Abstract:
A touch sensing apparatus is disclosed. The touch sensing apparatus includes a logic control module, at least one storage control module, and at least one decoding control module. The logic control module is used to generate a plurality of control signals having different control timings. The plurality of control signals includes a storage control signal and a decoding control signal. Each storage control module includes a plurality of storage capacitors, and respectively stores each of sensed voltages in different storage capacitors at different times according to a storage control timing of the storage control signal. The sensed voltages are analog data sensed from scan lines of an ITO sensor. The decoding control module performs analog adding process to the sensed voltages stored in the storage capacitors according to a decoding control timing of the decoding control signal to output decoded analog data with high signal-to-noise ratio (SNR).
Abstract:
A touch sensing apparatus is disclosed. The touch sensing apparatus includes a logic control module, at least one storage control module, and at least one decoding control module. The logic control module is used to generate a plurality of control signals having different control timings. The plurality of control signals includes a storage control signal and a decoding control signal. Each storage control module includes a plurality of storage capacitors, and respectively stores each of sensed voltages in different storage capacitors at different times according to a storage control timing of the storage control signal. The sensed voltages are analog data sensed from scan lines of an ITO sensor. The decoding control module performs analog adding process to the sensed voltages stored in the storage capacitors according to a decoding control timing of the decoding control signal to output decoded analog data with high signal-to-noise ratio (SNR).
Abstract:
A touch sensing apparatus includes a logic control module and at least one input control module. The logic control module generates a plurality of control signals having different control timings, wherein the control signals include an input control signal. The input control module is coupled with the logic control module, wherein each input control module includes a positive input switch and a negative input switch. The input control module controls, according to the input control signal, the positive input switch and the negative input switch to be deactivated or activated to control an input mode of a first sensing voltage and a second sensing voltage, which are analog data respectively sensed through a first sensing line and a second sensing line of a conductive thin film sensor, wherein the first sensing line and the second sensing line are sensing lines of adjacent channels.
Abstract:
A method of treating brain tissue damage, including administering to a subject in need thereof an effective amount of secretoneurin. Disclosed are methods of promoting angiogenesis or neurogenesis in the brain of subject. Also disclosed are a method of homing of stem cells to the brain of a subject and a method of protecting a neuronal cell from cell death.
Abstract:
Disclosed is a cultured pluripotent animal cell that is prepared from nasal polyps. Also disclosed are methods for making the cell and methods of treating a brain tissue damage or of promoting cerebral angiogenesis, cerebral neurogenesis, stem cell homing to the brain, neurotrophic factor expression in the brain.
Abstract:
The invention provides methods and compositions useful in pearl oyster cultivation. Polynucleotide and polypeptides relating to the nacre gene of Pinctada margaritifera are provided. Antibodies related to these polypeptides, and compositions comprising polynucleotides, polypeptides and/or antibodies of the invention are also provided. The invention provides methods of using these polynucleotides, polypeptides and antibodies, including methods related to pearl oyster cultivation. Arrays comprising polynucleotides, polypeptides and/or antibodies of the invention are also provided.
Abstract:
Disclosed is a cultured pluripotent animal cell that is prepared from nasal polyps. Also disclosed are methods for making the cell and methods of treating a brain tissue damage or of promoting cerebral angiogenesis, cerebral neurogenesis, stem cell homing to the brain, neurotrophic factor expression in the brain.