Author

S. M. Nicoloro

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioengineering· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Assay:CRISPR screen· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

A. Desai· 1 shared B. Yenilmez· 1 shared E. Tsagkaraki· 1 shared F. Henriques· 1 shared H. Wang· 1 shared J. K. Kim· 1 shared J. L. Cohen· 1 shared J. Solivan-Rivera· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

A. Desai

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Author profile →

2 papers

Recent·Most cited

Regulation of lipolysis by 14-3-3 proteins on human adipocyte lipid droplets.

Q. Yang, Z. Yang Loureiro, A. Desai, T. DeSouza, K. Li, H. Wang, S. M. Nicoloro, J. Solivan-Rivera, S. Corvera

This study identifies 14-3-3 proteins as regulators of lipolysis in human adipocytes by analyzing the PLIN1 interactome using proximity labeling.

bioRxiv · May 1, 2023Cell Biology

CRISPR delivery particles for developing therapeutic strategies in metabolic disease

Y. Shen, J. L. Cohen, S. M. Nicoloro, M. Kelly, B. Yenilmez, F. Henriques, E. Tsagkaraki, Y. J. K. Edwards, X. Hu, R. H. Friedline, J. K. Kim, M. P. Czech

This study develops CRISPR delivery particles (CriPs) for efficient gene editing in cultured cells and in vivo, demonstrating their potential for therapeutic applications in metabolic disease.

bioRxiv · Jun 21, 2018Bioengineering