Abstract:
The present invention discloses a method for indicating a modulation mode in HSDPA, comprising the following steps: a NodeB receiving capability information reported by a terminal, if determining that the terminal supports 64QAM modulation mode, determining a transmission block size, a modulation mode and code channel resource to be indicated based on an capability constraint condition and the capability information, and if the determined modulation mode is the same as a basic modulation mode satisfying requirement of the transmission block size, setting modulation mode information of a HS-SCCH as 0, otherwise setting the modulation mode information of the HS-SCCH as 1, and then sending the HS-SCCH to the terminal. Application of the present invention is compatible with a UE device which supports or does not support 64QAM high order modulation, without changing the current frame structure of the HS-SCCH, thereby achieving functional support of the 64QAM modulation mode.
Abstract:
The present invention discloses a method for indicating a modulation mode in HSDPA, comprising the following steps: a NodeB receiving capability information reported by a terminal, if determining that the terminal supports 64QAM modulation mode, determining a transmission block size, a modulation mode and code channel resource to be indicated based on an capability constraint condition and the capability information, and if the determined modulation mode is the same as a basic modulation mode satisfying requirement of the transmission block size, setting modulation mode information of a HS-SCCH as 0, otherwise setting the modulation mode information of the HS-SCCH as 1, and then sending the HS-SCCH to the terminal. Application of the present invention is compatible with a UE device which supports or does not support 64QAM high order modulation, without changing the current frame structure of the HS-SCCH, thereby achieving functional support of the 64QAM modulation mode.
Abstract:
Selective neuronal nitric oxide synthase (nNOS) inhibitor compounds designed with one or more thiophene-2-carboximidamide substituents for improved bioavailability.
Abstract:
This disclosure provides a method of making polylactic acid using carbon dioxide adducts of carbenes, wherein the adducts of carbenes have a structure represented by formula (I) as follows:
Abstract:
A method for modifying Multiple Input Multiple Output (MIMO) mode across Radio Network Controllers (RNCs) is provided by the present disclosure. In the method of the present disclosure, a Serving RNC (SRNC) transmits a request message to a Drift RNC (DRNC), wherein the request message requests the DRNC to set a radio link for a mobile equipment in a cell controlled by the DRNC, and the DRNC feeds back a response message to the SRNC based on the capability of the DRNC and the cell controlled by the DRNC, wherein the response message contains the element used for configuring the radio link in the non-MIMO mode. As a result, when the DRNC and the cell controlled by the DRNC support the MIMO mode, the SRNC configures the radio link to be in the MIMO mode for the mobile equipment, and when the DRNC and the cell controlled by the DRNC do not support the MIMO mode, the SRNC configures the radio link to be in the non-MIMO mode for the mobile equipment. Therefore, a mobile equipment handover or a radio link reconfiguration is completed, and the success rate of the handover or the configuration is improved.
Abstract:
Selective neuronal nitric oxide synthase (nNOS) inhibitor compounds designed with one or more thiophene-2-carboximidamide substituents for improved bioavailability.
Abstract:
Selective neuronal nitric oxide synthase (nNOS) inhibitor compounds designed with one or more thiophene-2-carboximidamide substituents for improved bioavailability.
Abstract:
This disclosure provides a method of making polylactic acid using carbon dioxide adducts of carbenes, wherein the adducts of carbenes have a structure represented by formula (I) as follows:
Abstract:
This disclosure provides methods of controlled polymerization of cyclic compounds catalyzed by carbene derivatives having a general formula as shown below, and to obtain a biodegradable polymeric material having a large molecular weight, a narrow dispersity, and no metallic impurity.
Abstract:
A method for identifying neuronal spikes (extracellular action potentials) is described wherein measured microelectrode readings from tissue are reviewed to identify spikes (successive readings having prolonged rises and/or falls). The frequency of such spikes as a function of their amplitude assumes a bimodal distribution wherein higher amplitude spikes represent neuronal spikes (signal) and lower amplitude spikes represent noise, and thus the higher amplitude spikes can be assumed to be neuronal spikes. Neuronal spikes from the same neuron can then be assumed to have substantially the same waveform shape and period, with the only significant difference between them being the scaling of their amplitudes (i.e., the amplitudes of spikes from the same neuron tend to be proportionate at any given time along their period). Thus, by testing identified neuronal spikes for matching timing and for proportional amplitudes, the neuronal spikes may further be identified as coming from the same or different neurons.