Y. Mashima

发表

Decreased substance P concentrations in tears from patients with corneal hypesthesia.

M. Yamada, M. Ogata, M. Kawai, 2000, American journal of ophthalmology.

The myocilin (MYOC) gene expression in the human trabecular meshwork

S. Minoshima, S. Noda, N. Shimizu, 2000 .

Multifocal Magnetoencephalogram Applied to Objective Visual Field Analysis

Y. Haruta, H. Ohde, Y. Mashima, 2004, Japanese Journal of Ophthalmology.

Clinical application of the multifocal VEPs

H. Ohde, Y. Mashima, Y. Oguchi, 2001, Current eye research.

Rapid and efficient molecular analysis of gyrate atrophy using denaturing gradient gel electrophoresis.

G. Inana, Y. Mashima, T. Shiono, 1994, Investigative ophthalmology & visual science.

Discordance between subjective perimetric visual fields and objective multifocal visual evoked potential-determined visual fields in patients with hemianopsia.

I. Kimura, K. Shinoda, H. Ohde, 2007, American journal of ophthalmology.

Unoprostone reduces oxidative stress- and light-induced retinal cell death, and phagocytotic dysfunction, by activating BK channels

H. Hara, M. Shimazawa, K. Tsuruma, 2011, Molecular vision.

Low levels of plasma endothelin-1 in patients with retinitis pigmentosa

H. Ohguro, M. Nakazawa, Y. Mashima, 2010, Clinical ophthalmology.

The myocilin (MYOC) gene expression in the human trabecular meshwork.

N. Shimizu, S. Minoshima, S. Noda, 2000, Current Eye Research.

Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma

M. Araie, Yasuyuki Suzuki, Y. Suzuki, 2003, The British journal of ophthalmology.

Increased Microcirculation on Optic Nerve Head by Laser Speckle Flowgraphy at Early Stage of Leber Hereditary Optic Neuropathy

M. Shimura, A. Hirakata, Y. Mashima, 2018, Neuro-ophthalmology.

Fluorophotometric measurement of pH of human tears in vivo.

M. Yamada, M. Kawai, Y. Mashima, 1997, Current eye research.

Optic disc excavation in the atrophic stage of Leber's hereditary optic neuropathy: comparison with normal tension glaucoma

I. Kimura, G. Tomita, H. Ohde, 2003, Graefe's Archive for Clinical and Experimental Ophthalmology.

Orbital high resolution magnetic resonance imaging with fast spin echo in the acute stage of Leber’s hereditary optic neuropathy

S. Momoshima, H. Shiga, Y. Imamura, 1998, Journal of neurology, neurosurgery, and psychiatry.

High-resolution magnetic resonance imaging of the intraorbital optic nerve and subarachnoid space in patients with papilledema and optic atrophy.

S. Momoshima, H. Shiga, Y. Imamura, 1996, Archives of ophthalmology.

Soluble vascular adhesion protein-1 accumulates in proliferative diabetic retinopathy.

Y. Okada, S. Kase, A. Kanda, 2012, Investigative ophthalmology & visual science.

Microcirculation in the macular area of eyes with an idiopathic epiretinal membrane

I. Kimura, S. Ishida, K. Shinoda, 2001, Graefe's Archive for Clinical and Experimental Ophthalmology.

Dry eye after haematopoietic stem cell transplantation

K. Tsubota, Y. Ikeda, R. Watanabe, 1999, The British journal of ophthalmology.

Rapid detection of M1S1 mutations by the protein truncation test.

Y. Tano, N. Maeda, Y. Shimomura, 2000, Investigative ophthalmology & visual science.

Association Between Open-Angle Glaucoma and Gene Polymorphism for Heat-Shock Protein 70-1

Y. Mashima, Y. Ohtake, Karin Tosaka, 2007, Japanese Journal of Ophthalmology.

Variants of the Myocilin Gene in Japanese Patients with Normal-Tension Glaucoma

T. Iwata, Y. Mashima, Y. Ohtake, 2003, Ophthalmic Research.

VAP-1-mediated M2 macrophage infiltration underlies IL-1β- but not VEGF-A-induced lymph- and angiogenesis.

A. Schering, A. Hafezi-Moghadam, Dawei Sun, 2011, The American journal of pathology.

Vascular adhesion protein‐1 blockade suppresses choroidal neovascularization

Joan W. Miller, T. Nakazawa, E. Gragoudas, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Involvement of insulin-like growth factor-I and insulin-like growth factor binding protein-3 in corneal fibroblasts during corneal wound healing.

K. Tsubota, D. Kurosaka, T. Iwata, 2006, Investigative ophthalmology & visual science.

A significant role of stromal fibroblasts in rapidly progressive dry eye in patients with chronic GVHD.

K. Tsubota, I. Toda, K. Yamazaki, 2001, Investigative ophthalmology & visual science.

Paraoxonase 1 gene polymorphisms influence clinical features of open-angle glaucoma

A. Murakami, N. Fuse, T. Fukuchi, 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.

Quantitative Evaluation of Tear Meniscus Height From Fluorescein Photographs

K. Tsubota, M. Kawashima, M. Inoue, 2007, Cornea.

Myocilin expression in the astrocytes of the optic nerve head.

N. Shimizu, S. Minoshima, S. Noda, 2000, Biochemical and biophysical research communications.

Woman with atypical unilateral Leber's hereditary optic neuropathy with visual improvement.

K. Shinoda, H. Ohde, Y. Mashima, 2007, Clinical & experimental ophthalmology.

Characterization of AOC2 gene encoding a copper-binding amine oxidase expressed specifically in retina.

S. Noda, N. Shimizu, J. Kudoh, 2003, Gene.

Docosahexaenoic acid (DHA) has neuroprotective effects against oxidative stress in retinal ganglion cells

H. Hara, M. Shimazawa, Y. Mashima, 2009, Brain Research.

Ex vivo Delivery of Suicide Genes into Melanoma Cells Using Epidermal Growth Factor Receptor‐specific Fab Immunogene

N. Shimizu, A. Takayanagi, Y. Mashima, 1999, Japanese journal of cancer research : Gann.

Nonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.

R. Weleber, G. Inana, Y. Mashima, 1992, American journal of human genetics.

Detection of human papillomavirus infection in squamous tumours of the conjunctiva and lacrimal sac by immunohistochemistry, in situ hybridisation, and polymerase chain reaction

M. Mukai, K. Kameyama, Y. Mashima, 1997, The British journal of ophthalmology.

Effect of Topical Unoprostone Isopropyl on Optic Nerve Head Circulation in Controls and in Normal-Tension Glaucoma Patients

I. Kimura, K. Shinoda, Y. Mashima, 2005, Japanese Journal of Ophthalmology.

The effect of selective cyclooxygenase-2 inhibitor on corneal angiogenesis in the rat.

Y. Kawai, M. Yamada, M. Kawai, 1999, Current eye research.

A deletion in the ornithine aminotransferase gene in gyrate atrophy.

R. Weleber, G. Inana, Y. Hotta, 1992, The Journal of biological chemistry.

Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma

M. Araie, Yasuyuki Suzuki, Y. Suzuki, 2003, The British journal of ophthalmology.

Novel compound heterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma.

Y. Mashima, R. Kubota, Y. Ohtake, 2000 .

Novel compound heterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma

Y. Mashima, R. Kubota, Y. Ohtake, 2000, Ophthalmic genetics.

Dissociation of damage to spatial and luminance channels in early Leber's hereditary optic neuropathy manifested by the visual evoked potential

Y. Imamura, Y. Mashima, Y. Oguchi, 1997, Eye.

Visual prognosis better in eyes with less severe reduction of visual acuity one year after onset of Leber hereditary optic neuropathy caused by the 11,778 mutation

M. Wakakura, K. Shinoda, Y. Mashima, 2017, BMC Ophthalmology.

Do Idebenone and Vitamin Therapy Shorten the Time to Achieve Visual Recovery in Leber Hereditary Optic Neuropathy?

M. Wakakura, Y. Mashima, Y. Oguchi, 2000, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Unusual phenotype of an individual with the R124C mutation in the TGFBI gene.

T. Chikama, T. Nishida, N. Morishige, 2004, Archives of ophthalmology.

Genetic variants of TP53 and EPHX1 in Leber’s hereditary optic neuropathy and their relationship to age at onset

H. Ohde, Y. Mashima, Tomoyo Funayama, 2005, Japanese Journal of Ophthalmology.

Retinal Blood Flow in the Macular Area Before and After Scleral Buckling Procedures for Rhegmatogenous Retinal Detachment Without Macular Involvement

I. Kimura, S. Ishida, K. Shinoda, 2004, Japanese Journal of Ophthalmology.

Clinical characteristics of 14 Japanese patients with X-linked juvenile retinoschisis associated with XLRS1 mutation

S. Ishida, K. Shinoda, Y. Mashima, 2000, Ophthalmic genetics.

ON-pathway disturbance in two siblings.

S. Ishida, K. Shinoda, H. Ohde, 2002, Acta ophthalmologica Scandinavica.

On- and off-responses of the photopic electroretinograms in X-linked juvenile retinoschisis.

S. Kawashima, S. Ishida, K. Shinoda, 2001, American journal of ophthalmology.

Specular microscopy of posterior polymorphous endothelial dystrophy.

T. Hida, Y. Mashima, S. Akiya, 1986, Ophthalmic paediatrics and genetics.

Quantitative analysis of lipid deposits from Schnyder’s corneal dystrophy

M. Yamada, Y. Mashima, H. Mochizuki, 1998, The British journal of ophthalmology.

Autologous serum eye drops for the treatment of severe dry eye in patients with chronic graft-versus-host disease

K. Tsubota, Y. Ikeda, R. Watanabe, 2003, Bone Marrow Transplantation.

Sodium hyaluronate eyedrops in the treatment of dry eyes.

K. Tsubota, E. Takamura, I. Toda, 1995, The British journal of ophthalmology.

A piggyback contact lens for the correction of irregular astigmatism in keratoconus.

K. Tsubota, M. Yamada, Y. Mashima, 1994, Ophthalmology (Rochester, Minn.).

Substance P in Human Tears

T. Nishida, M. Yamada, M. Ogata, 2003, Cornea.

Topical diclofenac sodium decreases the substance P content of tears.

M. Yamada, M. Ogata, M. Kawai, 2002, Archives of ophthalmology.

Simultaneous recording of visual evoked potentials and electroretinograms in patients with unilateral opaque media

Y. Mashima, Y. Oguchi, M. Matsuhashi, 1988, Acta ophthalmologica.

Aqueous humor levels of topically applied levofloxacin, norfloxacin, and lomefloxacin in the same human eyes

M. Yamada, M. Kawai, Y. Mashima, 2003 .

Corneal epithelium following penetrating keratoplasty.

K. Tsubota, M. Yamada, Y. Mashima, 1995, The British journal of ophthalmology.

Successful Treatment of Dry Eye in Two Patients With Chronic Graft-versus-host Disease With Systemic Administration of FK506 and Corticosteroids

K. Tsubota, R. Watanabe, M. Kuwana, 2001, Cornea.

Amyloid and Non-amyloid Forms of 5q31-linked Corneal Dystrophy Resulting from Kerato-epithelin Mutations at Arg-124 Are Associated with Abnormal Turnover of the Protein*

D. Schorderet, H. Henry, F. Munier, 2000, The Journal of Biological Chemistry.

Granular-lattice (Avellino) corneal dystrophy in Japanese patients.

H. Sugiura, M. Yamada, Y. Mashima, 1997, Cornea.

Periductal area as the primary site for T-cell activation in lacrimal gland chronic graft-versus-host disease.

K. Yamazaki, Y. Kawakami, M. Kuwana, 2003, Investigative ophthalmology & visual science.

Aqueous humor levels of topically applied levofloxacin, norfloxacin, and lomefloxacin in the same human eyes.

M. Yamada, M. Kawai, Y. Mashima, 2002, Journal of cataract and refractive surgery.

Aqueous humor levels of topically applied levofloxacin in human eyes

M. Yamada, M. Kawai, Y. Mashima, 2002, Current eye research.

Fluorophotometric measurement of the buffering action of human tears in vivo.

M. Yamada, M. Kawai, Y. Mashima, 1998, Current eye research.

Increasing ofloxacin resistance of bacterial flora from conjunctival sac of preoperative ophthalmic patients in Japan.

M. Yamada, Y. Mashima, T. Noda, 2002, Japanese journal of ophthalmology.

Varied appearance of cornea of patients with corneal dystrophy associated with R124H mutation in the BIGH3 gene.

M. Yamada, Y. Mashima, Y. Nakamura, 1999, Cornea.

Homogeneity of kerato-epithelin codon 124 mutations in Japanese patients with either of two types of corneal stromal dystrophy.

M Yamada, Y Mashima, N. Shimizu, 1997, American journal of human genetics.

On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies.

D. Schorderet, S. Uffer, F. Munier, 1999, Investigative ophthalmology & visual science.

Severe form of juvenile corneal stromal dystrophy with homozygous R124H mutation in the keratoepithelin gene in five Japanese patients

N. Shimizu, T. Ogata, J. Kudoh, 1998, The British journal of ophthalmology.

Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan.

N. Maeda, S. Kinoshita, S. Yamamoto, 2000, American journal of ophthalmology.

Fat adherence syndrome after retinal surgery treated with amniotic membrane transplantation.

K. Shinoda, S. Nishina, M. Yamada, 2001, American journal of ophthalmology.

Preventing symblepharon formation with a gelatin sponge in the eye of a patient with an alkali burn.

Y. Mashima, Y. Sano, M. Yamada, 1997, American journal of ophthalmology.

Corneal Stromal Penetration Of Topically Applied Levofloxacin, Norfloxacin, And Lomefloxacin In The Same Human Eyes

M. Yamada, M. Kawai, Y. Mashima, 2002 .

Corneal ulcer associated with deposits of norfloxacin.

M. Yamada, Y. Mashima, M. Konishi, 1998, American journal of ophthalmology.

Corneal Epithelium in Keratoconus

Y Mashima, K. Tsubota, T. Ogata, 1995, Cornea.

Evaluation of Corneal Endothelial Pump Function With a Cold Stress Test

M. Yamada, M. Kawai, Y. Mashima, 2005, Cornea.

Dry eye associated with chronic graft-versus-host disease.

K. Tsubota, K. Yamazaki, Y. Kawakami, 2002, Advances in experimental medicine and biology.

Electrolysis for corneal opacities in a young patient with superficial variant of granular corneal dystrophy (Reis-Bücklers corneal dystrophy).

K. Tsubota, M. Kawashima, Y. Mashima, 2005, American journal of ophthalmology.

Immunohistology of kerato-epithelin in corneal stromal dystrophies associated with R124 mutations of the BIGH3 gene

M. Yamada, Y. Mashima, Y. Nakamura, 2000, Current eye research.

Specular microscopic observation of corneal epithelium following penetrating keratoplasty

K. Tsubota, M. Yamada, Y. Mashima, 1990 .

Inhibition of vascular adhesion protein‐1 enhances the anti‐tumor effects of immune checkpoint inhibitors

H. Asamura, S. Ohta, Y. Kawakami, 2021, Cancer science.

Mouse myocilin (Myoc) gene expression in ocular tissues.

N. Shimizu, S. Noda, J. Kudoh, 1998, Biochemical and biophysical research communications.

Cloning of the cDNA for a new member of the immunoglobulin superfamily (ISLR) containing leucine-rich repeat (LRR).

S Minoshima, Y Mashima, N. Shimizu, 1997, Genomics.

Gene Analysis and Evaluation of the Single Founder Effect in Japanese Patients with Oguchi Disease

N. Shimizu, J. Kudoh, Y. Mashima, 2004, Japanese Journal of Ophthalmology.

Polymorphism of beta-adrenergic receptors and susceptibility to open-angle glaucoma.

K. Tsubota, A. Murakami, N. Fuse, 2006, Molecular vision.

Mitochondrial DNA Mutations with Leber's Hereditary Optic Neuropathy in Japanese Patients with Open-Angle Glaucoma

N. Fuse, T. Fukuchi, Y. Mashima, 2006, Japanese Journal of Ophthalmology.

Novel cytochrome P4501B1 (CYP1B1) gene mutations in Japanese patients with primary congenital glaucoma.

I. Kimura, M. Araie, M. Aihara, 2001, Investigative ophthalmology & visual science.

Scanning laser Doppler flowmeter study of retinal blood flow in macular area of healthy volunteers

Y Mashima, I. Kimura, K. Shinoda, 2003, The British journal of ophthalmology.

Identification of an Interstitial Deletion in an Adult Female with Schizophrenia , Mental Retardation , and Dysmorphic Features : Further Support for a Putative Schizophrenia-Susceptibility Locus

N. Shimizu, J. Kudoh, M. Yamada, 1997 .

A novel mtDNA C11777A mutation in Leigh syndrome.

Y. Goto, I. Nonaka, Takao Takahashi, 2003, Mitochondrion.

Visual evoked potential in the management of pituitary tumor during pregnancy

Y. Mashima, Y. Oguchi, 2004, Documenta Ophthalmologica.

Inhibition of Vascular Adhesion Protein‐1 for Treatment of Graft‐Versus‐Host Disease in Mice

K. Tsubota, Y. Kawakami, Y. Mashima, 2018, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

A Platform for Controlled Dual‐Drug Delivery to the Retina: Protective Effects against Light‐Induced Retinal Damage in Rats

Noriko Osumi, Matsuhiko Nishizawa, Hirokazu Kaji, 2014, Advanced healthcare materials.

Human and mouse ISLR (immunoglobulin superfamily containing leucine-rich repeat) genes: genomic structure and tissue expression.

N. Shimizu, S. Noda, J. Kudoh, 1999, Genomics.

REP-1 gene mutations in Japanese patients with choroideremia

A. Murakami, K. Fujiki, A. Kanai, 1999, Graefe's Archive for Clinical and Experimental Ophthalmology.

Mutation Spectrum in the Rep-1 Gene of Japanese Choroideremia Patients

A. Murakami, K. Fujiki, A. Kanai, 1999 .

Novel 473-bp deletion in XLRS1 gene in a Japanese family with X-linked juvenile retinoschisis

S. Ishida, K. Shinoda, M. Inoue, 2004, Graefe's Archive for Clinical and Experimental Ophthalmology.

Severe juvenile retinoschisis associated with a 33-bps deletion in XLRS1 gene.

S. Ishida, K. Shinoda, Y. Mashima, 1999, Ophthalmic genetics.

[Two cases of digitalis toxicity with reversible and severe decrease of visual acuity].

H. Ohde, Y. Mashima, Y. Oguchi, 2001, Nippon Ganka Gakkai zasshi.

A novel myosin-like protein (myocilin) expressed in the connecting cilium of the photoreceptor: molecular cloning, tissue expression, and chromosomal mapping.

S Minoshima, Y Mashima, N. Shimizu, 1997, Genomics.

Tranilast inhibits cell proliferation and collagen synthesis by rabbit corneal and Tenon’s capsule fibroblasts

D. Kurosaka, Y. Mashima, S. Tajima, 2000 .

Variants in optineurin gene and their association with tumor necrosis factor-alpha polymorphisms in Japanese patients with glaucoma.

H. Ideta, I. Kimura, N. Shimizu, 2004, Investigative ophthalmology & visual science.

Human retina-specific amine oxidase (RAO): cDNA cloning, tissue expression, and chromosomal mapping.

Y Mashima, N. Shimizu, S. Asakawa, 1997, Genomics.

Association of HK2 and NCK2 with Normal Tension Glaucoma in the Japanese Population

H. Ideta, T. Nakazawa, K. Nishida, 2013, PloS one.

Association of Toll-like receptor 4 gene polymorphisms in Japanese subjects with primary open-angle, normal-tension, and exfoliation glaucoma.

H. Ideta, T. Nakazawa, K. Nishida, 2012, American journal of ophthalmology.

Association between glaucoma and gene polymorphism of endothelin type A receptor.

H. Ideta, I. Kimura, A. Murakami, 2005, Molecular vision.

SNPs and interaction analyses of noelin 2, myocilin, and optineurin genes in Japanese patients with open-angle glaucoma.

A. Murakami, N. Fuse, T. Fukuchi, 2006, Investigative ophthalmology & visual science.

The influence of aniseikonia on the VEP by random‐dot stereogram

Y. Mashima, Y. Oguchi, 1989, Acta ophthalmologica.

Inhibition of vascular adhesion protein‐1 suppresses endotoxin‐induced uveitis

Joan W. Miller, T. Nakazawa, E. Gragoudas, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Multicenter study on the frequency of three primary mutations of mitochondrial DNA in Japanese pedigrees with Leber’s hereditary optic neuropathy: comparison with American and British counterparts

Makoto Nakamura, Y. Isashiki, Y. Hotta, 1999 .

Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.

K. Fujiki, A. Kanai, M. Hayakawa, 1995, Japanese journal of ophthalmology.

Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophy.

R. Weleber, G. Inana, Y. Mashima, 1999, Ophthalmic genetics.

Heterogeneity and uniqueness of ornithine aminotransferase mutations found in Japanese gyrate atrophy patients.

M. Tamai, G. Inana, Y. Mashima, 1996, Current Eye Research.

A single-base change at a splice acceptor site in the ornithine aminotransferase gene causes abnormal RNA splicing in gyrate atrophy

R. Weleber, G. Inana, Y. Mashima, 1992, Human Genetics.

Decreased blood flow at neuroretinal rim of optic nerve head corresponds with visual field deficit in eyes with normal tension glaucoma

Kei Shinoda, Itaru Kimura, Yuichiro Ohtake, 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.

The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients.

N. Shimizu, J. Kudoh, M. Yamada, 1998, American journal of ophthalmology.

Macular nerve fibers temporal to fovea may have a greater potential to recover function in patients with Leber's hereditary optic neuropathy.

H. Ohde, Y. Mashima, Y. Oguchi, 2002, Japanese journal of ophthalmology.

Human retina-specific amine oxidase: genomic structure of the gene (AOC2), alternatively spliced variant, and mRNA expression in retina.

Y Mashima, N. Shimizu, S. Noda, 1998, Genomics.

Electrolytic removal of recurrence of granular corneal dystrophy

M. Kawashima, M. Yamada, Y. Mashima, 2003, Eye.

Corneal electrolysis for recurrence of corneal stromal dystrophy after keratoplasty

M. Yamada, M. Kawai, Y. Mashima, 2002, The British journal of ophthalmology.

A novel mutation at codon 124 (R124L) in the BIGH3 gene is associated with a superficial variant of granular corneal dystrophy.

N. Shimizu, J. Kudoh, M. Yamada, 1999, Archives of ophthalmology.

Relaxation of Encircling Buckle Improved Choroidal Blood Flow in a Patient with Visual Field Defect Following Encircling Procedure

I. Kimura, K. Shinoda, M. Inoue, 2006, Japanese Journal of Ophthalmology.

In situ confirmation of retinal blood flow improvement after carotid endarterectomy in a patient with ocular ischemic syndrome.

I. Kimura, K. Shinoda, M. Inoue, 2002, American journal of ophthalmology.

Remission of Leber's hereditary optic neuropathy with idebenone

Y. Mashima, Y. Oguchi, Y. Hiida, 1992, The Lancet.

Novel Cytochrome P 4501 B 1 ( CYP 1 B 1 ) Gene Mutations in Japanese Patients with Primary Congenital Glaucoma

I. Kimura, M. Araie, M. Aihara, 2001 .

Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism.

N. Shimizu, J. Kudoh, M. Wakakura, 1995, Investigative ophthalmology & visual science.

Vascular Adhesion Protein-1 Blockade Suppresses Ocular Inflammation After Retinal Laser Photocoagulation in Mice.

A. Kanda, K. Noda, S. Ishida, 2017, Investigative ophthalmology & visual science.

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy.

N. Shimizu, J. Kudoh, M. Wakakura, 1998, Current eye research.

Detection of fenestrated central scotoma by scanning laser ophthalmoscope microperimetry in a patient with Leber’s hereditary optic neuropathy after visual recovery

Y. Mashima, Y. Oguchi, E. Sato, 2001 .

DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens.

N. Shimizu, J. Kudoh, Y. Mashima, 1994, American journal of ophthalmology.

[DNA diagnosis of Leber's hereditary optic neuropathy].

N. Shimizu, J. Kudoh, K. Sakai, 1993, Nippon Ganka Gakkai zasshi.

Visual recovery in a case of hereditary optic neuropathy of Leber with 3460 mutation

H. Takahashi, Y. Mashima, S. Akiya, 1996 .

[Molecular genetic analysis of Leber's hereditary optic neuropathy with the 3460 mutation in Japanese pedigrees].

N. Shimizu, J. Kudoh, Y. Mashima, 1995, Nippon Ganka Gakkai zasshi.

Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.

N. Shimizu, M. Nagano, T. Egashira, 2004, Clinical biochemistry.

High incidence of pre‐excitation syndrome in Japanese families with Leber's hereditary optic neuropathy

Y. Mashima, Y. Oguchi, K. Kigasawa, 1996, Clinical genetics.

Mitochondrial DNA analysis of Leber's hereditary optic neuropathy.

N. Shimizu, J. Kudoh, K. Sakai, 1991, Japanese journal of ophthalmology.

High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy

N. Shimizu, J. Kudoh, Y. Mashima, 1993, Human Genetics.

Effect of unoprostone on topographic and blood flow changes in the ischemic optic nerve head of rabbits.

Y. Mashima, T. Sugiyama, H. Oku, 2009, Archives of ophthalmology.

Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family.

Y Mashima, N. Shimizu, J. Kudoh, 1994, Ophthalmic genetics.

Polymorphism of β-adrenergic receptors and susceptibility to open-angle glaucoma

K. Tsubota, A. Murakami, N. Fuse, 2006 .

Topical Isopropyl Unoprostone for Retinitis Pigmentosa: Microperimetric Results of the Phase 2 Clinical Study

A. Murakami, M. Nakazawa, Y. Mashima, 2012, Ophthalmology and Therapy.

A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa

N. Shimizu, J. Kudoh, Y. Mashima, 1993, Human Genetics.

SHORT COMMUNICATION: A novel homozygous Ile535Asn mutation in the rod cGMP phosphodiesterase ß-subunit gene in two brothers of a Japanese family with autosomal recessive retinitis pigmentosa

Nobuyoshi Shimizu, Yoshihisa Oguchi, Masamichi Saga, 1998 .

Genetic polymorphisms in the angiotensin II receptor gene and their association with open-angle glaucoma in a Japanese population.

I. Kimura, R. Asaoka, T. Kanamoto, 2005, Investigative ophthalmology & visual science.

Long-Term Protection of Genetically Ablated Rabbit Retinal Degeneration by Sustained Transscleral Unoprostone Delivery.

H. Kaji, T. Nakazawa, M. Nishizawa, 2016, Investigative ophthalmology & visual science.

Protective effects of sustained transscleral unoprostone delivery against retinal degeneration in S334ter rhodopsin mutant rats.

H. Kaji, T. Nakazawa, M. Nishizawa, 2016, Journal of biomedical materials research. Part B, Applied biomaterials.

Novel mutations in the myocilin gene in Japanese glaucoma patients

A. Kanai, Y. Inoue, M. Inatani, 2000, Human mutation.

Novel MYOC Gene Mutation, Phe369Leu, in Japanese Patients with Primary Open-Angle Glaucoma Detected by Denaturing High-Performance Liquid Chromatography

H. Ideta, D. Kurosaka, R. Asaoka, 2004, Journal of glaucoma.

Analysis of porcine optineurin and myocilin expression in trabecular meshwork cells and astrocytes from optic nerve head.

S. Noda, N. Shimizu, J. Kudoh, 2004, Investigative ophthalmology & visual science.

Genomic organization of the human myocilin gene (MYOC) responsible for primary open angle glaucoma (GLC1A).

S Minoshima, Y Mashima, N. Shimizu, 1998, Biochemical and biophysical research communications.

Identification of four novel mutations of the XLRS1 gene in Japanese patients with X‐linked juvenile retinoschisis

J. Kudoh, Y. Ozawa, S. Ishida, 1999, Human mutation.

Substance P and its metabolites in normal human tears.

T. Nishida, M. Yamada, M. Ogata, 2002, Investigative ophthalmology & visual science.

Serum vascular adhesion protein-1 correlates with vascular endothelial growth factor in patients with type II diabetes.

K. Tsubota, Y. Ozawa, K. Noda, 2013, Journal of diabetes and its complications.

Vascular adhesion protein-1 regulates leukocyte transmigration rate in the retina during diabetes.

A. Hafezi-Moghadam, K. Noda, S. Zandi, 2009, Experimental eye research.

High Incidence of Visual Recovery Among Four Japanese Patients with Leber's Hereditary Optic Neuropathy with the 14484 Mutation

M. Wakakura, Y. Mashima, Y. Oguchi, 1997, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Blockade of vascular adhesion protein-1 attenuates choroidal neovascularization

K. Tsubota, Y. Ozawa, K. Noda, 2012, Molecular vision.

Haplotype analysis of Japanese families with a superficial variant of granular corneal dystrophy: evidence for multiple origins of R124L mutation of kerato-epithelin

D. Schorderet, F. Munier, E. Korvatska, 2000 .

[The role of the basal cell layer in the maintenance of normal corneal epithelium].

M. Yamada, Y. Mashima, 1995, Nippon Ganka Gakkai zasshi.

SCANNING ELECTRON MICROSCOPIC OBSERVATION OF BASAL CELLS FOLLOWING

K. Tsubota, M. Yamada, Y. Mashima, 1996 .

Scanning electron microscopic observation of basal cells following corneal epithelial abrasion

K. Tsubota, M. Yamada, Y. Mashima, 1996, Eye.

Mapping of the human gene for a melanocyte protein Pmel 17 (D12S53E) to chromosome 12q13-q14.

N. Shimizu, S. Minoshima, J. Kudoh, 1995, Genomics.

Transforming growth factor-beta 1 promotes contraction of collagen gel by bovine corneal fibroblasts through differentiation of myofibroblasts.

D. Kurosaka, Y. Mashima, Katsuhiko Kato, 1998, Investigative ophthalmology & visual science.

Clinical Case Notes

K. Shinoda, H. Ohde, Y. Mashima, 2007 .

New method for detecting misrouted retinofugal fibers in humans with albinism by magnetoencephalography

Y. Haruta, H. Kado, K. Shinoda, 2004, Vision Research.

Effect of unoprostone on topographic and blood flow changes in the ischemic optic nerve head of rabbits.

Y. Mashima, T. Sugiyama, H. Oku, 2009, Archives of ophthalmology.

Genetic polymorphisms in the angiotensin II receptor gene and their association with open-angle glaucoma in a Japanese population.

I. Kimura, R. Asaoka, T. Kanamoto, 2005, Investigative ophthalmology & visual science.

Clinical study of the pattern electroretinogram in patients with optic nerve damage

Y. Mashima, Y. Oguchi, 1985, Documenta Ophthalmologica.

Involvement of insulin-like growth factor-I and insulin-like growth factor binding protein-3 in corneal fibroblasts during corneal wound healing.

K. Tsubota, D. Kurosaka, T. Iwata, 2006, Investigative ophthalmology & visual science.

Low levels of plasma endothelin-1 in patients with retinitis pigmentosa

H. Ohguro, M. Nakazawa, Y. Mashima, 2010, Clinical ophthalmology.

Vascular adhesion protein‐1 blockade suppresses choroidal neovascularization

Joan W. Miller, T. Nakazawa, E. Gragoudas, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

A new contact lens for specular microscopic photography

K. Tsubota, Y. Mashima, S. Naoi, 1989 .