Author

Martí Aldea

Consejo Superior de Investigaciones CientíficasORCID 0000-0002-8710-5336Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Molecular Biology· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:cell-cell communication· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Organism:yeast· 1

Frequent Co-Authors

David F. MorenoiD· 2 shared Galal YahyaiD· 2 shared Adriana Soria-Villalba· 1 shared Attila Csikász‐NagyiD· 1 shared Carme GallegoiD· 1 shared Chao TangiD· 1 shared Doug Kellogg· 1 shared Eva ParisiiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 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 papersMolecular Biology

David F. MorenoORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Concerted remodelling of the postsynaptic spine and RNA granule by cLTP

Mònica B. Mendoza, Galal Yahya, Kimberly Alomoto, Adriana Soria-Villalba, Martí Aldea, Carme Gallego

The paper investigates how synaptic activation modulates RNA granule dynamics by analyzing protein accessibility and proximity changes during cLTP.

bioRxiv · Jul 16, 2025 · PreprintNeuroscience

Whi5 is diluted and protein synthesis does not dramatically increase in pre-Start G1

Kurt M. Schmoller, Michael Charles Lanz, Jacob Kim, Mardo Kõivomägi, Yimiao Qu, Chao Tang, I. V. Kukhtevich, Robert Schneider, Fabian Rudolf, David F. Moreno, Martí Aldea, Rafael Lucena, Doug Kellogg, Jan Marcel Skotheim

The paper challenges a model proposing that protein synthesis increases in pre-Start G1, finding that Whi5 concentration remains constant and Cln3 increase is not due to synthesis.

bioRxiv · Jun 1, 2020 · PreprintMolecular Biology

The chaperone-client network subordinates cell-cycle entry to growth and stress

David F. Moreno, Eva Parisi, Galal Yahya, Federico Vaggi, Attila Csikász‐Nagy, Martí Aldea

This study identifies chaperone systems as limiting factors for cell-cycle entry, showing their role in regulating nuclear accumulation of the G1 Cdk-cyclin complex and linking cell-cycle progression to growth and stress conditions.

Life Science Alliance · Apr 1, 2019Peer-reviewedMolecular Biology