Disposable 1-Day Acuvue® contact lenses for the delivery of lomefloxacin to rabbits'eyesXIN TIAN; IWATSU, Minoru; KANAI, Atsushi et al.The CLAO journal. 2001, Vol 27, Num 4, pp 212-215, issn 0733-8902Article

Endogenous substance P in corneal epithelial cells and keratocytesWATANABE, Michifumi; NAKAYASU, Kiyo; IWATSU, Minoru et al.Japanese journal of ophthalmology. 2002, Vol 46, Num 6, pp 616-620, issn 0021-5155, 5 p.Article

The expression of laminin-5 and ultrastructure of the interface between basal cells and underlying stroma in the keratoconus corneaEBIHARA, Nobuyuki; WATANABE, Yasuo; NAKAYASU, Kiyoo et al.Japanese journal of ophthalmology. 2001, Vol 45, Num 3, pp 209-215, issn 0021-5155Article

Secondary keratoconus with corneal epithelial iron ring similar to Fleischer's ringHIRATSUKA, Yoshimune; NAKAYASU, Kiyoo; KANAI, Atsushi et al.Japanese journal of ophthalmology. 2000, Vol 44, Num 4, pp 381-386, issn 0021-5155Article

Transferrin-polyethylenimine conjugate, FuGENE6 and TransIT-LT as nonviral vectors for gene transfer to the corneal endotheliumHA NGUYEN THANH; MURAKAMI, Akira; FUJIKI, Keiko et al.Japanese journal of ophthalmology. 2002, Vol 46, Num 2, pp 140-146, issn 0021-5155Article

A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophyNGUYEN THANH HA; HOANG MINH CHAU; LE XUAN CUNG et al.American journal of ophthalmology. 2003, Vol 135, Num 3, pp 390-393, issn 0002-9394, 4 p.Article

OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484YAMADA, Tetsuya; HAYASAKA, Seiji; KANAI, Atsushi et al.Japanese journal of ophthalmology. 2003, Vol 47, Num 4, pp 409-411, issn 0021-5155, 3 p.Article

Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese with meesmann's corneal dystrophyTAKAHASHI, Kozo; TAKAHASHI, Kenzo; MURAKAMI, Akira et al.Japanese journal of ophthalmology. 2002, Vol 46, Num 6, pp 673-674, issn 0021-5155, 2 p.Article

Multiplex polymerase chain reaction for detection of herpes simplex virus type 1, type 2, cytomegalovirus, and Varicella-Zoster virus in ocular viral infectionsYAN ZHANG; KIMURA, Tairo; FUJIKI, Keiko et al.Japanese journal of ophthalmology. 2003, Vol 47, Num 3, pp 260-264, issn 0021-5155, 5 p.Article

Transthyretin Ser-44 mutation in a case with vitreous amyloidosisMURAKAMI, Akira; FUJIKI, Keiko; HASEGAWA, Sachiko et al.American journal of ophthalmology. 2002, Vol 133, Num 2, pp 272-273, issn 0002-9394Article

Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2LI, Anren; XIAODONG JIAO; HECKENLIVELY, John et al.American journal of human genetics. 2004, Vol 74, Num 5, pp 817-826, issn 0002-9297, 10 p.Article

Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy : The P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophyNGUYEN THANH HA; FUJIKI, Keiko; HOTTA, Yoshihiro et al.American journal of ophthalmology. 2000, Vol 130, Num 1, pp 119-120, issn 0002-9394Article

Decreased GlcNAc 6-o-sulfotransferase activity in the cornea with macular corneal dystrophyHASEGAWA, Nobuko; TORII, Takayoshi; KATO, Takuji et al.Investigative ophthalmology & visual science. 2000, Vol 41, Num 12, pp 3670-3677, issn 0146-0404Article

Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35XIAODONG JIAO; MUNIER, Francis L; IWATA, Fumino et al.American journal of human genetics. 2000, Vol 67, Num 5, pp 1309-1313, issn 0002-9297Article