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Showing results (251-260 of 282) with videos related to

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Human Molecular Genetics|June 25, 2016
Cilia gene mutations cause atrioventricular septal defects by multiple mechanismsOzanna Burnicka-Turek, Jeffrey D Steimle, Wenhui Huang, et al.
Journal of Cellular and Molecular Medicine|January 8, 2021
Prognostic role of Wnt and Fzd gene families in acute myeloid leukaemiaYifeng Dai, Zhiheng Cheng, Doerte R Fricke, et al.
Nature Genetics|July 30, 2013
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeChristie M Buchovecky, Stephen D Turley, Hannah M Brown, et al.
Nature Communications|July 27, 2024
Adenosine triggers early astrocyte reactivity that provokes microglial responses and drives the pathogenesis of sepsis-associated encephalopathy in miceQilin Guo, Davide Gobbo, Na Zhao, et al.
The Pharmacogenomics Journal|January 29, 2020
Prognostic role of SCAMP family in acute myeloid leukemiaTingting Qian, Zhiheng Cheng, Liang Quan, et al.
Journal of the Neurological Sciences|March 23, 2016
Role of glyoxalase I gene polymorphisms in late-onset epilepsy and drug-resistant epilepsyHua Tao, Ligang Si, Xu Zhou, et al.
Plos One|June 9, 2017
Probabilistic Entity-Relationship Diagram: A correlation between functional connectivity and spontaneous brain activity during resting state in major depressive disorderLu Zhang, Lin Shi, Bin Zhang, et al.
The Pharmacogenomics Journal|January 7, 2020
High expression of chaperonin-containing TCP1 subunit 3 may induce dismal prognosis in multiple myelomaTingting Qian, Longzhen Cui, Yan Liu, et al.
Nature Communications|September 26, 2025
Noise-induced quantum synchronization with entangled oscillationsZiyu Tao, Finn Schmolke, Chang-Kang Hu, et al.
International Journal of Biological Sciences|April 15, 2024
Colchicine Blocks Abdominal Aortic Aneurysm Development by Maintaining Vascular Smooth Muscle Cell HomeostasisMin Chen, Dafeng Yang, Yangzhao Zhou, et al.
Pageof 29

Showing results (251-260 of 282) with videos related to

Sort By:
Pageof 29
Human Molecular Genetics|June 25, 2016
Cilia gene mutations cause atrioventricular septal defects by multiple mechanismsOzanna Burnicka-Turek, Jeffrey D Steimle, Wenhui Huang, et al.
Journal of Cellular and Molecular Medicine|January 8, 2021
Prognostic role of Wnt and Fzd gene families in acute myeloid leukaemiaYifeng Dai, Zhiheng Cheng, Doerte R Fricke, et al.
Nature Genetics|July 30, 2013
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeChristie M Buchovecky, Stephen D Turley, Hannah M Brown, et al.
Nature Communications|July 27, 2024
Adenosine triggers early astrocyte reactivity that provokes microglial responses and drives the pathogenesis of sepsis-associated encephalopathy in miceQilin Guo, Davide Gobbo, Na Zhao, et al.
The Pharmacogenomics Journal|January 29, 2020
Prognostic role of SCAMP family in acute myeloid leukemiaTingting Qian, Zhiheng Cheng, Liang Quan, et al.
Journal of the Neurological Sciences|March 23, 2016
Role of glyoxalase I gene polymorphisms in late-onset epilepsy and drug-resistant epilepsyHua Tao, Ligang Si, Xu Zhou, et al.
Plos One|June 9, 2017
Probabilistic Entity-Relationship Diagram: A correlation between functional connectivity and spontaneous brain activity during resting state in major depressive disorderLu Zhang, Lin Shi, Bin Zhang, et al.
The Pharmacogenomics Journal|January 7, 2020
High expression of chaperonin-containing TCP1 subunit 3 may induce dismal prognosis in multiple myelomaTingting Qian, Longzhen Cui, Yan Liu, et al.
Nature Communications|September 26, 2025
Noise-induced quantum synchronization with entangled oscillationsZiyu Tao, Finn Schmolke, Chang-Kang Hu, et al.
International Journal of Biological Sciences|April 15, 2024
Colchicine Blocks Abdominal Aortic Aneurysm Development by Maintaining Vascular Smooth Muscle Cell HomeostasisMin Chen, Dafeng Yang, Yangzhao Zhou, et al.
Pageof 29