スポンサーリンク
Div. Of Environ. Biol. Res. Inst. Rad. Biol. Med. Hiroshima University. | 論文
- 血中コレステロールと味噌--味噌食が食事性代謝障害に及ぼす影響の研究
- 誘発突然変異と損傷乗り越えDNA合成を制御するPCNAのモノユビキチン化反応の解析 (第50回原子爆弾後障害研究会 特集号)
- Two Major Factors Involved in the Reverse Dose-rate Effect for Somatic Mutation Induction are the Cell Cycle Position and LET Value
- 242 Analysis of apoptosis induction in Nbs1 deficient cells(Apoptosis related, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
- 206 Functional Domain Analysis of NBS1 Gene in Homologous Recombinational Repair(Physics, chemistry and DNA damage, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
- 182 Effect of gravity stress on homologous recombination(Environmental effects of radiation, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
- 98 Localization of Rad51 protein in cells from patients with Fanconi Anemia D1 group(Repair of radiation damage, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society)
- Induction of dominant lethality and teratogenesis in F_1 mice following paternal ^Cf neutron-irradiation at pre-meiotic and post-meiotic stages of germ cells.
- Mutation Induction and RBE of Monoenergetic Neutrons in V79 Cells
- Radiosensitization by PI3-kinase inhibitor wortmannin in human osteosarcoma cells in vitro
- The scid Mutation Does Not Affect Slowly Repairing Potentially Lethal Damage That Is Sensitive To 0.23 M NaCl.
- Scid mutation affects the rate of PLD repair
- Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients
- 誘発突然変異と損傷乗り越えDNA合成 : REV1の構造と生化学的機能
- 損傷乗り越えDNA合成と発癌 (特集 DNAの損傷・修復と疾患)
- P054 Effect of REV1 on the survival of human cells after various DNA damages(Poster Session)
- W2-2 Effect of REV1 on the survival of human cells after various DNA damages(Workshop(2) : Translesion DNA Synthesis and Mutagenesis)
- 放射線発がんのメカニズム (第46回原子爆弾後障害研究会) -- (シンポジウム 原子爆弾後障害研究の将来の展望--これからの10年間に期待される成果)
- シンポジウム-1 広島大学21世紀COEプログラム「放射線災害医療開発の先端的研究教育拠点-ゲノム障害科学に基づく学術基盤の確立と医療展開-」の概要
- Nijmegen Breakage Syndrome (NBS) gene, NBS1, is involved in telomeric length maintenance.