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Neuromolecular Medicine|May 29, 2019
eIF2B Mutations Cause Mitochondrial Malfunction in OligodendrocytesMelisa Herrero, Shir Mandelboum, Orna Elroy-SteinCells|August 27, 2021
The Energy Status of Astrocytes Is the Achilles' Heel of eIF2B-LeukodystrophyMelisa Herrero, Maron Daw, Andrea Atzmon, et al.Nucleic Acids Research|March 7, 2023
Effective extraction of polyribosomes exposes gene expression strategies in primary astrocytesShir Mandelboum, Melisa Herrero, Andrea Atzmon, et al.Frontiers in Molecular Neuroscience|October 4, 2018
Drug Screening Identifies Sigma-1-Receptor as a Target for the Therapy of VWM LeukodystrophyAndrea Atzmon, Melisa Herrero, Reut Sharet-Eshed, et al.Journal of Neurochemistry|March 18, 2017
Mutant eIF2B leads to impaired mitochondrial oxidative phosphorylation in vanishing white matter diseaseGali Raini, Reut Sharet, Melisa Herrero, et al.NAR Molecular Medicine|November 19, 2025
The translational landscape of reactive astrocytes reveals the impact of eIF2B-mediated dysregulation in VWM diseaseShir Mandelboum, Liat Lev-Ari, Andrea Atzmon, et al.Cell Death & Disease|December 7, 2021
Oligodendrocytes depend on MCL-1 to prevent spontaneous apoptosis and white matter degenerationAbigail H Cleveland, Alejandra Romero-Morales, Laurent Alfonso Azcona, et al.Circulation Research|September 27, 2024
Blunted Cardiac Mitophagy in Response to Metabolic Stress Contributes to HFpEFAkira Yoshii, Timothy S McMillen, Yajun Wang, et al.Pageof 1