Author

T. P. Rodriguez

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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Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Organism:C. elegans· 2 Organism:Drosophila· 2 Research Focus:drug response / drug discovery· 2 Assay:bulk RNA-seq· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

F. S. Sam· 2 shared H. Tsang· 2 shared J. D. Mast· 2 shared M. Prangley· 2 shared N. DiPrimio· 2 shared S. Iyer· 2 shared A. Hadjikyriacou· 1 shared B. Nyfeler· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersCell Biology

F. S. Sam

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Multi-Species Phenotypic Screening across Disease Models of Mucolipidosis Type IV

A. Hadjikyriacou, S. Iyer, J. D. Mast, N. DiPrimio, J. Concannon, J. Ketterman, F. Sigoillot, T. P. Rodriguez, F. S. Sam, H. Tsang, M. Prangley, J. Bilen, K. Murthy, T. A. Hartl, C. Antczak, , S. M. Canham

The paper screens a compound library across invertebrate and human models of mucolipidosis IV to identify conserved disease modifiers, finding cyclin-dependent kinase inhibition as a potential therapeutic strategy.

bioRxiv · Mar 5, 2021 · PreprintCell Biology

Drug screens of NGLY1 Deficiency worm and fly models reveal catecholamine, NRF2 and anti-inflammatory pathway activation as potential clinical approaches

S. Iyer, J. D. Mast, H. Tsang, T. P. Rodriguez, N. DiPrimio, M. Prangley, F. S. Sam, Z. M. Parton, E. Perlstein

The paper identifies drug candidates that rescue growth in NGLY1-deficient worm and fly models by targeting NRF2, anti-inflammatory pathways, and catecholamine signaling.

bioRxiv · Aug 28, 2019Pharmacology & Toxicology