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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 genes
Feng 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 pathway
Feng-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 categories
Brent 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 strategy
Xiu-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' disease
Shuang-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 Hypothyroidism
Qian-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 japonicum
Feng 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 response
Qiu-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 progression
Rebecca 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 study
Wei Liu, Hai-Ning Wang, Zhao-Hui Gu, et al.
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of 90
Search research articles
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Showing results (871-880 of 898) with videos related to
Sort By:
Page
of 90
European Journal of Endocrinology
|
April 14, 2018
The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes
Feng 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 pathway
Feng-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 categories
Brent 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 strategy
Xiu-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' disease
Shuang-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 Hypothyroidism
Qian-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 japonicum
Feng 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 response
Qiu-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 progression
Rebecca 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 study
Wei Liu, Hai-Ning Wang, Zhao-Hui Gu, et al.
Page
of 90