Asadollah Aghaie
Paris, 75012, France
Last Updated: 09/26/2026
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Found 8 publications
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 08, 2025
CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival.
Journal: EMBO molecular medicine
Published: November 01, 2017
Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment.
Journal: The Journal of cell biology
Published: December 06, 2016
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
Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.
Journal: The Journal of cell biology
Published: September 02, 2015
Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes.
Journal: Cell
Published: April 24, 2015
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.
Journal: The Journal of cell biology
Published: October 10, 2012
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.
Journal: Human molecular genetics
Published: June 09, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026