Author

M. de la Rosa

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

Biology Disciplines

Click to filter author papers

Biochemistry· 1 Bioengineering· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Organism:human· 2 Assay:CRISPR screen· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

A. E. Martelli· 1 shared A. Reik· 1 shared A. Rendina· 1 shared A. Rutkowska· 1 shared C. F. Dupont· 1 shared C. Jeanneau· 1 shared C. Ng· 1 shared C. Zhang· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperBioengineering

A. E. Martelli

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Epigenetic control of multiple genes with a single lentiviral vector encoding transcriptional repressors fused to compact zinc finger arrays

D. Monteferrario, M. David, S. K. Tadi, Y. Zhou, I. Marchetti, C. Jeanneau, G. Saviane, C. F. Dupont, A. E. Martelli, L. Truong, J. Eshleman, C. Ng, M. Huston, G. D. Davis, J. D. Fontenot, , D. Fenard

This paper develops a lentiviral system to simultaneously repress multiple genes using zinc finger repressors, showing efficient and long-term gene silencing without DNA editing.

bioRxiv · Jan 17, 2024Bioengineering

Characterization of apo-form selective inhibition of indoleamine 2,3-dioxygenase.

R. F. Ortiz-Meoz, L. Wang, R. Matico, A. Rutkowska, M. De la Rosa, S. Bedard, R. Midgett, K. Strohmer, D. Thomson, C. Zhang, M. Mebrahtu, J. Guss, R. Totoritis, T. Consler, N. Campobasso, , G. Zhang

This study compares two IDO1 inhibitors, showing GSK5628 selectively inhibits apo-IDO1 by competing with heme, while epacadostat binds to the heme cofactor, leading to longer-lasting inhibition.

bioRxiv · May 7, 2020Biochemistry