Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2011: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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Research Abstract |
The analyses of spectral karyotyping (SKY) and fluorescence in situ hybridization (FISH) were performed to human pancreatic cell lines. The frequent chromosomal disorder was detected in 8p12. NRG1 in 8p12 was considered as the possibility of fusion gene. The breakpoints of NRG1 was t(8;17)(p11.2;q23), t(8;18)(p23;q12) and t(7;8)(q11.2;p11.2) i(8q). We performed genomic array and bubble PCR to candidate cell lines. The detail breakpoints of NRG1 were exon 1, and exon9-17. We have performed further analyses for these breakpoints to find the fusion gene.
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