Photoactivation of Strong Photoluminescence in Superacid-Treated Monolayer Molybdenum Disulfide
Yamada, Yuki, Shinokita, Keisuke, Okajima, Yasuo, Takeda, Sakura N, Matsushita, Yuji, Takei, Kuniharu, Yoshimura, Takeshi, Ashida, Atsushi, Fujimura, Norifumi, Matsuda, Kazunari, Kiriya, Daisuke
Published in ACS applied materials & interfaces (12.08.2020)
Published in ACS applied materials & interfaces (12.08.2020)
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Lattice distortion of porous Si by Li absorption using two-dimensional photoelectron diffraction
Nouh, El Said A., Takeda, Sakura N., Matsui, Fumihiko, Hattori, Ken, Sakata, Tomohiro, Maejima, Naoyuki, Matsui, Hirosuke, Matsuda, Hiroyuki, Matsushita, Tomohiro, Tóth, László, Morita, Makoto, Kitagawa, Satoshi, Ishii, Ryo, Fujita, Masayoshi, Yasuda, Kaoru, Daimon, Hiroshi
Published in Journal of materials science (01.01.2014)
Published in Journal of materials science (01.01.2014)
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Differential diagnosis of neonatal mild hypergalactosaemia detected by mass screening: Clinical significance of portal vein imaging
Nishimura, Y., Tajima, G., Bahagia, A. Dwi, Sakamoto, A., Ono, H., Sakura, N., Naito, K., Hamakawa, M., Yoshii, C., Kubota, M., Kobayashi, K., Saheki, T.
Published in Journal of inherited metabolic disease (01.01.2004)
Published in Journal of inherited metabolic disease (01.01.2004)
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Total analysis of surface structure and properties by UHV transfer system
Yamatani, Hiroshi, Hattori, Ken, Matsuta, Takahisa, Ito, Takuji, Nohno, Tomohito, Hori, Madoka, Miyatake, Yutaka, Konno, Shigenori, Tanaka, Tsukasa, Hamada, Yoji, Katagiri, Hiroshi, Hibi, Mikiharu, Miyai, Toshiki, Hashimoto, Mie, Kataoka, Keita, Tatsuta, Takeshi, Hattori, Azusa N., Higashi, Naoto, Honda, Mitsunori, Masunaga, Norifumi, Mino, Hiroaki, Yasui, Shintaro, Nayeem, Janathul, Shimizu, Tatsuya, Takahashi, Nobuaki, Kato, Yukako, Sakai, Chikako, Yoshimura, Masashi, Takeda, Sakura N., Matsui, Fumihiko, Daimon, Hiroshi
Published in Surface science (15.11.2007)
Published in Surface science (15.11.2007)
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Conference Proceeding
Gas chromatographic–mass spectrometric newborn screening for propionic acidaemia by targeting methylcitrate in dried filter‐paper urine samples
Kuhara, T., Ohse, M., Inoue, Y., Yorifuji, T., Sakura, N., Mitsubuchi, H., Endo, F., Ishimatu, J.
Published in Journal of inherited metabolic disease (01.05.2002)
Published in Journal of inherited metabolic disease (01.05.2002)
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Novel drug delivery system to bone using acidic oligopeptide: pharmacokinetic characteristics and pharmacological potential
Sekido, T, Sakura, N, Higashi, Y, Miya, K, Nitta, Y, Nomura, M, Sawanishi, H, Morito, K, Masamune, Y, Kasugai, S, Yokogawa, K, Miyamoto, K
Published in Journal of drug targeting (01.01.2001)
Published in Journal of drug targeting (01.01.2001)
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Type II Citrullinaemia (Citrin Deficiency) in a Neonate with Hypergalactosaemia Detected by Mass Screening
Naito, E., Ito, M., Matsuura, S., Yokota, I., Saijo, T., Ogawa, Y., Kitamura, S., Kobayashi, K., Saheki, T., Nishimura, Y., Sakura, N., Kuroda, Y.
Published in Journal of inherited metabolic disease (01.02.2002)
Published in Journal of inherited metabolic disease (01.02.2002)
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Spectroscopic measurements of excited particles in a N2 gas RF plasma-assisted carbon laser ablation
BRATESCU, M. A, SAKURA, N, YAMAOKA, D, SAKAI, Y, SUGAWARA, H, SUDA, Y
Published in Applied physics. A, Materials science & processing (01.09.2004)
Published in Applied physics. A, Materials science & processing (01.09.2004)
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Conference Proceeding
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Selective screening for fatty acid oxidation disorders by tandem mass spectrometry: difficulties in practical discrimination
Shigematsu, Yosuke, Hirano, Satoko, Hata, Ikue, Tanaka, Yukie, Sudo, Masakatsu, Tajima, Tsuyoshi, Sakura, Nobuo, Yamaguchi, Seiji, Takayanagi, Masaki
Published in Journal of chromatography. B (15.07.2003)
Published in Journal of chromatography. B (15.07.2003)
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Conference Proceeding
The mitochondrial acetoacetyl‐CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2‐deficient patients with some residual T2 activity
Fukao, T., Zhang, G.‐X., Sakura, N., Kubo, T., Yamaga, H., Hazama, A., Kohno, Y., Matsuo, N., Kondo, M., Yamaguchi, S., Shigematsu, Y., Kondo, N.
Published in Journal of inherited metabolic disease (01.01.2003)
Published in Journal of inherited metabolic disease (01.01.2003)
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Methylenetetrahydrofolate reductase 677C>T mutation and epilepsy
Ono, H., Sakamoto, A., Mizoguchi, N., Sakura, N.
Published in Journal of inherited metabolic disease (01.07.2000)
Published in Journal of inherited metabolic disease (01.07.2000)
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Journal Article
Congenital porto–left renal venous shunt as a cause of galactosaemia
Mizoguchi, N., Sakura, N., Ono, H., Naito, K., Hamakawa, M.
Published in Journal of inherited metabolic disease (01.02.2001)
Published in Journal of inherited metabolic disease (01.02.2001)
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Journal Article
A simple and rapid enzymatic assay for the branched‐chain α‐ketoacid dehydrogenase complex using high‐performance liquid chromatography
Tajima, G., Yofune, H., Bahagia Febriani, A. D., Nishimura, Y., Ono, H., Sakura, N.
Published in Journal of inherited metabolic disease (01.01.2004)
Published in Journal of inherited metabolic disease (01.01.2004)
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