Amel Bahloul

5PUBLICATIONS
49CO-AUTHORS
Sensory systemsEpigenetics (incl. genome methylation and epigenomics)Lasers and quantum electronicsMedical molecular engineering of nucleic acids and proteins
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Publications (5)

|Feb 11, 2023
Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder.

Anissa Rym Saidia, Jérôme Ruel, Amel Bahloul

|Nov 24, 2020
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.

Sophie Boucher, Fabienne Wong Jun Tai, Sedigheh Delmaghani

|Dec 21, 2019
A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in USH1C That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss.

Ju Sun Song, Amel Bahloul, Christine Petit

|Nov 08, 2017
Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses.

Nicolas Michalski, Juan D Goutman, Sarah Marie Auclair

|Jun 28, 2017
Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery.

Amel Bahloul, Elise Pepermans, Bertrand Raynal

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Frequent Collaborators

3 joint publications

Christine Petit

2 joint publications

Nicolas Michalski

1 joint publications

Jacques Boutet de Monvel

1 joint publications

Danica Ciric