MP
Malgorzata Piechota
International Institute of Molecular and Cell Biology
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Ubiquitin and proteasome pathways · Glaucoma and retinal disorders · Mitochondrial Function and Pathology
Employment
- 2019 - Present
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (19)
- CHIP, VCP, and Nucleolar Gatekeepers Remodel the Nucleolus into a Stress-Responsive Proteostasis Hub Save
- Floxuridine supports UPS independent of germline signaling and proteostasis regulators via involvement of detoxification in C. elegans Save
- DEGRONOPEDIA: a web server for proteome-wide inspection of degrons Save
- Sterility-Independent Enhancement of Proteasome Function via Floxuridine-Triggered Detoxification inC. elegans Save
- DEGRONOPEDIA - a web server for proteome-wide inspection of degrons Save
- CHIP ubiquitin ligase is involved in the nucleolar stress management Save
- Muscle-derived exophers promote reproductive fitness Save
- Nutritional status and fecundity are synchronised by muscular exopheresis Save
- Generation of silent synapses in dentate gyrus correlates with development of alcohol addiction Save
- Cellular Senescence in Age-Related Macular Degeneration: Can Autophagy and DNA Damage Response Play a Role? Save
- Is senescence-associated β-galactosidase a marker of neuronal senescence? Save
- Polyploidy Formation in Doxorubicin-Treated Cancer Cells Can Favor Escape from Senescence Save
- Resveratrol Derivative, 3,3′,4,4′-Tetrahydroxy-trans-Stilbene, Retards Senescence of Mesothelial Cells via Hormetic-Like Prooxidative Mechanism Save
- [Neuronal ageing]. Save
- Opa1 is essential for retinal ganglion cell synaptic architecture and connectivity Save
- Secondary mtDNA Defects Do Not Cause Optic Nerve Dysfunction in a Mouse Model of Dominant Optic Atrophy Save
- OPA1 Deficiency Associated with Increased Autophagy in Retinal Ganglion Cells in a Murine Model of Dominant Optic Atrophy Save
- A missense mutation in the murine Opa3 gene models human Costeff syndrome Save
- Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function Save