Oshimura Mitsuo | 鳥取大学医学部分子細胞生物学講座ゲノム医工学分野

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著作論文

Introduction of a CD40L genomic fragment via a human artificial chromosome vector permits cell-type-specific gene expression and induces immunoglobulin secretion
Increased Frequencies of Gene and Chromosome Mutations after X-Irradiation in Mouse Embryonal Carcinoma Cells Transfected with the bcl-2 Gene
The Effect of Caffeine on p53-Dependent Radioresponses in Undifferentiated Mouse Embryonal Carcinoma Cells after X-ray and UV-irradiations
Radiosensitivity of undifferentiated mouse teratocarcinoma cells.
Introduction of a Normal Human Chromosome 8 Corrects Abnormal Phenotypes of Werner Syndrome Cells Immortalized by Expressing an hTERT Gene
Delayed Induction of Telomere Instability in Normal Human Fibroblast Cells by Ionizing Radiation
226 Radiation-induced delayed chromosomal instability caused by large deletion(Genetic instability, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
223 Radiation-Induced Delayed Chromosomal Instability(Genetic instability, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
221 A Role of DNA Double Strand Break Repair in the Induction of Genetic Instability(Genetic instability, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
214 The complementation of abnormal phenotypes of Werner syndrome cells by expressing WRN gene(Physics, chemistry and DNA damage, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
S-2-3 Radiation-Induced Delayed Chromosome Aberrations(Radiation Induced Genetical Instability : What Is the Mechanism That a Cell Memorizes Being Irradiated?, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
Instability of a Human Chromosome Exposed to Radiation in Unirradiated Mouse Cells
The Role of DNA-PKcs Function on Induction of Genetic Instability by Radiation
Radiation-induced genomic instability caused by large deletion (position)
Thermosensitization by Inhibition of Gap Junctional Intercellular Communication
Phenotypic Reversion of an X-Ray-Induced Transformant of Mouse m5S by Introduction of a Human Chromosome 11
The Effect of DNA Repair Defects on the Induction of Delayed Chromosome Aberrations by Radiation
The Examination of the Exclusion Mechanism of Apoptosis against the Cells with Unrepairable DNA Damage Using Undifferentiated Mouse Terarocarcinoma Cells
Mapping of the underlying gene for rare genetic complementation group Fanconi anemia
Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells
Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6
Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb
Exogenous gene expression and growth regulation of hematopoietic cells via a novel human artificial chromosome
A new method of microcell-mediated transfer of human artificial chromosomes using a hemagglutinating virus of Japan envelope
A novel expression system for genomic DNA loci using a human artificial chromosome vector with transformation-associated recombination cloning
Germline transmission of a transferred human chromosome 21 fragment in transchromosomal mice
Reconstructing chromosomes : Functional studies using genomic engineering(Symposium : Manipulating Chromosomes)(Abstracts of the 52nd Annual Meeting of the Society of Chromosome Research)

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