Research Project
Grant-in-Aid for Young Scientists (B)
Deficits in prepulse inhibition (PPI) are a biological marker for psychiatric illnesses such as schizophrenia and bipolar disorder. To unravel PPI-controlling mechanisms, we previously performed quantitative trait loci analysis in mice, and identified Fabp7, that encodes a brain-type fatty acid binding protein (Fabp), as a causative gene. FABPs constitute a gene family, of which members FABP5 and FABP3 are also expressed in the brain. In this project, I examined the genetic roles of these FABP genes in schizophrenia and bipolar disorder. FABP7 showed nominal association with bipolar disorder (we previously reported an association of FABP7 with schizophrenia). We could not obtain evidence for associations of FABP5 and FABP3 with either disease.
All 2010 2008 Other
All Journal Article (14 results) (of which Peer Reviewed: 14 results) Presentation (2 results) Remarks (2 results)
Am. J. Med. Genet. Part B. 153B
Pages: 484-493
J. Hum. Genet. 55
Pages: 127-130
Am.J.Med.Genet.Part B (in press)
J.Hum.Genet (in press)
Schizophrenia Research 99
Pages: 359-364
Psychiatric Genetics 18
Pages: 1-10
Mol. Psychiatry 13
Pages: 385-397
Biol. Psychiatry 63
Pages: 678-685
Am. J. Med. Genet. B Neuropsychiatr. Genet. 147B
Pages: 1019-1027
The International Journal of Neuropsychopharmacology 11
Pages: 1073-1084
Am. J. Med. Genet. B Neuropsychiatr. Genet. (in press)
Eur. J. Hum. Genet. (in press)
Neuropsychiatr. Genet. (in press)
http://www.riken.jp/engn/r-world/research/lab/nokagaku/age/molecular/index.html