Satake W - Search Results

1

TUBB3 E410K Syndrome With Childhood-Onset Nonalcoholic Steatohepatitis.

Mori J, Umemura A, Satake W, Cha PC, Suzuki Y, Itoh K, Chiyonobu T. Mori J, et al. Among authors: satake w. J Clin Endocrinol Metab. 2022 Jan 1;107(1):e38-e43. doi: 10.1210/clinem/dgab628. J Clin Endocrinol Metab. 2022. PMID: 34435630

2

A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child.

Saida K, Inaba Y, Hirano M, Satake W, Toda T, Suzuki Y, Sudo A, Noda S, Hidaka Y, Hirabayashi K, Imai H, Kurokawa T, Koike K. Saida K, et al. Among authors: satake w. Brain Dev. 2014 Sep;36(8):721-4. doi: 10.1016/j.braindev.2013.10.013. Epub 2013 Nov 26. Brain Dev. 2014. PMID: 24290075

3

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: satake w. PLoS One. 2015 Jul 1;10(7):e0130329. doi: 10.1371/journal.pone.0130329. eCollection 2015. PLoS One. 2015. PMID: 26132555 Free PMC article.

4

The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan.

Hirano M, Satake W, Ihara K, Tsuge I, Kondo S, Saida K, Betsui H, Okubo K, Sakamoto H, Ueno S, Ikuno Y, Ishihara R, Iwahashi H, Ohishi M, Mano T, Yamashita T, Suzuki Y, Nakamura Y, Kusunoki S, Toda T. Hirano M, et al. Among authors: satake w. PLoS One. 2015 Sep 1;10(9):e0136317. doi: 10.1371/journal.pone.0136317. eCollection 2015. PLoS One. 2015. PMID: 26325687 Free PMC article.

5

A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy.

Oda T, Xiong H, Kobayashi K, Wang S, Satake W, Jiao H, Yang Y, Cha PC, Hayashi YK, Nishino I, Suzuki Y, Sugano S, Wu X, Toda T. Oda T, et al. Among authors: satake w. Hum Genome Var. 2015 Jul 16;2:15022. doi: 10.1038/hgv.2015.22. eCollection 2015. Hum Genome Var. 2015. PMID: 27081534 Free PMC article.

6

Japanese WDR45 de novo mutation diagnosed by exome analysis: A case report.

Endo H, Uenaka T, Satake W, Suzuki Y, Tachibana H, Chihara N, Ueda T, Sekiguchi K, Mariko TI, Kowa H, Kanda F, Toda T. Endo H, et al. Among authors: satake w. Neurol Clin Neurosci. 2017 Jul;5(4):131-133. doi: 10.1111/ncn3.12132. Epub 2017 Jun 29. Neurol Clin Neurosci. 2017. PMID: 28932395 Free PMC article.

7

In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson's disease.

Uenaka T, Satake W, Cha PC, Hayakawa H, Baba K, Jiang S, Kobayashi K, Kanagawa M, Okada Y, Mochizuki H, Toda T. Uenaka T, et al. Among authors: satake w. Hum Mol Genet. 2018 Nov 15;27(22):3974-3985. doi: 10.1093/hmg/ddy279. Hum Mol Genet. 2018. PMID: 30137437 Free PMC article.

8

Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients.

Cha PC, Satake W, Ando-Kanagawa Y, Yamamoto K, Murata M, Toda T. Cha PC, et al. Among authors: satake w. J Hum Genet. 2020 Aug;65(8):693-704. doi: 10.1038/s10038-020-0760-8. Epub 2020 May 1. J Hum Genet. 2020. PMID: 32355309 Free PMC article.

9

Bardet-Biedl syndrome and related disorders in Japan.

Hirano M, Satake W, Moriyama N, Saida K, Okamoto N, Cha PC, Suzuki Y, Kusunoki S, Toda T. Hirano M, et al. Among authors: satake w. J Hum Genet. 2020 Oct;65(10):847-853. doi: 10.1038/s10038-020-0778-y. Epub 2020 May 25. J Hum Genet. 2020. PMID: 32451492

10

Comparative whole transcriptome analysis of Parkinson's disease focusing on the efficacy of zonisamide.

Naito T, Satake W, Cha PC, Kobayashi K, Murata M, Toda T. Naito T, et al. Among authors: satake w. J Neurol Neurosurg Psychiatry. 2022 May;93(5):509-512. doi: 10.1136/jnnp-2021-328742. Epub 2022 Mar 9. J Neurol Neurosurg Psychiatry. 2022. PMID: 35264450 Free PMC article.

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