Author

A. Naldi

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

Immunology· 2 Physiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:cell signaling & trafficking· 2 Approach:statistical model· 2 Assay:ChIP-seq· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

D. Thieffry· 2 shared M. A. Santana· 2 shared A. Medina-Rivera· 1 shared A. Sanchez-Jimenez· 1 shared A. V. Leon-Apodaca· 1 shared B. Desvergne· 1 shared C. Casals Casas· 1 shared C. Hernandez· 1 shared

Activity by Year

2019-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 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

2 shared papersImmunology

D. Thieffry

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Logical modeling of dendritic cells in vitro differentiation from human monocytes unravels novel transcriptional regulatory interactions

K. J. Nunez-Reza, A. Naldi, A. Sanchez-Jimenez, A. V. Leon-Apodaca, M. A. Santana, M. Thomas-Chollier, D. Thieffry, A. Medina-Rivera

The paper builds a logical model of human monocyte-to-dendritic cell differentiation using ChIP-seq and RNA-seq data to identify novel transcriptional regulatory interactions.

bioRxiv · Aug 14, 2020Immunology

An altered metabolism could contribute to the low activation of neonatal CD8+T cells

J. A. Sanchez-Villanueva, O. Rodriguez-Jorge, O. Ramirez-Pliego, G. Rosas-Salgado, W. Abou-Jaoude, C. Hernandez, A. Naldi, D. Thieffry, M. A. Santana

The paper investigates how altered metabolism and ROS levels affect neonatal CD8+T cell activation, showing that lower ROS status explains reduced activation rates compared to adult cells.

bioRxiv · Aug 8, 2019 · PreprintImmunology

System analysis of cross-talk between nuclear receptors reveals an opposite regulation of the cell cycle by LXR and FXR in human HepaRG liver cells

L. Wigger, C. Casals Casas, M. Baruchet, K. B. Trang, S. Pradervand, A. Naldi, B. Desvergne

The paper analyzes the cross-talk between nuclear receptors LXR, FXR, and PPAR in HepaRG liver cells, revealing opposite effects of FXR and LXR on cell cycle regulation and hepatocyte differentiation.

bioRxiv · Mar 25, 2019Physiology