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京都大学放射線生物研究センター | 論文
- Mutation screening of the NBS1 gene in sporadic malignant lymphoma
- Genetic Disease 毛細血管拡張性運動失調症と関連疾患の遺伝子機能
- ナイミーヘン染色体不安定症候群の原因遺伝子BS1のクローニング
- Morphometric Evaluation of Late Normal Tissue Damage after Neon Beam Irradiation in Mouse Hind Legs
- RBE of Heavy Ions (proton, carbon,neon) for Acute Cell Death of Pancreatic Islet Cells of the Golden Hamster(Mesocricetus auratus)
- Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia
- Comparative Studies on Protective Effect of Various Sulfhydryl Compounds Against Cell Death and DNA Strand Breaks Induced by X-Ravs in Cultured Mouse L Cells
- Radiobiological Studies on Cultured Mouse Bone Marrow Cells in vitro
- Emerging Connection Between Centrosome and DNA Repair Machinery
- Nijmegen染色体不安定症候群と発がん (第1土曜特集 発がん過程における染色体ダイナミクス) -- (各種疾患における染色体異常と発がん)
- Dose-response Relationship of Lymphocyte Chromosome Aberrations in Locally lrradiated Persons
- Analysis of Junction Sequences of Double-Strand Breaks in Plasmid DNA by Nuclear Extracts from X-Irradiated Mouse Cells
- Analysis of Mutations at the FANCC and FANCG genes in Japanese Fanconi anemia patients
- チェックポイントとDNA修復のクロストーク (特集 DNA修復機構--DNA複製,チェックポイントとのクロストーク)
- O-15. Chromosome instability and cancer predisposition in the PCS (premature chromatid separation) syndrome(Abstracts of the oral and poster presentations,Abstracts of the 55th Annual Meeting of the Society of Chromosome Research)
- O-11. The optimal conditions for cytological diagnosis of total premature chromatid separation (PCS), a novel cancer-prone genetic trait associated with mitotic checkpoint defect(Abstracts of the oral and poster presentations)(The 53rd Annual Meeting of t
- 染色体異常と発癌 (染色体-2-)
- 遺伝性のがん--網膜芽細胞腫 (遺伝子診断)
- ファンコニ貧血症
- 放射線と染色体異常 (第6回国際放射線研究会議から)