Author

C. Sepulveda

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 Plant Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

A. Fasano· 1 shared A. M. Guercio· 1 shared A. M. Lozano· 1 shared C. Burns· 1 shared C. E. Conn· 1 shared C. Hetz· 1 shared C. J. Fiscus· 1 shared C. S. Asensio· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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1 shared paperCell Biology

A. Fasano

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BAX and BAK expression triggers multiple IRE1 signaling outputs under ER stress

C. Sepulveda, M. Milani, V. Morales, G. Tamburini, N. Montes, C. Hetz

This study shows that BAX and BAK deficiency increases ER stress threshold for XBP1 splicing and reduces RIDD substrate degradation and IRE1 phosphorylation.

bioRxiv · Mar 26, 2024 · PreprintCell Biology

A KARRIKIN INSENSITIVE2 paralog in lettuce mediates highly sensitive germination responses to karrikinolide

S. E. Martinez, C. E. Conn, A. M. Guercio, C. Sepulveda, C. J. Fiscus, D. Koenig, N. Shabek, D. C. Nelson

This study identifies LsKAI2b as the lettuce receptor mediating sensitive KAR1 germination responses, with specific residues determining ligand specificity.

bioRxiv · Oct 13, 2021Plant Biology

VPS41 recessive mutation causes ataxia and dystonia with retinal dystrophy and mental retardation by inhibiting HOPS function and mTORC1 signaling

R. E. N. van der Welle, R. Jobling, C. Burns, P. Sanza, C. ten Brink, A. Fasano, L. Chen, F. J. Zwartkruis, S. Zwakenberg, E. F. Griffin, J. van der Beek, T. Veenendaal, N. Liv, S. Blaser, C. Sepulveda, , J. Klumperman

This paper identifies VPS41 mutations causing neurodegenerative disease by disrupting HOPS function and mTORC1 signaling, leading to lysosomal dysfunction and impaired autophagy.

bioRxiv · Dec 18, 2019 · PreprintCell Biology