act(p(HGNC:MTOR)) negativeCorrelation path(MESH:Schizophrenia)

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PubMed:30061532

Remarkably, the identification of rare genetic variants of ULK1 in a cohort of schizophrenic patients by means of exome sequence analysis strengthens the idea of a key role of both disrupted mTOR signaling and autophagy in the pathophysiology and susceptibility to schizophrenia

Related Edges 5

• bp(GO:autophagy) negativeCorrelation path(MESH:Schizophrenia)
• p(HGNC:ULK1, var("?")) association path(MESH:Schizophrenia)
• path(MESH:Schizophrenia) negativeCorrelation act(p(HGNC:MTOR))
• path(MESH:Schizophrenia) association p(HGNC:ULK1, var("?"))
• path(MESH:Schizophrenia) negativeCorrelation bp(GO:autophagy)

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