Author

M. Valadares

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 Physiology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:rat· 1

Frequent Co-Authors

E. Cruvinel· 2 shared I. Ogusuku· 2 shared R. Dariolli· 2 shared A. C. Campos de Carvalho· 1 shared A. C. Silva· 1 shared A. F. Ribeiro· 1 shared A. Pereira· 1 shared D. B. Mello· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersPhysiology

E. Cruvinel

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

In situ maturated early-stage human induced pluripotent stem cell-derived cardiomyocytes improve cardiac function by enhancing segmentary contraction in infarcted rats

D. Biagi, E. T. Fantozzi, J. C. Campos-Oliveira, M. V. Naghetini, A. F. Ribeiro, S. Rodrigues, I. Ogusuku, R. Vanderlinde, M. L. A. Christie, D. B. Mello, A. C. Campos de Carvalho, M. Valadares, E. Cruvinel, R. Dariolli

bioRxiv · Mar 9, 2021Physiology

Long-term single-cell passaging of human iPSC fully supports pluripotency and high-efficient trilineage differentiation capacity

E. Cruvinel, I. Ogusuku, R. Cerioni, J. Goncalves, M. E. Goes, A. C. Silva, J. Alvim, A. Pereira, R. Dariolli, M. Valadares, D. G. Biagi

This study validates a long-term single-cell passaging method for human iPSC that maintains pluripotency and efficient trilineage differentiation.

bioRxiv · Apr 8, 2020Cell Biology