Literature DB >> 17438657

[Gene polymorphism and gene expression in schizophrenia].

Trixler Mátyás1.   

Abstract

The author reviews relevant data on the neuropathology and molecular genetics of schizophrenia. Anatomical alterations are localized mainly in the hippocampus, dorsal thalamus and dorsolateral prefrontal cortex, and involve the morphology and molecular structure of the neurons and synapses. Several susceptibility genes [including COMT, dysbindin, neuregulin, DISCI, RGS4, GRM3, G72, PPP3CC, CHRNA7, PRODH2, Aktl, 5qGABA(A)] having physiological function in the brain have been identified and this supports the view of schizophrenia as a disorder of cerebral synaptic function. NMDA receptor-mediated glutamate transmission may be particularly involved, but disturbances of dopamine and GABA signalling seem to be linked as well. Based on recent data, an agreement is emerging between the roles of the genes on the molecular and synaptic levels and the understanding of the disorder at the neural systems level.

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Year:  2006        PMID: 17438657

Source DB:  PubMed          Journal:  Psychiatr Hung        ISSN: 0237-7896


  2 in total

1.  Catechol O-methyltransferase pharmacogenomics: human liver genotype-phenotype correlation and proximal promoter studies.

Authors:  Jianping Zhang; Yuan Ji; Irene Moon; Linda L Pelleymounter; Oreste Ezequel Salavaggione; Yanhong Wu; Gregory D Jenkins; Anthony J Batzler; Daniel J Schaid; Richard M Weinshilboum
Journal:  Pharmacogenet Genomics       Date:  2009-08       Impact factor: 2.089

2.  GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders.

Authors:  Tobias Hornig; Björn Grüning; Kousik Kundu; Torsten Houwaart; Rolf Backofen; Knut Biber; Claus Normann
Journal:  Genet Res (Camb)       Date:  2017-01-30       Impact factor: 1.588

  2 in total

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