Endogenous Substance P in Corneal Epithelial Cells and Keratocytes

スポンサーリンク

概要

論文の詳細を見る
2002-11-01

著者

関連論文

CLINICAL FEATURES OF JAPANESE LEBER'S HEREDITARY OPTIC NEUROPATHY WITH 11778 MUTATION OF MITOCHONDRIAL DNA
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
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
Corneal dystrophies in Japan
Plus/Minus Screening of Rabbit Corneal Endothelial cDNA Library
Analysis of Peripherin/RDS Gene for Japanese Retinal Dystrophies
FREQUENCIES OF POLYMORPHISMS IN THE RHODOPSIN GENE OF JAPANESE RETINITIS PIGMENTOSA AND NORMAL INDIVIDUALS
Trial for New Intraocular Lens Power Calculation Following Phototherapeutic Keratectomy
Molecular Cloning of ELOVL4 Gene from Cynomolgus Monkey (Masasa fascicularis)
Heterozygous Ala137Pro Mutation in Keratin 12 Gene Found in Japanese with Meesmann's Corneal Dystrophy
Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778
Effect of Cyclosporin A Eyedrops on Tear Secretion in Rabbit
Corneal Wound Healing : Immunohistological Features of Extracellular Matrix Following Penetrating Keratoplasty in Rabbits
Arg124Cys Mutation of the βig-h3 Gene in a Japanese Family With Lattice Corneal Dystrophy Type I
The Ultrastructure of the Lens Capsule Abnormalities in Alport's Syndrome
High Level of Fc Epsilon Receptor I-Bindable Immunoglobulin E in the Tear Fluid and Increased Immunoglobulin E-saturated Cells in the Giant Papillae of Vernal Keratoconjunctivitis Patients
The Expression of Laminin-5 and Ultrastructure of the Interface Between Basal Cells and Underlying Stroma in the Keratoconus Cornea
Secondary Keratoconus with Corneal Epithelial Iron Ring Similar to Fleischer's Ring
CLONING AND HIGH EXPRESSION OF RABBIT FKBP25 IN CORNEA
Ocular Fundus Lesions in Systemic Lupus Erythematosus Model Mice
Endogenous Substance P in Corneal Epithelial Cells and Keratocytes
The Effects of Vitamin A Compounds on Hyaluronic Acid Released from Cultured Rabbit Corneal Epithelial Cells and Keratocytes
Influences of Long-term Tolbutamide Administration on Diabetic Syndrome in Alloxan Rabbits

もっと見る

スポンサーリンク