Naruto T - Search Results

1

Construction of a combinatorial pipeline using two somatic variant calling methods for whole exome sequence data of gastric cancer.

Kohmoto T, Masuda K, Naruto T, Tange S, Shoda K, Hamada J, Saito M, Ichikawa D, Tajima A, Otsuji E, Imoto I. Kohmoto T, et al. Among authors: naruto t. J Med Invest. 2017;64(3.4):233-240. doi: 10.2152/jmi.64.233. J Med Invest. 2017. PMID: 28954988 Free article.

2

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.

3

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.

4

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

5

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.

6

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.

7

A FRMD7 variant in a Japanese family causes congenital nystagmus.

Kohmoto T, Okamoto N, Satomura S, Naruto T, Komori T, Hashimoto T, Imoto I. Kohmoto T, et al. Among authors: naruto t. Hum Genome Var. 2015 Feb 12;2:15002. doi: 10.1038/hgv.2015.2. eCollection 2015. Hum Genome Var. 2015. PMID: 27081518 Free PMC article.

8

A novel COL11A1 mutation affecting splicing in a patient with Stickler syndrome.

Kohmoto T, Naruto T, Kobayashi H, Watanabe M, Okamoto N, Masuda K, Imoto I, Okamoto N. Kohmoto T, et al. Among authors: naruto t. Hum Genome Var. 2015 Nov 12;2:15043. doi: 10.1038/hgv.2015.43. eCollection 2015. Hum Genome Var. 2015. PMID: 27081549 Free PMC article.

9

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.

10

A novel frameshift mutation of CHD7 in a Japanese patient with CHARGE syndrome.

Kohmoto T, Shono M, Naruto T, Watanabe M, Suga K, Nakagawa R, Kagami S, Masuda K, Imoto I. Kohmoto T, et al. Among authors: naruto t. Hum Genome Var. 2016 Apr 7;3:16004. doi: 10.1038/hgv.2016.4. eCollection 2016. Hum Genome Var. 2016. PMID: 27081570 Free PMC article.

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