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Chunjiang Zhu

Showing results (1-10 of 17) with videos related to

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Proceedings of the ... AAAI Conference on Artificial Intelligence. AAAI Conference on Artificial Intelligence|November 8, 2021
An Efficient Algorithm for Deep Stochastic Contextual BanditsTan Zhu, Guannan Liang, Chunjiang Zhu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 9, 2022
[Genetic diagnosis of a case of Smith-Magenis syndrome due to a rare small-scale deletion]Baodong Tian, Donglan Yu, Guangli Wang, et al.
Parallel Computing|December 28, 2020
Asynchronous Parallel Stochastic Quasi-Newton MethodsQianqian Tong, Guannan Liang, Xingyu Cai, et al.
Systems Biology in Reproductive Medicine|October 21, 2022
Resveratrol improves follicular development of PCOS rats via regulating glycolysis pathway and targeting SIRT1Peng Huo, Man Li, Jianghua Le, et al.
Health Science Reports|November 3, 2025
Metabolites and Immune Cells Mediated the Causal Relationship Between the Gut Microbiota and Osteosarcoma: A Mendelian Randomization StudyGuanjun Chen, Zhenyu Song, Imtiaz Abdullah, et al.
Medicine|March 8, 2024
Compound heterozygosity for Southeast Asian hereditary persistence of fetal hemoglobin and β0-thalassemia results in thalassemia intermedia: Pedigree analysis and genetic research in a family from South China. A case reportGuangli Wang, Huiping Deng, Peng Peng, et al.
Clinical Chemistry and Laboratory Medicine|September 10, 2015
Rapid detection of non-deletional mutations causing α-thalassemia by multicolor melting curve analysisQiuying Huang, Xudong Wang, Ning Tang, et al.
Annals of Translational Medicine|November 17, 2022
Accurate genotype diagnosis of Hong Kongαα thalassemia based on third-generation sequencingJun Li, Guimei Ye, Dan Zeng, et al.
Blood Cells, Molecules & Diseases|August 10, 2010
Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boyChunjiang Zhu, Wenfang Yu, Jiansheng Xie, et al.
Journal of Molecular Graphics & Modelling|February 28, 2021
OctSurf: Efficient hierarchical voxel-based molecular surface representation for protein-ligand affinity predictionQinqing Liu, Peng-Shuai Wang, Chunjiang Zhu, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Proceedings of the ... AAAI Conference on Artificial Intelligence. AAAI Conference on Artificial Intelligence|November 8, 2021
An Efficient Algorithm for Deep Stochastic Contextual BanditsTan Zhu, Guannan Liang, Chunjiang Zhu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 9, 2022
[Genetic diagnosis of a case of Smith-Magenis syndrome due to a rare small-scale deletion]Baodong Tian, Donglan Yu, Guangli Wang, et al.
Parallel Computing|December 28, 2020
Asynchronous Parallel Stochastic Quasi-Newton MethodsQianqian Tong, Guannan Liang, Xingyu Cai, et al.
Systems Biology in Reproductive Medicine|October 21, 2022
Resveratrol improves follicular development of PCOS rats via regulating glycolysis pathway and targeting SIRT1Peng Huo, Man Li, Jianghua Le, et al.
Health Science Reports|November 3, 2025
Metabolites and Immune Cells Mediated the Causal Relationship Between the Gut Microbiota and Osteosarcoma: A Mendelian Randomization StudyGuanjun Chen, Zhenyu Song, Imtiaz Abdullah, et al.
Medicine|March 8, 2024
Compound heterozygosity for Southeast Asian hereditary persistence of fetal hemoglobin and β0-thalassemia results in thalassemia intermedia: Pedigree analysis and genetic research in a family from South China. A case reportGuangli Wang, Huiping Deng, Peng Peng, et al.
Clinical Chemistry and Laboratory Medicine|September 10, 2015
Rapid detection of non-deletional mutations causing α-thalassemia by multicolor melting curve analysisQiuying Huang, Xudong Wang, Ning Tang, et al.
Annals of Translational Medicine|November 17, 2022
Accurate genotype diagnosis of Hong Kongαα thalassemia based on third-generation sequencingJun Li, Guimei Ye, Dan Zeng, et al.
Blood Cells, Molecules & Diseases|August 10, 2010
Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boyChunjiang Zhu, Wenfang Yu, Jiansheng Xie, et al.
Journal of Molecular Graphics & Modelling|February 28, 2021
OctSurf: Efficient hierarchical voxel-based molecular surface representation for protein-ligand affinity predictionQinqing Liu, Peng-Shuai Wang, Chunjiang Zhu, et al.
Pageof 2