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Copyright of Food & Machinery is the property of Food & Machinery Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The colors of tea porcelain, as the most significant color combination and aesthetic object, offer endless imagination and delight for tea drinkers through their richness, depth, and poetic and picturesque beauty. The contrasting beauty found in the interactions during tea ceremonies, the ever-changing beauty of diverse atmospheres, and the purest and most authentic natural beauty enrich the aesthetic material, expanding the aesthetic dimension, and enhancing the artistic conception of tea appreciation. The bold color innovation and practice by people of the Song Dynasty in tea ceremonies deepened the aesthetic value of color, enhanced the theory of tea evaluation, set up lofty aesthetic standards, and made indelible contributions to Chinese tea culture. [ABSTRACT FROM AUTHOR]

Copyright of Science & Technology of Food Industry is the property of Science & Technology of Food Industry Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Guangxi Normal University - Natural Science Edition is the property of Gai Kan Bian Wei Hui and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Shandong Medical Journal is the property of Shandong Medical Health Newspapers and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Harbin Institute of Technology. Social Sciences Edition / Haerbin Gongye Daxue Xuebao. Shehui Kexue Ban is the property of Harbin Institute of Technology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Objective To investigate the relationship between newborn jaundice of Guangxi population and the gene mutation in exon 1 and TATA box of bilirubin uridine diphosphate-glucuronosyl transferase (UGT1A1). Methods Totally 102 cases with newborn hyperbilirubinemia (case group) and 50 neonates without newborn jaundice (control group) were included. TATA box and exon 1 genotypes of UGT1A1 in the two groups were detected by PCR and direct sequencing. UGT1A1 G71R genotype distribution and the differences in allele frequencies were compared between these two groups. The types of UGT1A1 mutation in the case group and the total serum bilirubin (TSB) levels in children patients at 72 hours after birth with different genotypes were observed. Results Significant difference was found in the UGT1A1 G71R genotype distribution and allele frequencies between these two groups (all P < 0. 01) . There were 40 cases with G71R missense mutation，2 cases with (TA) 7 insertion mutation， and 1 case with 715C→T heterozygous nonsense mutation in the case group. In the case group，the TSB level of G71R homozygous children patients was higher than that of the wild type and heterozygous children (all P <0. 0 5 ). Conclusions The G71R mutation of UGT1A1 gene is the main mutation type and closely related with newborn hyperbilirubinemia in Guangxi region. The new-found 715C→T nonsense mutation may be one of the important causes of neonatal bilirubin encephalopathy. [ABSTRACT FROM AUTHOR]