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- Category: News
- Monday, 13 January 2014 14:13
Presentation of the Institute
The Institute for Neurosciences of Montpellier (INM) will celebrate its 10th anniversary in February 2014. It is located in the Neuroscience (Head and Neck) hospital, closed to the University Campus.
The INM houses 200 people working on vision, hearing, somatosensory wiring, and myelination. Molecular to systems level investigations are carried-out through core technical facilities, which are opened to academic and private users outside the INM. Team competences cover expertise in genetic, molecular and cellular biology, electrophysiology, computational neurosciences pre-clinical and clinical researches. Research outputs favor the development of new treatments for sensory and motor deficits, with a strong interest in inherited retinal and optic blindness, auditory neuropathies, neurodegenerative diseases (amyotrophic lateral sclerosis, giant axonal neuropathy), somatosensation disorders (touch and pain) and glial pathologies (gliomas and Charcot Marie Tooth disease).
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- Category: News
- Monday, 13 January 2014 18:50
Relevant Publications (2009-2014)
Otsmane B, Moumen A, Aebischer J, Coque E, Sar C, Sunyach C, Salsac C, Valmier J, Salinas S, Bowerman M, Raoul C. Somatic and axonal LIGHT signaling elicit degenerative and regenerative responses in motoneurons, respectively. EMBO Rep., in press.
Sendin G, Bourien J, Rassendren F, Puel JL, Nouvian R. Spatiotemporal pattern of action potential firing in developing inner hair cells of the mouse cochlea. Proc Natl Acad Sci U S A. 2014, 111(5):1999-2004.
Martino J, De Witt Hamer PC, Berger MS, Lawton MT, Arnold CM, de Lucas EM, Duffau H. Analysis of the subcomponents and cortical terminations of the perisylvian superior longitudinal fasciculus: a fiber dissection and DTI tractography study. Brain Struct Funct. 2013, 218(1):105-21.
Manes G, Meunier I, Avila-Fernández A, Banfi S, Le Meur G, Zanlonghi X, Corton, M, Simonelli F, Brabet P, Labesse G, Audo I, Mohand-Said S, Zeitz C, Sahel JA, Weber M, Dollfus H, Dhaenens CM, Allorge D, De Baere E, Koenekoop RK, Kohl S, Cremers FP, Hollyfield JG, Sénéchal A, Hebrard M, Bocquet B, Ayuso García C, Hamel CP. Mutations in IMPG1 cause vitelliform macular dystrophies. Am J Hum Genet. 2013, 93(3):571-8.
