Christine Petit

Institut Pasteur, Paris, Paris, France 
"Christine Petit"
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Sarah M. Auclair collaborator 2016-2017 Institut Pasteur (Chemistry Tree)
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Michalski N, Petit C. (2021) Central auditory deficits associated with genetic forms of peripheral deafness. Human Genetics
Elrharchi S, Riahi Z, Salime S, et al. (2021) Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family. Human Heredity. 1-5
Boucher S, Wong Jun Tai F, Delmaghani S, et al. (2020) Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis. Proceedings of the National Academy of Sciences of the United States of America
Postal O, Dupont T, Bakay W, et al. (2020) Spontaneous Mouse Behavior in Presence of Dissonance and Acoustic Roughness. Frontiers in Behavioral Neuroscience. 14: 588834
Michel V, Pepermans E, Boutet de Monvel J, et al. (2020) Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells. Scientific Reports. 10: 16430
Avan P, Le Gal S, Michel V, et al. (2019) Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane. Proceedings of the National Academy of Sciences of the United States of America
Dunbar LA, Patni P, Aguilar C, et al. (2019) Clarin-2 is essential for hearing by maintaining stereocilia integrity and function. Embo Molecular Medicine. e10288
Michalski N, Petit C. (2019) Genes Involved in the Development and Physiology of Both the Peripheral and Central Auditory Systems. Annual Review of Neuroscience
Richardson GP, Petit C. (2019) Hair-Bundle Links: Genetics as the Gateway to Function. Cold Spring Harbor Perspectives in Medicine
Corns LF, Johnson SL, Roberts T, et al. (2018) Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation. Nature Communications. 9: 4015
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