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Division of Cellular and Gene Therapy Products, National Institute of Health Sciences | 論文
- Clastogenicity of Quinoline Derivatives in the Liver Micronucleus Assay Using Rats and Mice
- Clastogenicity of Quinoline and Monofluorinated Quinolines in Chinese Hamster Lung Cells
- Neutralizing Antibody Evasion Ability of Adenovirus Vector Induced by the Bioconjugation of Methoxypolyethylene Glycol Succinimidyl Propionate(MPEG-SPA)(Biopharmacy)
- Tumor Necrosis Factor α-Gene Therapy for an Established Murine Melanoma Using RGD (Arg-Gly-Asp) Fiber-mutant Adenovirus Vectors
- OJ-015 Retinoic acid and thyroid hormones play an important role in the transcriptional regulation of sarcolipin(Excitation-Contraction Coupling/Ion Channel (A) : OJ3)(Oral Presentation (Japanese))
- 3 Regulation of Activity of Sarcoplasmic Reticulum Calcium ATPase in the Failing Heart(Plenary Session 5 (PL-5) (M) Calcium Handling Abnormality in Heart Failure,Special Program,The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- Gene expression profiles of hepatotoxin-treated human hepatocytes can be used to cluster unknown compounds according to their mode of action(Toxicogenomics, Toxicoproteomics, Proceedings of the 32nd Annual Meeting)
- Gene Expression Profiling of Human Mesenchymal Stem Cells for Identification of Novel Markers in Early- and Late-Stage Cell Culture
- A NEW TYPE OF HEMOCLIP DEVICE
- CLINICAL SIGNIFICANCE OF THE USE OF MAGNETIC ENDOSCOPE IMAGING FOR COLONOSCOPY
- Differential Gene Expression Induced by Two Genotoxic N-nitroso Carcinogens, Phenobarbital and Ethanol in Mouse Liver Examined with Oligonucleotide Microarray and Quantitative Real-time PCR
- Microcystin-LR is not Mutagenic in vivo in the λ/lacZ Transgenic Mouse (Muta^ Mouse)
- Comparison of the Efficiency and Safety of Non-viral Vector-Mediated Gene Transfer into a Wide Range of Human Cells
- Genotoxicity of microcystin-LR in vitro and in vivo
- P-039 Topoisomerase II inhibition invovled in DNA Double-Strand Breaks by Emodin and its genotoxocity(Poster Session)
- Foreword
- Tumorigenicity Studies for Human Pluripotent Stem Cell-Derived Products