スポンサーリンク
Dept. Genome Repair Dynam., RBC, Kyoto Univ. | 論文
- Accelerated telomere shortening by disruption of DNA repair protein NBS1
- Construction of Nbs1 knockout cell line using chicken DT40
- Nijmegen Breakage Syndrome (NBS) gene, NBS1, is involved in telomeric length maintenance.
- Positional cloning of the gene for Nijmegen breakage syndrome
- Genetic Mapping of Nijmegen Breakage Syndrome using Functional Complementation Assays and Homozygosity Mapping
- Haplotype Analysis of Nijmegen Breakage Syndrome and Construction of Physical Map of Candidate Region.
- Complementation Assay between Radiation-Sensitive irs2 Mutant and Ataxia-Telangiectasia Cell
- The Genetic Homogeneity of Nijmegen Breakage Syndrome V1 and V2.
- Mapping of the underlying gene for rare genetic complementation group Fanconi anemia
- NBS1 Regulates Apoptosis Induced by γ-Irradiation in Lymphoblastoid
- Mutation screening of the NBS1 gene in sporadic malignant lymphoma
- LET, cell cycle dependence for mutation induction and spectrum in HPRT locus
- Mutation Analysis of the Fanconi Anemia Gene FAA in Japanese patients
- Mutation Analysis of the Fanconi Anemia Genes in Japanese Patients
- Function of NBS1 in Activation of ATM kinase in Response to IR.
- 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
- The genetic complementation assay of Nijmegen breakage syndrome witit ataxia telangiectasia on the basis of radiation sensitivity to cell killing.
- A polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locus
- Nijmegen breakage syndrome : Sequence analysis of an 800-kb genomic region on chromosome 8q21.
- The relationship between NBS1 and cell death induced by γ-ray irradiation in lymphoblastoid