{"id":2137,"date":"2019-10-02T00:58:47","date_gmt":"2019-10-01T22:58:47","guid":{"rendered":"https:\/\/idibell.cat\/?page_id=2137"},"modified":"2024-06-20T10:37:32","modified_gmt":"2024-06-20T08:37:32","slug":"cellular-and-molecular-basis-of-sensory-disorders","status":"publish","type":"page","link":"https:\/\/idibell.cat\/en\/research\/neuroscience-area\/neuroscience-program\/cellular-and-molecular-basis-of-sensory-disorders\/","title":{"rendered":"Cellular and molecular basis of sensory disorders"},"content":{"rendered":"\n

\n\t\tCellular and molecular basis of sensory disorders\n\t<\/h1>\n

\n\t\tSummary\n\t<\/h3>\n\t

The group undertakes the challenges of treating sensory disorders and preserving sensory functions during ageing, through the study of original animal models in the vestibular system and retina. The group develops models which enable it to obtain therapeutically relevant information on these highly complex sensory systems through the use of first-line methodologies, such as super-resolution fluorescence microscopy, RNA-seq and proteomics.<\/p>\n

149<\/h2>\n

Publications<\/h2>\n\t\t\t\t\"208-basescelmoltrastsensorials-jllorens-def\"\n\t\t\t\t\tStrategic lines<\/a>\n\t\t\t\t\t\t\t\t\t\t\tExpand<\/i><\/a>\n\t\t\t\t\tStudy of cellular and molecular mechanisms of vestibular dysfunction using chronic toxicity models and in vitro models
\nRodent models to assess vestibular function
\nZebrafish models to study hair cell degeneration
\nCauses of vestibular loss in vestibular schwannoma patients
\nPhotoreceptor cell physiology
\nMolecular and cellular basis of light adaptation
\nPhosphoproteome of the dark\/light retina
\nRetinal metabolism
\nPolarized ciliary trafficking in photoreceptor cells
\nMouse models of inherited retinal dystrophies and testing of new therapeutic approaches\n\t\t\t\t\tSelected Publications<\/a>\n\t\t\t\t\t\t\t\t\t\t\tExpand<\/i><\/a>\n\t\t\t\t\t