摘要:
An apparatus and method for implementing multi-traffic load monitoring and prediction in a CDMA cellular mobile communication system includes a received signal strength indication (RSSI) measuring unit for measuring total interference power and processing a measured value to eliminate jitters; a parameter accounting or statistic unit for accounting for some traffic parameters associated to the load monitoring and prediction; a load monitoring unit for calculating the load monitoring based on the measured value and statistic results; and a load prediction unit for calculating an increased amount of an up link load after receiving or accessing new traffic and a total load value after receiving or accessing the new traffic based on parameters requested by the new traffic and calculation results transmitted in real time by the load monitoring unit.
摘要:
Content transfer involving a gesture is described. In an implementation, a method is implemented by a mobile communications device that includes recognizing a gesture input via a touchscreen of the mobile communications device that is indicative of a direction, the touchscreen including a display of content. One or more other mobile communications devices are located that are positioned, approximately, along the indicated direction of the gesture. A communication is formed to transfer the content to the located one or more other mobile communications devices.
摘要:
Novel human polyadenylation binding Protein 20.13 and polynucleotide encoding it. The invention also concerns the process of producing the polypeptide by recombinant DNA technique, and methods for treating many diseases e.g. disorder of embryo development, growth developmental disturbant diseases etc. The invention also discloses antagonists against the polypeptide.
摘要:
A novel polypeptide-human retinoic acid-responsive protein 53.57 and a polynucleotide encoding the same, as well as a method of producing the polypeptide by DNA recombinant technique. The present invention also discloses methods of using the polypeptide in treatment of various disease, such as arhythmia, bronchial asthma, peptic ulcer, diabetes mellitus, tumor, developmental deformation of embryo and so on. Also disclosed are antagonists against the polypeptide and the therapeutic use of the same.
摘要:
The present invention discloses a novel polypeptide-Human SNARE protein 25 and polynucleotide encoding the same, as well as a method of producing the polypeptide by DNA recombinant technology. The present invention also discloses methods of using the polypeptide in treatment of various diseases, such as malignant tumor, blood disease, HIV infection, immunological disease and various inflammations. The present invention also discloses an antagonist against the polypeptide and the therapeutic use of the same. The present invention also discloses the use of such polynucleotide encoding Human SNARE protein 25.
摘要:
The present invention discloses a new polypeptide-calcitonin 11, the polynucleotide encoding it and a method producing the polypeptide by recombinant DNA technology. The present invention further discloses a method using the polypeptide to treat various disorders, e.g. malignant neoplasm, hematopathy, HIV infection and immunological disease and various inflammation etc. The present invention also discloses agonists of the polypeptide and their therapeutic uses. The present invention further discloses the use of the polynucleotide encoding the new calcitonin 11.
摘要:
Minimal Motifs of linear B-cell epitopes in L1 structure protein from human papillomavirus type 58 (HPV 58) and their applications are disclosed. Eighteen linear epitope motifs and their extended 8-mer peptides in the L1 protein from HPV 58 are described, which can be used as antigens separately or in combination to specifically detect the serum from subjects with HPV 58 infection, or to develop preventive or therapeutic multi-epitope peptide vaccines against HPV 58 by inducing humoral immunity. Of the eighteen B-cell epitope motifs, ten of them are 100% conservative and one is highly conservative among many homologous proteins of high-risk HPVs. They can be used as candidate “universal” epitopes to develop preventive or therapeutic HPV vaccines. The amino acid sequences of the epitope motifs and the 8-mer peptide formula of the invention are shown below in SEQ ID No. 1-2, 2B, 3, 3B, 4-18, 18B, 19, 19B, and 20-32.
摘要:
The invention discloses a novle human vacuolar H+-ATPase C subunit 42 and a polynucleotide encoding it. The invention also concerns a process of producing the polypeptide by recombinant DNA techniques. Methods are also disclosed for treating many diseases, e.g. malignant tumors, hemopathies, HIV infections, immune diseases and inflammations utilizing the ploypeptide. The invention discloses antagonists of the polypeptide and therapeutics comprising the same. The invention also discloses the uses of the polynucleotide, which encodes the human vacuolar H+-ATPase C subunit 42.
摘要:
A micro-actuator that reduces suspension tongue stiffness and a method of manufacturing the micro-actuator are disclosed. In one embodiment, the micro-actuator has a base piece with two arms extending from the base piece. The electric contact pads for the arms are situated on the exterior of the arms at the end opposite the base piece. In one embodiment, the electric contact pads are electrically coupled to the same connection plate that the magnetic read/write head is coupled to, reducing the number of connection traces.
摘要:
A new polypeptide, human zinc finger protein FPM315-17, the polynucleotide encoding it and a method for producing the polypeptide by DNA recombinant technology. The present invention further discloses a method for using the polypeptide or polynucleotide for treating various disorders, e.g., various tumors, nervous system disorders, hemopathy, developmental disorders, and HIV infections. The present invention also discloses an antagonist of the polypeptide and its therapeutic application.