TWI615614B - 疾病樣本分析裝置、分析系統及分析方法 - Google Patents
疾病樣本分析裝置、分析系統及分析方法 Download PDFInfo
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| GB0417887D0 (en) * | 2004-08-11 | 2004-09-15 | Ares Trading Sa | Protein |
| CN101142483A (zh) * | 2005-03-18 | 2008-03-12 | 株式会社资生堂 | 以鳞状上皮细胞癌抗原为指标的皮肤性状的评价方法 |
| CN101189243A (zh) * | 2005-04-06 | 2008-05-28 | 阿斯利康(瑞典)有限公司 | 取代的杂环及其作为chk1、pdk1和pak抑制剂的应用 |
| JP2007077104A (ja) * | 2005-09-16 | 2007-03-29 | Shiseido Co Ltd | 血管内皮増殖因子阻害剤 |
| EP1996923B1 (en) * | 2006-03-02 | 2012-06-27 | PerkinElmer Health Sciences, Inc. | Methods for distinguishing isomers using mass spectrometry |
| US20070258899A1 (en) * | 2006-03-31 | 2007-11-08 | Karyon-Ctt Ltd | Diagnostic and therapeutic agents |
| JP5005955B2 (ja) * | 2006-05-24 | 2012-08-22 | 田辺三菱製薬株式会社 | 被験物質の脂質代謝異常症誘発可能性を予測する方法 |
| EP2405270B1 (en) * | 2006-06-30 | 2013-07-17 | Merck Sharp & Dohme Corp. | IGFBP2-Biomarker |
| CN101578287B (zh) * | 2006-09-06 | 2012-09-05 | 阿特纳赞塔里斯有限公司 | 地索拉唑及其衍生物与细胞结合分子的轭合物，新的地索拉唑衍生物，其制备方法及其应用 |
| EP1900742A1 (en) * | 2006-09-07 | 2008-03-19 | AEterna Zentaris GmbH | Conjugates of disorazoles and their derivatives with cell-binding molecules, novel disorazole derivatives, processes of manufacturing and uses thereof |
| US20090075284A1 (en) * | 2006-09-19 | 2009-03-19 | The Regents Of The University Of Michigan | Metabolomic profiling of prostate cancer |
| WO2008089453A2 (en) * | 2007-01-18 | 2008-07-24 | Sepracor Inc. | Inhibitors of d-amino acid oxidase |
| MX2009008559A (es) * | 2007-02-12 | 2009-08-21 | Anthrogenesis Corp | Hepatocitos y condorcitos de celulas madre de la placenta adherentes, y poblaciones de celulas enriquecidas con celulas madre de la placenta cd34+, cd45-. |
| US8034780B2 (en) * | 2007-07-16 | 2011-10-11 | Mcphail Kerry Leigh | Isolation, purification, and structure elucidation of the antiproliferative compound coibamide A |
| US20110045495A1 (en) * | 2008-01-17 | 2011-02-24 | Yoshinori Tanaka | Composition and method for diagnosis or detection of renal cancer |
| JP2009184981A (ja) * | 2008-02-07 | 2009-08-20 | Shiseido Co Ltd | 抗ｄ−アミノ酸モノクローナル抗体及び、抗ｄ−アミノ酸モノクローナル抗体を用いたｄ−アミノ酸の免疫学的分析方法 |
| CL2009001156A1 (es) * | 2008-05-14 | 2010-08-27 | Canbas Co Ltd | Acetato de un peptido de 12 aminoacidos; metodo de preparacion; composicion farmaceutica y agente que lo contiene, solo o conjuntamente con un principio activo que dana el acido nucleico; util para el tratamiento o profilaxis de trastornos proliferativos celulares. |
| WO2009143489A2 (en) * | 2008-05-22 | 2009-11-26 | Archer Pharmaceuticals, Inc. | Modulation of angiogenesis by a-beta peptide fragments |
| WO2010005982A2 (en) * | 2008-07-07 | 2010-01-14 | The General Hospital Corporation | Multiplexed biomarkers of insulin resistance |
| JP2010038796A (ja) * | 2008-08-06 | 2010-02-18 | Human Metabolome Technologies Inc | 疾患マーカー、および、疾患マーカーの測定方法 |
| JP5639890B2 (ja) * | 2008-08-26 | 2014-12-10 | 国立大学法人九州大学 | Ｄａｏ１−／−マウスを活用したＤ−アミノ酸関連疾患の評価・スクリーニング方法 |
| US8722343B2 (en) * | 2008-11-21 | 2014-05-13 | Carla Perego | Methods and compositions for the diagnosis and treatment of diabetes |
| ES2799327T3 (es) * | 2009-05-05 | 2020-12-16 | Infandx Ag | Método para diagnosticar asfixia |
| CN101619092B (zh) * | 2009-08-06 | 2012-08-15 | 中国人民解放军第三军医大学第二附属医院 | 肿瘤抗原trag-3模拟表位肽及其应用 |
| US20110064828A1 (en) * | 2009-09-11 | 2011-03-17 | Novelos Therapeutics, Incorporated | Treatment of metastatic tumors and other conditions |
| JP2011247869A (ja) * | 2010-04-27 | 2011-12-08 | Kobe Univ | メタボローム解析手法を用いた特定疾患の検査方法 |
| CN102079771B (zh) * | 2010-12-10 | 2012-10-03 | 郑州大学 | 具有抗肿瘤活性的雌甾氨基酸酯化合物及其合成方法 |
-
2013
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- 2013-03-18 WO PCT/JP2013/001849 patent/WO2013140785A1/ja not_active Ceased
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Non-Patent Citations (6)
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