Tsunoda T - Search Results

1

Sudden death in a case of megalencephaly capillary malformation associated with a de novo mutation in AKT3.

Harada A, Miya F, Utsunomiya H, Kato M, Yamanaka T, Tsunoda T, Kosaki K, Kanemura Y, Yamasaki M. Harada A, et al. Among authors: tsunoda t. Childs Nerv Syst. 2015 Mar;31(3):465-71. doi: 10.1007/s00381-014-2589-y. Epub 2014 Nov 22. Childs Nerv Syst. 2015. PMID: 25416470

2

Recombination rates of genes expressed in human tissues.

Kato M, Miya F, Kanemura Y, Tanaka T, Nakamura Y, Tsunoda T. Kato M, et al. Among authors: tsunoda t. Hum Mol Genet. 2008 Feb 15;17(4):577-86. doi: 10.1093/hmg/ddm332. Epub 2007 Nov 13. Hum Mol Genet. 2008. PMID: 18000027

3

Targeted next-generation sequencing in the diagnosis of neurodevelopmental disorders.

Okamoto N, Miya F, Tsunoda T, Kato M, Saitoh S, Yamasaki M, Shimizu A, Torii C, Kanemura Y, Kosaki K. Okamoto N, et al. Among authors: tsunoda t. Clin Genet. 2015 Sep;88(3):288-92. doi: 10.1111/cge.12492. Epub 2014 Nov 13. Clin Genet. 2015. PMID: 25156961

4

KIF1A mutation in a patient with progressive neurodegeneration.

Okamoto N, Miya F, Tsunoda T, Yanagihara K, Kato M, Saitoh S, Yamasaki M, Kanemura Y, Kosaki K. Okamoto N, et al. Among authors: tsunoda t. J Hum Genet. 2014 Nov;59(11):639-41. doi: 10.1038/jhg.2014.80. Epub 2014 Sep 25. J Hum Genet. 2014. PMID: 25253658

5

Primary microcephaly with anterior predominant pachygyria caused by novel compound heterozygous mutations in ASPM.

Nakamura K, Inui T, Miya F, Kanemura Y, Okamoto N, Saitoh S, Yamasaki M, Tsunoda T, Kosaki K, Tanaka S, Kato M. Nakamura K, et al. Among authors: tsunoda t. Pediatr Neurol. 2015 May;52(5):e7-8. doi: 10.1016/j.pediatrneurol.2015.01.019. Epub 2015 Feb 7. Pediatr Neurol. 2015. PMID: 25765464 No abstract available.

6

A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations.

Miya F, Kato M, Shiohama T, Okamoto N, Saitoh S, Yamasaki M, Shigemizu D, Abe T, Morizono T, Boroevich KA, Kosaki K, Kanemura Y, Tsunoda T. Miya F, et al. Among authors: tsunoda t. Sci Rep. 2015 Mar 19;5:9331. doi: 10.1038/srep09331. Sci Rep. 2015. PMID: 25786579 Free PMC article.

7

Attenuation of progressive hearing loss in DBA/2J mice by reagents that affect epigenetic modifications is associated with up-regulation of the zinc importer Zip4.

Mutai H, Miya F, Fujii M, Tsunoda T, Matsunaga T. Mutai H, et al. Among authors: tsunoda t. PLoS One. 2015 Apr 14;10(4):e0124301. doi: 10.1371/journal.pone.0124301. eCollection 2015. PLoS One. 2015. PMID: 25875282 Free PMC article.

8

A deletion mutation in myosin heavy chain 11 causing familial thoracic aortic dissection in two Japanese pedigrees.

Imai Y, Morita H, Takeda N, Miya F, Hyodo H, Fujita D, Tajima T, Tsunoda T, Nagai R, Kubo M, Komuro I. Imai Y, et al. Among authors: tsunoda t. Int J Cardiol. 2015 Sep 15;195:290-2. doi: 10.1016/j.ijcard.2015.05.178. Epub 2015 Jun 3. Int J Cardiol. 2015. PMID: 26056961 No abstract available.

9

Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.

Shigemizu D, Aiba T, Nakagawa H, Ozaki K, Miya F, Satake W, Toda T, Miyamoto Y, Fujimoto A, Suzuki Y, Kubo M, Tsunoda T, Shimizu W, Tanaka T. Shigemizu D, et al. Among authors: tsunoda t. PLoS One. 2015 Jul 1;10(7):e0130329. doi: 10.1371/journal.pone.0130329. eCollection 2015. PLoS One. 2015. PMID: 26132555 Free PMC article.

10

Gene expression profiling of DBA/2J mice cochleae treated with l-methionine and valproic acid.

Miya F, Mutai H, Fujii M, Boroevich KA, Matsunaga T, Tsunoda T. Miya F, et al. Among authors: tsunoda t. Genom Data. 2015 Jul 2;5:323-5. doi: 10.1016/j.gdata.2015.06.022. eCollection 2015 Sep. Genom Data. 2015. PMID: 26484279 Free PMC article.

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