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Pediatric Neurology
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April 25, 2022
Novel RARS2 Variants: Updating the Diagnosis and Pathogenesis of Pontocerebellar Hypoplasia Type 6
Yi Zhang, Yafen Yu, Xiangyue Zhao, et al.
Frontiers in Plant Science
|
January 5, 2023
Design of field real-time target spraying system based on improved YOLOv5
He Li, Changle Guo, Zishang Yang, et al.
Insects
|
January 20, 2023
Evaluation of Rearing Factors Affecting <i>Clanis bilineata tsingtauica</i> Mell Larvae Fed by Susceptible Soybean Variety NN89-29 in Spring and Autumn Sowing
Xiaofeng Liu, Yulu Yan, Nan Liu, et al.
Journal of Food Science
|
March 4, 2020
Influence of refining processes on the bioactive composition, in vitro antioxidant capacity, and their correlation of perilla seed oil
Fengguang Pan, Baoli Wen, Xiangdan Luo, et al.
Neurogenetics
|
October 30, 2021
Novel compound heterozygous variant of TOE1 results in a mild type of pontocerebellar hypoplasia type 7: an expansion of the clinical phenotype
Hongzhu Chen, Niu Li, Yufei Xu, et al.
Journal of Child Neurology
|
February 15, 2017
Exome Sequencing Identifies De Novo DYNC1H1 Mutations Associated With Distal Spinal Muscular Atrophy and Malformations of Cortical Development
Yulin Chen, Yufei Xu, Guoqiang Li, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
October 8, 2024
An Efficient Approach for Advancing Performance in Rapid Detection Based on Molybdenum Disulfide Nanoflower Supported Binary Transition Metal Oxides
Meiyi Liu, Yijian Zhao, Shuai Zhou, et al.
Journal of Nursing Management
|
April 14, 2025
Knowledge, Attitudes, and Practices of Bedside Nurses regarding Antimicrobial Stewardship in China: An Explanatory Sequential Mixed Methods Study
Wenting Zhao, Yufei Xu, Ru Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
July 15, 2019
[Analysis of SATB2 gene mutation in a child with Glass syndrome]
Meili Lin, Ruen Yao, Jing Lu, et al.
Scientific Reports
|
December 5, 2020
Clinical and molecular analysis in a cohort of Chinese children with Cornelia de Lange syndrome
Qun Li, Guoying Chang, Lei Yin, et al.
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of 10
Search research articles
Search
Showing results (51-60 of 92) with videos related to
Sort By:
Page
of 10
Pediatric Neurology
|
April 25, 2022
Novel RARS2 Variants: Updating the Diagnosis and Pathogenesis of Pontocerebellar Hypoplasia Type 6
Yi Zhang, Yafen Yu, Xiangyue Zhao, et al.
Frontiers in Plant Science
|
January 5, 2023
Design of field real-time target spraying system based on improved YOLOv5
He Li, Changle Guo, Zishang Yang, et al.
Insects
|
January 20, 2023
Evaluation of Rearing Factors Affecting <i>Clanis bilineata tsingtauica</i> Mell Larvae Fed by Susceptible Soybean Variety NN89-29 in Spring and Autumn Sowing
Xiaofeng Liu, Yulu Yan, Nan Liu, et al.
Journal of Food Science
|
March 4, 2020
Influence of refining processes on the bioactive composition, in vitro antioxidant capacity, and their correlation of perilla seed oil
Fengguang Pan, Baoli Wen, Xiangdan Luo, et al.
Neurogenetics
|
October 30, 2021
Novel compound heterozygous variant of TOE1 results in a mild type of pontocerebellar hypoplasia type 7: an expansion of the clinical phenotype
Hongzhu Chen, Niu Li, Yufei Xu, et al.
Journal of Child Neurology
|
February 15, 2017
Exome Sequencing Identifies De Novo DYNC1H1 Mutations Associated With Distal Spinal Muscular Atrophy and Malformations of Cortical Development
Yulin Chen, Yufei Xu, Guoqiang Li, et al.
Langmuir : the ACS Journal of Surfaces and Colloids
|
October 8, 2024
An Efficient Approach for Advancing Performance in Rapid Detection Based on Molybdenum Disulfide Nanoflower Supported Binary Transition Metal Oxides
Meiyi Liu, Yijian Zhao, Shuai Zhou, et al.
Journal of Nursing Management
|
April 14, 2025
Knowledge, Attitudes, and Practices of Bedside Nurses regarding Antimicrobial Stewardship in China: An Explanatory Sequential Mixed Methods Study
Wenting Zhao, Yufei Xu, Ru Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
July 15, 2019
[Analysis of SATB2 gene mutation in a child with Glass syndrome]
Meili Lin, Ruen Yao, Jing Lu, et al.
Scientific Reports
|
December 5, 2020
Clinical and molecular analysis in a cohort of Chinese children with Cornelia de Lange syndrome
Qun Li, Guoying Chang, Lei Yin, et al.
Page
of 10