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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 Proteome
Zeng 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 NHPs
Yue 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 mice
Seemin Seher Ahmed, Huapeng Li, Chunyan Cao, et al.
Nature Methods
|
March 6, 2012
Long-term, efficient inhibition of microRNA function in mice using rAAV vectors
Jun 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 fibroblasts
Ronghui 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 protein
Maoxue Tang, Guangping Gao, Carlos B Rueda, et al.
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of 4
Search research articles
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Showing results (31-40 of 36) with videos related to
Sort By:
Page
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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 Proteome
Zeng 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 NHPs
Yue 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 mice
Seemin Seher Ahmed, Huapeng Li, Chunyan Cao, et al.
Nature Methods
|
March 6, 2012
Long-term, efficient inhibition of microRNA function in mice using rAAV vectors
Jun 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 fibroblasts
Ronghui 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 protein
Maoxue Tang, Guangping Gao, Carlos B Rueda, et al.
Page
of 4