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au.\*:("GOTO, Yu-Ichi")

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Results 1 to 25 of 46

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Defect in normal developmental increase of the brain biogenic amine concentrations in the mecp2-null mouseIDE, Shuhei; ITOH, Masayuki; GOTO, Yu-Ichi et al.Neuroscience letters. 2005, Vol 386, Num 1, pp 14-17, issn 0304-3940, 4 p.Article

Granular Swollen Epithelial Cells: A Histologic and Diagnostic Marker for Mitochondrial NephropathyKOBAYASHI, Akimitsu; GOTO, Yu-Ichi; NAGATA, Michio et al.The American journal of surgical pathology. 2010, Vol 34, Num 2, pp 262-270, issn 0147-5185, 9 p.Article

The P86L Common Allele of CALHM1 Does Not Influence for Alzheimer Disease in Japanese CohortsINOUE, Ken; TANAKA, Noriko; YAMASHITA, Fumio et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 2, pp 532-535, issn 1552-4841, 4 p.Article

A novel D104G mutation in the adenine nucleotide translocator 1 gene in autosomal dominant progressive external ophthalmoplegia patients with mitochondrial DNAKOMAKI, Hirofumi; FUKAZAWA, Toshiyuki; HOUZEN, Hideki et al.Annals of neurology. 2002, Vol 51, Num 5, pp 645-648, issn 0364-5134Article

Elevated expression of beta-site amyloid precursor protein cleaving enzyme 2 in brains of patients with Down syndromeMOTONAGA, Kozo; ITOH, Masayuki; BECKER, Laurence E et al.Neuroscience letters. 2002, Vol 326, Num 1, pp 64-66, issn 0304-3940Article

An infant with a mitochondrial A3243G mutation demonstrating the melas phenotypeKANAUMI, Takeshi; HIROSE, Shinichi; GOTO, Yu-Ichi et al.Pediatric neurology. 2006, Vol 34, Num 3, pp 235-238, issn 0887-8994, 4 p.Article

Blockade of bombesin-like peptide receptors impairs inhibitory avoidance learning in miceSANTO-YAMADA, Yuko; YAMADA, Kazuyuki; WADA, Etsuko et al.Neuroscience letters. 2003, Vol 340, Num 1, pp 65-68, issn 0304-3940, 4 p.Article

Clinical and Genetic Features in a MELAS Child With a 3271T>C MutationCHOU, Hsiao-Feng; LIANG, Wen-Chen; QING ZHANG et al.Pediatric neurology. 2008, Vol 38, Num 2, pp 143-146, issn 0887-8994, 4 p.Article

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient miceFUKUDA, Tetsuya; ITOH, Masayuki; ICHIKAWA, Tomio et al.Journal of neuropathology and experimental neurology. 2005, Vol 64, Num 6, pp 537-544, issn 0022-3069, 8 p.Article

Fewer GABAergic interneurons, heightened anxiety and decreased high-frequency electroencephalogram components in Bronx waltzer mice, a model of hereditary deafnessMATSUDA, Yoshiki; INOUE, Yuki; IZUMI, Hitomi et al.Brain research. 2011, Vol 1373, pp 202-210, issn 0006-8993, 9 p.Article

Edaravone Inhibits DNA Peroxidation and Neuronal Cell Death in Neonatal Hypoxic-Ischemic Encephalopathy Model RatTAKIZAWA, Yuji; MIYAZAWA, Takahito; NONOYAMA, Shigeaki et al.Pediatric research. 2009, Vol 65, Num 6, pp 636-641, issn 0031-3998, 6 p.Article

Cochlear damage due to germanium-induced mitochondrial dysfunction in guinea pigsYAMASOBA, Tatsuya; GOTO, Yu-Ichi; KOMAKI, Hirofumi et al.Neuroscience letters. 2006, Vol 395, Num 1, pp 18-22, issn 0304-3940, 5 p.Article

Leber's hereditary optic neuropathy with dystonia in a Japanese familyWATANABE, Masaki; MITA, Shuji; TAKITA, Tomohiro et al.Journal of the neurological sciences. 2006, Vol 243, Num 1-2, pp 31-34, issn 0022-510X, 4 p.Article

Clinical implications of duplicated mtDNA in Pearson syndromeMURAKI, Kae; SAKURA, Nobuo; UEDA, Haruo et al.American journal of medical genetics. 2001, Vol 98, Num 3, pp 205-209, issn 0148-7299Conference Paper

Brainstem monoamine pathology of neonatal hypoxic-ischemic brain damage : A model of acute stage of neonatal asphyxiaSHIRAISHI, Mika; TAKIZAWA, Yuji; IDE, Shuhei et al.Brain research. 2008, Vol 1213, pp 120-126, issn 0006-8993, 7 p.Article

Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycosideMATSUNAGA, Tatsuo; KUMANOMIDO, Hiroshi; GOTO, Yu-Ichi et al.The Annals of otology, rhinology & laryngology. 2005, Vol 114, Num 2, pp 153-160, issn 0003-4894, 8 p.Article

Apoptosis is suspended in muscle of mitochondrial encephalomyopathiesIKEZOE, Koji; NAKAGAWA, Masahiro; YAN, Chuanzhu et al.Acta neuropathologica. 2002, Vol 103, Num 6, pp 531-540, issn 0001-6322Article

CYP2C8 haplotype structures and their influence on pharmacokinetics of paclitaxel in a Japanese populationSAITO, Yoshiro; KATORI, Noriko; KAMATANI, Naoyuki et al.Pharmacogenetics and genomics (Print). 2007, Vol 17, Num 7, pp 461-471, issn 1744-6872, 11 p.Article

ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutationKUBOTA, Takeo; FURUUMI, Hiroyasu; KAMODA, Tomohiro et al.American journal of medical genetics. 2004, Vol 129A, Num 3, pp 290-293, issn 0148-7299, 4 p.Article

Up-regulation of E2F-1 in Down's syndrome brain exhibiting neuropathological features of Alzheimer-type dementiaMOTONAGA, Kozo; ITOH, Masayuki; HIRAYAMA, Aya et al.Brain research. 2001, Vol 905, Num 1-2, pp 250-253, issn 0006-8993Article

Importance of CAG repeat length in childhood-onset dentatorubral―pallidoluysian atrophyMARUYAMA, Shinsuke; SAITO, Yoshiaki; MINAMI, Narihiro et al.Journal of neurology. 2012, Vol 259, Num 11, pp 2329-2334, issn 0340-5354, 6 p.Article

A Loss-of-Function Mutation in the FTSJ1 Gene Causes Nonsyndromic X-Linked Mental Retardation in a Japanese FamilyTAKANO, Kyoko; NAKAGAWA, Eiji; INOUE, Ken et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 4, pp 479-484, issn 1552-4841, 6 p.Article

Functional characterization of five novel CYP2C8 variants, G171s, R186x, R186g, K247R, and K383N, found in a Japanese populationHICHIYA, Hiroyuki; TANAKA-KAGAWA, Toshiko; MINAMI, Narihiro et al.Drug metabolism and disposition. 2005, Vol 33, Num 5, pp 630-636, issn 0090-9556, 7 p.Article

Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutationTAKESHITA, Eri; SAITO, Yoshiaki; GOTO, Yu-Ichi et al.Journal of the neurological sciences. 2011, Vol 308, Num 1-2, pp 168-172, issn 0022-510X, 5 p.Article

Sexually Dimorphic Effect of the Val66Met Polymorphism of BDNF on Susceptibility to Alzheimer's Disease: New Data and Meta-AnalysisFUKUMOTO, Noriko; FUJII, Takashi; HYMAN, Bradley T et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 1, pp 235-242, issn 1552-4841, 8 p.Article

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