Результаты поиска - Watkins, Hugh

Multiple disease genes cause hypertrophic cardiomyopathy по Watkins, Hugh

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Waiting for the working draft from the human genome project: A huge achievement, but not of immediate medical use по Cardon, Lon R, Watkins, Hugh

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Localization of the binding site of the C-terminal domain of cardiac myosin-binding protein-C on the myosin rod по Flashman, Emily, Watkins, Hugh, Redwood, Charles

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Personalized medicine: hope or hype? по Salari, Keyan, Watkins, Hugh, Ashley, Euan A.

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Localisation of AMPK γ subunits in cardiac and skeletal muscles по Pinter, Katalin, Grignani, Robert T., Watkins, Hugh, Redwood, Charles

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Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers по Grace, Christopher, Farrall, Martin, Watkins, Hugh, Goel, Anuj

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Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: Insights into disease pathogenesis and troponin function по Sweeney, H. Lee, Feng, Huisheng S., Yang, Zhaouhui, Watkins, Hugh

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Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications по Ormondroyd, Elizabeth, Oates, Stephanie, Parker, Michael, Blair, Edward, Watkins, Hugh

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Subunit composition of AMPK trimers present in the cytokinetic apparatus: Implications for drug target identification по Pinter, Katalin, Jefferson, Andrew, Czibik, Gabor, Watkins, Hugh, Redwood, Charles

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Determination of AMP-activated protein kinase phosphorylation sites in recombinant protein expressed using the pET28a vector: A cautionary tale по Renz, Bernhard, Davies, Joanna K., Carling, David, Watkins, Hugh, Redwood, Charles

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Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies по Mackley, Michael P., Fletcher, Benjamin, Parker, Michael, Watkins, Hugh, Ormondroyd, Elizabeth

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From Genotype to Phenotype: Clinical Assessment and Participant Perspective of a Secondary Genomic Finding Associated with Long QT Syndrome по Mackley, Michael, McGuire, Karen, Taylor, Jenny, Watkins, Hugh, Ormondroyd, Elizabeth

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Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes по Grace, Christopher, Hopewell, Jemma C., Watkins, Hugh, Farrall, Martin, Goel, Anuj

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Embryonic expression of AMPK γ subunits and the identification of a novel γ2 transcript variant in adult heart по Pinter, Katalin, Grignani, Robert T., Czibik, Gabor, Farza, Hend, Watkins, Hugh, Redwood, Charles

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Discrepancy Between Pathological Progression and Clinical Stability in a Young Patient with Hypertrophic Cardiomyopathy по Raman, Betty, Wen, David, Chan, Kenneth, Watkins, Hugh, Neubauer, Stefan, Mahmod, Masliza

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Mavacamten rescues increased myofilament calcium sensitivity and dysregulation of Ca(2+) flux caused by thin filament hypertrophic cardiomyopathy mutations по Sparrow, Alexander J., Watkins, Hugh, Daniels, Matthew J., Redwood, Charles, Robinson, Paul

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Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease по Grace, Christopher, Clarke, Robert, Goel, Anuj, Farrall, Martin, Watkins, Hugh, Hopewell, Jemma C.

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Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study по Mackley, Michael P, Blair, Edward, Parker, Michael, Taylor, Jenny C, Watkins, Hugh, Ormondroyd, Elizabeth

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Patients with hypertrophic cardiomyopathy (HCM) and HCM gene carriers have attenuated myocardial oxygenation response to vasodilator stress - a potential mechanism for sudden cardi... по Dass, Sairia, Karamitsos, Theodoros, Suttie, Joseph, Sever, Emily, Jerosch-Herold, Michael, Watkins, Hugh, Neubauer, Stefan

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In vivo mouse cardiac hyperpolarized magnetic resonance spectroscopy по Dodd, Michael S, Ball, Vicky, Bray, Rosalind, Ashrafian, Houman, Watkins, Hugh, Clarke, Kieran, Tyler, Damian J

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