Expert Nutritional and Medical Solutions
Greetings and welcome to our PhD nutritional and medical science consultation service. We are dedicated to providing one-on-one online health consultations for weight loss, medical conditions, and more. Our comprehensive ebooks offer valuable medical information and specialised diet meal plans tailored just for you.
Our mission
To bring nutritional and medical science to everyone.
To provide clients with the latest scientific data so they can make informed decisions about their health and diet.
To empower and inspire clients to live life to their optimal potential.
To let clients take control of their health.
You only have one life and we will help you make the most of it.
Our approach
We use PhD-level nutritional and medical research experience to expertly guide our clients.
All advice is based on published scientific research that is cross-referenced to ensure accuracy and no bias.
We do not sell supplements or provide unsubstantiated or error-prone biological analyses.
We use expert medical research skills to provide the most accurate advice tailored to you.
Experience and skills
OUR STORY
Dr. Simon Miller Ph.D.
Postdoctoral Medical Research Scientist
I am a University of Cambridge graduate with a Ph.D. in Molecular Biology. I have 18 years of medical research experience in cancer, heart disease, diabetes, neurodegeneration, inflammation, and aging.
My research has revealed insights into genetic diseases and contributed to the development of therapeutic drugs. I have published numerous first-author primary research and review manuscripts in elite scientific journals. I am also a review editor for Frontiers in Chemical Biology.
In addition to molecular biology, I am also a graduate in Biochemistry and Nutrition where I obtained a First-Class (1:1) Bachelor of Science (Combined Honours) degree.
Simon Miller
Education and qualifications
University of Cambridge
Ph.D. (Doctorate) in Molecular Biology
2006-2010
University of Southampton
First class (1:1) Bachelor's degree (combined honours) in Biochemistry and Nutrition
2003-2006
St. John's College, University of Cambridge
Selected Publications
Simon Miller et al., (2022). CRY2 isoform selectivity of a circadian clock modulator with anti-glioblastoma efficacy. PNAS. 119 (40) e2203936119. https://doi.org/10.1073/pnas.2203936119
Simon Miller and Tsuyoshi Hirota. (2022). De-Crypting Cryptochromes: Structural and chemical biology approaches reveal isoform-selective mechanisms of ligand interactions in mammalian Cryptochromes. Front. Physiol. (Chronobiology). 13:837280. https://doi.org/10.3389/fphys.2022.837280
Simon Miller et al., (2021). Structural differences in the FAD-binding pockets and lid loops of mammalian CRY1 and CRY2 for compound selectivity. PNAS. 118, e2026191118. https://doi.org/10.1073/pnas.2026191118
Dušan Kolarski, Simon Miller (joint first author), Ben L. Feringa* et al., (2021). Photopharmacological Manipulation of Mammalian CRY1 for Regulation of the Circadian Clock. J Am Chem Soc. 143, 2078-2087. https://doi.org/10.1021/jacs.0c12280 *Nobel Prize winner
Simon Miller et al., (2020). An isoform-selective modulator of Cryptochrome 1 regulates circadian rhythms in mammals. Cell Chemical Biology. 27, 1192-1198. https://doi.org/10.1016/j.chembiol.2020.05.008
Simon Miller et al., (2020). Isoform-selective regulation of mammalian Cryptochromes. Nature Chemical Biology. 16, 676-685.https://doi.org/10.1038/s41589-020-0505-1
Simon Miller and Tsuyoshi Hirota. (2020). Pharmacological interventions to circadian clocks and their molecular bases. Journal of Molecular Biology. 432, 3498-3514. https://doi.org/10.1016/j.jmb.2020.01.003
Simon Miller et al., (2010). Shaping Development of Autophagy Inhibitors with the Structure of the Lipid Kinase Vps34. Science. 327, 1638-1642. DOI: 10.1126/science.1184429
Alex Berndt, Simon Miller, Olusegan Williams, Daniel D Le, Benjamin T Houseman, et al., (2010). The crystal structures of the class IA PI3-kinase p110δ uncover the mechanisms for specificity and potency of novel PI3Kδ inhibitors. Nature Chemical Biology. 6, 117-124. https://doi.org/10.1038/nchembio.293
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