Abstract |
Glutamate dysfunction has been hypothesized to be involved in the pathophysiology of schizophrenia. The human homolog of Drosophila discs large protein (hDLG) and post-synaptic density-95-associated protein-1 (DAP-1) is one of the major proteins that are involved in intracellular signal transduction via N-methyl-d-aspartate receptors. In the present study 33 Japanese patients with schizophrenia were screened for mutations in the DAP-1 gene. A single nucleotide polymorphism was identified in the DAP-1 gene (1618A/G). A case-control study using a larger sample of unrelated patients and controls did not reveal a significant association between this polymorphism and schizophrenia. The results do not provide evidence that the DAP-1 gene is involved in vulnerability to schizophrenia.
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Authors | Shinsuke Aoyama, Osamu Shirakawa, Hisae Ono, Takeshi Hashimoto, Yasuo Kajimoto, Kiyoshi Maeda |
Journal | Psychiatry and clinical neurosciences
(Psychiatry Clin Neurosci)
Vol. 57
Issue 5
Pg. 545-7
(Oct 2003)
ISSN: 1323-1316 [Print] Australia |
PMID | 12950712
(Publication Type: Journal Article)
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Chemical References |
- DLGAP1 protein, human
- Nerve Tissue Proteins
- SAP90-PSD95 Associated Proteins
- DNA
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Topics |
- Case-Control Studies
- DNA
(genetics)
- DNA Mutational Analysis
- Female
- Gene Frequency
- Genotype
- Humans
- Male
- Middle Aged
- Mutation
- Nerve Tissue Proteins
(genetics)
- Polymerase Chain Reaction
- Polymorphism, Single-Stranded Conformational
- SAP90-PSD95 Associated Proteins
- Schizophrenia
(genetics)
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