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Development (Cambridge, England)
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February 18, 2017
A histone H4 lysine 20 methyltransferase couples environmental cues to sensory neuron control of developmental plasticity
Colin E Delaney, Albert T Chen, Jacqueline V Graniel, et al.
Nature Cardiovascular Research
|
May 16, 2022
A High-Efficiency AAV for Endothelial Cell Transduction Throughout the Central Nervous System
Trevor Krolak, Ken Y Chan, Luke Kaplan, et al.
Nature Communications
|
August 3, 2024
Systematic multi-trait AAV capsid engineering for efficient gene delivery
Fatma-Elzahraa Eid, Albert T Chen, Ken Y Chan, et al.
Science (New York, N.Y.)
|
May 15, 2025
Programmable gene insertion in human cells with a laboratory-evolved CRISPR-associated transposase
Isaac P Witte, George D Lampe, Simon Eitzinger, et al.
Plos Biology
|
July 19, 2023
Targeting AAV vectors to the central nervous system by engineering capsid-receptor interactions that enable crossing of the blood-brain barrier
Qin Huang, Albert T Chen, Ken Y Chan, et al.
Biorxiv : the Preprint Server for Biology
|
January 8, 2024
An AAV capsid reprogrammed to bind human Transferrin Receptor mediates brain-wide gene delivery
Qin Huang, Ken Y Chan, Shan Lou, et al.
Science (New York, N.Y.)
|
May 16, 2024
An AAV capsid reprogrammed to bind human transferrin receptor mediates brain-wide gene delivery
Qin Huang, Ken Y Chan, Jason Wu, et al.
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Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Development (Cambridge, England)
|
February 18, 2017
A histone H4 lysine 20 methyltransferase couples environmental cues to sensory neuron control of developmental plasticity
Colin E Delaney, Albert T Chen, Jacqueline V Graniel, et al.
Nature Cardiovascular Research
|
May 16, 2022
A High-Efficiency AAV for Endothelial Cell Transduction Throughout the Central Nervous System
Trevor Krolak, Ken Y Chan, Luke Kaplan, et al.
Nature Communications
|
August 3, 2024
Systematic multi-trait AAV capsid engineering for efficient gene delivery
Fatma-Elzahraa Eid, Albert T Chen, Ken Y Chan, et al.
Science (New York, N.Y.)
|
May 15, 2025
Programmable gene insertion in human cells with a laboratory-evolved CRISPR-associated transposase
Isaac P Witte, George D Lampe, Simon Eitzinger, et al.
Plos Biology
|
July 19, 2023
Targeting AAV vectors to the central nervous system by engineering capsid-receptor interactions that enable crossing of the blood-brain barrier
Qin Huang, Albert T Chen, Ken Y Chan, et al.
Biorxiv : the Preprint Server for Biology
|
January 8, 2024
An AAV capsid reprogrammed to bind human Transferrin Receptor mediates brain-wide gene delivery
Qin Huang, Ken Y Chan, Shan Lou, et al.
Science (New York, N.Y.)
|
May 16, 2024
An AAV capsid reprogrammed to bind human transferrin receptor mediates brain-wide gene delivery
Qin Huang, Ken Y Chan, Jason Wu, et al.
Page
of 1