摘要:
Methods and compositions for treating retinal diseases comprising therapeutic amounts of a compound selected from a normal Puf-A gene product, an active polypeptide fragment thereof, an analog thereof or a peptidomimetic thereof. Vectors, including AAV vectors comprising the therapeutic compound are provided. Puf-A compositions suitable for subretinal, intravitreal, topical, subconjunctival, retrobulbar, periocular, suprachoroidal, or intraocular administration are provided. Methods for screening siRNA, RNAi and shRNA, small molecules and monoclonal antibodies that inhibit Puf-A target activity and reduce apoptosis are provided.
摘要:
A touch panel module includes a frame unit and a touch panel unit. The frame unit includes a hollow frame body. The hollow frame body has a receiving space concaved downwardly from the top side thereof, a surrounding positioning portion formed on an inner bottom surface thereof, and an inner ladder structure formed on an inner surrounding peripheral surface thereof. The touch panel unit includes a transparent substrate received in the receiving space and disposed on the surrounding positioning portion by a plurality of adhesive elements and a transparent conductive film received in the receiving space and disposed on the transparent substrate. Therefore, the touch panel unit can naturally aim at the center position inside the hollow frame body due to the design of the inner ladder structure of the hollow frame body.
摘要:
Methods and compositions for treating retinal diseases comprising therapeutic amounts of a compound selected from a normal Puf-A gene product, an active polypeptide fragment thereof, an analog thereof or a peptidomimetic thereof. Vectors, including AAV vectors comprising the therapeutic compound are provided. Puf-A compositions suitable for subretinal, intravitreal, topical, subconjunctival, retrobulbar, periocular, suprachoroidal, or intraocular administration are provided. Methods for screening siRNA, RNAi and shRNA, small molecules and monoclonal antibodies that inhibit Puf-A target activity and reduce apoptosis are provided.