Keywords

Aging; Autophagy; Cell Biology; Inflammation; Neuromuscular Diseases; Neurosciences; Stem Cell Research

Techniques, methods & infrastructure

Investigation of trangenic mouse models and patient samples

Selected publications

1. Sukseree, S. et al., 2021. Sequestosome 1/p62 enhances chronic skin inflammation. Journal of Allergy and Clinical Immunology, 147(6), pp.2386–2393.e4. Available at: http://dx.doi.org/10.1016/j.jaci.2021.02.028.
2. Rossiter, H. et al., 2021. Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile. Autophagy, pp.1–15. Available at: http://dx.doi.org/10.1080/15548627.2021.1966716.
3. Sukseree, S. et al., 2020. ATG7 is essential for secretion of iron from ameloblasts and normal growth of murine incisors during aging. Autophagy, 16(10), pp.1851–1857. Available at: http://dx.doi.org/10.1080/15548627.2019.1709764.
4. Sukseree, S. et al., 2018. Suppression of Epithelial Autophagy Compromises the Homeostasis of Sweat Glands during Aging. Journal of Investigative Dermatology, 138(9), pp.2061–2063. Available at: http://dx.doi.org/10.1016/j.jid.2018.03.1502.
5. Sukseree, S. et al., 2018. Filamentous Aggregation of Sequestosome-1/p62 in Brain Neurons and Neuroepithelial Cells upon Tyr-Cre-Mediated Deletion of the Autophagy Gene Atg7. Molecular Neurobiology, 55(11), pp.8425–8437. Available at: http://dx.doi.org/10.1007/s12035-018-0996-x.