Author
Carolina Eliscovich
Albert Einstein College of MedicineORCID 0000-0001-7653-5536Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
Click to filter author papersSignature Assays, Organisms & Methods
Click to filter · or open tagActivity by Year
2024-2026 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 29 mutual co-author links5 papers
Recent·Most cited
- Molecular BiologyNature MetabolismPeer-reviewed
Spatial hepatocyte plasticity of gluconeogenesis during the metabolic transitions between fed, fasted and starvation states
Junichi Okada, Austin Landgraf, Alus M. Xiaoli…·Jeffrey E. Pessin
The paper shows that gluconeogenic gene expression and activity in liver hepatocytes change spatially and temporally during feeding, fasting, and starvation states.
- Developmental BiologybioRxivPreprint
Identification and classification of abundant RNA-binding proteins in the mouse lens and interactions of Carhsp1, Igf2bp1/ZBP1, and Ybx1 with crystallin and β-actin mRNAs
Danielle Rayêe, Dong-Woo Hwang, William K. Chang…·Aleš Cvekl
The paper identifies abundant RNA-binding proteins in mouse lenses and characterizes their interactions with crystallin and β-actin mRNAs using proteomic, transcriptomic, and imaging techniques.
2 citations - Developmental BiologybioRxivPreprint
Continuous nucleolar ribosomal RNA synthesis in differentiating lens fiber cells until abrupt nuclear degradation required for ocular lens transparency
Danielle Rayêe, U. Thomas Meier, Carolina Eliscovich, Aleš Cvekl
The paper shows that rRNA transcription continues in differentiating lens fiber cells until nuclear degradation, supporting translational mechanisms for crystallin protein production.
DOI 10.1101/2024.10.21.619434 - Molecular BiologybioRxivPreprint
Co-translational sorting enables a single mRNA to generate distinct polysomes with different localizations and protein fates
Soha Salloum, Martial Sevéno, Khadija El Koulali…·Édouard Bertrand
The paper shows that co-translational interactions sort β-catenin mRNAs into distinct polysome populations with different localizations and protein fates.