Kurahashi H - Search Results

1

Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations.

Suzuki E, Shima H, Toki M, Hanew K, Matsubara K, Kurahashi H, Narumi S, Ogata T, Kamimaki T, Fukami M. Suzuki E, et al. Among authors: kurahashi h. Cytogenet Genome Res. 2016;150(2):86-92. doi: 10.1159/000455026. Epub 2017 Jan 19. Cytogenet Genome Res. 2016. PMID: 28099951

2

Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis.

Kato T, Ouchi Y, Inagaki H, Makita Y, Mizuno S, Kajita M, Ikeda T, Takeuchi K, Kurahashi H. Kato T, et al. Among authors: kurahashi h. Cytogenet Genome Res. 2017;153(1):1-9. doi: 10.1159/000481586. Epub 2017 Oct 27. Cytogenet Genome Res. 2017. PMID: 29073611 Free article.

3

Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events.

Fukami M, Kurahashi H. Fukami M, et al. Among authors: kurahashi h. Methods Mol Biol. 2018;1769:21-33. doi: 10.1007/978-1-4939-7780-2_2. Methods Mol Biol. 2018. PMID: 29564815 Review.

4

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. 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.

5

Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.

Inagaki H, Ohye T, Kogo H, Kato T, Bolor H, Taniguchi M, Shaikh TH, Emanuel BS, Kurahashi H. Inagaki H, et al. Among authors: kurahashi h. Genome Res. 2009 Feb;19(2):191-8. doi: 10.1101/gr.079244.108. Epub 2008 Nov 7. Genome Res. 2009. PMID: 18997000 Free PMC article.

6

Six years' accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures.

Takahashi Y, Date H, Oi H, Adachi T, Imanishi N, Kimura E, Takizawa H, Kosugi S, Matsumoto N, Kosaki K, Matsubara Y; IRUD Consortium; Mizusawa H. Takahashi Y, et al. J Hum Genet. 2022 Sep;67(9):505-513. doi: 10.1038/s10038-022-01025-0. Epub 2022 Mar 23. J Hum Genet. 2022. PMID: 35318459 Free PMC article.

7

Recent advance in our understanding of the molecular nature of chromosomal abnormalities.

Kurahashi H, Bolor H, Kato T, Kogo H, Tsutsumi M, Inagaki H, Ohye T. Kurahashi H, et al. J Hum Genet. 2009 May;54(5):253-60. doi: 10.1038/jhg.2009.35. Epub 2009 Apr 17. J Hum Genet. 2009. PMID: 19373258 Review.

8

Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations.

Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H. Inagaki H, et al. Among authors: kurahashi h. Nat Commun. 2013;4:1592. doi: 10.1038/ncomms2595. Nat Commun. 2013. PMID: 23481400 Free article.

9

Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases.

Kato T, Kawai M, Miyai S, Suzuki F, Tsutsumi M, Mizuno S, Ikeda T, Kurahashi H. Kato T, et al. Among authors: kurahashi h. Cytogenet Genome Res. 2020;160(3):118-123. doi: 10.1159/000507177. Epub 2020 Apr 4. Cytogenet Genome Res. 2020. PMID: 32248198

10

The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.

Kato T, Inagaki H, Miyai S, Suzuki F, Naru Y, Shinkai Y, Kato A, Kanyama K, Mizuno S, Muramatsu Y, Yamamoto T, Shinya M, Tazaki Y, Hiwatashi S, Ikeda T, Ozaki M, Kurahashi H. Kato T, et al. Among authors: kurahashi h. Hum Genet. 2020 Nov;139(11):1417-1427. doi: 10.1007/s00439-020-02186-8. Epub 2020 Jun 2. Hum Genet. 2020. PMID: 32488466

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