List of works - Nicolas Michalski

An organotypic slice culture to study the formation of calyx of Held synapses in-vitro.

scientific article

Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction

scientific article

BMP signaling specifies the development of a large and fast CNS synapse.

scientific article published on 26 May 2013

Central auditory deficits associated with genetic forms of peripheral deafness

scientific article published in 2021

Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells

scientific article

Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness

scientific article

Genetics of auditory mechano-electrical transduction

scientific article

Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells

scientific article published on November 2009

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

scientific journal article

Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly

scientific journal 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

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

scientific journal article

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

scientific article

Stiffness and tension gradients of the hair cell's tip-link complex in the mammalian cochlea

scientific article published on 01 April 2019

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

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

scientific journal article

List of works by Nicolas Michalski

An organotypic slice culture to study the formation of calyx of Held synapses in-vitro.

Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction

BMP signaling specifies the development of a large and fast CNS synapse.

Central auditory deficits associated with genetic forms of peripheral deafness

Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells

Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness

Genetics of auditory mechano-electrical transduction

Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells

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

Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly

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

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

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

Stiffness and tension gradients of the hair cell's tip-link complex in the mammalian cochlea

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

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells