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Department of Ophthalmology, Juntendo University School of Medicine | 論文
- Multicenter Genetic Study of Retinitis Pigmentosa in Japan : II. Prevalence of Autosomal Recessive Retinitis Pigmentosa
- Inhibitory Effects of 1'-Acetoxychavicol Acetate on N-Nitrosobis(2-oxopropyl)-amine-induced Initiation of Cholangiocarcinogenesis in Syrian Hamsters
- Experimantal Study of Inclusive Reaction ^C(γ,π^-) at 44.2°
- Protective effects of dimethyl amiloride, a Na^+/H^+ exchange inhibitor against ischemia-reperfusion injury of rabbit hearts : ^P-NMR study on ion dynamics and energy metabolism.
- Possible Anti-tumor Promoting Properties of Edible Plants from Thailand, and Identification of an Active Constituent, Cardamonin, of Boesenbergia pandurata
- 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
- A Novel Mutation of the TGFBI Gene Found in a Vietnamese Family with Atypical Granular Corneal Dystrophy
- Transferrin-Polyethylenimine Conjugate, FuGENE6 and TransIT-LT as Nonviral Vectors for Gene Transfer to the Corneal Endothelium
- MISSENSE MUTATION OF RHODOPSIN GENE CODON 15 FOUND IN JAPANESE AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA
- A Case of Oculodentodigital Dysplasia Syndrome with Novel GJA1 Gene Mutation
- Long-term Follow-up of Two Sisters with Leber's Hereditary Optic Neuropathy
- Corneal dystrophies in Japan
- Mathematical Theory of the Manifestation-rate in Human Genetics : IV. Further Study on the Genetical Constitution of the Offspring of Cousin Marriages of Both Normal
- Plus/Minus Screening of Rabbit Corneal Endothelial cDNA Library
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