Moriyama K - Search Results

1

Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system.

Morishita M, Muramatsu T, Suto Y, Hirai M, Konishi T, Hayashi S, Shigemizu D, Tsunoda T, Moriyama K, Inazawa J. Morishita M, et al. Among authors: moriyama k. Oncotarget. 2016 Mar 1;7(9):10182-92. doi: 10.18632/oncotarget.7186. Oncotarget. 2016. PMID: 26862731 Free PMC article.

2

Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion.

Okamoto N, Hayashi S, Masui A, Kosaki R, Oguri I, Hasegawa T, Imoto I, Makita Y, Hata A, Moriyama K, Inazawa J. Okamoto N, et al. Among authors: moriyama k. J Hum Genet. 2012 Mar;57(3):191-6. doi: 10.1038/jhg.2011.154. Epub 2012 Jan 19. J Hum Genet. 2012. PMID: 22258158

3

Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study.

Tumurkhuu T, Fujiwara T, Komazaki Y, Kawaguchi Y, Tanaka T, Inazawa J, Ganburged G, Bazar A, Ogawa T, Moriyama K. Tumurkhuu T, et al. Among authors: moriyama k. BMJ Open. 2016 Nov 1;6(11):e012283. doi: 10.1136/bmjopen-2016-012283. BMJ Open. 2016. PMID: 27803108 Free PMC article.

4

Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel.

Hirabayashi K, Uehara DT, Abe H, Ishii A, Moriyama K, Hirose S, Inazawa J. Hirabayashi K, et al. Among authors: moriyama k. J Hum Genet. 2019 Nov;64(11):1097-1106. doi: 10.1038/s10038-019-0661-x. Epub 2019 Aug 30. J Hum Genet. 2019. PMID: 31471553

5

Case report of de novo dup(18p)/del(18q) and r(18) mosaicism.

Gereltzul E, Baba Y, Suda N, Shiga M, Inoue MS, Tsuji M, Shin I, Hirata Y, Ohyama K, Moriyama K. Gereltzul E, et al. Among authors: moriyama k. J Hum Genet. 2008;53(10):941-946. doi: 10.1007/s10038-008-0326-7. Epub 2008 Aug 5. J Hum Genet. 2008. PMID: 18679767

6

The use of next-generation sequencing in molecular diagnosis of neurofibromatosis type 1: a validation study.

Maruoka R, Takenouchi T, Torii C, Shimizu A, Misu K, Higasa K, Matsuda F, Ota A, Tanito K, Kuramochi A, Arima Y, Otsuka F, Yoshida Y, Moriyama K, Niimura M, Saya H, Kosaki K. Maruoka R, et al. Among authors: moriyama k. Genet Test Mol Biomarkers. 2014 Nov;18(11):722-35. doi: 10.1089/gtmb.2014.0109. Epub 2014 Oct 17. Genet Test Mol Biomarkers. 2014. PMID: 25325900 Free PMC article. Clinical Trial.

7

Marfan syndrome and its disorder in periodontal tissues.

Suda N, Shiga M, Ganburged G, Moriyama K. Suda N, et al. Among authors: moriyama k. J Exp Zool B Mol Dev Evol. 2009 Jul 15;312B(5):503-9. doi: 10.1002/jez.b.21278. J Exp Zool B Mol Dev Evol. 2009. PMID: 19199346 Review.

8

A Mongolian patient with hypohidrotic ectodermal dysplasia with a novel P121S variant in EDARADD.

Suda N, Bazar A, Bold O, Jigjid B, Garidkhuu A, Ganburged G, Moriyama K. Suda N, et al. Among authors: moriyama k. Orthod Craniofac Res. 2010 May;13(2):114-7. doi: 10.1111/j.1601-6343.2010.01484.x. Orthod Craniofac Res. 2010. PMID: 20477971

9

Dilated capillaries, disorganized collagen fibers and differential gene expression in periodontal ligaments of hypomorphic fibrillin-1 mice.

Ganburged G, Suda N, Saito M, Yamazaki Y, Isokawa K, Moriyama K. Ganburged G, et al. Among authors: moriyama k. Cell Tissue Res. 2010 Sep;341(3):381-95. doi: 10.1007/s00441-010-1021-5. Epub 2010 Aug 17. Cell Tissue Res. 2010. PMID: 20714769

10

Non-syndromic oligodontia with a novel mutation of PAX9.

Suda N, Ogawa T, Kojima T, Saito C, Moriyama K. Suda N, et al. Among authors: moriyama k. J Dent Res. 2011 Mar;90(3):382-6. doi: 10.1177/0022034510390042. Epub 2010 Nov 22. J Dent Res. 2011. PMID: 21098475

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