Personal profile
Research interests
Medical Genetics is the main focus of our lab. Working on the foundation that the Human Genome Project has built, we are constantly trying to characterize un-annotated genes and proteins that are associated with hereditary disorders.
Lysosomes have always been a focused part of our research- characterizing lysosomal proteins can help us discover ways to fight back against lysosomal storage neurodegenerative diseases. Dr. Sardiello characterized TFEB (Transcription Factor EB) in 2009, with a groundbreaking study which refined the role of lysosomes. Since then, the Sardiello lab has been dedicated towards understanding lysosomal protein in an effort to cure or treat Neuronal Ceroid Lipofuscinoses, a specific category of lysosomal storage diseases.
Translational Medicine is one of our lab's biggest priorities. We believe strongly in bench-to-bedside approaches, and work hard to fulfill that ideal. Much of our research is focused on not only characterizing and discovering new scientific concepts, but also on how to deliver the fruit of our discoveries to the patients that need it. The Sardiello Lab is here to help.
Available to Mentor:
- PhD Students
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Collaborations and top research areas from the last five years
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A proteogenomic gene signature defines prognostic subgroups highlighting PI3K/AKT/mTOR signaling pathway as a therapeutic vulnerability in myeloid malignancies
He, F., Lin, S., Gao, B., Ramesh, V., Kim, A. B., Kong, T., Fisher, D. A. C., Letson, C. T., Brakhane, M., Fulbright, M., Yu, Y., Sardiello, M., Di Paola, J., Sykes, S. M. & Oh, S. T., Dec 2026, In: Cell Communication and Signaling. 24, 1, 61.Research output: Contribution to journal › Article › peer-review
Open Access -
CELF1 is a non-canonical eIF4E binding protein that promotes translation of epithelial-mesenchymal transition effector mRNAs
Chaudhury, A., Kongchan, N., Massey, S. A., Sharma, R., Pal, R., Zhao, N., Tsoi, P., Zhu, Y., Olokpa, E., Mao, S., Del Rincon, S., Reineke, L. C., Lloyd, R. E., Sardiello, M., Rosen, J. M., Kim, C., Ferreon, J. C. & Neilson, J. R., Mar 24 2026, In: Nucleic acids research. 54, 5, gkag123.Research output: Contribution to journal › Article › peer-review
Open Access -
Atypical free sialic acid storage disorder associated with tissue specific mosaicism of SLC17A5
Undiagnosed Diseases Network, Jan 2025, In: Molecular genetics and metabolism. 144, 1, 109004.Research output: Contribution to journal › Article › peer-review
Open Access -
Corrigendum to A CLN6-CLN8 complex recruits lysosomal enzymes at the ER for Golgi transfer
Bajaj, L., Sharma, J., di Ronza, A., Zhang, P., Eblimit, A., Pal, R., Roman, D., Collette, J. R., Booth, C., Chang, K. T., Sifers, R. N., Jung, S. Y., Weimer, J. M., Chen, R., Schekman, R. W. & Sardiello, M., Dec 15 2025, In: The Journal of clinical investigation. 135, 24Research output: Contribution to journal › Comment/debate
Open Access -
Enteric nervous system degeneration in human and murine CLN3 disease, is ameliorated by gene therapy in mice
Ziółkowska, E. A., Williams, L. L., Jansen, M. J., Wang, S. H., Eultgen, E. M., Sharma, J., Sardiello, M., Bradley, R. P., Whiteman, I. T., Sands, M., Heuckeroth, R. O. & Cooper, J. D., Dec 2025, In: Acta Neuropathologica Communications. 13, 1, 260.Research output: Contribution to journal › Article › peer-review
Open Access