Imoto I - Search Results

1

Manifestation of recessive combined D-2-, L-2-hydroxyglutaric aciduria in combination with 22q11.2 deletion syndrome.

Eguchi M, Ozaki E, Yamauchi T, Ohta M, Higaki T, Masuda K, Imoto I, Ishii E, Eguchi-Ishimae M. Eguchi M, et al. Among authors: imoto i. Am J Med Genet A. 2018 Feb;176(2):351-358. doi: 10.1002/ajmg.a.38578. Epub 2017 Dec 19. Am J Med Genet A. 2018. PMID: 29265763 Review.

2

Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.

Hayashi S, Kurosawa K, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: imoto i. Am J Med Genet A. 2005 Nov 15;139(1):32-6. doi: 10.1002/ajmg.a.30982. Am J Med Genet A. 2005. PMID: 16222686

3

Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia-de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array-based comparative genomic hybridization.

Hayashi S, Ono M, Makita Y, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: imoto i. Am J Med Genet A. 2007 Jun 1;143A(11):1191-7. doi: 10.1002/ajmg.a.31737. Am J Med Genet A. 2007. PMID: 17497725

4

Partial tandem duplication of GRIA3 in a male with mental retardation.

Chiyonobu T, Hayashi S, Kobayashi K, Morimoto M, Miyanomae Y, Nishimura A, Nishimoto A, Ito C, Imoto I, Sugimoto T, Jia Z, Inazawa J, Toda T. Chiyonobu T, et al. Among authors: imoto i. Am J Med Genet A. 2007 Jul 1;143A(13):1448-55. doi: 10.1002/ajmg.a.31798. Am J Med Genet A. 2007. PMID: 17568425

5

The incidence of hypoplasia of the corpus callosum in patients with dup (X)(q28) involving MECP2 is associated with the location of distal breakpoints.

Honda S, Hayashi S, Nakane T, Imoto I, Kurosawa K, Mizuno S, Okamoto N, Kato M, Yoshihashi H, Kubota T, Nakagawa E, Goto Y, Inazawa J. Honda S, et al. Among authors: imoto i. Am J Med Genet A. 2012 Jun;158A(6):1292-303. doi: 10.1002/ajmg.a.35321. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22528406

6

NF90 in posttranscriptional gene regulation and microRNA biogenesis.

Masuda K, Kuwano Y, Nishida K, Rokutan K, Imoto I. Masuda K, et al. Among authors: imoto i. Int J Mol Sci. 2013 Aug 19;14(8):17111-21. doi: 10.3390/ijms140817111. Int J Mol Sci. 2013. PMID: 23965975 Free PMC article. Review.

7

Novel PAX9 mutations cause non-syndromic tooth agenesis.

Mitsui SN, Yasue A, Masuda K, Watanabe K, Horiuchi S, Imoto I, Tanaka E. Mitsui SN, et al. Among authors: imoto i. J Dent Res. 2014 Mar;93(3):245-9. doi: 10.1177/0022034513519801. Epub 2014 Jan 16. J Dent Res. 2014. PMID: 24436340

8

HuR regulates alternative splicing of the TRA2β gene in human colon cancer cells under oxidative stress.

Akaike Y, Masuda K, Kuwano Y, Nishida K, Kajita K, Kurokawa K, Satake Y, Shoda K, Imoto I, Rokutan K. Akaike Y, et al. Among authors: imoto i. Mol Cell Biol. 2014 Aug;34(15):2857-73. doi: 10.1128/MCB.00333-14. Epub 2014 May 27. Mol Cell Biol. 2014. PMID: 24865968 Free PMC article.

9

HER2 amplification detected in the circulating DNA of patients with gastric cancer: a retrospective pilot study.

Shoda K, Masuda K, Ichikawa D, Arita T, Miyakami Y, Watanabe M, Konishi H, Imoto I, Otsuji E. Shoda K, et al. Among authors: imoto i. Gastric Cancer. 2015 Oct;18(4):698-710. doi: 10.1007/s10120-014-0432-5. Epub 2014 Oct 17. Gastric Cancer. 2015. PMID: 25322965

10

Deep intronic GPR143 mutation in a Japanese family with ocular albinism.

Naruto T, Okamoto N, Masuda K, Endo T, Hatsukawa Y, Kohmoto T, Imoto I. Naruto T, et al. Among authors: imoto i. Sci Rep. 2015 Jun 10;5:11334. doi: 10.1038/srep11334. Sci Rep. 2015. PMID: 26061757 Free PMC article.

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