Inagaki H - Search Results

1

Intragenic DOK7 deletion detected by whole-genome sequencing in congenital myasthenic syndromes.

Azuma Y, Töpf A, Evangelista T, Lorenzoni PJ, Roos A, Viana P, Inagaki H, Kurahashi H, Lochmüller H. Azuma Y, et al. Among authors: inagaki h. Neurol Genet. 2017 May 3;3(3):e152. doi: 10.1212/NXG.0000000000000152. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28508085 Free PMC article.

2

Cruciform DNA structure underlies the etiology for palindrome-mediated human chromosomal translocations.

Kurahashi H, Inagaki H, Yamada K, Ohye T, Taniguchi M, Emanuel BS, Toda T. Kurahashi H, et al. Among authors: inagaki h. J Biol Chem. 2004 Aug 20;279(34):35377-83. doi: 10.1074/jbc.M400354200. Epub 2004 Jun 20. J Biol Chem. 2004. PMID: 15208332 Free PMC article.

3

Palindromic AT-rich repeat in the NF1 gene is hypervariable in humans and evolutionarily conserved in primates.

Inagaki H, Ohye T, Kogo H, Yamada K, Kowa H, Shaikh TH, Emanuel BS, Kurahashi H. Inagaki H, et al. Hum Mutat. 2005 Oct;26(4):332-42. doi: 10.1002/humu.20228. Hum Mutat. 2005. PMID: 16116616 Free PMC article.

4

Genetic variation affects de novo translocation frequency.

Kato T, Inagaki H, Yamada K, Kogo H, Ohye T, Kowa H, Nagaoka K, Taniguchi M, Emanuel BS, Kurahashi H. Kato T, et al. Among authors: inagaki h. Science. 2006 Feb 17;311(5763):971. doi: 10.1126/science.1121452. Science. 2006. PMID: 16484486 Free PMC article.

5

Chromosomal translocations mediated by palindromic DNA.

Kurahashi H, Inagaki H, Ohye T, Kogo H, Kato T, Emanuel BS. Kurahashi H, et al. Among authors: inagaki h. Cell Cycle. 2006 Jun;5(12):1297-303. doi: 10.4161/cc.5.12.2809. Epub 2006 Jun 15. Cell Cycle. 2006. PMID: 16760666 Review.

6

Palindrome-mediated chromosomal translocations in humans.

Kurahashi H, Inagaki H, Ohye T, Kogo H, Kato T, Emanuel BS. Kurahashi H, et al. Among authors: inagaki h. DNA Repair (Amst). 2006 Sep 8;5(9-10):1136-45. doi: 10.1016/j.dnarep.2006.05.035. Epub 2006 Jul 10. DNA Repair (Amst). 2006. PMID: 16829213 Free PMC article. Review.

7

Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22).

Ashley T, Gaeth AP, Inagaki H, Seftel A, Cohen MM, Anderson LK, Kurahashi H, Emanuel BS. Ashley T, et al. Among authors: inagaki h. Am J Hum Genet. 2006 Sep;79(3):524-38. doi: 10.1086/507652. Epub 2006 Aug 1. Am J Hum Genet. 2006. PMID: 16909390 Free PMC article.

8

Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats.

Kogo H, Inagaki H, Ohye T, Kato T, Emanuel BS, Kurahashi H. Kogo H, et al. Among authors: inagaki h. Nucleic Acids Res. 2007;35(4):1198-208. doi: 10.1093/nar/gkm036. Epub 2007 Jan 30. Nucleic Acids Res. 2007. PMID: 17264116 Free PMC article.

9

Molecular cloning of a translocation breakpoint hotspot in 22q11.

Kurahashi H, Inagaki H, Hosoba E, Kato T, Ohye T, Kogo H, Emanuel BS. Kurahashi H, et al. Among authors: inagaki h. Genome Res. 2007 Apr;17(4):461-9. doi: 10.1101/gr.5769507. Epub 2007 Jan 31. Genome Res. 2007. PMID: 17267815 Free PMC article.

10

Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm.

Kato T, Yamada K, Inagaki H, Kogo H, Ohye T, Emanuel BS, Kurahashi H. Kato T, et al. Among authors: inagaki h. Fertil Steril. 2007 Nov;88(5):1446-8. doi: 10.1016/j.fertnstert.2007.01.019. Epub 2007 Apr 19. Fertil Steril. 2007. PMID: 17448469 Free PMC article.

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