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1
Massive layer of pure anorthosite on the Moon
Massive layer of pure anorthosite on the Moon
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Massive layer of pure anorthosite on the Moon

Yamamoto, 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 Ltd

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2
A new type of pyroclastic deposit on the Moon containing Fe-spinel and chromite
A new type of pyroclastic deposit on the Moon containing Fe-spinel and chromite
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A new type of pyroclastic deposit on the Moon containing Fe-spinel and chromite

Yamamoto, 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 Ltd

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3
Novel biallelic mutations in the PNPT1 gene encoding a mitochondrial‐RNA‐import protein PNPase cause delayed myelination
Novel biallelic mutations in the PNPT1 gene encoding a mitochondrial‐RNA‐import protein PNPase cause delayed myelination
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Novel biallelic mutations in the PNPT1 gene encoding a mitochondrial‐RNA‐import protein PNPase cause delayed myelination

Sato, 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 Ltd

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4
Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2
Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2
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Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2

Kishita, Yoshihito ; Shimura, Masaru ; Kohda, Masakazu ; Fushimi, Takuya ; Nitta, Kazuhiro R. ; Yatsuka, Yukiko ; Hirose, Shinichi ; Ideguchi, Hiroshi ; Ohtake, Akira ; Murayama, Kei ; Okazaki, Yasushi

Human mutation, 2021-11, Vol.42 (11), p.1422-1428 [Periódico revisado por pares]

United States: Wiley Periodicals Inc

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5
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency
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De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

McFarland, 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 Company

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6
A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency
A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency
Material Type:
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A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency

Yatsuka, Yukiko ; Kishita, Yoshihito ; Formosa, Luke E. ; Shimura, Masaru ; Nozaki, Fumihito ; Fujii, Tatsuya ; Nitta, Kazuhiro R. ; Ohtake, Akira ; Murayama, Kei ; Ryan, Michael T. ; Okazaki, Yasushi

Clinical genetics, 2020-08, Vol.98 (2), p.155-165 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Impact of measuring heteroplasmy of a pathogenic mitochondrial DNA variant at the single‐cell level in individuals with mitochondrial disease
Impact of measuring heteroplasmy of a pathogenic mitochondrial DNA variant at the single‐cell level in individuals with mitochondrial disease
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Impact of measuring heteroplasmy of a pathogenic mitochondrial DNA variant at the single‐cell level in individuals with mitochondrial disease

Imai‐Okazaki, Atsuko ; Nitta, Kazuhiro R. ; Yatsuka, Yukiko ; Sugiura, Ayumu ; Arao, Masato ; Shimura, Masaru ; Ebihara, Tomohiro ; Onuki, Takanori ; Ichimoto, Keiko ; Ohtake, Akira ; Murayama, Kei ; Okazaki, Yasushi

Journal of inherited metabolic disease, 2022-11, Vol.45 (6), p.1143-1150 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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8
Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease
Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease
Material Type:
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Low mutant load of mitochondrial DNA G13513A mutation can cause Leigh's disease

Kirby, 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 Company

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9
Featureless spectra on the Moon as evidence of residual lunar primordial crust
Featureless spectra on the Moon as evidence of residual lunar primordial crust
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Featureless spectra on the Moon as evidence of residual lunar primordial crust

Yamamoto, S. ; Nakamura, R. ; Matsunaga, T. ; Ogawa, Y. ; Ishihara, Y. ; Morota, T. ; Hirata, N. ; Ohtake, M. ; Hiroi, T. ; Yokota, Y. ; Haruyama, J.

Journal of geophysical research. Planets, 2015-12, Vol.120 (12), p.2190-2205 [Periódico revisado por pares]

Washington: Blackwell Publishing Ltd

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10
Molecular diagnosis of mitochondrial respiratory chain disorders in Japan: Focusing on mitochondrial DNA depletion syndrome
Molecular diagnosis of mitochondrial respiratory chain disorders in Japan: Focusing on mitochondrial DNA depletion syndrome
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Molecular diagnosis of mitochondrial respiratory chain disorders in Japan: Focusing on mitochondrial DNA depletion syndrome

Yamazaki, 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, Akira

Pediatrics international, 2014-04, Vol.56 (2), p.180-187 [Periódico revisado por pares]

Australia: Blackwell Publishing Ltd

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