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  4. Schizophrenia-derived hiPSC brain microvascular endothelial-like cells show impairments in angiogenesis and blood–brain barrier function
Details

Schizophrenia-derived hiPSC brain microvascular endothelial-like cells show impairments in angiogenesis and blood–brain barrier function

Journal
Molecular Psychiatry
ISSN
1359-4184
1476-5578
Date Issued
2022
Author(s)
Bárbara S. Casas
Gabriela Vitória
Catalina P. Prieto
Mariana Casas
Carlos Chacón
Markus Uhrig
EZQUER, EDUARDO FERNANDO  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Stevens K. Rehen
EZQUER, EDUARDO MARCELO  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Verónica Palma
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85131910097
WoS ID
WOS:000811467200003
DOI
10.1038/s41380-022-01653-0
URL
https://investigadores.udd.cl/handle/123456789/5086
URL Institutional Repository
http://hdl.handle.net/11447/6656
Cite this document
Casas, B. S., Vitória, G., Prieto, C. P., Casas, M., Chacón, C., Uhrig, M., Ezquer, F., Ezquer, M., Rehen, S. K., & Palma, V. (2022). Schizophrenia-derived hiPSC brain microvascular endothelial-like cells show impairments in angiogenesis and blood–brain barrier function. Molecular Psychiatry, 27(9), 3708-3718. https://doi.org/10.1038/s41380-022-01653-0
Subjects
growth-factor

; 

matrix-metalloproteinase-9 mmp-9

; 

neurotrophic factor

; 

gene

; 

polymorphism

; 

expression

; 

insights

; 

hypoxia

; 

pathway

; 

risk

; 

animals

; 

blood-brain barrier

; 

brain

; 

cell line

; 

humans

; 

induced pluripotent stem cells

; 

mice

; 

schizophrenia

; 

tight junction protein

; 

angiogenesis

; 

animal cell

; 

animal experiment

; 

article

; 

blood brain barrier

; 

brain cell

; 

capillary endothelial cell

; 

cell function

; 

controlled study

; 

disease association

; 

gene

; 

hcmec/d3 cell line

; 

immunofluorescence

; 

in vitro study

; 

in vivo study

; 

induced pluripotent stem cell

; 

male

; 

molecular interaction

; 

mouse

; 

nonhuman

; 

protein expression

; 

schizophrenia

; 

transcriptomics

; 

animal

; 

blood brain barrier

; 

brain

; 

cell line

; 

human

; 

metabolism
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