Eric A. Schon
Affiliations: | Columbia University, New York, NY |
Area:
Genetics, Microbiology BiologyGoogle:
"Eric Schon"Children
Sign in to add trainee| Yingying Tang | grad student | 2000 | Columbia |
| Yin M. Lim | grad student | 2009 | Columbia |
| Sonja Brosel | grad student | 2010 | Columbia |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Morcillo P, Kabra K, Velasco K, et al. (2024) Aberrant ER-mitochondria communication is a common pathomechanism in mitochondrial disease. Cell Death & Disease. 15: 405 |
| Adashi EY, Rubenstein DS, Mossman JA, et al. (2021) Mitochondrial disease: Replace or edit? Science (New York, N.Y.). 373: 1200-1201 |
| Larrea D, Pera M, Gonelli A, et al. (2019) MFN2 mutations in Charcot-Marie-Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics. Human Molecular Genetics |
| Area-Gomez E, Guardia-Laguarta C, Schon EA, et al. (2019) Mitochondria, OxPhos, and neurodegeneration: cells are not just running out of gas. The Journal of Clinical Investigation. 129: 34-45 |
| Schon EA. (2018) Bioenergetics through thick and thin. Science (New York, N.Y.). 362: 1114-1115 |
| Siegmund SE, Grassucci R, Carter SD, et al. (2018) Three-Dimensional Analysis of Mitochondrial Crista Ultrastructure in a Patient with Leigh Syndrome by In Situ Cryoelectron Tomography. Iscience. 6: 83-91 |
| Area-Gomez E, de Groof A, Bonilla E, et al. (2018) A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease. Cell Death & Disease. 9: 335 |
| Rebelo AP, Saade D, Pereira CP, et al. (2018) SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency. Brain : a Journal of Neurology |
| Pera M, Larrea D, Guardia-Laguarta C, et al. (2017) Increased localization of APP-C99 in mitochondria-associated ER membranes causes mitochondrial dysfunction in Alzheimer disease. The Embo Journal |
| Siegmund S, Yang H, Sharma R, et al. (2017) Low-dose rapamycin extends lifespan in a mouse model of mtDNA depletion syndrome. Human Molecular Genetics |