Naruto T - Search Results

1

Identification of target genes within an amplicon at 14q12-q13 in esophageal squamous cell carcinoma.

Yasui K, Imoto I, Fukuda Y, Pimkhaokham A, Yang ZQ, Naruto T, Shimada Y, Nakamura Y, Inazawa J. Yasui K, et al. Among authors: naruto t. Genes Chromosomes Cancer. 2001 Oct;32(2):112-8. doi: 10.1002/gcc.1172. Genes Chromosomes Cancer. 2001. PMID: 11550278

2

Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin Syndrome.

Morita K, Naruto T, Tanimoto K, Yasukawa C, Oikawa Y, Masuda K, Imoto I, Inazawa J, Omura K, Harada H. Morita K, et al. Among authors: naruto t. PLoS One. 2015 Nov 6;10(11):e0140480. doi: 10.1371/journal.pone.0140480. eCollection 2015. PLoS One. 2015. PMID: 26544948 Free PMC article.

3

Tumor-promoting function and prognostic significance of the RNA-binding protein T-cell intracellular antigen-1 in esophageal squamous cell carcinoma.

Hamada J, Shoda K, Masuda K, Fujita Y, Naruto T, Kohmoto T, Miyakami Y, Watanabe M, Kudo Y, Fujiwara H, Ichikawa D, Otsuji E, Imoto I. Hamada J, et al. Among authors: naruto t. Oncotarget. 2016 Mar 29;7(13):17111-28. doi: 10.18632/oncotarget.7937. Oncotarget. 2016. PMID: 26958940 Free PMC article.

4

A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndrome.

Kohmoto T, Tsuji A, Morita K, Naruto T, Masuda K, Kashimada K, Enomoto K, Morio T, Harada H, Imoto I. Kohmoto T, et al. Among authors: naruto t. Hum Genome Var. 2016 Apr 7;3:16003. doi: 10.1038/hgv.2016.3. eCollection 2016. Hum Genome Var. 2016. PMID: 27081569 Free PMC article.

5

Frequent silencing of the candidate tumor suppressor TRIM58 by promoter methylation in early-stage lung adenocarcinoma.

Kajiura K, Masuda K, Naruto T, Kohmoto T, Watabnabe M, Tsuboi M, Takizawa H, Kondo K, Tangoku A, Imoto I. Kajiura K, et al. Among authors: naruto t. Oncotarget. 2017 Jan 10;8(2):2890-2905. doi: 10.18632/oncotarget.13761. Oncotarget. 2017. PMID: 27926516 Free PMC article.

6

Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome.

Matsudate Y, Naruto T, Hayashi Y, Minami M, Tohyama M, Yokota K, Yamada D, Imoto I, Kubo Y. Matsudate Y, et al. Among authors: naruto t. J Dermatol Sci. 2017 Jun;86(3):206-211. doi: 10.1016/j.jdermsci.2017.02.282. Epub 2017 Mar 11. J Dermatol Sci. 2017. PMID: 28342698

7

KH-type splicing regulatory protein is involved in esophageal squamous cell carcinoma progression.

Fujita Y, Masuda K, Hamada J, Shoda K, Naruto T, Hamada S, Miyakami Y, Kohmoto T, Watanabe M, Takahashi R, Tange S, Saito M, Kudo Y, Fujiwara H, Ichikawa D, Tangoku A, Otsuji E, Imoto I. Fujita Y, et al. Among authors: naruto t. Oncotarget. 2017 Sep 15;8(60):101130-101145. doi: 10.18632/oncotarget.20926. eCollection 2017 Nov 24. Oncotarget. 2017. PMID: 29254151 Free PMC article.

8

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. Sci Rep. 2015 Jun 10;5:11334. doi: 10.1038/srep11334. Sci Rep. 2015. PMID: 26061757 Free PMC article.

9

A unique TBX5 microdeletion with microinsertion detected in patient with Holt-Oram syndrome.

Morine M, Kohmoto T, Masuda K, Inagaki H, Watanabe M, Naruto T, Kurahashi H, Maeda K, Imoto I. Morine M, et al. Among authors: naruto t. Am J Med Genet A. 2015 Dec;167A(12):3192-6. doi: 10.1002/ajmg.a.37359. Epub 2015 Sep 28. Am J Med Genet A. 2015. PMID: 26780237

10

A novel PTCH1 mutation in a patient with Gorlin syndrome.

Okamoto N, Naruto T, Kohmoto T, Komori T, Imoto I. Okamoto N, et al. Among authors: naruto t. Hum Genome Var. 2014 Nov 13;1:14022. doi: 10.1038/hgv.2014.22. eCollection 2014. Hum Genome Var. 2014. PMID: 27081512 Free PMC article.

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