Abstract: A redundancy termination panel includes first and second interfaces configured to be coupled to first and second I/O modules, respectively. The redundancy termination panel also includes a third interface configured to be coupled to a field device. The redundancy termination panel further includes an I/O channel circuit associated with an I/O channel between the I/O modules and the field device. The I/O channel circuit is configured to allow an input current used for receiving data from the field device to be split such that different portions of the input current are sourced by different ones of the I/O modules. The I/O channel circuit is also configured to combine multiple currents driven by different ones of the I/O modules and provide an output current used for sending data to the field device.

Abstract: With the scale of information available today along with the existing diverse channels of communication, manual processing of information is becoming a challenge and companies across industries are under tremendous pressure to lower transactional costs. Artificial Intelligence based automation of business transactions has seen regulatory hurdles due to probabilistic nature of the outcome. The main challenge lies in processing of transactions with unstructured information. Systems and methods of the present disclosure uses deterministic as well as probabilistic approaches to maximize accuracy. The larger use of deterministic approach with configurable components and ontologies helps to improvise accuracy, precision and reduce recall. The probabilistic approach is used when there is absence of quality information or less information for learning. Also, confidence indicators are provided at attribute level of data being processed and at each decision level.

Abstract: An operating shift apparatus for a manual transmission includes: an operating lever having an upper end at which a handle is disposed and a lower end extending toward a lever box; a shift lever having a shift joint disposed at a lower end of the shift lever; a connecting lever, an upper end of which is rotatably connected with the shift lever, having a cylinder joint which is downwardly protruded; a select lever having a select groove into which the cylinder joint is accommodated, a select joint disposed at a front end of the select lever, a return protrusion which is downwardly protruded, and a guide groove which is formed at both ends thereof, wherein the lever box has a guide rail which is engaged with the guide groove; and a return spring contacting the return protrusion to return the select lever to an original position.

Abstract: The present invention relates to a nucleic acid aptamer molecule that includes a domain that binds to an estrogen receptor, molecular complexes that include the nucleic acid aptamer molecule and an estrogen receptor, and constructed DMA molecules and expression systems, as well as host cells, that the contain an RNA aptamer molecule of the invention. Use of these aptamers and encoding constructs to inhibiting estrogen receptor activity in a cell and to treat estrogen receptor-positive cancers is also described.

Abstract: A transmission cable locking device for vehicles may include a plurality of opposing locking clips rotating with respect to each other wherein the rotation determines a grip or release state of a transmission cable; a locking band provided between the locking clips and providing interconnecting tension between the locking clips; and a housing accommodating the locking clips and the locking band, and in which a hinge shaft is formed wherein the locking clips are coupled to the internal surface to rotate.

Abstract: With the scale of information available today along with the existing diverse channels of communication, manual processing of information is becoming a challenge and companies across industries are under tremendous pressure to lower transactional costs. Artificial Intelligence based automation of business transactions has seen regulatory hurdles due to probabilistic nature of the outcome. The main challenge lies in processing of transactions with unstructured information. Systems and methods of the present disclosure uses deterministic as well as probabilistic approaches to maximize accuracy. The larger use of deterministic approach with configurable components and ontologies helps to improvise accuracy, precision and reduce recall. The probabilistic approach is used when there is absence of quality information or less information for learning. Also, confidence indicators are provided at attribute level of data being processed and at each decision level.

Abstract: Methods, systems, and devices for wireless communication are described. A user equipment (UE) may determine that a number of access stratum (AS) operations or communications have failed while attempting to communicate with a cell. Based on the AS failures, the UE may deprioritize the cell. For example, based on the deprioritization, the UE may bar certain cells from selection or reselection procedures. The UE may thus attempt to select or reselect a different cell even if the cell is ranked lower based on a selection criteria or reselection criteria. In some cases, UEs may store and share historical AS failure information that may also be used to determine when to deprioritize a cell. In some cases, a group of cells may be deprioritized (e.g., a group based on frequency, network, or tracking area).

Abstract: The present invention relates to pharmaceutically acceptable acid addition salts of sitagliptin, in particular anti-oxidant acid addition salts of sitagliptin and a process for its preparation. The present invention also provides a pharmaceutical composition using the pharmaceutically acceptable acid addition salts of sitagliptin.

Abstract: The present invention relates to pharmaceutically acceptable acid addition salts of sitagliptin, in particular anti-oxidant acid addition salts of sitagliptin and a process for its preparation. The present invention also provides a pharmaceutical composition using the pharmaceutically acceptable acid addition salts of sitagliptin.

Abstract: The present invention relates to a series of substituted compounds having the general formula (I), including their stereoisomers and/or their pharmaceutically acceptable salts. (I) Wherein A, m, R1s, R2, R3, R4 are as defined herein. This invention also relates to methods of making these compounds including intermediates. The compounds of this invention are effective at the kappa (?) opioid receptor (KOR) site. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic pain, and associated disorders, particularly functioning peripherally at the CNS.

Abstract: Methods implemented in a mobile communication device (e.g., a dual-SIM-dual-active or multi-SIM-multi-active communication device) for improving accuracy of radio-frequency (RF) output power measurements include opportunistically scheduling when a power detector takes RF output power measurements of a radio access technology (“RAT”). In various embodiments, a processor of the mobile communication device may ensure that the power detector takes an accurate RF output power measurement of the RAT by identifying an upcoming time window during which the RAT's transmit power is not artificially reduced as a result of performing transmit blanking/zeroing or artificially increased by transmissions originating from one or more other RATs operating on the device, and configuring or scheduling the power detector to take RF output power measurements of the RAT during that upcoming time window. A priority of the measured RAT may be increased in response to repeated delays in obtaining an RF output power measurement.

Abstract: The present invention relates to pharmaceutically acceptable acid addition salts of sitagliptin, in particular anti-oxidant acid addition salts of sitagliptin and a process for its preparation. The present invention also provides a pharmaceutical composition using the pharmaceutically acceptable acid addition salts of sitagliptin.

Abstract: Methods and apparatus for selecting one or more suitable antennas for use during power-up/initial acquisition and out of service modes are disclosed. In some examples, initial system acquisition may be performed for a particular receive circuit utilizing a selected one of a first antenna or a second antenna, based on a channel characteristic, such as an automatic gain control (AGC) value corresponding to a received signal energy utilizing either of the antennas. In another example, initial system acquisition utilizing either a receive diversity determination algorithm or an antenna switching determination algorithm may be performed based on a channel characteristic, such as an AGC value corresponding to a received signal energy utilizing one of the antennas coupled to one of the receive circuits.

Abstract: Methods and apparatus for selecting one or more suitable antennas for use during power-up/initial acquisition and out of service modes are disclosed. In some examples, initial system acquisition may be performed for a particular receive circuit utilizing a selected one of a first antenna or a second antenna, based on a channel characteristic, such as an automatic gain control (AGC) value corresponding to a received signal energy utilizing either of the antennas. In another example, initial system acquisition utilizing either a receive diversity determination algorithm or an antenna switching determination algorithm may be performed based on a channel characteristic, such as an AGC value corresponding to a received signal energy utilizing one of the antennas coupled to one of the receive circuits.

Abstract: The present invention relates to pharmaceutically acceptable acid addition salts of sitagliptin, in particular anti-oxidant acid addition salts of sitagliptin and a process for its preparation. The present invention also provides a pharmaceutical composition using the pharmaceutically acceptable acid addition salts of sitagliptin.

Abstract: The present invention relates to a series of substituted compounds having the general formula (I), including their stereoisomers and/or their pharmaceutically acceptable salts. (I) Wherein A, m, R1s, R2, R3, R4 are as defined herein. This invention also relates to methods of making these compounds including intermediates. The compounds of this invention are effective at the kappa (?) opioid receptor (KOR) site. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic pain, and associated disorders, particularly functioning peripherally at the CNS.

Abstract: Celecoxib crystalline Form Ill substantially free of celecoxib crystalline Forms I and II and a process for its preparation.

Abstract: The present invention provides new heterocyclic compounds, particularly substituted pyridines, methods and compositions for making and using these heterocyclic compounds, and methods for treating a variety of diseases and disease states, including atherosclerosis, arthritis, restenosis, diabetic nephropathy, or dyslipidemia, or disease states mediated by the low expression of Perlecan.

Abstract: Novel water soluble C-ring analogues of 20(S)-camptothecin having the general formula 1, All the compounds of the formula 1 are prepared from the compounds of the general formula 2 having 20(S)-chiral carbon where R1 to R5 have the meaning given above. The compounds of the formula 1 possess potent anti-cancer and anti-viral properties.

Abstract: A telecommunications switch (12) includes a dial plan database (300) used for creating, identifying, and verifying dial plan codes and dialing sequences of a desire dial plan (100). The dial plan (100) is created through a craft terminal (201) that communicates with a craft interface (200) of the telecommunications switch (12). The telecommunications switch (12) uses dial plans created and stored within the dial plan database (300) in performing a digit parsing routine. The digit parsing routine identifies dial plan codes and dialing sequences through digit collection by systematically eliminating possible dial plan codes until one is identified. The identified dial plan code is processed by performing valid or error actions associated with the identified dial plan code. The digit parsing routine continues with an incoming call until it has been appropriately handled and awaits for the next incoming call digits to be received.