Author

Carmela Galli

Institute for Research in Biomedicine

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· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Assay:proteomics· 2 Approach:biophysical modeling· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Organism:human· 1

Frequent Co-Authors

Maurizio MolinariiD· 3 shared Andrea RaimondiiD· 2 shared Tatiana SoldàiD· 2 shared Carolin Hoefner· 1 shared Concetta GuerraiD· 1 shared Diego MoroneiD· 1 shared Marco Del Fabbro· 1 shared Mikhail RudinskiyiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 17 mutual co-author links

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3 shared papersCell Biology

Maurizio MolinariORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

A reversible temperature block captures pre-lysosomal intermediates of starvation-induced ERphagy

Marco Del Fabbro, Tatiana Soldà, Diego Morone, Carmela Galli, Andrea Raimondi, Maurizio Molinari

This study identifies a reversible temperature block that captures pre-lysosomal intermediates of ERphagy, showing their formation requires autophagy machinery and reveals their structural features.

bioRxiv · Oct 8, 2026 · PreprintCell Biology

ER-phagy Receptors Intrinsically Disordered Modules Drive ER Fragmentation and ER-phagy

Mikhail Rudinskiy, Carmela Galli, Andrea Raimondi, Maurizio Molinari

This study shows that intrinsically disordered regions (IDRs) of ER-phagy receptors drive ER fragmentation, not their membrane-remodeling domains.

Nature Cell Biology · Aug 4, 2025Peer-reviewedCell Biology

TMX5/TXNDC15, a natural trapping mutant of the PDI family is a client of the proteostatic factor ERp44

Tatiana Soldà, Carmela Galli, Concetta Guerra, Carolin Hoefner, Maurizio Molinari

The paper identifies TMX5 as a PDI family member that interacts with ERp44 via disulfide bonds, controlling its ER retention and distribution.

Life Science Alliance · Sep 30, 2024Peer-reviewedCell Biology