Author

A. Monteiro da Rocha

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· 2 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:ATAC-seq· 2 Research Focus:cell signaling & trafficking· 2 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:deep learning· 1

Frequent Co-Authors

E. N. Jimenez-Vazquez· 2 shared G. Guerrero-Serna· 2 shared T. J. Herron· 2 shared A. J. Cuttita· 1 shared A. Macias· 1 shared A. Shcherbina· 1 shared B. A. Yang· 1 shared B. M. Baker· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersCell Biology

E. N. Jimenez-Vazquez

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Manipulation of the nucleoscaffold potentiates cellular reprogramming kinetics

B. A. Yang, A. Monteiro da Rocha, I. Newton, A. Shcherbina, S.-W. Wong, P. M. Fraczek, J. A. Larouche, H. L. Hiraki, B. M. Baker, J.-W. Shin, S. Takayama, M. D. Thouless, C. A. Aguilar

This study shows that manipulating Lamin A/C affects nuclear structure and reprogramming efficiency in human fibroblasts.

bioRxiv · Mar 12, 2023Cell Biology

SNTA1 GeneRescues Ion Channel Function in Cardiomyocytes Derived from Induced Pluripotent Stem Cells Reprogrammed from Muscular Dystrophy Patients with Arrhythmias

J. Jalife, E. N. Jimenez-Vazquez, M. Arad, A. Macias, M. L. Vera-Pedrosa, F. M. Cruz, A. J. Cuttita, A. Monteiro da Rocha, T. J. Herron, D. Ponce-Balbuena, G. Guerrero-Serna, O. Binah, D. E. Michele

This study shows that iPSC-CMs from DMD patients with arrhythmias have NaV1.5-Kir2.1 channelosome dysfunction, which can be rescued by 1-syntrophin.

bioRxiv · Jan 25, 2022 · PreprintCell Biology

From atoms to cells: bridging the gap between potency, efficacy, and safety of small molecules directed at a membrane protein

R. Aguayo-Ortiz, J. Creech, E. N. Jimenez-Vazquez, G. Guerrero-Serna, N. Wang, A. Monteiro da Rocha, T. J. Herron, L. M. Espinoza-Fonseca

This study combines computational and experimental methods to evaluate drug potency, efficacy, and safety for targeting membrane proteins, using SERCA2a as a model.

bioRxiv · Mar 19, 2021Pharmacology & Toxicology