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Yingjun Xie

Showing results (41-50 of 89) with videos related to

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Frontiers in Genetics|October 18, 2021
Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective StudyJianlong Zhuang, Na Zhang, Yuanbai Wang, et al.
Molecular Cytogenetics|June 7, 2022
Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese populationJianlong Zhuang, Chunnuan Chen, Rongfu Huang, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|March 30, 2017
B-cell lymphoma 2 inhibitor ABT-737 induces Beclin1- and reactive oxygen species-dependent autophagy in Adriamycin-resistant human hepatocellular carcinoma cellsXiaoxiao Yao, Xiaoning Li, Dan Zhang, et al.
BMC Medical Genetics|August 19, 2018
The phenomena of balanced effect between α-globin gene and of β-globin geneLiangying Zhong, Xin Gan, Lingling Xu, et al.
BMC Medical Genomics|March 17, 2023
A retrospective analysis of MS/MS screening for IEM in high-risk areasXiao He, Juan Kuang, Jiahong Lai, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the <i>KCNH2</i> Gene in a Fetus With Familial 2q14.2 DuplicationJianlong Zhuang, Chunnuan Chen, Yuanbai Wang, et al.
The Clinical Respiratory Journal|October 17, 2015
A new compound heterozygous CFTR mutation in a Chinese family with cystic fibrosisYingjun Xie, Xueqiong Huang, Yujian Liang, et al.
Frontiers in Pediatrics|November 1, 2021
The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray AnalysisYu'e Chen, Yingjun Xie, Yuying Jiang, et al.
Expert Review of Gastroenterology & Hepatology|July 9, 2019
Pancreatic reconstruction techniques after pancreaticoduodenectomy: a review of the literatureYien Xiang, Jiacheng Wu, Chao Lin, et al.
Hereditas|March 14, 2017
Psychomotor retardation with a 1q42.11-q42.12 deletionJialing He, Yingjun Xie, Shu Kong, et al.
Pageof 9

Showing results (41-50 of 89) with videos related to

Sort By:
Pageof 9
Frontiers in Genetics|October 18, 2021
Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective StudyJianlong Zhuang, Na Zhang, Yuanbai Wang, et al.
Molecular Cytogenetics|June 7, 2022
Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese populationJianlong Zhuang, Chunnuan Chen, Rongfu Huang, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|March 30, 2017
B-cell lymphoma 2 inhibitor ABT-737 induces Beclin1- and reactive oxygen species-dependent autophagy in Adriamycin-resistant human hepatocellular carcinoma cellsXiaoxiao Yao, Xiaoning Li, Dan Zhang, et al.
BMC Medical Genetics|August 19, 2018
The phenomena of balanced effect between α-globin gene and of β-globin geneLiangying Zhong, Xin Gan, Lingling Xu, et al.
BMC Medical Genomics|March 17, 2023
A retrospective analysis of MS/MS screening for IEM in high-risk areasXiao He, Juan Kuang, Jiahong Lai, et al.
Frontiers in Genetics|July 22, 2022
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the <i>KCNH2</i> Gene in a Fetus With Familial 2q14.2 DuplicationJianlong Zhuang, Chunnuan Chen, Yuanbai Wang, et al.
The Clinical Respiratory Journal|October 17, 2015
A new compound heterozygous CFTR mutation in a Chinese family with cystic fibrosisYingjun Xie, Xueqiong Huang, Yujian Liang, et al.
Frontiers in Pediatrics|November 1, 2021
The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray AnalysisYu'e Chen, Yingjun Xie, Yuying Jiang, et al.
Expert Review of Gastroenterology & Hepatology|July 9, 2019
Pancreatic reconstruction techniques after pancreaticoduodenectomy: a review of the literatureYien Xiang, Jiacheng Wu, Chao Lin, et al.
Hereditas|March 14, 2017
Psychomotor retardation with a 1q42.11-q42.12 deletionJialing He, Yingjun Xie, Shu Kong, et al.
Pageof 9