Murakami A | Juntendo Univ. School Of Medicine Tokyo Jpn

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著作論文

A Novel Mutation (967-970+2)delAAAGGT in the Choroideremia Gene Found in a Japanese Family and Related Clinical Findings
Mast Cells in Pterygium : Number and Phenotype
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
Expression of Stem Cell Factor in Pterygium
Heterozygous Ala137Pro Mutation in Keratin 12 Gene Found in Japanese with Meesmann's Corneal Dystrophy
In Vitro Shoot Development of Eucalyptus citriodora on Rockwool in the Film Culture Vessel under CO_2 Enrichment

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