スポンサーリンク
Department Of Biology Faculty Of Science Kumamoto University | 論文
- A Novel Mutation (967-970+2)delAAAGGT in the Choroideremia Gene Found in a Japanese Family and Related Clinical Findings
- Control of Inter-Dot Electrostatic Coupling by a Side Gate in a Silicon Double Quantum Dot Operating at 4.5K
- The influence of hepatitis B DNA level and antiviral therapy on recurrence after initial curative treatment in patients with hepatocellular carcinoma
- CLINICAL FEATURES OF JAPANESE LEBER'S HEREDITARY OPTIC NEUROPATHY WITH 11778 MUTATION OF MITOCHONDRIAL DNA
- Functional Results of Sleeve Lobectomy for Tuberculous Bronchial Stenosis
- Multicenter Genetic Study of Retinitis Pigmentosa in Japan : I. Genetic Heterogeneity in Typical Retinitis Pigmentosa
- Multicenter Genetic Study of Retinitis Pigmentosa in Japan : II. Prevalence of Autosomal Recessive Retinitis Pigmentosa
- Elevated levels of soluble fibrin in patients with venous thromboembolism
- Negative predictive value of D-dimer for diagnosis of venous thromboembolism
- Preparation and Characterization of Everted Membrane Vesicles from Cells of Staphylococcus aureus
- Molecular and Cellular Regulation of Renal Phosphate Transporters in X-Linked Hypophosphatemia
- Biomechanical Analysis of TMJ Soft Tissues under Asymmetric Jaw Movement(3D1 Dental Biomechanics)
- P-06 TRANSPORT MODEL OF PHYSIOLOGICAL SUBSTANCES IN CORTICAL BONE THROUGH POROUS CANAL NETWORK
- A Novel Mutation in the Cornea-Specific Keratin 12 Gene in Meesmann Corneal Dystrophy
- Novel Mutation (V505D) of the TGFBI Gene Found in A Chinese Family with Lattice Corneal Dystrophy, Type I
- Mutations in the Membrane Component, Chromosome 1, Surface Marker 1 (M1S1) Gene in Gelatinous Drop-like Corneal Dystrophy
- Analysis of COL8A2 Gene Mutation in Japanese Patients with Fuchs' Endothelial Dystrophy and Posterior Polymorphous Dystrophy
- Mutation Analysis of the TGFBI Gene in Vietnamese with Granular and Avellino Corneal Dystrophy
- OPA1 Gene Mutations in Japanese Patients with Bilateral Optic Atrophy Unassociated with Mitochondrial DNA Mutations at nt 11778, 3460, and 14484
- Multiplex Polymerase Chain Reaction for Detection of Herpes Simplex Virus Type 1, Type 2, Cytomegalovirus, and Varicella-Zoster Virus in Ocular Viral Infections