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Huapeng Li

Showing results (31-40 of 36) with videos related to

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Biorxiv : the Preprint Server for Biology|June 29, 2026
Dehydration/1,6-addition-based Site-specific Bioconjugation Unveils Norepinephrinylation as a Widespread Post-translational Modification in the Cellular ProteomeZeng Lin, Xingyu Ma, Zhengjun Cai, et al.
Molecular Therapy. Advances|May 18, 2026
Engineering novel AAV capsids by broadly attenuated and subsequent muscle-specific tropism in mice and NHPsYue Pan, Yujian Zhong, Huan Chen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 3, 2013
A single intravenous rAAV injection as late as P20 achieves efficacious and sustained CNS Gene therapy in Canavan miceSeemin Seher Ahmed, Huapeng Li, Chunyan Cao, et al.
Nature Methods|March 6, 2012
Long-term, efficient inhibition of microRNA function in mice using rAAV vectorsJun Xie, Stefan L Ameres, Randall Friedline, et al.
Cell Stem Cell|July 13, 2010
A mesenchymal-to-epithelial transition initiates and is required for the nuclear reprogramming of mouse fibroblastsRonghui Li, Jialiang Liang, Su Ni, et al.
Nature Communications|January 21, 2017
Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 proteinMaoxue Tang, Guangping Gao, Carlos B Rueda, et al.
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Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Biorxiv : the Preprint Server for Biology|June 29, 2026
Dehydration/1,6-addition-based Site-specific Bioconjugation Unveils Norepinephrinylation as a Widespread Post-translational Modification in the Cellular ProteomeZeng Lin, Xingyu Ma, Zhengjun Cai, et al.
Molecular Therapy. Advances|May 18, 2026
Engineering novel AAV capsids by broadly attenuated and subsequent muscle-specific tropism in mice and NHPsYue Pan, Yujian Zhong, Huan Chen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 3, 2013
A single intravenous rAAV injection as late as P20 achieves efficacious and sustained CNS Gene therapy in Canavan miceSeemin Seher Ahmed, Huapeng Li, Chunyan Cao, et al.
Nature Methods|March 6, 2012
Long-term, efficient inhibition of microRNA function in mice using rAAV vectorsJun Xie, Stefan L Ameres, Randall Friedline, et al.
Cell Stem Cell|July 13, 2010
A mesenchymal-to-epithelial transition initiates and is required for the nuclear reprogramming of mouse fibroblastsRonghui Li, Jialiang Liang, Su Ni, et al.
Nature Communications|January 21, 2017
Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 proteinMaoxue Tang, Guangping Gao, Carlos B Rueda, et al.
Pageof 4