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Department of Molecular Medicine, Nagasaki University Graduate School of Biomedical Sciences | 論文
- The Uteroglobin Gene G38A Polymorphism Is Not Associated with Kawasaki Disease
- Alteration of p53-binding protein 1 expression during skin carcinogenesis: association with genomic instability.
- Oncogenic role of miR-17-92 cluster in anaplastic thyroid cancer cells
- No Evidence of ARAF, CRAF and MET Mutations in BRAF^ Negative Human Papillary Thyroid Carcinoma
- No.37 Molecular epidemiology study of radiation-induced thyroid cancer as a main research project of Representative office of Nagasaki University in Belarus
- Ukraine Urinary Iodine Levels ; 20 years after the Chernobyl Accident
- Plasma Concentrations of Adrenomedullin and Ghrelin in Hemodialysis Patients with Sustained and Episodic Hypotension
- Steam Leak Accident at Nuclear Power Plant in Japan
- Thyroid Blockade during a Radiation Emergency in Iodine-rich Areas : Effect of a Stable-iodine Dosage
- Benign Thyroid Diseases among Chernobyl Liquidators
- No Evidence of Radiation Risk for Thyroid Gland among Schoolchildren around Semipalatinsk Nuclear Testing Site
- Mutation Analysis of RAP1 Gene in Papillary Thyroid Carcinomas
- Current concentration of artificial radionuclides and estimated radiation doses from 137Cs around the Chernobyl Nuclear Power Plant, the Semipalatinsk Nuclear Testing Site, and in Nagasaki
- Current Concentration of Artificial Radionuclides and Estimated Radiation Doses from 137Cs around the Chernobyl Nuclear Power Plant, the Semipalatinsk Nuclear Testing Site, and in Nagasaki
- Segmental Jumping Translocation of Ret Oncogene in Radiation-associated Thyroid Cancer
- DHMEQ, a novel NF-kappaB inhibitor, suppresses growth and type I collagen accumulation in keloid fibroblasts
- A Novel Role for Thyroid Hormone Receptor Beta in Cellular Radiosensitivity
- Urinary Iodine Levels and Thyroid Diseases in Children; Comparison between Nagasaki and Chernobyl
- Establishment of Telemedicine System for International Hibakushas' Medical Care
- A Single Missense Mutation in Codon 918 of the RET Proto-Oncogene in Sporadic Medullary Thyroid Carcinomas