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Plos One|December 17, 2016
Plasma Metabolites Predict Severity of Depression and Suicidal Ideation in Psychiatric Patients-A Multicenter Pilot AnalysisDaiki Setoyama, Takahiro A Kato, Ryota Hashimoto, et al.
European Journal of Clinical Pharmacology|February 5, 2005
Haplotype structures of EPHX1 and their effects on the metabolism of carbamazepine-10,11-epoxide in Japanese epileptic patientsYukiko Nakajima, Yoshiro Saito, Kisho Shiseki, et al.
Mitochondrion|January 13, 2010
Extensive screening system using suspension array technology to detect mitochondrial DNA point mutationsYutaka Nishigaki, Hitomi Ueno, Jorida Coku, et al.
The American Journal of Pathology|April 22, 2017
Pathologic Active mTOR Mutation in Brain Malformation with Intractable Epilepsy Leads to Cell-Autonomous Migration DelaySae Hanai, Sayuri Sukigara, Hongmei Dai, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 18, 2003
Six novel nonsynonymous CYP1A2 gene polymorphisms: catalytic activities of the naturally occurring variant enzymesNorie Murayama, Akiko Soyama, Yoshiro Saito, et al.
FEBS Open Bio|April 9, 2015
Impaired respiratory function in MELAS-induced pluripotent stem cells with high heteroplasmy levelsMasaki Kodaira, Hideyuki Hatakeyama, Shinsuke Yuasa, et al.
Drug Metabolism and Pharmacokinetics|March 17, 2005
Single nucleotide polymorphisms and haplotypes of CYP1A2 in a Japanese populationAkiko Soyama, Yoshiro Saito, Nobumitsu Hanioka, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 9, 2009
Sexually dimorphic effect of the Val66Met polymorphism of BDNF on susceptibility to Alzheimer's disease: New data and meta-analysisNoriko Fukumoto, Takashi Fujii, Onofre Combarros, et al.
Biomarker Research|October 12, 2017
Re-evaluation of soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for early diagnosis of dementia disordersWataru Araki, Kotaro Hattori, Kazutomi Kanemaru, et al.
Drug Metabolism and Pharmacokinetics|December 25, 2004
Eleven novel single nucleotide polymorphisms in the NR1I2 (PXR) gene, four of which induce non-synonymous amino acid alterationsSatoru Koyano, Kouichi Kurose, Shogo Ozawa, et al.
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