608 results about "Cell specific" patented technology

Disclosed is a method, a computer program product and a device that includes a receiver for receiving a downlink signal transmitted into a cell. The receiver is operable to obtain time, carrier frequency and cell-specific preamble synchronization to the received signal and includes a plurality of synchronization units that include a first detector to detect a frame boundary using preamble delay correlation; a second detector to detect the frame boundary with greater precision using a conjugate symmetry property over a region identified by the first detector; a cyclic prefix correlator to resolve symbol boundary repetition; an estimator, using the cyclic prefix, to estimate and correct a fractional carrier frequency offset; an operator to perform a Fast Fourier Transform of an identified preamble symbol and a frequency domain cross-correlator to identify cell-specific preamble sequences and an integer frequency offset in sub-carrier spacing. The transmitted signal may be a downlink signal transmitted into the cell from a base station that is compatible with IEEE 802.16e (WiMAX).

Endothelial cell attachment to an intravascular stent is promoted by coating the stent with an endothelial cell specific adhesion peptide. Coating is preferably carried out by activating the intravascular stent using plasma glow discharge, applying on the stent a layer or plurality of layers of a polymer such as poly(2-hydroxyethylmethacrylate), applying a tresylation solution containing pyridine and tresyl chloride, and applying a five amino acid peptide having the sequence glycine-arginine-glutamic acid-aspartic acid-valine.

Method for informing a mobile terminal on target cell-specific system information to facilitate a mobility procedure such as handover or cell reselection in a mobile communication network. Further a radio resource control apparatus, a mobile terminal and a system comprising the radio resource control apparatus and the mobile terminal are provided. The invention suggests improvements to current mobility procedures so as to reduce the interruption time implied by the procedures. More specifically, it is proposed to include at least one pointer to target cell-specific system information to a control message, such as a handover indication or connection release message, pointing the mobile terminal to system information in the target cell relevant for system access and / or to perform mobility procedures. Further, a portion of the target cell-specific system information may also be comprised in the control message.

A base stations (BS) are configured to perform a coordinated transmission to at least one user equipment (UE). The BS includes a plurality of antenna configured to communicate with the UE. The BS also includes processing circuitry coupled to the plurality of antennas and configured to transmit physical downlink control channel (PDCCH) to the at least one user equipment. The UE includes a plurality of antennas configured to communicate with the BS. The UE also includes a processing circuitry coupled to the plurality of antennas and configured to receive PDCCH from the BS. The PDCCH is included in one or more transmit (Tx) beams. A Tx beam is defined by the cell specific reference signal (CRS) transmitted through the Tx beam. A Tx beam is configured to carry a beam identifier, and the PDCCH is configured to include resource allocation information for the user equipment.

A base station communicating with a mobile station in a radio communication system by using OFDM for downlink is disclosed. The base station includes a sequence selecting unit configured to select multiple synchronization signal sequences; a synchronization signal generating unit configured to generate a secondary synchronization channel based on a part of the selected synchronization signal sequences and another part of the selected synchronization signal sequences; and a transmitting unit configured to transmit the secondary synchronization channel. The secondary synchronization channel is used to detect cell-specific information.

Methods and apparatus for remapping and regrouping transmission resources in a wireless communication system. First, a set of new permutation algorithms based on Galois field operation is proposed. Then the proposed algorithms and the known Pruned Bit Reversal Ordering (PBRO) algorithm are applied to several of various resource mapping schemes, including slot or symbol level Orthogonal Cover (OC) / Cyclic Shift (CS) mapping, cell-specific slot-level and symbol-level CS hopping patterns, and subframe and slot level base sequence hopping patterns.

The present invention provides a method of operating a base station transmitter. In one embodiment, the method includes providing a cellular downlink synchronization signal having primary and secondary portions, wherein the primary portion is common for all cells and the secondary portion is cell-specific and transmitting the cellular downlink synchronization signal. In another embodiment, the method includes providing a cellular downlink synchronization signal having primary and secondary portions wherein the primary portion employs a corresponding one of a plurality of different primary signals allocated to adjoining transmission cells. The method also includes further providing cell-specific information in the secondary portion and transmitting the cellular downlink synchronization signal. The present invention also provides a method of operating user equipment. The method includes receiving a cellular downlink synchronization signal having primary and secondary portions wherein the secondary portion provides cell-specific parameters and identifying and extracting the secondary portion.

Physical layer structures and related access schemes for unsynchronized communication networks are provided. Access channel information, preferably including a common synchronization code associated with all transceiver stations in a communication network and a cell-specific synchronization code uniquely associated with one of the transceiver stations, is modulated onto at least one set of time-continuous signal components of a communication signal. In order to access the communication network, communication terminals search for the access channel information in one or more sets of time-continuous signal components and synchronization parameters are then determined based on a location of the access channel information in the sets of time-continuous signal components. Some embodiments of the invention provide for joint frame synchronization and coarse timing synchronization. In further embodiments, the communication signal also includes a scattered pilot channel onto which a portion of the access channel information, preferably the cell-specific synchronization code, is modulated. The pilot channels may then be re-used for initial access operations in addition to its conventional uses for such operations as channel estimation.

In one aspect, the present invention provides a simple method of signaling reference signal muting information to receiving radio equipment, such as items of user equipment (UEs). The reference signals may be positioning reference signals and / or cell-specific reference signals, for example. In one or more embodiments, the present invention proposes a general solution whereby the receiving radio equipment is informed not only on whether muting is used in general in a cell, but also the particular timing and formatting of such muting. Further, the contemplated method provides for the use of dynamic muting patterns, and thus avoids the need for statically defined muting patterns, and provides for coordinated muting control, across two or more network cells. In at least one embodiment, static or less dynamic aspects of the muting configuration is signaled via higher-layer signaling, while lower-layer signaling is used to signal more dynamic aspects of the muting configuration.

Changes in wireless service user behavior are encouraged and produced to shape utilization patterns among cells within a rate plan region by using shaping rules which define potential discounts from a standard charge rate under certain cell-specific utilization conditions, analyzing the shaping rules and utilization statistics of a cell upon service initiation, generating a discount from the standard rate for underutilized cells. The user is notified of these discount opportunities using text messages, icons, or other means. Over time, the users learn that at certain places and times, significant discounts are offered, and thus changes their behavior to take advantage of those discounts, thereby shaping traffic in a manner desired by the service provider.

A base station for use in an OFDM / OFDMA wireless network. The base station transmits system-specific broadcast control channel (BCCH) information in a first group of time-frequency slots and transmits cell-specific BCCH information in a second group of time-frequency slots. The time-frequency slots in the first group are orthogonal to the time-frequency slots in the second group. The base station transmits the system-specific BCCH information in the same time-frequency slots as a neighboring base station. The neighboring base station transmits cell-specific BCCH information in a third group of time-frequency slots that may or may not be orthogonal to the time-frequency slots in the second group.

The present invention provides DNA encoding a TADG-15 protein as well as a TADG-15 protein. Also provided is a vector capable of expressing the DNA of the present invention adapted for expression in a recombinant cell and regulatory elements necessary for expression of the DNA in the cell. The present invention further provides for methods of inhibiting TADG-15 expression and / or protease activity, methods of detecting TADG-15 mRNA and / or protein and methods of screening for TADG-15 inhibitors. Additionally, the present invention provides for cell-specific targeting via TADG-15 and methods of vaccinating an individual against TADG-15. The methods described are useful in the diagnosis, treatment and prevention of cancer, particularly breast and ovarian cancer.

The present invention provides a method of operating a base station transmitter. The method includes providing a cellular downlink synchronization signal having primary and secondary portions, wherein the primary portion employs a corresponding one of a plurality of different primary signals allocated to adjoining transmission cells. The method also includes further providing cell-specific information in the secondary portion and transmitting the cellular downlink synchronization signal. In one embodiment, the primary portion explicitly indicates a partial cell identification information and the remaining cell identification information is carried in the secondary portion. In another embodiment, the plurality of different primary signals are simply used to avoid the channel mismatch effect. The present invention also provides a method of operating user equipment. The method includes receiving a cellular downlink synchronization signal having primary and secondary portions wherein the timing acquisition is performed in conjunction with the primary synchronization sequence index detection via the primary portion. In addition, the secondary portion provides cell-specific parameters and identifying and extracting the secondary portion.

Disclosed is an apparatus and method for transmitting the synchronization signal in an Orthogonal Frequency Division Multiplexing (OFDM) based cellular system. The cell search process widely used in the OFDM based cellular system is divided into two steps for obtaining the frame timing synchronization and obtaining the cell-specific scrambling code. When designing the channel for obtaining the frame timing synchronization and the channel for obtaining the cell-specific scrambling code, different frequency reuse factors are applied to the synchronization channels of different steps according to the characteristics of each synchronization obtainment step in order to improve the performance of each step.

Oligonucleotides bearing free, uncapped 5′ phosphate group(s) are recognized by RIG-I, leading to the induction of type I IFN, IL-18 and IL-1β production. Bacterial RNA also induces type I IFN production. 5′ phosphate oligonucleotides and bacterial RNA can be used for inducing an anti-viral response or an anti-bacterial response, in particular, type I IFN and / or IL-18 and / or IL-1β production, in vitro and in vivo and for treating various disorders and diseases such as viral infections, bacterial infections, parasitic infections, tumors, allergies, autoimmune diseases, immunodeficiencies and immunosuppression. Single-stranded 5′ triphosphate RNA can be used for inducing an anti-viral response, an anti-bacterial response, or an anti-tumor response, in particular, type I IFN and / or IL-18 and / or IL-1β production, in a target cell-specific manner.

Provided are a cell search method, a frame transmission method thereof, and a forward link frame structure thereof. The cell search method used by a terminal to search a target cell using reception signals received from a plurality of base stations, each base station transmitting a frame of its cell, in an Orthogonal Frequency-Division Multiplexing (OFDM) cellular system comprising a plurality cells to which a cell-specific scrambling code is assigned includes: detecting a hopping pattern of the target cell using reception sync channel symbols, which are signals corresponding to sync channel symbol positions of the reception signals, wherein the frame of each cell comprises M sync channel symbols code-hopped according to a hopping pattern of the cell, where M is a natural number equal to or greater than 2, each hopping pattern containing M sync channel code sequences and respectively corresponding to each code group to which a scrambling code of each cell belongs, and an arbitrary hopping pattern used in the OFDM cellular system differs from a cyclically shifted result of the hopping pattern, other hopping patterns, or cyclically shifted results of the other hopping patterns; and detecting a code group of the target cell based on the detected hopping pattern. Accordingly, a cell search time and the complexity of the cell search can be reduced.

Methods and compositions are provided for delivering a polynucleotide encoding a gene of interest to a target cell using a virus. The virus envelope comprises a cell-specific binding determinant that recognizes and binds to a component on the target cell surface, leading to endocytosis of the virus. A separate fusogenic molecule is also present on the envelope and facilitates delivery of the polynucleotide across the membrane and into the cytosol of the target cell. The methods and related compositions can be used for treating patients having suffering from a wide range of conditions, including infection, such as HIV; cancers, such as non-Hodgkin's lymphoma and breast cancer; and hematological disorders, such as severe combined immunodeficiency.

Disclosed is a method, a computer program product and a device that includes a receiver for receiving a downlink signal transmitted into a cell. The receiver is operable to obtain time, carrier frequency and cell-specific preamble synchronization to the received signal and includes a plurality of synchronization units that include a first detector to detect a frame boundary using preamble delay correlation; a second detector to detect the frame boundary with greater precision using a conjugate symmetry property over a region identified by the first detector; a cyclic prefix correlator to resolve symbol boundary repetition; an estimator, using the cyclic prefix, to estimate and correct a fractional carrier frequency offset; an operator to perform a Fast Fourier Transform of an identified preamble symbol and a frequency domain cross-correlator to identify cell-specific preamble sequences and an integer frequency offset in sub-carrier spacing. The transmitted signal may be a downlink signal transmitted into the cell from a base station that is compatible with IEEE 802.16e (WiMAX).

The invention relates to the use of a light-gated ion channel for the manufacture of a medicament for the treatment of blindness and a method for expressing said cell specific fashion, e.g. in ON-bipolar cells, ON-ganglion cells, or AII amacrine cells.

Isolated polynucleotide sequences exhibiting endothelial cell specific promoter activity, novel cis regulatory elements and methods of use thereof enabling treatment of diseases characterized by aberrant neovascularization or cell growth are disclosed.

A method and apparatus for performing mobility measurement in a communication network (100) is described. The method comprises of receiving a subframe sequence pattern from a node in the communication network (100). The subframe sequence pattern indicates types of subframes being transmitted by a neighboring cell node (104) in a neighboring cell (112). The method includes receiving a subframe from a sequence of subframes transmitted by the neighboring cell node (104) in the neighboring cell (112), and determining that the received subframe is a multicast subframe based on the subframe sequence pattern. The method then includes performing a single cell-specific reference symbol measurement in response to determining that the received subframe is the multicast subframe.

The present invention relates to novel process for the preparation of glycoproteins by mammalian cell culture wherein the sialic acid content of the glycoprotein produced is controlled over a broad range of values by manipulating the cell culture environment. The invention provides for processes in which the sialic acid content of the glycoprotein is modified by changes in cell culture parameters which affect cell specific productivity. Preferred embodiments of the invention include cell culture processes in the osmolality of the cell culture is controlled as well as the concentration of a transcription enhancer during the production phase of the cell culture. The invention further provides for novel preparations of soluble type 1 tumor necrosis factor immunoglobulin G1 and their uses in the treatment of inflammatory or immune related disorders.

Disclosed is a method for radio link monitoring in a wireless communication system and an apparatus for the method. More specifically, a method for a user equipment (UE) to perform Radio Link Monitoring (RLM) in a wireless communication system comprises performing second RLM on a cell based on a Reference Signal (RS) other than a Cell-specific Reference Signal (CRS) and determining an Radio Link Failure (RLF) with respect to the cell based on the second RLM, wherein a condition for determining an RLF applied to the second RLM is different from the condition for determining an RLF applied to CRS-based first RLM.

A method and apparatus for transmitting a dedicated reference signal (DRS) are provided, the method including determining, by a base station, whether user equipments (UEs) participating in multiple users-multiple input multiple output (MU-MIMO) at the same physical resource block (PRB) belong to the same cell, if yes, configuring that the UEs adopt a cell-specific scrambling code sequence; otherwise, configuring that the UEs located in the cells belonging to the same cell group adopt a cell group-specific scrambling code sequence; sending, by the base station, configuration information to the UE, and sending a DRS to the UE by using the scrambling code sequence configured for the UE; an initialization code of the cell-specific scrambling code sequence is determined according to an identity of the cell in which the UE is located; an initialization code of the cell group-specific scrambling code sequence is determined according to an identity of the cell group. As such, the UE can restrain DRS interferences between different cells when receiving the DRS and improve the precision of the channel estimation.

Provided are a method and an apparatus for measuring channel quality indicator in a wireless communication system. User equipment receives, from a base station, at least one of a cell-specific reference signal (CRS) which is cell-specifically transmitted and a channel state information reference signal (CSI RS). The user equipment also receives, from the base station, a demodulation reference signal (DMRS) which is user equipment-specifically transmitted in an enhanced physical downlink control channel (e-PDCCH) region constituted in a physical downlink shared channel (PDSCH) region. The terminal measures the CQI based on either at least one of the CRS and the CSI RS or the DMRS.

A method and apparatus is provided for transmitting an orthogonal frequency domain multiple access (OFDMA) signal including a synchronization channel signal transmitted within a localized portion of a bandwidth of the OFDMA signal (818), the synchronization channel signal having predetermined time domain symmetry within the localized portion of the bandwidth (816). The synchronization channel signal enables an initial acquisition and cell search method with low computational load which provides OFDMA symbol timing detection and frequency error detection by differential processing of sequence elements of the synchronization channel signal (1112) and frame boundary detection and cell specific information detection (1114) in an OFDMA system supporting multiple system bandwidths, both synchronized and un-synchronized systems, a large cell index and an OFDMA symbol structure with both short and long cyclic prefix length.

Notifying served user equipments (UEs) of the presence or absence of cell-specific reference signal (CRS) symbols transmitted by neighboring base stations in the physical downlink shared channel (PDSCH) region of a subframe can be achieved through various of signaling techniques. The served UE may be notified by communicating a one or multi-bit indicator in a physical layer signaling channel of the serving cell, such as the physical downlink control channel (PDCCH) of the subframe. Alternatively, the served UE may be notified through higher layer signaling.

Isolated polynucleotide sequences exhibiting endothelial cell specific promoter activity, novel cis regulatory elements and methods of use thereof enabling treatment of diseases characterized by aberrant neovascularization or cell growth are disclosed.