Genome-wide association study for abnormal cranio-facial morphology
Project/Area Number |
23890011
|
Research Category |
Grant-in-Aid for Research Activity Start-up
|
Allocation Type | Single-year Grants |
Research Field |
Orthodontic/Pediatric dentistry
|
Research Institution | Hokkaido University |
Principal Investigator |
SAITO Fumio 北海道大学, 北海道大学病院, 医員 (00612889)
|
Project Period (FY) |
2011 – 2012
|
Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2012: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2011: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
|
Keywords | 歯学 / ゲノム / 形態異常 |
Research Abstract |
Two loci (1q32.2 and 1p22.3) were likely to be as novel susceptibility regions of mandibular prognathism.PLXNA2 and SSX2IP genes were considered as a genetic candidate.PLXNA2 gene is a gene encoding semaphorin co-receptors, and the relations to bone metabolism are reported in semaphorin 3A.SSX2IP gene is related to a Synovium Sarcoma and the temporomandibular joint that is related to mandibular growth has synovial tissue. We speculate that these genes may be also associated with mandibular prognathism.
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Report
(3 results)
Research Products
(4 results)