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De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activity.
Nishi A, Numata S, Tajima A, Zhu X, Ito K, Saito A, Kato Y, Kinoshita M, Shimodera S, Ono S, Ochi S, Imamura A, Kurotaki N, Ueno SI, Iwata N, Fukui K, Imoto I, Kamiya A, Ohmori T. Nishi A, et al. Among authors: kinoshita m. Sci Rep. 2017 Jun 6;7(1):2887. doi: 10.1038/s41598-017-02792-z. Sci Rep. 2017. PMID: 28588275 Free PMC article.
DNA methylation signatures of peripheral leukocytes in schizophrenia.
Kinoshita M, Numata S, Tajima A, Shimodera S, Ono S, Imamura A, Iga J, Watanabe S, Kikuchi K, Kubo H, Nakataki M, Sumitani S, Imoto I, Okazaki Y, Ohmori T. Kinoshita M, et al. Neuromolecular Med. 2013 Mar;15(1):95-101. doi: 10.1007/s12017-012-8198-6. Epub 2012 Sep 9. Neuromolecular Med. 2013. PMID: 22961555
Missense variants of the alanine:glyoxylate aminotransferase 2 gene are not associated with Japanese schizophrenia patients.
Yoshino Y, Abe M, Numata S, Ochi S, Mori Y, Ishimaru T, Kinoshita M, Umehara H, Yamazaki K, Mori T, Ohmori T, Ueno S. Yoshino Y, et al. Among authors: kinoshita m. Prog Neuropsychopharmacol Biol Psychiatry. 2014 Aug 4;53:137-41. doi: 10.1016/j.pnpbp.2014.04.002. Epub 2014 Apr 12. Prog Neuropsychopharmacol Biol Psychiatry. 2014. PMID: 24727203
Blood diagnostic biomarkers for major depressive disorder using multiplex DNA methylation profiles: discovery and validation.
Numata S, Ishii K, Tajima A, Iga J, Kinoshita M, Watanabe S, Umehara H, Fuchikami M, Okada S, Boku S, Hishimoto A, Shimodera S, Imoto I, Morinobu S, Ohmori T. Numata S, et al. Among authors: kinoshita m. Epigenetics. 2015;10(2):135-41. doi: 10.1080/15592294.2014.1003743. Epub 2015 Jan 14. Epigenetics. 2015. PMID: 25587773 Free PMC article.
3,418 results