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Peiwei Zhao

Showing results (11-20 of 42) with videos related to

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BMC Medical Genetics|December 2, 2017
Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature reviewLi Tan, Bo Bi, Peiwei Zhao, et al.
Pediatric Nephrology (Berlin, Germany)|March 30, 2022
Gross hematuria, edema, and hypocomplementemia in a 9-year-old boy: QuestionsJuanjuan Ding, Panli Liao, Gaohong Zhu, et al.
Frontiers in Immunology|August 22, 2025
Clinical and functional characterization of a novel <i>TNFRSF9</i> variant causing immune dysregulation with predisposition to EBV-driven lymphomagenesisPeiwei Zhao, Kailan Chen, Li Yang, et al.
Chempluschem|March 26, 2025
Multifactor Multilevel Optimization of MOF Derivatives for Promoting Catalyst FabricationPeiwei Zhao, Yuqing Zhang, Lele Gao, et al.
Plos One|May 1, 2013
Suppression of mitochondrial complex I influences cell metastatic propertiesXuelian He, Aifen Zhou, Hao Lu, et al.
Molecular Genetics & Genomic Medicine|July 31, 2021
Genetic analysis and prenatal diagnosis in a Chinese with growth retardation, abnormal liver function, and microcephalyPeiwei Zhao, Lei Zhang, Li Tan, et al.
Seizure|September 11, 2024
Identification of two novel variants in ALG11 causing congenital disorder of glycosylationPeiwei Zhao, Xiankai Zhang, Zhengrong Duan, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|January 27, 2016
GRIM-19 inhibition induced autophagy through activation of ERK and HIF-1α not STAT3 in Hela cellsXin Yue, Peiwei Zhao, Kongming Wu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|July 26, 2021
[Novel duplication mutation of <i>EYA1</i> causes branchio-oto-renal syndrome in a Chinese family]Jun Li, Peiwei Zhao, Zhijie Xia, et al.
Pediatric Nephrology (Berlin, Germany)|May 1, 2012
C1GALT1 polymorphisms are associated with Henoch-Schönlein purpura nephritisXuelian He, Peiwei Zhao, Shixiu Kang, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
BMC Medical Genetics|December 2, 2017
Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature reviewLi Tan, Bo Bi, Peiwei Zhao, et al.
Pediatric Nephrology (Berlin, Germany)|March 30, 2022
Gross hematuria, edema, and hypocomplementemia in a 9-year-old boy: QuestionsJuanjuan Ding, Panli Liao, Gaohong Zhu, et al.
Frontiers in Immunology|August 22, 2025
Clinical and functional characterization of a novel <i>TNFRSF9</i> variant causing immune dysregulation with predisposition to EBV-driven lymphomagenesisPeiwei Zhao, Kailan Chen, Li Yang, et al.
Chempluschem|March 26, 2025
Multifactor Multilevel Optimization of MOF Derivatives for Promoting Catalyst FabricationPeiwei Zhao, Yuqing Zhang, Lele Gao, et al.
Plos One|May 1, 2013
Suppression of mitochondrial complex I influences cell metastatic propertiesXuelian He, Aifen Zhou, Hao Lu, et al.
Molecular Genetics & Genomic Medicine|July 31, 2021
Genetic analysis and prenatal diagnosis in a Chinese with growth retardation, abnormal liver function, and microcephalyPeiwei Zhao, Lei Zhang, Li Tan, et al.
Seizure|September 11, 2024
Identification of two novel variants in ALG11 causing congenital disorder of glycosylationPeiwei Zhao, Xiankai Zhang, Zhengrong Duan, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|January 27, 2016
GRIM-19 inhibition induced autophagy through activation of ERK and HIF-1α not STAT3 in Hela cellsXin Yue, Peiwei Zhao, Kongming Wu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|July 26, 2021
[Novel duplication mutation of <i>EYA1</i> causes branchio-oto-renal syndrome in a Chinese family]Jun Li, Peiwei Zhao, Zhijie Xia, et al.
Pediatric Nephrology (Berlin, Germany)|May 1, 2012
C1GALT1 polymorphisms are associated with Henoch-Schönlein purpura nephritisXuelian He, Peiwei Zhao, Shixiu Kang, et al.
Pageof 5