Cha PC - Search Results

1

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. 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.

2

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: cha pc. Hum Mol Genet. 2018 Nov 15;27(22):3974-3985. doi: 10.1093/hmg/ddy279. Hum Mol Genet. 2018. PMID: 30137437 Free PMC article.

3

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: cha pc. 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.

4

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: cha pc. 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.

5

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: cha pc. 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

6

Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese.

Cha PC, Mushiroda T, Takahashi A, Kubo M, Minami S, Kamatani N, Nakamura Y. Cha PC, et al. Hum Mol Genet. 2010 Dec 1;19(23):4735-44. doi: 10.1093/hmg/ddq389. Epub 2010 Sep 10. Hum Mol Genet. 2010. PMID: 20833655

7

Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.

Low SK, Takahashi A, Cha PC, Zembutsu H, Kamatani N, Kubo M, Nakamura Y. Low SK, et al. Among authors: cha pc. Hum Mol Genet. 2012 May 1;21(9):2102-10. doi: 10.1093/hmg/dds020. Epub 2012 Jan 27. Hum Mol Genet. 2012. PMID: 22286173

8

A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.

Cha PC, Zembutsu H, Takahashi A, Kubo M, Kamatani N, Nakamura Y. Cha PC, et al. J Hum Genet. 2012 Apr;57(4):235-7. doi: 10.1038/jhg.2012.9. Epub 2012 Feb 9. J Hum Genet. 2012. PMID: 22318345

9

Genome-wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels.

Yu CC, Furukawa M, Kobayashi K, Shikishima C, Cha PC, Sese J, Sugawara H, Iwamoto K, Kato T, Ando J, Toda T. Yu CC, et al. Among authors: cha pc. PLoS One. 2012;7(10):e47081. doi: 10.1371/journal.pone.0047081. Epub 2012 Oct 17. PLoS One. 2012. PMID: 23082141 Free PMC article.

10

Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium-glucose cotransporter 2 inhibitor.

Hamaguchi T, Hirota Y, Takeuchi T, Nakagawa Y, Matsuoka A, Matsumoto M, Awano H, Iijima K, Cha PC, Satake W, Toda T, Ogawa W. Hamaguchi T, et al. Among authors: cha pc. J Diabetes Investig. 2018 Sep;9(5):1224-1227. doi: 10.1111/jdi.12825. Epub 2018 Mar 25. J Diabetes Investig. 2018. PMID: 29476696 Free PMC article.

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