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30 results on '"Yang, Yanling"'

4. Back Cover: Atomic cerium modulated palladium nanoclusters exsolved ferrite catalysts for lean methane conversion (EXP2 6/2022)

Author

Yang, Yanling, primary, Wang, Si, additional, Tu, Xin, additional, Hu, Zhiwei, additional, Zhu, Yinlong, additional, Guo, Hongquan, additional, Li, Zhishan, additional, Zhang, Li, additional, Peng, Meilan, additional, Jia, Lichao, additional, Yang, Meiting, additional, Yang, Guangming, additional, Qiao, Xurong, additional, Sun, Jiahui, additional, Liang, Xiaolu, additional, Zhang, Zhen, additional, Zhu, Yanru, additional, Shi, Lei, additional, Jiang, Chenxing, additional, Zhao, Yingru, additional, Li, Jianhui, additional, Shao, Zongping, additional, Zhang, Xin, additional, and Sun, Yifei, additional

Published
2022
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5. Atomic cerium modulated palladium nanoclusters exsolved ferrite catalysts for lean methane conversion

Author

Yang, Yanling, primary, Wang, Si, additional, Tu, Xin, additional, Hu, Zhiwei, additional, Zhu, Yinlong, additional, Guo, Hongquan, additional, Li, Zhishan, additional, Zhang, Li, additional, Peng, Meilan, additional, Jia, Lichao, additional, Yang, Meiting, additional, Yang, Guangming, additional, Qiao, Xurong, additional, Sun, Jiahui, additional, Liang, Xiaolu, additional, Zhang, Zhen, additional, Zhu, Yanru, additional, Shi, Lei, additional, Jiang, Chenxing, additional, Zhao, Yingru, additional, Li, Jianhui, additional, Shao, Zongping, additional, Zhang, Xin, additional, and Sun, Yifei, additional

Published
2022
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16. A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia

Author

Kang, Lulu, primary, Liu, Yupeng, additional, Shen, Ming, additional, Liu, Yi, additional, He, Ruxuan, additional, Song, Jinqing, additional, Jin, Ying, additional, Li, Mengqiu, additional, Zhang, Yao, additional, Dong, Hui, additional, Liu, Xueqin, additional, Yan, Hui, additional, Qin, Jiong, additional, Zheng, Hong, additional, Chen, Yongxing, additional, Li, Dongxiao, additional, Wei, Haiyan, additional, Zhang, Huifeng, additional, Sun, Liying, additional, Zhu, Zhijun, additional, Liang, Desheng, additional, and Yang, Yanling, additional

Published
2019
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17. Pattern Directive Sensing Selectivity of Graphene for Wearable Multifunctional Sensors via Femtosecond Laser Fabrication

Author

Feng Lei, Yang Yanling, Suo Guoquan, Ye Xiaohui, Zhang Li, Xuebing Yuan, Yang Yifan, Jinying Zhang, Miao Yu, Ting Huang, Ming Qi, and Xiaojiang Hou

Subjects
Materials science, Mechanics of Materials, Graphene, law, Laser fabrication, Femtosecond, Wearable computer, General Materials Science, Nanotechnology, Selectivity, Industrial and Manufacturing Engineering, law.invention
Published
2020

29. A study on a cohort of 301 Chinese patients with isolated methylmalonic acidemia.

Author

Kang L, Liu Y, Shen M, Liu Y, He R, Song J, Jin Y, Li M, Zhang Y, Dong H, Liu X, Yan H, Qin J, Zheng H, Chen Y, Li D, Wei H, Zhang H, Sun L, Zhu Z, Liang D, and Yang Y

Subjects
Adolescent, Age of Onset, Amino Acid Metabolism, Inborn Errors diagnosis, Asian People, Child, Child, Preschool, China, Cohort Studies, Female, Genetic Predisposition to Disease, Genotype, Humans, Infant, Infant, Newborn, Male, Methylmalonic Acid, Mutation, Phenotype, Young Adult, Amino Acid Metabolism, Inborn Errors genetics
Abstract

Methylmalonic acidemia (MMA) is the most common organic acidemia in China. This study aimed to characterise the genotypic and phenotypic variabilities, and the molecular epidemiology of Chinese patients with isolated MMA. Patients (n = 301) with isolated MMA were diagnosed by clinical examination, biochemical assays, and genetic analysis. Fifty-eight patients (19.3%) were detected by newborn screening and 243 patients (80.7%) were clinically diagnosed after onset. Clinical onset ranged from the age of 3 days to 23 years (mean age = 1.01 ± 0.15 years). Among 234 MMA patients whose detailed clinical data were available, 170 (72.6%) had early onset disease (before the age of 1 year), and 64 (27.4%) had late-onset disease. The 234 MMA patients manifested with neuropsychiatric impairment (65.4%), haematological abnormality (31.6%), renal damage (8.5%), and metabolic crises (67.1%). Haematological abnormality was significantly more common in early-onset patients than that in late-onset patients. The incidence of metabolic crises was significantly high (P < 0.001) in patients with mut type than those with other types of isolated MMA. Variations (n = 122) were identified in MMUT, MMAA, MMAB, MMADHC, SUCLG1, and SUCLA2, of which 45 were novel. c.729&#95;730insTT was the most frequent MMUT mutation, with a significantly higher frequency in our patients than that in 151 reported European patients. The frequency of c.914T>C in MMUT in our cohort was also higher than that in 151 European patients. MMUT mutations c.729&#95;730insTT and c.914T>C are specific for the Chinese population. Our study expanded the spectrum of phenotypes and genotypes in isolated MMA., (© 2019 SSIEM.)

Published
2020
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30. Demographics, diagnosis and treatment of 256 patients with tetrahydrobiopterin deficiency in mainland China: results of a retrospective, multicentre study.

Author

Ye J, Yang Y, Yu W, Zou H, Jiang J, Yang R, Shang S, and Gu X

Subjects
Adolescent, Adult, Child, Child, Preschool, China, Female, Humans, Infant, Infant, Newborn, Male, Mutation, Neonatal Screening methods, Phenylalanine blood, Phenylketonurias blood, Phenylketonurias genetics, Phosphorus-Oxygen Lyases blood, Phosphorus-Oxygen Lyases deficiency, Phosphorus-Oxygen Lyases drug effects, Phosphorus-Oxygen Lyases genetics, Retrospective Studies, Young Adult, Phenylketonurias diagnosis, Phenylketonurias drug therapy
Abstract

Background: National coverage of neonatal screening for hyperphenylalaninaemia (HPA) in China is still low and tests to differentiate causes of HPA are not performed in many centres. This study aimed to describe the demographics, geographic distribution, diagnosis, treatment and clinical outcomes of treatment, including intellectual development, in patients with tetrahydrobiopterin (BH4) deficiency in mainland China., Methods: This was a retrospective, multicentre, chart review in patients with BH4 deficiency across mainland China born 1985-2010., Results: Two hundred fifty six patients were included; 59.9 % (267/446) of parents were from eastern China. Median (interquartile range) age at diagnosis decreased from 12.0 (5.5, 102.0) months to 2.0 (1.0, 3.5) months in patients born 1985-1999 (n = 28) and 2005-2010 (n = 152), respectively. 6-Pyruvoyl-tetrahydropterin synthase (PTPS) deficiency was the primary cause of BH4 deficiency (96.0 %); four hotspot mutations accounted for 76.6 % of PTS gene mutations; two novel variants in the QDPR gene were identified. Most patients (83.6 %) received treatment with BH4, L-dopa, 5-hydroxytryptophan and/or diet therapy. Target blood Phe concentration was confirmed at 88.9 % of visits; median (Q1, Q3) blood Phe concentration was 106.8 (73.0, 120.0) μmol/L during therapy and 117.0 (67.1, 120.0) μmol/L at last visit. Median (Q1, Q3) WISC IQ score was 80.0 (69.0, 90.0) in 33 patients. DQ scores were within normal range (≥85) for 37/59 (62.7 %) patients. Physical development indicators were within normal ranges. Treatment-related adverse events, reported in 20/256 (7.8 %) patients, were mild-to-moderate in severity., Conclusion: This study provides valuable information on the current and historical situation of BH4 deficiency in mainland China.

Published
2013
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