Noemi Esteras

15PUBLICATIONS
113CO-AUTHORS
Neurology and neuromuscular diseasesCellular nervous systemMedical biochemistry - proteins and peptides (incl. medical proteomics)MicrotechnologyMolecular targets
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Publications (15)

|Apr 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality.

|Oct 29, 2025
Melatonin-Mediated Nrf2 Activation as a Potential Therapeutic Strategy in Mutation-Driven Neurodegenerative Diseases.

Lucía Íñigo-Catalina, María Ortiz-Cabello, Elisa Navarro

|Jan 08, 2025
Multitarget Effects of Nrf2 Signalling in the Brain: Common and Specific Functions in Different Cell Types.

Elisa Navarro, Noemí Esteras

|Aug 16, 2024
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality and disrupt mitochondrial function.

Francesca Magrinelli, Christelle Tesson, Plamena R Angelova

|May 22, 2024
KAT8 compound inhibition inhibits the initial steps of PINK1-dependant mitophagy.

Capucine de Talhouët, Noemi Esteras, Marc P M Soutar

|May 06, 2024
A new mutation in the Parkinson's-related FBXO7 gene impairs mitochondrial and proteasomal function.

Elisa Navarro, Noemí Esteras

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Frequent Collaborators

8 joint publications

Andrey Y Abramov

6 joint publications

Plamena R Angelova

4 joint publications

Sonia Gandhi

3 joint publications

Benjamin O'Callaghan