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Yu Ding

Showing results (521-530 of 1,643) with videos related to

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Yao Xue Xue Bao = Acta Pharmaceutica Sinica|July 10, 2013
[Sequence analysis of LEAFY homologous gene from Dendrobium moniliforme and application for identification of medicinal Dendrobium]Wen-Rui Xing, Bei-Wei Hou, Jing-Jiao Guan, et al.
Frontiers in Pediatrics|December 26, 2022
Deterioration in glycemic control on schooldays among children and adolescents with type 1 diabetes: A continuous glucose monitoring-based studyYu Ding, Wenhao Zhang, Xiumei Wu, et al.
Frontiers in Chemistry|December 5, 2022
Research advances of femtosecond laser-induced nanogratings for transparent materialsYue Lu, Yunfei Li, Xiaofan Xie, et al.
Oncotargets and Therapy|October 2, 2019
Long noncoding RNA ZFAS1 promotes progression of papillary thyroid carcinoma by sponging miR-590-3p and upregulating HMGA2 expressionHouchao Tong, Xi Zhuang, Jingsheng Cai, et al.
Endocrine Journal|November 9, 2018
Premature ovarian insufficiency may be associated with the mutations in mitochondrial tRNA genesYu Ding, Bo-Hou Xia, Guang-Chao Zhuo, et al.
Oncotarget|November 19, 2016
LncRNA GAS5 contributes to lymphatic metastasis in colorectal cancerYongbin Zheng, Dan Song, Kuang Xiao, et al.
Plos One|March 4, 2014
Elevated expression of miR-210 predicts poor survival of cancer patients: a systematic review and meta-analysisJian Wang, Jiqing Zhao, Mengjing Shi, et al.
Analytical Chemistry|April 7, 2017
Modulation of the Singlet Oxygen Generation from the Double Strand DNA-SYBR Green I Complex Mediated by T-Melamine-T Mismatch for Visual Detection of MelamineHao Hu, Jinyi Zhang, Yu Ding, et al.
Current Molecular Medicine|March 12, 2019
The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese PedigreeYu Ding, Yao-Shu Teng, Guang-Chao Zhuo, et al.
BMC Pediatrics|July 13, 2019
TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case reportXin Li, Qing Cheng, Yu Ding, et al.
Pageof 165

Showing results (521-530 of 1,643) with videos related to

Sort By:
Pageof 165
Yao Xue Xue Bao = Acta Pharmaceutica Sinica|July 10, 2013
[Sequence analysis of LEAFY homologous gene from Dendrobium moniliforme and application for identification of medicinal Dendrobium]Wen-Rui Xing, Bei-Wei Hou, Jing-Jiao Guan, et al.
Frontiers in Pediatrics|December 26, 2022
Deterioration in glycemic control on schooldays among children and adolescents with type 1 diabetes: A continuous glucose monitoring-based studyYu Ding, Wenhao Zhang, Xiumei Wu, et al.
Frontiers in Chemistry|December 5, 2022
Research advances of femtosecond laser-induced nanogratings for transparent materialsYue Lu, Yunfei Li, Xiaofan Xie, et al.
Oncotargets and Therapy|October 2, 2019
Long noncoding RNA ZFAS1 promotes progression of papillary thyroid carcinoma by sponging miR-590-3p and upregulating HMGA2 expressionHouchao Tong, Xi Zhuang, Jingsheng Cai, et al.
Endocrine Journal|November 9, 2018
Premature ovarian insufficiency may be associated with the mutations in mitochondrial tRNA genesYu Ding, Bo-Hou Xia, Guang-Chao Zhuo, et al.
Oncotarget|November 19, 2016
LncRNA GAS5 contributes to lymphatic metastasis in colorectal cancerYongbin Zheng, Dan Song, Kuang Xiao, et al.
Plos One|March 4, 2014
Elevated expression of miR-210 predicts poor survival of cancer patients: a systematic review and meta-analysisJian Wang, Jiqing Zhao, Mengjing Shi, et al.
Analytical Chemistry|April 7, 2017
Modulation of the Singlet Oxygen Generation from the Double Strand DNA-SYBR Green I Complex Mediated by T-Melamine-T Mismatch for Visual Detection of MelamineHao Hu, Jinyi Zhang, Yu Ding, et al.
Current Molecular Medicine|March 12, 2019
The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese PedigreeYu Ding, Yao-Shu Teng, Guang-Chao Zhuo, et al.
BMC Pediatrics|July 13, 2019
TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case reportXin Li, Qing Cheng, Yu Ding, et al.
Pageof 165