho, Patrick Shea, et al.
Plos One|April 7, 2009
Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretionStephen Newhouse, Martin Farrall, Chris Wallace, et al.
The Lancet. Digital Health|September 1, 2022
CODE-EHR best-practice framework for the use of structured electronic health-care records in clinical researchDipak Kotecha, Folkert W Asselbergs, Stephan Achenbach, et al.
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