Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Massive layer of pure anorthosite on the MoonYamamoto, S. ; Nakamura, R. ; Matsunaga, T. ; Ogawa, Y. ; Ishihara, Y. ; Morota, T. ; Hirata, N. ; Ohtake, M. ; Hiroi, T. ; Yokota, Y. ; Haruyama, J.Geophysical research letters, 2012-07, Vol.39 (13), p.np-n/a [Periódico revisado por pares]Washington, DC: Blackwell Publishing LtdTexto completo disponível |
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2 |
Material Type: Artigo
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A new type of pyroclastic deposit on the Moon containing Fe-spinel and chromiteYamamoto, S. ; Nakamura, R. ; Matsunaga, T. ; Ogawa, Y. ; Ishihara, Y. ; Morota, T. ; Hirata, N. ; Ohtake, M. ; Hiroi, T. ; Yokota, Y. ; Haruyama, J.Geophysical research letters, 2013-09, Vol.40 (17), p.4549-4554 [Periódico revisado por pares]Washington, DC: Blackwell Publishing LtdTexto completo disponível |
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3 |
Material Type: Artigo
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Novel biallelic mutations in the PNPT1 gene encoding a mitochondrial‐RNA‐import protein PNPase cause delayed myelinationSato, R. ; Arai‐Ichinoi, N. ; Kikuchi, A. ; Matsuhashi, T. ; Numata‐Uematsu, Y. ; Uematsu, M. ; Fujii, Y. ; Murayama, K. ; Ohtake, A. ; Abe, T. ; Kure, S.Clinical genetics, 2018-02, Vol.93 (2), p.242-247 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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4 |
Material Type: Artigo
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Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2Kishita, Yoshihito ; Shimura, Masaru ; Kohda, Masakazu ; Fushimi, Takuya ; Nitta, Kazuhiro R. ; Yatsuka, Yukiko ; Hirose, Shinichi ; Ideguchi, Hiroshi ; Ohtake, Akira ; Murayama, Kei ; Okazaki, YasushiHuman mutation, 2021-11, Vol.42 (11), p.1422-1428 [Periódico revisado por pares]United States: Hindawi LimitedTexto completo disponível |
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5 |
Material Type: Artigo
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De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiencyMcFarland, Robert ; Kirby, Denise M. ; Fowler, Kerry J. ; Ohtake, Akira ; Ryan, Michael T. ; Amor, David J. ; Fletcher, Janice M. ; Dixon, Joanne W. ; Collins, Felicity A. ; Turnbull, Douglass M. ; Taylor, Robert W. ; Thorburn, David R.Annals of neurology, 2004-01, Vol.55 (1), p.58-64 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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6 |
Material Type: Artigo
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The widespread occurrence of high-calcium pyroxene in bright-ray craters on the Moon and implications for lunar-crust compositionOgawa, Y. ; Matsunaga, T. ; Nakamura, R. ; Saiki, K. ; Ohtake, M. ; Hiroi, T. ; Takeda, H. ; Arai, T. ; Yokota, Y. ; Yamamoto, S. ; Hirata, N. ; Sugihara, T. ; Sasaki, S. ; Haruyama, J. ; Morota, T. ; Honda, C. ; Demura, H. ; Kitazato, K. ; Terazono, J. ; Asada, N.Geophysical research letters, 2011-09, Vol.38 (17), p.n/a [Periódico revisado por pares]Washington, DC: Blackwell Publishing LtdTexto completo disponível |
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7 |
Material Type: Artigo
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A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiencyYatsuka, Yukiko ; Kishita, Yoshihito ; Formosa, Luke E. ; Shimura, Masaru ; Nozaki, Fumihito ; Fujii, Tatsuya ; Nitta, Kazuhiro R. ; Ohtake, Akira ; Murayama, Kei ; Ryan, Michael T. ; Okazaki, YasushiClinical genetics, 2020-08, Vol.98 (2), p.155-165 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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8 |
Material Type: Artigo
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Impact of measuring heteroplasmy of a pathogenic mitochondrial DNA variant at the single‐cell level in individuals with mitochondrial diseaseImai‐Okazaki, Atsuko ; Nitta, Kazuhiro R. ; Yatsuka, Yukiko ; Sugiura, Ayumu ; Arao, Masato ; Shimura, Masaru ; Ebihara, Tomohiro ; Onuki, Takanori ; Ichimoto, Keiko ; Ohtake, Akira ; Murayama, Kei ; Okazaki, YasushiJournal of inherited metabolic disease, 2022-11, Vol.45 (6), p.1143-1150 [Periódico revisado por pares]Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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9 |
Material Type: Artigo
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Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's diseaseKirby, Denise M. ; Boneh, Avihu ; Chow, C. W. ; Ohtake, Akira ; Ryan, Michael T. ; Thyagarajan, Dominic ; Thorburn, David R.Annals of neurology, 2003-10, Vol.54 (4), p.473-478 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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10 |
Material Type: Artigo
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Molecular diagnosis of mitochondrial respiratory chain disorders in Japan: Focusing on mitochondrial DNA depletion syndromeYamazaki, Taro ; Murayama, Kei ; Compton, Alison G ; Sugiana, Canny ; Harashima, Hiroko ; Amemiya, Shin ; Ajima, Masami ; Tsuruoka, Tomoko ; Fujinami, Ayako ; Kawachi, Emi ; Kurashige, Yoshiko ; Matsushita, Kenshi ; Wakiguchi, Hiroshi ; Mori, Masato ; Iwasa, Hiroyasu ; Okazaki, Yasushi ; Thorburn, David R ; Ohtake, AkiraPediatrics international, 2014-04, Vol.56 (2), p.180-187 [Periódico revisado por pares]Australia: Blackwell Publishing LtdTexto completo disponível |