未登录Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: A cybrid study
Chen, Jing; Hattori, Yukiko; Nakajima, Kazuo; Eizawa, Takayuki; Ehara, Takashi; Koyama, Masamichi; Hirai, Tetsuya; Fukuda, Youji; Kinoshita, Moritoshi; Sugiyama, Atsushi; Hayashi, Jun-Ichi; Onaya, Toshimasa; Kobayashi, Tetsuro; Tawata, Masato
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收藏Thermolabile phenotype of carnitine palmitoyltransferase II variations as a predisposing factor for influenza-associated encephalopathy
Chen, Y; Mizuguchi, H; Yao, D; Ide, M; Kuroda, Y; Shigematsu, Y; Yamaguchi, S; Yamaguchi, M; Kinoshita, M; Kido, H
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收藏Diverse p53 gene aberration in hepatocellular carcinoma detected by dual-color fluorescence in situ hybridization
Kondo, M; Marusawa, H; Ueda, Y; Katsurada, A; Kawasome, C; Takami, S; Kinoshita, M; Ikai, I; Kondo, M; Chiba, T
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收藏Heteroplasmic mitochondrial DNA 3310 mutation in NADN dehydrogenase subunit 1 associated with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation in a single patient
Hattori, Y; Nakajima, K; Eizawa, T; Ehara, T; Koyama, M; Hirai, T; Fukuda, Y; Kinoshita, M
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收藏A new mutation of the fukutin gene in a non-Japanese patient
Silan, F; Yoshioka, M; Kobayashi, K; Simsek, E; Tunc, M; Alper, M; Cam, M; Guven, A; Fukuda, Y; Kinoshita, M; Kocabay, K; Toda, T
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收藏Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin
Kobayashi, K; Sasaki, J; Kondo-Iida, E; Fukuda, Y; Kinoshita, M; Sunada, Y; Nakamura, Y; Toda, T
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收藏Association of amino acid sequence in the PKR-eIF2 phosphorylation homology domain and response to interferon therapy
Chayama, K; Suzuki, F; Tsubota, A; Kobayashi, M; Arase, Y; Saitoh, S; Suzuki, Y; Murashima, N; Ikeda, K; Takahashi, N; Kinoshita, M; Kumada, H
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收藏Real-time automated PCR for early diagnosis and monitoring of cytomegalovirus infection after bone marrow transplantation
Machida, U; Kami, M; Fukui, T; Kazuyama, Y; Kinoshita, M; Tanaka, Y; Kanda, Y; Ogawa, S; Honda, H; Chiba, S; Mitani, K; Muto, Y; Osumi, K; Kimura, S; Hirai, H
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收藏Hepatitis delta virus genotype IIb predominates in an endemic area, Okinawa, Japan
Sakugawa, H; Nakasone, H; Nakayoshi, T; Kawakami, Y; Miyazato, S; Kinjo, F; Saito, A; Ma, SP; Hotta, H; Kinoshita, M
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收藏Heterogeneous point mutations of the p53 gene in pulmonary fibrosis
Hojo, S; Fujita, J; Yamadori, I; Kamei, T; Yoshinouchi, T; Ohtsuki, Y; Okada, H; Bandoh, S; Yamaji, Y; Takahara, J; Fukui, T; Kinoshita, M
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收藏The relationship among HBV genome integration, p53 gene mutation, telomerase activity and genetic instability in HBsAg-negative and anti-HCV positive hepatocellular carcinoma in Japan.
Matsuzaki, Y; Chiba, T; Saito, Y; Doy, M; Itoh, S; Asaoka, H; Shoda, J; Tanaka, N; Hadama, T; Kinoshita, M
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