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Entity

Name
protein kinase B signaling
Namespace
go
Namespace Version
20190224
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/c328ad964c08967a0417a887510b97b965a62fa5/external/go-names.belns

Appears in Networks 2

In-Edges 6

a(CHEBI:chlorpromazine) decreases bp(GO:"protein kinase B signaling") View Subject | View Object

In contrast, chlorpromazine, which is a typical antipsychotic agent, induces autophagy by inhibiting the Akt/mTOR pathway PubMed:30061532

p(HGNC:NRG1) association bp(GO:"protein kinase B signaling") View Subject | View Object

Moreover, it has been demonstrated that NRG1 also regulates DISC1 expression [230], thus further worsening the aberrancy of the Akt–mTOR pathway and the pathogenesis of schizophrenia and related behaviors. PubMed:30061532

p(MGI:Rictor) decreases bp(GO:"protein kinase B signaling") View Subject | View Object

Again, an impaired Akt signaling, achieved by neuronal deletion of rictor, a key regulatory subunit of mTORC2, contributes to schizophrenia-like phenotypes in rictor-null (KO) mice PubMed:30061532

path(MESH:Schizophrenia) association bp(GO:"protein kinase B signaling") View Subject | View Object

Again, an impaired Akt signaling, achieved by neuronal deletion of rictor, a key regulatory subunit of mTORC2, contributes to schizophrenia-like phenotypes in rictor-null (KO) mice PubMed:30061532

path(MESH:Schizophrenia) decreases bp(GO:"protein kinase B signaling") View Subject | View Object

Dysregulation in Akt signaling and altered Akt protein levels were found in the frontal cortex and hippocampus of post-mortem brain samples from individuals affected by schizophrenia PubMed:30061532

path(MESH:Schizophrenia) association bp(GO:"protein kinase B signaling") View Subject | View Object

Moreover, it has been demonstrated that NRG1 also regulates DISC1 expression [230], thus further worsening the aberrancy of the Akt–mTOR pathway and the pathogenesis of schizophrenia and related behaviors. PubMed:30061532

Out-Edges 4

bp(GO:"protein kinase B signaling") increases act(p(FPLX:NFkappaB)) View Subject | View Object

NF-κB is a ubiquitous transcriptional factor, which can be activated by AKT pathway. PubMed:27288790

bp(GO:"protein kinase B signaling") association path(MESH:Schizophrenia) View Subject | View Object

Again, an impaired Akt signaling, achieved by neuronal deletion of rictor, a key regulatory subunit of mTORC2, contributes to schizophrenia-like phenotypes in rictor-null (KO) mice PubMed:30061532

bp(GO:"protein kinase B signaling") association path(MESH:Schizophrenia) View Subject | View Object

Moreover, it has been demonstrated that NRG1 also regulates DISC1 expression [230], thus further worsening the aberrancy of the Akt–mTOR pathway and the pathogenesis of schizophrenia and related behaviors. PubMed:30061532

bp(GO:"protein kinase B signaling") association p(HGNC:NRG1) View Subject | View Object

Moreover, it has been demonstrated that NRG1 also regulates DISC1 expression [230], thus further worsening the aberrancy of the Akt–mTOR pathway and the pathogenesis of schizophrenia and related behaviors. PubMed:30061532

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.