Friday Lecture Series
Understanding Hearing Mechanisms: Advances Rooted in the Genetic Approach
Christine Petit, M.D., Ph.D., professor,College de France;
Chair of Genetics & Cellular Physiology; head, Unit of Genetics and Physiology of Hearing,
Institut Pasteur
April 30, 2010
3:45 p.m.-5:00 p.m. (Refreshments, 3:15 p.m., Abby Lounge)
Caspary Auditorium
Recommended Readings:
Cohen-Salmon, M., B. Regnault, N. Cayet, D. Caille, K. Demuth, J. -P Hardelin, N. Janel, P. Meda, and C. Petit. 2007. Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis. Proceedings of the National Academy of Sciences of the United States of America 104, (15): 6229-6234
Lagresle-Peyrou, C., E. M. Six, C. Picard, F. Rieux-Laucat, V. Michel, A. Ditadi, C. D. -D Chappedelaine, et al. 2009. Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness. Nature genetics 41, (1): 106-111
Petit, C. 2006. From deafness genes to hearing mechanisms: Harmony and counterpoint. Trends in molecular medicine 12, (2): 57-64
Roux, I., S. Safieddine, R. Nouvian, M. Grati, M. -C Simmler, A. Bahloul, I. Perfettini, et al. 2006. Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell 127, (2): 277-289
Wei, D., S. Levic, L. Nie, W. -Q Gao, C. Petit, E. G. Jones, and E. N. Yamoah. 2008. Cells of adult brain germinal zone have properties akin to hair cells and can be used to replace inner ear sensory cells after damage. Proceedings of the National Academy of Sciences of the United States of America 105, (52): 21000-21005