Abstract: Some aspects of the disclosure provide a method for camera operation control in an electronic device. The method includes obtaining, based on a plurality of frames associated with a target time slice, a first target parameter to be met by a camera of a virtual camera system in the target time slice. Then, the method includes determining a target operation speed of the camera in the target time slice at least partially based on the first target parameter and a time-speed change magnification curve, and controlling the camera to operate based on the target operation speed. Apparatus and non-transitory computer-readable storage medium counterpart embodiments are also contemplated.

Abstract: The present disclosure relates to a backlight module, a method for designing the same, and a display device. The backlight module includes: a first substrate; a plurality of LED chips on the first substrate; and a light control structure on the first substrate. The backlight module includes a plurality of light control region groups in one-to-one correspondence with the plurality of light-emitting diode chips, each light control region group includes at least a first light control region and a second light control region. The light control structure includes a plurality of light control substructure groups respectively located in the plurality of light control region groups. Each light control substructure group includes at least a first light control substructure in the first light control region and a second light control substructure in the second light control region.

Abstract: The present invention encompasses compounds of formula (I) wherein R1a, R1b, R2a, R2b, Z, R3 to R5, A, p, U, V, W, L and E have the meanings given in the claims and specification, their use as inhibitors of mutant Ras family proteins, pharmaceutical compositions and preparations containing such compounds and their use as medicaments/medical uses, especially as agents for treatment and/or prevention of oncological diseases.

Abstract: A method for detecting abnormal direct current voltage measurement in a modular multilevel converter high voltage direct current transmission system is provided. In the method, a valve group voltage at a detection pole is obtained, voltages at voltage measurement points at the detection pole are collected, and comparison and determination are performed based on the actual arrangement of the voltage measurement points, and then whether an abnormal measurement occurs at each of the voltage measurement points is determined.

Abstract: This application relates to an identity verification method performed at a computer device and a computer-readable storage medium.

Abstract: Disclosed are a pyrazole compound or a salt thereof, a preparation method therefor, a herbicidal composition and use thereof. The pyrazole compound or a salt thereof has a structure as shown in formula (I): wherein, R represents wherein, R?, R?, and R?? represent hydrogen, C1-C4 alkyl, C1-C4 halogenated alkyl, C1-C4 alkoxy or halogen, R?, R?, and R?? may be the same or different; R1 represents C1-C3 alkyl; R2 represents hydrogen or C1-C4 alkyl; R3 represents hydrogen or C1-C6 alkyl, optionally substituted phenyl, optionally substituted pyridyl, optionally substituted alkenyl, optionally substituted alkynyl, C1-C6 alkyl carbonyl, C1-C6 alkoxyl carbonyl, C1-C6 alkyl carbonyl methyl, etc. A compound having a pyrazole structure not only has excellent herbicidal effect on barnyard grass, but also is safe to rice in post-emergence application. More surprisingly, it also has good control efficacy on barnyard grass resistant to major herbicides, such as penoxsulam, quinclorac, cyhalofop-butyl, propanil, etc.

Abstract: Embodiments of the present disclosure relate to the field of network technologies, including a resource transfer method and apparatus and a storage medium. The method includes: storing a graphic code in the specified application client, the graphic code being sent by a specified server when a network is already connected, the graphic code including a user identifier used by the specified application client to log in to the specified server, and the graphic code being obtained by the specified server from a third-party server accessed by an interface of the specified server, and presenting a stored graphic code when detecting a graphic code calling operation.

Abstract: The invention relates to the field of pesticide technology, and in particular a type of carboxylic acid derivative-substituted iminoaryl compound, preparation method, herbicidal composition and use thereof. The compound, as shown in general formula I: wherein, Q represents Y represents halogen, haloalkyl or cyano; Z represents halogen; M represents CH or N; W represents OX5, SX5 or N(X5)2; X represents —CX1X2-(alkyl)n-, -alkyl-CX1X2-(alkyl)n- or —(CH2)r—; X3 and X4 each independently represent O, S, NH or N-alkyl, etc. The compound has excellent herbicidal activity against gramineous weeds, broadleaf weeds, cyperaceae weeds and so on even at low application rates, and has high selectivity for crops.

Abstract: The invention belongs to the technical field of pesticides, and specifically relates to a 4-pyridinyl formamide compound or a derivative thereof, a preparation method therefor, a herbicidal composition and the use thereof. The 4-pyridinyl formamide compound is as represented by formula (I), wherein, X and Y each independently represent nitro, halogen, cyano, formyl, thiocyano, mercapto, etc.; and M represents an unsubstituted or substituted structure (II). The compound, and the derivative and the composition thereof have excellent herbicidal activity and a higher crop safety, and establish good selectivity, especially for key crops such as wheat and rice.

Abstract: The invention relates to the field of pesticide technology, and in particular a type of fused-ring substituted aromatic compound, preparation method, herbicidal composition and use thereof. The fused-ring substituted aromatic compound, represented by general formula I: wherein, Q represents etc.; Y represents halogen, haloalkyl, cyano, nitro or amino; Z represents H, halogen or hydroxy; M represents CH or N; Het represents a cyclic structure that shares two carbon atoms at 4- and 5-positions with isoxazoline ring to form a fused ring; X1, X2 each independently represent H, halogen or nitro etc. The compound has excellent herbicidal activity against gramineous weeds, broadleaf weeds, etc. even at low application rates, and has high selectivity for crops.

Abstract: The present invention belongs to the technical field of pesticides, and specifically relates to an isoxazoline oxime formate compound, a preparation method therefor, and a herbicidal composition and a use thereof. The isoxazoline oxime formate compound is shown in general formula I. Wherein, Y represents halogen, haloalkyl, cyano, nitro or amino; Z represents hydrogen, halogen or hydroxyl; Q represents M represents CH or N; X1, X2 and X3 each independently represent hydrogen, etc.; X4 and X5 each independently represent hydrogen, halogen, cyano or nitro, etc. The compound also has an excellent herbicidal activity against grassy weeds, broadleaf weeds, etc. at a low application rate, and has a high selectivity to crops.

Abstract: The invention relates to the field of pesticide technology, and in particular a type of substituted 1,2,4-triazolo[4,3-a]pyridine derivatives, preparation method, herbicidal composition and use thereof. A substituted 1,2,4-triazolo[4,3-a]pyridine derivative, as shown in Formula I: wherein, Q represents X and Z each independently represent hydrogen, halogen, cyano or nitro, etc.; Y represents hydrogen, halogen, formyl, cyanoalkyl; or an alkyl, alkenyl or alkynyl, each of which contains or does not contain a halogen, etc. The compound and its composition have excellent herbicidal activity and higher crop safety, especially good selectivity for key crops such as rice.

Abstract: The invention belongs to the technical field of pesticides, and specifically relates to a type of substituted-isoxazoline-containing aromatic compound, preparation method therefor, herbicidal composition and use thereof. The compound is as shown in general formula I: Wherein, Q represents Y represents halogen, halogenated alkyl or cyano; Z represents halogen; X1, X2 each independently represent hydrogen, halogen, alkyl, etc.; X3 represents halogen, cyano, etc.; X4 each independently represents —COOR5 or -alkyl-COOR5; R5 each independently represents hydrogen, alkyl, etc.. The compound has excellent herbicidal activity against gramineous weeds, broadleaf weeds, and so on even at low application rates, and has high selectivity for crops.

Abstract: The invention belongs to the technical field of agricultural chemicals, and particularly relates to an N-(1,3,4-oxadiazol-2-yl)arylcarboxamide compound or a salt thereof, a preparation method, a herbicidal composition and a use thereof. The compound is as shown in the following Formula I: wherein X represents O, S, SO, SO2 or NR1; Y represents halogen, cyano, cyanoalkyl, carboxyl, nitro, etc.; or —X—Y represents unsubstituted or substituted five- or six-membered heterocyclyl or heteroaryl; Z represents hydrogen, halogen, cyano, OR4, -alkyl-OR4, —O-alkyl-N(R5)2, etc., M represents hydrogen, OR6, SR6, COR6, COOR6, CON(R7)2, etc. The compound has advantages of a low dosage for use, excellent herbicidal activity, and higher crop safety, especially good selectivity for key crops such as rice.

Abstract: Methods and compositions capable of modulating activity of TLX (NR2E1), a nuclear receptor essential for neural stem cell self-renewal are provided. The modulation may comprise downregulating TLX expression and/or modulating TET3. In addition, methods of delivering shRNAs using dendrimer nanoparticles into glioblastoma stem cells are provided. The methods and compositions are useful for treating and preventing the progression of brain cancer, e.g., glioblastoma.

Abstract: A substituted thiazole aromatic ring compound and a preparation method therefor, a herbicidal composition and use thereof. The substituted thiazole aromatic ring compound is as shown in general formula I: Wherein, Y represents halogen, halogenated alkyl, cyano, nitro or amino; Q represents M represents CH or N; X represents X1 represents O or S; X2 represents OX3, SX3 or N(X3)2. The compound has excellent herbicidal activity against gramineous weeds, broadleaf weeds, and so on even at low application rates, and has high selectivity for crops.

Abstract: The present invention belongs to the technical field of pesticides, and in particular relates to a pyridazinol compound, a derivative thereof, a preparation method therefor, a herbicidal composition and the use thereof. The pyridazinol compound is as represented by general formula I, wherein X represents and the ring is an unsubstituted or substituted aryl or unsubstituted or substituted heterocyclyl containing a carbon atom at the 1-position; Y represents haloalkyl; and Z represents halogen, cyano, hydroxy, etc. The derivative refers to an agriculturally acceptable derivative of the hydroxyl group at the 4-position of the pyridazine ring in the general formula I, including a salt, an ester, an oxime, a hydroxylamine and an ether derivative, etc. The compound, the derivative thereof and the composition thereof have good herbicidal activity and crop safety.