List of works - Amel Bahloul

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

scientific article published on 01 May 2020

CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival

scientific article published on 30 October 2017

Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids

scientific article

Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery

scientific article published on 27 June 2017

Crystal Structure of Two Anti-Porphyrin Antibodies with Peroxidase Activity

scientific article

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

scientific article

Electrospray ionization mass spectrometry studies of noncovalent myosin VI complexes reveal a new specific calmodulin binding site

scientific article published on 01 August 2005

Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells

scientific article published on 02 October 2020

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

scientific article

Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning

scientific journal article

Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses

scientific article

Myosin VII

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

scientific article

Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses

scientific article published on 7 November 2017

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse

scientific article

PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa

scientific journal article

The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells

scientific article

The structure of the myosin VI motor reveals the mechanism of directionality reversal

scientific article

The unique insert in myosin VI is a structural calcium-calmodulin binding site.

scholarly article

Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis

scientific article published on 23 November 2020

Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia

scientific article

Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells

scientific article

List of works by Amel Bahloul

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

CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival

Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids

Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery

Crystal Structure of Two Anti-Porphyrin Antibodies with Peroxidase Activity

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

Electrospray ionization mass spectrometry studies of noncovalent myosin VI complexes reveal a new specific calmodulin binding site

Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning

Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses

Myosin VII

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse

PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa

The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells

The structure of the myosin VI motor reveals the mechanism of directionality reversal

The unique insert in myosin VI is a structural calcium-calmodulin binding site.

Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis

Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia

Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells