中学1年：生き方を探る - 人から学び共に考えよう -(II.キャリア形成を軸とした総合人間科の取り組み) (2006)
中野, 和之,
NAKANO, K.,
今村, 敦司,
IMAMURA, A.,
西川, 陽子,
NISHIKAWA, Y.,
...
国立情報学研究所で電子化したコンテンツを使用している。
4．SSH評価部会中間報告 A: SSH評価グループ (VI.研究グループ中間報告) (2006)
今村, 敦司,
IMAMURA, A.,
藤田, 高弘,
FUJITA, T.,
嘉賀, 正泰,
KAGA, M.,
...
国立情報学研究所で電子化したコンテンツを使用している。
中学3年生 : 「国際理解と平和Ⅰ」 : 広島から平和を科学する （Ⅱ. キャリア形成を軸とした総合人間科の取り組み） (2005)
仲田, 恵子,
Nakata, K.,
川田, 基生,
Kawata, M.,
今村, 敦司,
Imamura, A.,
...
国立情報学研究所で電子文書化したコンテンツを使用している。
高校１年生 : 生命と環境Ⅱ : 共に生きる！地球と私たち （Ⅱ. キャリア形成を軸とした総合人間科の取り組み） (2004)
山田, 孝,
Yamada, T.,
三小田, 博昭,
Sankoda, H.,
高橋, 伸行,
Takahashi, N.,
...
国立情報学研究所で電子化したコンテンツを使用している。
高校3年生 : 生き方を探るII : 丘を越え行こうよ 口笛吹きつつ(III.キャリア形成を軸とした総合人間科の取り組み) (2003)
渡辺, 武志,
WATANABE, T.,
飯島, 幸久,
IIJIMA, Y.,
高橋, 伸行,
TAKAHASHI, N.,
...
国立情報学研究所で電子化したコンテンツを使用している。
Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient (2000)
Shimozawa, N.,
Zhang, Z.,
Imamura, A.,
Suzuki, Y.,
Fujiki, Y.,
Tsukamoto, T.,
...
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1 (2000)
Imamura, A.,
Shimozawa, N.,
Suzuki, Y.,
Zhang, Z.,
Tsukamoto, T.,
Fujiki, Y.,
...
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients (1999)
Shimozawa, N.,
Zhang, Z.,
Suzuki, S.,
Imamura, A.,
Tsukamoto, T.,
Osumi, T.,
...
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders (1999)
Shimozawa, N.,
Suzuki, Y.,
Zhang, Z.,
Imamura, A.,
Toyama, R.,
Mukai, S.,
...
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders (1999)
Zhang, Z.,
Suzuki, Y.,
Shimozawa, N.,
Fukuda, S.,
Imamura, A.,
Tsukamoto, T.,
...
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders (1999)
Shimozawa, N.,
Imamura, A.,
Zhang, Z.,
Suzuki, Y.,
Orii, T.,
Tsukamoto, T.,
...
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders (1999)
Shimozawa, N,
Suzuki, Y,
Zhang, Z,
Imamura, A,
Toyama, R,
Mukai, S,
...
Transmission Electron Microscopy Studies of Growth and Interface Structure of Chemically Vapour Deposited TiC and TiN Films on WC-Co Alloy Substrates. (1998)
Echigoya, J.,
Liu, Zheng-Tang,
Imamura, A.,
Takatsu, S.
The interface structures between deposits and substrates and the growth microstructure of deposits are important factors in the wear resistance of coating films. tin and tic films prepared by the...
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13 (1998)
Shimozawa, N.,
Suzuki, Y.,
Zhang, Z.,
Imamura, A.,
Tsukamoto, T.,
Osumi, T.,
...
Genetic basis of peroxisomes-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts (letter) (1998)
Shimozawa, N.,
Suzuki, Y.,
Zhang, Z.,
Imamura, A.,
Kondo, N.,
Kinoshita, N.,
...
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders (1998)
Imamura, A,
Tamura, S,
Shimozawa, N,
Suzuki, Y,
Zhang, Z,
Tsukamoto, T,
...
Identification of a novel frameshift mutation in a Japanese adrenoleukodystrophy patient (1995)
Song, X.Q.,
Fukao, T.,
Suzuki, Y.,
Imamura, A.,
Uchiyama, A.,
Shimozawa, N.,
...
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
Tamura, S,
Matsumoto, N,
Imamura, A,
Shimozawa, N,
Suzuki, Y,
Kondo, N,
...
The peroxisome biogenesis disorders (PBDs), including Zellweger syndrome (ZS), neonatal adrenoleucodystrophy (NALD) and infantile Refsum disease (IRD), are fatal autosomal recessive diseases caused...
Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.
Imamura, A,
Tsukamoto, T,
Shimozawa, N,
Suzuki, Y,
Zhang, Z,
Imanaka, T,
...
Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.
Shimozawa, N,
Suzuki, Y,
Zhang, Z,
Imamura, A,
Kondo, N,
Kinoshita, N,
...
Preoperative assessment for laparoscopic cholecystectomy: feasibility of using spiral computed tomography.
Kwon, A H,
Inui, H,
Imamura, A,
Uetsuji, S,
Kamiyama, Y
OBJECTIVE: The authors investigated the preoperative feasibility of using spiral computed tomography (SCT) after intravenous infusion cholangiography (IVC-SCT) for laparoscopic cholecystectomy....
Preoperative assessment for laparoscopic cholecystectomy: feasibility of using spiral computed tomography.
Kwon, A H,
Inui, H,
Imamura, A,
Uetsuji, S,
Kamiyama, Y
OBJECTIVE: The authors investigated the preoperative feasibility of using spiral computed tomography (SCT) after intravenous infusion cholangiography (IVC-SCT) for laparoscopic cholecystectomy....
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
Tamura, S,
Matsumoto, N,
Imamura, A,
Shimozawa, N,
Suzuki, Y,
Kondo, N,
...
The peroxisome biogenesis disorders (PBDs), including Zellweger syndrome (ZS), neonatal adrenoleucodystrophy (NALD) and infantile Refsum disease (IRD), are fatal autosomal recessive diseases caused...
Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.
Imamura, A,
Tsukamoto, T,
Shimozawa, N,
Suzuki, Y,
Zhang, Z,
Imanaka, T,
...
Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.
Shimozawa, N,
Suzuki, Y,
Zhang, Z,
Imamura, A,
Kondo, N,
Kinoshita, N,
...
Mucosal immune defence mechanisms in enterocolitis complicating Hirschsprung's disease.
Imamura, A,
Puri, P,
O'Briain, D S,
Reen, D J
Enterocolitis remains an important cause of morbidity and mortality in Hirschsprung's disease. The aetiology of enterocolitis is uncertain-ischaemic and bacterial causes and recently, rotavirus...
Microsatellite instability in patients with multiple primary cancers of the gastrointestinal tract
Yamashita, K,
Arimura, Y,
Kurokawa, S,
Itoh, F,
Endo, T,
Hirata, K,
...
BACKGROUND—Little is known about the genetic alterations in multiple primary cancers of the gastrointestinal tract. Microsatellite instability (MSI) is frequently observed in hereditary...
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders
Shimozawa, N.,
Imamura, A.,
Zhang, Z.,
Suzuki, Y.,
Orii, T.,
Tsukamoto, T.,
...
Peroxisome biogenesis disorders (PBD) comprise three phenotypes including Zellweger syndrome (ZS) (the most severe), neonatal adrenoleucodystrophy, and infantile Refsum disease (IRD) (the most mild),...
Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disorders
Imamura, A.,
Shimozawa, N.,
Suzuki, Y.,
Zhang, Z.,
Tsukamoto, T.,
Orii, T.,
...