Michelle Fry
myfry.bsky.social
Michelle Fry
@myfry.bsky.social
🙋‍♀️🐚💴🍟,👩‍🔬
This is such a great idea! Thank you for making this. Could you please add me?✋
November 22, 2024 at 2:59 PM
Thank you
November 18, 2024 at 1:23 AM
Is there still space?
November 17, 2024 at 11:05 PM
6/ Many thanks to Chen and Tom for inviting us to collaborate and expand on our shared interest in how Opa1 perturbations drive changes in mitochondrial ultrastructure.
November 14, 2024 at 3:01 PM
5/ Our findings bring us closer to understanding the molecular mechanisms behind ADOA and open new avenues for developing targeted therapies to prevent neurodegeneration.
October 3, 2024 at 1:58 PM
4/ We've identified Sarm1 as a key driver of RGC degeneration in our mouse model. Remarkably, knocking out SARM1 nearly completely suppresses these degeneration phenotypes, offering new hope for potential therapies.
October 3, 2024 at 1:58 PM
3/ Using cryo-ET, we quantified architectural changes in mitochondrial ultrastructure, giving us detailed insights into how this pathogenic OPA1 mutation affect mitochondrial integrity at the nanoscale level.
October 3, 2024 at 1:58 PM
2/ Our novel mouse model carrying the Opa1R290Q/+ allele recapitulates key features of human ADOA, including mitochondrial defects, age-related RGC loss, optic nerve degeneration, and reduced RGC function.
October 3, 2024 at 1:57 PM
1/ ADOA, a common inherited optic neuropathy, leads to RGC degeneration and vision loss. It's primarily caused by mutations in the OPA1 gene, a key player in mitochondrial inner membrane dynamics.
October 3, 2024 at 1:57 PM
4/ We've identified Sarm1 as a key driver of RGC degeneration in our mouse model. Remarkably, knocking out SARM1 nearly completely suppresses these degeneration phenotypes, offering new hope for potential therapies.
October 3, 2024 at 1:53 PM
3/ Using cryo-ET, we quantified architectural changes in mitochondrial ultrastructure, giving us detailed insights into how this pathogenic OPA1 mutation affect mitochondrial integrity at the nanoscale level.
October 3, 2024 at 1:53 PM
2/ Our novel mouse model carrying the Opa1R290Q/+ allele recapitulates key features of human ADOA, including mitochondrial defects, age-related RGC loss, optic nerve degeneration, and reduced RGC function.
October 3, 2024 at 1:53 PM
1/ ADOA, a common inherited optic neuropathy, leads to RGC degeneration and vision loss. It's primarily caused by mutations in the OPA1 gene, a key player in mitochondrial inner membrane dynamics.
October 3, 2024 at 1:52 PM