Investigation of neurodevelopmental deficits of 22 q11.2 deletion syndrome with a patient-ipsc-derived blood–brain barrier model

Li, Y., Xia, Y., Zhu, H., Luu, E., Huang, G., Sun, Y., Sun, K., Markx, S., Leong, K. W., Xu, B., & Fu, B. M. (2021). Investigation of Neurodevelopmental Deficits of 22 q11.2 Deletion Syndrome with a Patient-iPSC-Derived Blood–Brain Barrier Model. Cells, 10(10), 2576. https://doi.org/10.3390/cells10102576
Authors:
Yunfei Li
Yifan Xia
Huixiang Zhu
Eric Luu
Guangyao Huang
Yan Sun
Kevin Sun
Sander Markx
Kam W. Leong
Bin Xu
Bingmei M. Fu
Affiliated Authors:
Huixiang Zhu
Yan Sun
Kevin Sun
Sander Markx
Kam W. Leong
Bin Xu
Columbia Affiliation:
Author Keywords:
blood-brain barrier
digeorge syndrome
endothelial glycocalyx
tight junction
permeability
transcription network
blood–brain barrier
elink
Publication Type:
Article
Unique ID:
10.3390/cells10102576
PMID:
34685556
DOI:
10.3390/cells10102576
Journal:
Cells
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record
View Web of Science Record

Record Created: