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Sheng Yi

Showing results (281-290 of 461) with videos related to

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Animals : an Open Access Journal From MDPI|May 2, 2020
Serum Metabolomics Revealed the Differential Metabolic Pathway in Calves with Severe Clinical Diarrhea SymptomsMei-Zhou Huang, Dong-An Cui, Xiao-Hu Wu, et al.
Guang Pu Xue Yu Guang Pu Fen Xi = Guang Pu|July 27, 2018
[Study of the Detection of Histidine Based on “On-Off” Fluorescence Probe of Carbon Dots]Hui-lin Tao, Xiu-fen Liao, Chao Sun, et al.
Chronic Diseases and Translational Medicine|October 25, 2017
Identifying at-risk foot among hospitalized patients with type 2 diabetes: A cross-sectional study in one Chinese tertiary hospitalSheng-Yi Zou, Yuan Zhao, Yue-Ping Shen, et al.
Molecular Genetics & Genomic Medicine|June 18, 2023
Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing-site variant and a missense variant in the ROBO3 geneSheng Yi, Zailong Qin, Xunzhao Zhou, et al.
Biomedical Journal|January 2, 2022
Phosphorylated α-synuclein in diluted human serum as a biomarker for Parkinson's diseaseWei-Ru Chen, Jin-Chung Chen, Sheng-Yi Chang, et al.
Molecular Genetics and Genomics : MGG|March 23, 2016
Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese familiesLingling Hu, Xuan Shang, Sheng Yi, et al.
Frontiers in Genetics|March 29, 2020
PREPL Deficiency: A Homozygous Splice Site PREPL Mutation in a Patient With Congenital Myasthenic Syndrome and Absence of Ovaries and Hypoplasia of UterusQi Yang, Rong Hua, Jiale Qian, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 28, 2020
A novel splicing mutation in F8 causes various aberrant transcripts in a hemophilia A patient and identifies a new transcript from healthy individualsSheng Yi, Yangjin Zuo, Qiuxia Yu, et al.
Food & Function|November 22, 2018
In silico assessment and structural characterization of antioxidant peptides from major yolk protein of sea urchin Strongylocentrotus nudusWen-Hui Shang, Yue Tang, Sheng-Yi Su, et al.
Frontiers in Neurology|April 15, 2026
Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the <i>NDUFAF6</i> geneQi Yang, Qiang Zhang, Xunzhao Zhou, et al.
Pageof 47

Showing results (281-290 of 461) with videos related to

Sort By:
Pageof 47
Animals : an Open Access Journal From MDPI|May 2, 2020
Serum Metabolomics Revealed the Differential Metabolic Pathway in Calves with Severe Clinical Diarrhea SymptomsMei-Zhou Huang, Dong-An Cui, Xiao-Hu Wu, et al.
Guang Pu Xue Yu Guang Pu Fen Xi = Guang Pu|July 27, 2018
[Study of the Detection of Histidine Based on “On-Off” Fluorescence Probe of Carbon Dots]Hui-lin Tao, Xiu-fen Liao, Chao Sun, et al.
Chronic Diseases and Translational Medicine|October 25, 2017
Identifying at-risk foot among hospitalized patients with type 2 diabetes: A cross-sectional study in one Chinese tertiary hospitalSheng-Yi Zou, Yuan Zhao, Yue-Ping Shen, et al.
Molecular Genetics & Genomic Medicine|June 18, 2023
Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing-site variant and a missense variant in the ROBO3 geneSheng Yi, Zailong Qin, Xunzhao Zhou, et al.
Biomedical Journal|January 2, 2022
Phosphorylated α-synuclein in diluted human serum as a biomarker for Parkinson's diseaseWei-Ru Chen, Jin-Chung Chen, Sheng-Yi Chang, et al.
Molecular Genetics and Genomics : MGG|March 23, 2016
Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese familiesLingling Hu, Xuan Shang, Sheng Yi, et al.
Frontiers in Genetics|March 29, 2020
PREPL Deficiency: A Homozygous Splice Site PREPL Mutation in a Patient With Congenital Myasthenic Syndrome and Absence of Ovaries and Hypoplasia of UterusQi Yang, Rong Hua, Jiale Qian, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 28, 2020
A novel splicing mutation in F8 causes various aberrant transcripts in a hemophilia A patient and identifies a new transcript from healthy individualsSheng Yi, Yangjin Zuo, Qiuxia Yu, et al.
Food & Function|November 22, 2018
In silico assessment and structural characterization of antioxidant peptides from major yolk protein of sea urchin Strongylocentrotus nudusWen-Hui Shang, Yue Tang, Sheng-Yi Su, et al.
Frontiers in Neurology|April 15, 2026
Clinical and genetic analysis of Chinese patients with Leigh syndrome caused by biallelic loss-of-function variants of the <i>NDUFAF6</i> geneQi Yang, Qiang Zhang, Xunzhao Zhou, et al.
Pageof 47