https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-1044-7
Ziemann, M., Eren, Y., & El-Osta, A. (2016). Gene name errors are widespread in the scientific literature. Genome Biology, 17(1). https://doi.org/10.1186/s13059-016-1044-7
https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-1044-7
Ziemann, M., Eren, Y., & El-Osta, A. (2016). Gene name errors are widespread in the scientific literature. Genome Biology, 17(1). https://doi.org/10.1186/s13059-016-1044-7
https://www.science.org/doi/10.1126/science.adv9817
Lewis, S., Hempel, T., Jiménez-Luna, J., Gastegger, M., Xie, Y., Foong, A. Y. K., Satorras, V. G., Abdin, O., Veeling, B. S., Zaporozhets, I., Chen, Y., Yang, S., Foster, A. E., Schneuing, A., Nigam, J., Barbero, F., Stimper, V., Campbell, A., Yim, J., . . . Noé, F. (2025, July 10). Scalable emulation of protein equilibrium ensembles with generative deep learning. Science.
https://www.science.org/doi/10.1126/science.adv9817
https://pmc.ncbi.nlm.nih.gov/articles/PMC10905009/
Liu, P., Lapcinski, I. P., Hlynialuk, C. J., Steuer, E. L., Loude, T. J., Shapiro, S. L., Kemper, L. J., & Ashe, K. H. (2024). Aβ∗56 is a stable oligomer that impairs memory function in mice. iScience, 27(3), 109239. https://doi.org/10.1016/j.isci.2024.109239
Aβ∗56 is a ∼56-kDa, SDS-stable, A11-reactive, non-plaque-dependent, water-soluble, brain-derived oligomer containing canonical Aβ(1-40).
https://pmc.ncbi.nlm.nih.gov/articles/PMC11513550/
Ponce‐Bobadilla, A. V., Schmitt, V., Maier, C. S., Mensing, S., & Stodtmann, S. (2024). Practical guide to SHAP analysis: Explaining supervised machine learning model predictions in drug development. Clinical and Translational Science, 17(11).
https://doi.org/10.1111/cts.70056
https://www.nature.com/articles/s41586-025-08744-2
Hafner, D., Pasukonis, J., Ba, J., & Lillicrap, T. (2025). Mastering diverse control tasks through world models. Nature.
https://doi.org/10.1038/s41586-025-08744-2
Guarente, L., Sinclair, D. A., & Kroemer, G. (2024). Human trials exploring anti-aging medicines. Cell Metabolism, 36(2), 354–376. https://doi.org/10.1016/j.cmet.2023.12.007
https://www.cell.com/cell-metabolism/fulltext/S1550-4131(23)00458-8
QT:{{”
In a recent issue of Cell Metabolism, Guarente co-authored a review article about human trials exploring compounds that target pathways and mechanisms of aging along with David Sinclair, Ph.D., one of Dr. Guarente’s postdoctoral mentees and now a professor of genetics at Harvard Medical School, and Guido Kroemer, M.D., Ph.D., a professor at the Université Paris Cité. Guarente and his colleagues focus on eight drugs and compounds: metformin, NAD+ precursors, glucagon-like peptide-1 receptor agonists, TORC1 inhibitors, spermidine, senolytics, probiotics, and anti-inflammatories.
These interventions made the list for four reasons: 1) they’re well-represented in ongoing or completed human clinical trials; 2) they’ve been shown to slow aging in preclinical studies; 3) they’re thought to be sufficiently safe for long-term use in humans; and 4) they work by targeting the hallmarks of aging.
“}}
https://onlinelibrary.wiley.com/doi/10.1111/php.13866
Görlitz, M., Justen, L., Rochette, P. J., Buonanno, M., Welch, D., Kleiman, N. J., Eadie, E., Kaidzu, S., Bradshaw, W. J., Javorsky, E., Cridland, N., Galor, A., Guttmann, M., Meinke, M. C., Schleusener, J., Jensen, P., Söderberg, P., Yamano, N., Nishigori, C., . . . Esvelt, K. (2023). Assessing the safety of new germicidal far‐UVC technologies. Photochemistry and Photobiology, 100(3), 501–520.
https://doi.org/10.1111/php.13866
Has detailed setup for ELBO
https://arxiv.org/abs/1906.02691
Kingma, D. P., & Welling, M. (2019). An introduction to variational autoencoders. Foundations and Trends® in Machine Learning, 12(4), 307–392. https://doi.org/10.1561/2200000056