Abstract: A substrate is disclosed. The substrate includes a transparent underlayer, a plurality of signal lines on the transparent underlayer, and a plurality of labels on the transparent underlayer. The plurality of labels respectively correspond to the plurality of signal lines in a one-to-one relationship and are configured to identify the corresponding signal lines, and one of at least two adjacent labels is a forward pattern label, and another one of the at least two adjacent labels is a reverse pattern label.

Abstract: Provided by the invention are methods for identifying therapeutic agents for treating multiple myeloma or another hematological malignancy, as well as methods for determining the prognosis of a patient with multiple myeloma or another hematological malignancy. The methods are based in part on the inventors' discovery that an extracellular form of cyclophilin A binds to CD147 expressed on multiple myeloma cells.

Abstract: The present application provides a display panel. The display panel includes an array substrate which includes a display region and a frame region. The frame region includes a gate circuit drive unit, the gate circuit drive unit comprises a thin film transistor, and the thin film transistor comprises a source, a drain and a gate. The frame region further includes a driving circuit and a first signal lead line, the first signal lead line is arranged on a single layer and arranged on a same layer as the signal transmission wire layer, one end of the first signal lead line is electrically connected to the gate and the other end of the first signal lead line is electrically connected to the driving circuit.

Abstract: The present disclosure provides a display panel and a method for forming an array substrate of a display panel. The display panel includes an array substrate which includes a display region and a frame region. The frame region includes a wire region in which first signal wires are formed. Each of the first signal wires includes a first conductive layer and a second conductive layer which are stacked with each other and electrically connected. As such, to obtain the same resistance value as that in prior art, the first signal wires in the present disclosure can be formed with a reduced width. Therefore, the wire region of the array substrate can have a smaller size, and thus the whole frame region of the display panel can be smaller.

Abstract: Methods for the photoreduction of molecules are provided. The methods use diamond having a negative electron affinity as a photocatalyst, taking advantage of its ability to act as a solid-state electron emitter that is capable of inducing reductions without the need for reactants to adsorb onto its surface. The methods comprise illuminating a fluid sample comprising the molecules to be reduced and hydrogen surface-terminated diamond having a negative electron affinity with light comprising a wavelength that induces the emission of electrons from the diamond directly into the fluid sample. The emitted electrons induce the reduction of the molecules to form a reduction product.

Abstract: A process for plasmonic-based high resolution color printing is provided. The process includes a) providing a nanostructured substrate surface having a reverse structure geometry comprised of nanopits and nanoposts on a support, and b) forming a conformal continuous metal coating over the nanostructured substrate surface to generate a continuous metal film, the continuous metal film defining nanostructures for the plasmonic-based high resolution color printing, wherein a periodicity of the nanostructures is equal to or less than a diffraction limit of visible light. A nanostructured metal film or metal-film coated support obtained by the process and a method for generating a color image are also provided.

Abstract: A method, device and user equipment (UE) for transmitting multi-cell scheduling information is provided. When at least two cells are serving the UE, the method for transmitting multi-cell scheduling information includes determining a main cell of the UE from the at least two cells and transmitting, in the main cell, the scheduling information of the main cell and an auxiliary cell which are serving the UE.

Abstract: Methods for the photoreduction of molecules are provided, the methods comprising illuminating an amino-terminated diamond surface comprising amino groups covalently bound to the surface of diamond with light comprising a wavelength sufficient to excite an electronic transition defined by the energy band structure of the amino-terminated diamond, thereby inducing the emission of electrons from the amino-terminated diamond surface into a sample comprising molecules to be reduced, wherein the emitted electrons induce the reduction of the molecules to form a reduction product; and collecting the reduction product.

Abstract: The present disclosure provides a display panel and a method for forming an array substrate of a display panel. The display panel includes an array substrate which includes a display region and a frame region. The frame region includes a wire region in which first signal wires are formed. Each of the first signal wires includes a first conductive layer and a second conductive layer which are stacked with each other and electrically connected. As such, to obtain the same resistance value as that in prior art, the first signal wires in the present disclosure can be formed with a reduced width. Therefore, the wire region of the array substrate can have a smaller size, and thus the whole frame region of the display panel can be smaller.

Abstract: Methods for the photoreduction of molecules are provided. The methods use diamond having a negative electron affinity as a photocatalyst, taking advantage of its ability to act as a solid-state electron emitter that is capable of inducing reductions without the need for reactants to adsorb onto its surface. The methods comprise illuminating a fluid sample comprising the molecules to be reduced and hydrogen surface-terminated diamond having a negative electron affinity with light comprising a wavelength that induces the emission of electrons from the diamond directly into the fluid sample. The emitted electrons induce the reduction of the molecules to form a reduction product.

Abstract: A substrate is disclosed. The substrate includes a transparent underlayer, a plurality of signal lines on the transparent underlayer, and a plurality of labels on the transparent underlayer. The plurality of labels respectively correspond to the plurality of signal lines in a one-to-one relationship and are configured to identify the corresponding signal lines, and one of at least two adjacent labels is a forward pattern label, and another one of the at least two adjacent labels is a reverse pattern label.

Abstract: Methods for the photoreduction of molecules are provided. The methods use diamond having a negative electron affinity as a photocatalyst, taking advantage of its ability to act as a solid-state electron emitter that is capable of inducing reductions without the need for reactants to adsorb onto its surface. The methods comprise illuminating a fluid sample comprising the molecules to be reduced and hydrogen surface-terminated diamond having a negative electron affinity with light comprising a wavelength that induces the emission of electrons from the diamond directly into the fluid sample. The emitted electrons induce the reduction of the molecules to form a reduction product.

Abstract: A method, device and user equipment (UE) for transmitting multi-cell scheduling information is provided. When at least two cells are serving the UE, the method for transmitting multi-cell scheduling information includes determining a main cell of the UE from the at least two cells and transmitting, in the main cell, the scheduling information of the main cell and an auxiliary cell which are serving the UE.

Abstract: A method, device and user equipment (UE) for transmitting multi-cell scheduling information is provided. When at least two cells are serving the UE, the method for transmitting multi-cell scheduling information includes the following steps: determining a main cell of the UE from the at least two cells; transmitting, in the main cell, the scheduling information of the main cell and an auxiliary cell which are serving the UE.

Abstract: Disclosed is a process of enantioselectively forming an aminoxy compound of Formula (3) In formula (3) R1 is one of an aliphatic group and an alicyclic group. R2 is one of hydrogen, an aliphatic group, an alicyclic group, an aromatic group, an arylaliphatic group and an arylalicyclic group. R3 is one of hydrogen, halogen, hydroxyl, and an aliphatic group with a main chain having 1 to about 10 carbon atoms. The respective aliphatic, alicyclic, aromatic, arylaliphatic or arylalicyclic groups of R1, R2, and R3 comprise 0 to about 3 heteroatoms independently selected from the group consisting of N, O, S, Se and Si. The process includes contacting a carbonyl compound of Formula (1) and a nitroso compound of Formula (2) in the presence of a chiral catalyst.

Abstract: Embodiments of the present invention provide a networking method applied to a multi-site cell, a base band unit, a remote RF unit and a system. The method includes: connecting at least one RRU of one or more remote end remote units RRUs under a base station of a local cell to at least two base stations. The at least two base stations include the base station of the local cell and at least one other base station. Communication, is continued by using the at least one other base station when the communication between the one RRU of the one or more RRUs and the base station of the local cell fails.

Abstract: Disclosed is a process of enantioselectively forming an aminoxy compound of Formula (3) In formula (3) R1 is one of an aliphatic group and an alicyclic group. R2 is one of hydrogen, an aliphatic group, an alicyclic group, an aromatic group, an arylaliphatic group and an arylalicyclic group. R3 is one of hydrogen, halogen, hydroxyl, and an aliphatic group with a main chain having 1 to about 10 carbon atoms. The respective aliphatic, alicyclic, aromatic, arylaliphatic or arylalicyclic groups of R1, R2, and R3 comprise 0 to about 3 heteroatoms independently selected from the group consisting of N, O, S, Se and Si. The process includes contacting a carbonyl compound of Formula (1) and a nitroso compound of Formula (2) in the presence of a chiral catalyst.

Abstract: Methods for the photoreduction of molecules are provided. The methods use diamond having a negative electron affinity as a photocatalyst, taking advantage of its ability to act as a solid-state electron emitter that is capable of inducing reductions without the need for reactants to adsorb onto its surface. The methods comprise illuminating a fluid sample comprising the molecules to be reduced and hydrogen surface-terminated diamond having a negative electron affinity with light comprising a wavelength that induces the emission of electrons from the diamond directly into the fluid sample. The emitted electrons induce the reduction of the molecules to form a reduction product.

Abstract: Tailored doping of barrier layers enables balancing of the radiative recombination among the multiple-quantum-wells in III-Nitride light-emitting diodes. This tailored doping enables more symmetric carrier transport and uniform carrier distribution which help to reduce electron leakage and thus reduce the efficiency droop in high-power III-Nitride LEDs. Mitigation of the efficiency droop in III-Nitride LEDs may enable the pervasive market penetration of solid-state-lighting technologies in high-power lighting and illumination.

Abstract: Disclosed is a process of enantioselectively forming an aminoxy compound of Formula (3) In formula (3) R1 is one of an aliphatic group and an alicyclic group. R2 is one of hydrogen, an aliphatic group, an alicyclic group, an aromatic group, an arylaliphatic group and an arylalicyclic group. R3 is one of hydrogen, halogen, hydroxyl, and an aliphatic group with a main chain having 1 to about 10 carbon atoms. The respective aliphatic, alicyclic, aromatic, arylaliphatic or arylalicyclic groups of R1, R2, and R3 comprise 0 to about 3 heteroatoms independently selected from the group consisting of N, O, S, Se and Si. The process includes contacting a carbonyl compound of Formula (1) and a nitroso compound of Formula (2) in the presence of a chiral catalyst.