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Peiwei Zhao

Showing results (1-10 of 42) with videos related to

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Microbiology (Reading, England)|August 22, 2009
Identification and characterization of a novel spore-associated subtilase from Thermoactinomyces sp. CDFGuyue Cheng, Peiwei Zhao, Xiao-Feng Tang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 10, 2018
[Clinical features and genetic analysis of a case with Coffin-Siris syndrome]Peiwei Zhao, Dan Gao, Yufeng Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 1, 2019
[Genome-wide copy number microarray analysis for a boy with autism]Xuelian He, Peiwei Zhao, Yufeng Huang, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|May 18, 2021
Influence of <i>UGT2B7</i> and <i>UGT1A6</i> polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic childrenZhaosong Du, Hua Xu, Peiwei Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 29, 2021
[Clinical features and genetic analysis of a case with Perlman syndrome due to variant of DIS3L2 gene]Jing Chen, Chunhui Hu, Lanfen Ren, et al.
Epilepsy Research|October 23, 2020
Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic childrenMaochang Liu, Junjun Mao, Hua Xu, et al.
Plos One|May 13, 2014
Association of mTOR polymorphisms with cancer risk and clinical outcomes: a meta-analysisJianbo Shao, Ying Li, Peiwei Zhao, et al.
Pediatric Nephrology (Berlin, Germany)|March 30, 2022
Gross hematuria, edema, and hypocomplementemia in a 9-year-old boy: AnswersJuanjuan Ding, Panli Liao, Gaohong Zhu, et al.
International Journal of Pediatric Otorhinolaryngology|May 6, 2018
2q24 deletion in a 9-month old girl with anal atresia, hearing impairment, and hypotoniaPeiwei Zhao, Bing Mao, Xiaonan Cai, et al.
Neurogenetics|January 12, 2020
Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spamsPeiwei Zhao, Xuehua Peng, Sukun Luo, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Microbiology (Reading, England)|August 22, 2009
Identification and characterization of a novel spore-associated subtilase from Thermoactinomyces sp. CDFGuyue Cheng, Peiwei Zhao, Xiao-Feng Tang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 10, 2018
[Clinical features and genetic analysis of a case with Coffin-Siris syndrome]Peiwei Zhao, Dan Gao, Yufeng Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 1, 2019
[Genome-wide copy number microarray analysis for a boy with autism]Xuelian He, Peiwei Zhao, Yufeng Huang, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|May 18, 2021
Influence of <i>UGT2B7</i> and <i>UGT1A6</i> polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic childrenZhaosong Du, Hua Xu, Peiwei Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 29, 2021
[Clinical features and genetic analysis of a case with Perlman syndrome due to variant of DIS3L2 gene]Jing Chen, Chunhui Hu, Lanfen Ren, et al.
Epilepsy Research|October 23, 2020
Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic childrenMaochang Liu, Junjun Mao, Hua Xu, et al.
Plos One|May 13, 2014
Association of mTOR polymorphisms with cancer risk and clinical outcomes: a meta-analysisJianbo Shao, Ying Li, Peiwei Zhao, et al.
Pediatric Nephrology (Berlin, Germany)|March 30, 2022
Gross hematuria, edema, and hypocomplementemia in a 9-year-old boy: AnswersJuanjuan Ding, Panli Liao, Gaohong Zhu, et al.
International Journal of Pediatric Otorhinolaryngology|May 6, 2018
2q24 deletion in a 9-month old girl with anal atresia, hearing impairment, and hypotoniaPeiwei Zhao, Bing Mao, Xiaonan Cai, et al.
Neurogenetics|January 12, 2020
Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spamsPeiwei Zhao, Xuehua Peng, Sukun Luo, et al.
Pageof 5