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Dong Song

Showing results (871-880 of 898) with videos related to

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European Journal of Endocrinology|April 14, 2018
The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genesFeng Sun, Jun-Xiu Zhang, Chang-Yi Yang, et al.
Journal of Medical Genetics|March 10, 2023
Pathogenic variations in <i>MAML2</i> and <i>MAMLD1</i> contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathwayFeng-Yao Wu, Rui-Meng Yang, Hai-Yang Zhang, et al.
Frontiers in Computational Neuroscience|February 23, 2024
Developing a hippocampal neural prosthetic to facilitate human memory encoding and recall of stimulus features and categoriesBrent M Roeder, Xiwei She, Alexander S Dakos, et al.
The Journal of Biological Chemistry|June 28, 2005
Identification of two critical amino acid residues of the severe acute respiratory syndrome coronavirus spike protein for its variation in zoonotic tropism transition via a double substitution strategyXiu-Xia Qu, Pei Hao, Xi-Jun Song, et al.
Plos One|March 19, 2013
A refined study of FCRL genes from a genome-wide association study for Graves' diseaseShuang-Xia Zhao, Wei Liu, Ming Zhan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 5, 2020
Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's HypothyroidismQian-Yue Zhang, Wei Liu, Lu Li, et al.
Plos Pathogens|April 18, 2006
New perspectives on host-parasite interplay by comparative transcriptomic and proteomic analyses of Schistosoma japonicumFeng Liu, Jiong Lu, Wei Hu, et al.
Vaccine|January 31, 2021
Recombinant SARS-CoV-2 RBD with a built in T helper epitope induces strong neutralization antibody responseQiu-Dong Su, Ye-Ning Zou, Yao Yi, et al.
Nature Genetics|December 4, 2023
Noncoding mutations cause super-enhancer retargeting resulting in protein synthesis dysregulation during B cell lymphoma progressionRebecca J Leeman-Neill, Dong Song, Jonathan Bizarro, et al.
Human Genetics|December 19, 2013
Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association studyWei Liu, Hai-Ning Wang, Zhao-Hui Gu, et al.
Pageof 90

Showing results (871-880 of 898) with videos related to

Sort By:
Pageof 90
European Journal of Endocrinology|April 14, 2018
The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genesFeng Sun, Jun-Xiu Zhang, Chang-Yi Yang, et al.
Journal of Medical Genetics|March 10, 2023
Pathogenic variations in <i>MAML2</i> and <i>MAMLD1</i> contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathwayFeng-Yao Wu, Rui-Meng Yang, Hai-Yang Zhang, et al.
Frontiers in Computational Neuroscience|February 23, 2024
Developing a hippocampal neural prosthetic to facilitate human memory encoding and recall of stimulus features and categoriesBrent M Roeder, Xiwei She, Alexander S Dakos, et al.
The Journal of Biological Chemistry|June 28, 2005
Identification of two critical amino acid residues of the severe acute respiratory syndrome coronavirus spike protein for its variation in zoonotic tropism transition via a double substitution strategyXiu-Xia Qu, Pei Hao, Xi-Jun Song, et al.
Plos One|March 19, 2013
A refined study of FCRL genes from a genome-wide association study for Graves' diseaseShuang-Xia Zhao, Wei Liu, Ming Zhan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 5, 2020
Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's HypothyroidismQian-Yue Zhang, Wei Liu, Lu Li, et al.
Plos Pathogens|April 18, 2006
New perspectives on host-parasite interplay by comparative transcriptomic and proteomic analyses of Schistosoma japonicumFeng Liu, Jiong Lu, Wei Hu, et al.
Vaccine|January 31, 2021
Recombinant SARS-CoV-2 RBD with a built in T helper epitope induces strong neutralization antibody responseQiu-Dong Su, Ye-Ning Zou, Yao Yi, et al.
Nature Genetics|December 4, 2023
Noncoding mutations cause super-enhancer retargeting resulting in protein synthesis dysregulation during B cell lymphoma progressionRebecca J Leeman-Neill, Dong Song, Jonathan Bizarro, et al.
Human Genetics|December 19, 2013
Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association studyWei Liu, Hai-Ning Wang, Zhao-Hui Gu, et al.
Pageof 90