Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kunyi Wang"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 40, Iss , Pp 101127- (2024)
Background and aims: 3-Methylcrotonyl-CoA carboxylase deficiency (3-MCCD) is an autosomal recessive leucine catabolism condition caused by 3-methylcrotonyl-CoA carboxylase (3-MCC) deficiency due to MCCC1/MCCC2 variants. We investigated its incidence
Externí odkaz:
https://doaj.org/article/1251bedb27f54d1aba3f5e99702759a9
Autor:
Jiadong Wang, Junjie Lin, Yujie Zheng, Minxia Hua, Kunyi Wang, Kexin Lu, Yu Zhang, Weijun Zheng, Rucheng Chen, Fuquan Lin
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundStroke, prevalent globally, particularly impacts low- and middle-income countries. Decreased lung function is one of the risk factors for stroke, and there is a lack of sufficient research on the association between the two, especially base
Externí odkaz:
https://doaj.org/article/759c0363bdca44dfaaf44e5e0d6ef8b4
Autor:
Qingkai Wu1 wuqingkai@stu.xidian.edu.cn, Kunyi Wang1, Zhongchao Lin1 zclin@xidian.edu.com, Yu Zhang1, Xunwang Zhao1
Publikováno v:
Applied Computational Electromagnetics Society Journal. Aug2023, Vol. 38 Issue 8, p558-565. 8p.
Autor:
Junjie Lin, Yu Zhang, Kunyi Wang, Junping Wang, Shuo Kou, Kan Chen, Weijun Zheng, Rucheng Chen
Publikováno v:
European Journal of Nutrition.
Publikováno v:
Journal of Ambient Intelligence and Humanized Computing. 13:3807-3817
As a computing service platform closer to users, fog computing has many advantages such as extremely low latency, good mobility, accurate location perception and wide distribution. It has developed rapidly in recent years. However, due to the wide di
Publikováno v:
Clinica Chimica Acta. 512:166-171
Background and aims Primary carnitine deficiency (PCD) is an autosomal recessive disease caused by functional defects in the carnitine transporter OCTN2 due to mutations in SLC22A5. Here, we aimed to understand the incidence, clinical, biochemical, a
Employment relationship (ER) is a social exchange relationship in nature with uncertainty and incongruence during the exchange process. Previous studies has been stuck on regression-based methods, examining and exploring related issue by studying the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::772b900ae22e0f732798686b890ad7c3
https://doi.org/10.3233/faia200739
https://doi.org/10.3233/faia200739
Autor:
Min Li, Weilin Peng, Yiming Lin, Jianlong Zhuang, Weihua Lin, Dongmei Chen, Kunyi Wang, Qingliu Fu, Zhenzhu Zheng
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 509
Background Isovaleric acidemia (IVA) is a rare autosomal recessive disorder of leucine metabolism caused by a defective isovaleryl-CoA dehydrogenase (IVD) gene. Reports of IVA diagnoses following newborn screening (NBS) in the Chinese population are
Autor:
Zhong-Jian Yang, Chao Huang, Renming Liu, Rongling Su, Zhang-Kai Zhou, Li Jiang, Xue-Hua Wang, Kunyi Wang
Publikováno v:
The Journal of Physical Chemistry C. 121:10071-10077
Perovskite nanocrystals open up a bright future for nanolasers, for their various instinct advantages (such as large absorption cross section and optical gain, high fluorescence quantum yields, etc.) can greatly benefit the design and fabrication of