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鳥取大学生命機能研究支援センター遺伝子探索 | 論文
- 筋強直性ジストロフィー症 (特集 筋疾患の病態と診断,治療戦略の最前線) -- (病態と診断)
- Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers
- 授乳を介して 1,2,3,4-tetrachlorodibenzo-ρ-dioxin (1,2,3,4-TCDD) に暴露された新生仔ラット肝における抗酸化酵素 (antioxidant enzymes, AOE) mRNAの反応
- Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex
- Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn
- Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
- MOLECULAR EPIDEMIOLOGY OF TUBEROUS SCLEROSIS
- 序論
- 先天代謝異常症 (特集 小児科医に役立つ臨床遺伝学) -- (分子遺伝学の基礎と臨床:bedsideからbenchへ)
- 遺伝子多型の新技術について
- 精神遅滞
- Integration of a transposon into the Gli3 gene in the Pdn mouse
- Regulation of Cigarette Smoke-Induced Cytochrome P4501A1 Gene Expression in Osteogenic Disorder Shionogi Rat Liver and in Lung by Large Ascorbic Acid Dose(Biochemistry & Molecular Biology)
- Altered Sensitivities to Potential Inhibitors of Cholesterol Biosynthesis in Niemann-Pick Type C Fibroblasts
- 脆弱X症候群の分子機構と治療 (第1土曜特集 精神発達遅滞・自閉症の分子医学) -- (既知の遺伝子異常による発達障害・精神遅滞の分子医学)
- The Level of Orally Ingested Vitamin C Affected the Expression of Vitamin C Transporters and Vitamin C Accumulation in the Livers of ODS Rats