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Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.
Ishizuka K, Fujita Y, Kawabata T, Kimura H, Iwayama Y, Inada T, Okahisa Y, Egawa J, Usami M, Kushima I, Uno Y, Okada T, Ikeda M, Aleksic B, Mori D, Someya T, Yoshikawa T, Iwata N, Nakamura H, Yamashita T, Ozaki N. Ishizuka K, et al. Among authors: yamashita t. Transl Psychiatry. 2017 Aug 1;7(8):e1184. doi: 10.1038/tp.2017.173. Transl Psychiatry. 2017. PMID: 28763059 Free PMC article.
A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.
Kimura H, Fujita Y, Kawabata T, Ishizuka K, Wang C, Iwayama Y, Okahisa Y, Kushima I, Morikawa M, Uno Y, Okada T, Ikeda M, Inada T, Branko A, Mori D, Yoshikawa T, Iwata N, Nakamura H, Yamashita T, Ozaki N. Kimura H, et al. Among authors: yamashita t. Transl Psychiatry. 2017 Aug 22;7(8):e1214. doi: 10.1038/tp.2017.170. Transl Psychiatry. 2017. PMID: 28892071 Free PMC article.
[Risk factors and preventive measures].
Nakamura H, Yamashita T. Nakamura H, et al. Among authors: yamashita t. Nihon Rinsho. 1999 Jul;57(7):1609-13. Nihon Rinsho. 1999. PMID: 10429465 Review. Japanese.
[Fenofibrate].
Yamashita T, Nakamura H. Yamashita T, et al. Nihon Rinsho. 2001 Mar;59 Suppl 3:618-24. Nihon Rinsho. 2001. PMID: 11347142 Review. Japanese. No abstract available.
6,895 results