Sedigheh Delmaghani
Paris, France
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: October 30, 2025
Deciphering Auditory Hyperexcitability in Otogl Mutant Mice Unravels an Auditory Neuropathy Mechanism.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: September 04, 2024
Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: October 20, 2023
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 24, 2020
Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges.
Journal: Journal of clinical medicine
Published: June 27, 2020
Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 03, 2019
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.
Journal: EMBO molecular medicine
Published: January 09, 2019
Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome.
Journal: The Journal of clinical investigation
Published: March 31, 2017
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.
Journal: American journal of human genetics
Published: February 18, 2016
Last Updated: 09/26/2026