| A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies Y Goto, I Nonaka, S Horai Nature 348 (6302), 651-653, 1990 | 2494 | 1990 |
| Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice N Ishihara, M Nomura, A Jofuku, H Kato, SO Suzuki, K Masuda, H Otera, ... Nature cell biology 11 (8), 958-966, 2009 | 1136 | 2009 |
| Hydrogen sulfide increases glutathione production and suppresses oxidative stress in mitochondria Y Kimura, YI Goto, H Kimura Antioxidants & redox signaling 12 (1), 1-13, 2010 | 778 | 2010 |
| A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA T Kadowaki, H Kadowaki, Y Mori, K Tobe, R Sakuta, Y Suzuki, Y Tanabe, ... New England Journal of Medicine 330 (14), 962-968, 1994 | 759 | 1994 |
| Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction. JL Hayashi, S Ohta, A Kikuchi, M Takemitsu, Y Goto, I Nonaka Proceedings of the National Academy of Sciences 88 (23), 10614-10618, 1991 | 715 | 1991 |
| Inter-mitochondrial complementation: mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA K Nakada, K Inoue, T Ono, K Isobe, A Ogura, YI Goto, I Nonaka, ... Nature medicine 7 (8), 934-940, 2001 | 511 | 2001 |
| Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS) A correlative study of the clinical features and mitochondrial DNA mutation Y Goto, S Horai, T Matsuoka, Y Koga, K Nihei, M Kobayashi, I Nonaka Neurology 42 (3), 545-545, 1992 | 507 | 1992 |
| Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes K Inoue, K Nakada, A Ogura, K Isobe, Y Goto, I Nonaka, JI Hayashi Nature genetics 26 (2), 176-181, 2000 | 458 | 2000 |
| Mutations in the integrin α7 gene cause congenital myopathy YK Hayashi, FL Chou, E Engvall, M Ogawa, C Matsuda, S Hirabayashi, ... Nature genetics 19 (1), 94-97, 1998 | 455 | 1998 |
| A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) Y Goto, I Nonaka, S Horai Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1097 (3), 238-240, 1991 | 414 | 1991 |
| Mitochondrial Lon protease regulates mitochondrial DNA copy number and transcription by selective degradation of mitochondrial transcription factor A (TFAM) Y Matsushima, Y Goto, LS Kaguni Proceedings of the National Academy of Sciences 107 (43), 18410-18415, 2010 | 310 | 2010 |
| Delayed Maturation of Neuronal Architecture and Synaptogenesis in Cerebral Cortex of Mecp2-Deficient Mice T Fukuda, M Itoh, T Ichikawa, K Washiyama, Y Goto Journal of Neuropathology & Experimental Neurology 64 (6), 537-544, 2005 | 271 | 2005 |
| Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population H Fukushima‐Uesaka, Y Saito, H Watanabe, K Shiseki, M Saeki, ... Human mutation 23 (1), 100-100, 2004 | 239 | 2004 |
| Comparative analyses of copy-number variation in autism spectrum disorder and schizophrenia reveal etiological overlap and biological insights I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Okada, Y Uno, ... Cell reports 24 (11), 2838-2856, 2018 | 214 | 2018 |
| Strongly succinate dehydrogenase–reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes H Hasegawa, T Matsuoka, Y Goto, I Nonaka Annals of Neurology: Official Journal of the American Neurological …, 1991 | 209 | 1991 |
| Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease Y Kirino, Y Goto, Y Campos, J Arenas, T Suzuki Proceedings of the National Academy of Sciences 102 (20), 7127-7132, 2005 | 201 | 2005 |
| Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23. 3-q24. 1 M Mikami, T Yasuda, A Terao, M Nakamura, S Ueno, H Tanabe, T Tanaka, ... The American Journal of Human Genetics 65 (3), 745-751, 1999 | 191 | 1999 |
| Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles S Noguchi, Y Keira, K Murayama, M Ogawa, M Fujita, G Kawahara, Y Oya, ... Journal of Biological Chemistry 279 (12), 11402-11407, 2004 | 183 | 2004 |
| Human mitochondria and mitochondrial genome function as a single dynamic cellular unit. JL Hayashi, M Takemitsu, Y Goto, I Nonaka The journal of cell biology 125 (1), 43-50, 1994 | 169 | 1994 |
| Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca2+ channels Y Endo, S Noguchi, Y Hara, YK Hayashi, K Motomura, S Miyatake, ... Human molecular genetics 24 (3), 637-648, 2015 | 161 | 2015 |
