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Serum metabolome profiles characterized by patients with hepatocellular carcinoma associated with hepatitis B and C
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作者 Takafumi Saito Masahiro Sugimoto +10 位作者 Kazuo Okumoto Hiroaki Haga Tomohiro Katsumi Kei Mizuno Taketo Nishina Sonoko Sato Kaori Igarashi Hiroko Maki masaru tomita Yoshiyuki Ueno Tomoyoshi Soga 《World Journal of Gastroenterology》 SCIE CAS 2016年第27期6224-6234,共11页
AIM: To clarify the characteristics of metabolite profiles in virus-related hepatocellular carcinoma (HCC) patients using serum metabolome analysis.METHODS: The serum levels of low-molecular-weight metabolites in 68 p... AIM: To clarify the characteristics of metabolite profiles in virus-related hepatocellular carcinoma (HCC) patients using serum metabolome analysis.METHODS: The serum levels of low-molecular-weight metabolites in 68 patients with HCC were quantified using capillary electrophoresis chromatography and mass spectrometry. Thirty and 38 of the patients suffered from hepatitis B virus-related HCC (HCC-B) and hepatitis C virus-related HCC (HCC-C), respectively.RESULTS: The main metabolites characteristic of HCC were those associated with glutathione metabolism, notably 13 &#x003b3;-glutamyl peptides, which are by-products of glutathione induction. Two major profiles, i.e., concentration patterns, of metabolites were identified in HCC patients, and these were classified into two groups: an HCC-B group and an HCC-C group including some of the HCC-B cases. The receiver operating characteristic curve for the multiple logistic regression model discriminating HCC-B from HCC-C incorporating the concentrations of glutamic acid, methionine and &#x003b3;-glutamyl-glycine-glycine showed a highly significant area under the curve value of 0.94 (95%CI: 0.89-1.0, P &#x0003c; 0.0001).CONCLUSION: The serum levels of &#x003b3;-glutamyl peptides, as well as their concentration patterns, contribute to the development of potential biomarkers for virus-related HCC. The difference in metabolite profiles between HCC-B and HCC-C may reflect the respective metabolic reactions that underlie the different pathogeneses of these two types of HCC. 展开更多
关键词 METABOLOME Hepatocellular carcinoma γ -glutamyl peptides GLUTATHIONE Oxidative stress
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Restauro-G:A Rapid Genome Re-Annotation System for Comparative Genomics 被引量:1
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作者 Satoshi Tamaki Kazuharu Arakawa +1 位作者 Nobuaki Kono masaru tomita 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2007年第1期53-58,共6页
of complete genome sequences submitted directly from sequencing projects are diverse in terms of annotation strategies and update frequencies. These inconsistencies make comparative studies difficult. To allow rapid d... of complete genome sequences submitted directly from sequencing projects are diverse in terms of annotation strategies and update frequencies. These inconsistencies make comparative studies difficult. To allow rapid data preparation of a large number of complete genomes, automation and speed are important for genome re-annotation. Here we introduce an open-source rapid genome re-annotation software system, Restauro-G, specialized for bacterial genomes. Restauro-G re-annotates a genome by similarity searches utilizing the BLASTLike Alignment Tool, referring to protein databases such as UniProt KB, NCBI nr, NCBI COGs, Pfam, and PSORTb. Re-annotation by Restauro-G achieved over 98% accuracy for most bacterial chromosomes in comparison with the original manually curated annotation of EMBL releases. Restauro-G was developed in the generic bioinformatics workbench G-language Genome Analysis Environment and is distributed at http://restauro-g.iab.keio.ac.jp/ under the GNU General Public License. 展开更多
关键词 BIOINFORMATICS SOFTWARE ANNOTATION G-language Genome Analysis Environment complete genomes
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A COMPREHENSIVE SOFTWARE SUITE FOR THE ANALYSIS OF CDNAS
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作者 KAZUHARU ARAKAWA HARUO SUZUKI +4 位作者 KOSUKE FUJISHIMA KENJI FUJIMOTO SHO UEDA MOTOMU MATSUI masaru tomita 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2005年第3期179-188,共10页
We have developed a comprehensive software suite for bioinformatics research of cDNAs; it is aimed at rapid characterization of the features of genes and the proteins they code. Methods implemented include the detecti... We have developed a comprehensive software suite for bioinformatics research of cDNAs; it is aimed at rapid characterization of the features of genes and the proteins they code. Methods implemented include the detection of translation initia- tion and termination signals, statistical analysis of codon usage, comparative study of amino acid composition, comparative modeling of the structures of product proteins, prediction of alternative splice forms, and metabolic pathway reconstruction. The software package is freely available under the GNU General Public License at http: / /www.g-language.org/ data/cdna/. 展开更多
关键词 CDNA bioinformatics software
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