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Tiansen Li

Showing results (51-60 of 105) with videos related to

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Biorxiv : the Preprint Server for Biology|December 18, 2025
Visualization of photoreceptor outer segment renewal using AAV-delivered Dendra2-tagged rhodopsinLijing Xie, Dianlei Guo, Xiaoyu Zhang, et al.
Experimental and Therapeutic Medicine|December 2, 2015
<i>Brucella melitensis</i> 16MΔTcfSR as a potential live vaccine allows for the differentiation between natural and vaccinated infectionZhiqiang Li, Junbo Zhang, K E Zhang, et al.
Human Molecular Genetics|September 2, 2011
Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosisCristy A Ku, Vince A Chiodo, Sanford L Boye, et al.
Molecular & Cellular Proteomics : MCP|May 15, 2007
The proteome of the mouse photoreceptor sensory cilium complexQin Liu, Glenn Tan, Natasha Levenkova, et al.
Cell|November 27, 2012
Three-dimensional architecture of the rod sensory cilium and its disruption in retinal neurodegenerationJared C Gilliam, Juan T Chang, Ivette M Sandoval, et al.
World Journal of Microbiology & Biotechnology|March 2, 2016
The Brucella melitensis M5-90 phosphoglucomutase (PGM) mutant is attenuated and confers protection against wild-type challenge in BALB/c miceYu Zhang, Tiansen Li, Jing Zhang, et al.
Plos Genetics|May 27, 2010
Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing lossJun Yang, Xiaoqing Liu, Yun Zhao, et al.
Experimental and Therapeutic Medicine|October 5, 2016
Expression and regulation of the <i>ery</i> operon of <i>Brucella melitensis</i> in human trophoblast cellsHui Zhang, Xiaoxia Dou, Zhiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIPBasil S Pawlyk, Alexander J Smith, Prateek K Buch, et al.
Human Molecular Genetics|February 20, 2013
Prickle1 is expressed in distinct cell populations of the central nervous system and contributes to neuronal morphogenesisChunqiao Liu, Chen Lin, D Thad Whitaker, et al.
Pageof 11

Showing results (51-60 of 105) with videos related to

Sort By:
Pageof 11
Biorxiv : the Preprint Server for Biology|December 18, 2025
Visualization of photoreceptor outer segment renewal using AAV-delivered Dendra2-tagged rhodopsinLijing Xie, Dianlei Guo, Xiaoyu Zhang, et al.
Experimental and Therapeutic Medicine|December 2, 2015
<i>Brucella melitensis</i> 16MΔTcfSR as a potential live vaccine allows for the differentiation between natural and vaccinated infectionZhiqiang Li, Junbo Zhang, K E Zhang, et al.
Human Molecular Genetics|September 2, 2011
Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosisCristy A Ku, Vince A Chiodo, Sanford L Boye, et al.
Molecular & Cellular Proteomics : MCP|May 15, 2007
The proteome of the mouse photoreceptor sensory cilium complexQin Liu, Glenn Tan, Natasha Levenkova, et al.
Cell|November 27, 2012
Three-dimensional architecture of the rod sensory cilium and its disruption in retinal neurodegenerationJared C Gilliam, Juan T Chang, Ivette M Sandoval, et al.
World Journal of Microbiology & Biotechnology|March 2, 2016
The Brucella melitensis M5-90 phosphoglucomutase (PGM) mutant is attenuated and confers protection against wild-type challenge in BALB/c miceYu Zhang, Tiansen Li, Jing Zhang, et al.
Plos Genetics|May 27, 2010
Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing lossJun Yang, Xiaoqing Liu, Yun Zhao, et al.
Experimental and Therapeutic Medicine|October 5, 2016
Expression and regulation of the <i>ery</i> operon of <i>Brucella melitensis</i> in human trophoblast cellsHui Zhang, Xiaoxia Dou, Zhiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIPBasil S Pawlyk, Alexander J Smith, Prateek K Buch, et al.
Human Molecular Genetics|February 20, 2013
Prickle1 is expressed in distinct cell populations of the central nervous system and contributes to neuronal morphogenesisChunqiao Liu, Chen Lin, D Thad Whitaker, et al.
Pageof 11