Abstract: A liquid crystal composition includes one or more compounds represented by Formula I and one or more compounds represented by Formula II and/or Formula III. The liquid crystal composition has excellent flicker level and a relatively large elastic constant K11 and a relatively small rotational viscosity ?1 while maintaining a suitable optical anisotropy and a suitable clear point, that is, the liquid crystal composition has a relatively small ?1/K11 ratio, so that the liquid crystal display element and the liquid crystal display have a relatively fast response speed.

Abstract: A liquid crystal composition, a liquid crystal display element and a liquid crystal display comprising the liquid crystal composition belong to the field of liquid crystal display. The liquid crystal composition of the present disclosure comprises a compound represented by formula I, a compound represented by formula II, one or more compounds represented by formula III, one or more compounds represented by formula IV and more than three compounds represented by formula V. The liquid crystal composition has low rotational viscosity ?1 and high stability to heat and light on the basis of maintaining appropriate optical anisotropy ?n, which can realize fast response of liquid crystal display.

Abstract: A liquid crystal composition, a liquid crystal display element and a liquid crystal display comprising the liquid crystal composition belong to the field of liquid crystal display. The liquid crystal composition of the present disclosure comprises a compound represented by formula I, a compound represented by formula II, one or more compounds represented by formula III, one or more compounds represented by formula IV and more than three compounds represented by formula V. The liquid crystal composition has low rotational viscosity ?1 and high stability to heat and light on the basis of maintaining appropriate optical anisotropy ?n, which can realize fast response of liquid crystal display.

Abstract: The identification, function and application of m6A methylation site in the FAM134B mRNA. The main steps include confirming the m6A methylation site in FAM134B mRNA by comparative analyzing m6A-seq results of Landrace and Jinhua pigs, corresponding with highly conserved motif RRACH (R=G, A; H=A, C, T) and the prediction website; altering the m6A methylation in FAM134B mRNA via mutating synonymous codon of FAM134B gene (C1358 to T1358) without changing the amino acid sequence; designing qPCR primers according to the m6A peak region and a control region of FAM134B mRNA; extracting total RNA and determining the relative m6A level of a single gene by protein immunoprecipitation and qPCR. The m6A methylation site of FAM134B mRNA plays a critical rule on fat deposition, which serves as a novel molecular marker and a drug target for treating obesity.