Typhaine Dupont

发表

Spontaneous Mouse Behavior in Presence of Dissonance and Acoustic Roughness

C. Petit, N. Michalski, B. Gourévitch, 2020, Frontiers in Behavioral Neuroscience.

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

Fabienne Wong Jun Tai, P. Avan, C. Petit, 2020, Proceedings of the National Academy of Sciences.

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

P. Avan, C. Petit, Vincent Michel, 2014, EMBO Molecular Medicine.

Characterizing subcutaneous cortical auditory evoked potentials in mice

C. Petit, N. Michalski, A. Buck, 2022, Hearing Research.

Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G

P. Avan, C. Petit, Vincent Michel, 2017, Proceedings of the National Academy of Sciences.

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

Steve D. M. Brown, P. Avan, S. Picaud, 2017, EMBO molecular medicine.

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth

P. Avan, C. Petit, A. El-Amraoui, 2016, The Journal of cell biology.

Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane

P. Avan, C. Petit, Vincent Michel, 2019, Proceedings of the National Academy of Sciences.

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

C. Métin, P. Avan, C. Petit, 2017, Proceedings of the National Academy of Sciences.

Detecting Central Auditory Processing Disorders in Awake Mice

T. Bourgeron, Typhaine Dupont, Camille Dejean, 2023, Brain sciences.

Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G

P. Avan, C. Petit, Vincent Michel, 2017, Proceedings of the National Academy of Sciences.