A protein-centric view of in vitro biological model systems for schizophrenia
Research output: Contribution to journal › Review › Research › peer-review
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A protein-centric view of in vitro biological model systems for schizophrenia. / Chandrasekaran, Abinaya; Jensen, Pia; Mohamed, Fadumo A; Lancaster, Madeline; Benros, Michael E; Larsen, Martin R; Freude, Kristine K.
In: Stem Cells, Vol. 39, No. 12, 2021, p. 1569-1578.Research output: Contribution to journal › Review › Research › peer-review
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TY - JOUR
T1 - A protein-centric view of in vitro biological model systems for schizophrenia
AU - Chandrasekaran, Abinaya
AU - Jensen, Pia
AU - Mohamed, Fadumo A
AU - Lancaster, Madeline
AU - Benros, Michael E
AU - Larsen, Martin R
AU - Freude, Kristine K
N1 - ©2021 The Authors. Stem Cells published by Wiley Periodicals LLC on behalf of AlphaMed Press 2021.
PY - 2021
Y1 - 2021
N2 - Schizophrenia (SCZ) is a severe brain disorder, characterized by psychotic, negative, and cognitive symptoms, affecting 1% of the population worldwide. The precise etiology of SCZ is still unknown; however, SCZ has a high heritability, and is associated with genetic, environmental, and social risk factors. Even though the genetic contribution is indisputable, the discrepancies between transcriptomics and proteomics in brain tissues are consistently challenging the field to decipher the disease pathology. Here we provide an overview of the state of the art of neuronal two-dimensional and three-dimensional model systems that can be combined with proteomics analyses to decipher specific brain pathology and detection of alternative entry points for drug development.
AB - Schizophrenia (SCZ) is a severe brain disorder, characterized by psychotic, negative, and cognitive symptoms, affecting 1% of the population worldwide. The precise etiology of SCZ is still unknown; however, SCZ has a high heritability, and is associated with genetic, environmental, and social risk factors. Even though the genetic contribution is indisputable, the discrepancies between transcriptomics and proteomics in brain tissues are consistently challenging the field to decipher the disease pathology. Here we provide an overview of the state of the art of neuronal two-dimensional and three-dimensional model systems that can be combined with proteomics analyses to decipher specific brain pathology and detection of alternative entry points for drug development.
U2 - 10.1002/stem.3447
DO - 10.1002/stem.3447
M3 - Review
C2 - 34431581
VL - 39
SP - 1569
EP - 1578
JO - Stem Cells
JF - Stem Cells
SN - 1066-5099
IS - 12
ER -
ID: 279189471