Plus/Minus Screening of Rabbit Corneal Endothelial cDNA Library
スポンサーリンク
概要
- 論文の詳細を見る
- 1997-11-01
著者
-
FUJIMAKI Takuro
Department of Ophthalmology, Juntendo University School of Medicine
-
FUJIKI Keiko
Department of Ophthalmology, Juntendo University School of Medicine
-
Fujiki Keiko
Department Of Ophthalmology Juntendo University School Of Medicine
-
Fujiki Keiko
Department Of Biology Faculty Of Science Kumamoto University
-
HOTTA Yoshihiro
Department of Ophthalmology, Juntendo University School of Medicine
-
KANAI Atsushi
Department of Ophthalmology, Juntendo University School of Medicine
-
KITAGAWA Hitoshi
Departments of Veterinary Internal Medicine, Faculty of Agriculture, Gifu Unviersity
-
Hotta Yoshihiro
Department Of Ophthalmology Juntendo University School Of Medicine
-
Kanai Atsushi
Department Of Ophthalmology Juntendo University School Of Medicine
-
Fujimaki Takuro
Department Of Ophthalmology Juntendo University School Of Medicine
-
NAKAYASU Kiyoo
Department of Ophthalmology, Juntendo University School of Medicine
-
SAKUMA Hitoshi
Department of Ophthalmology, Juntendo University School of Medicine
-
Hotta Yoshihiro
Department Of Ophthalmology Hamamatsu University School Of Medicine
-
OHNUKI Hisashi
Department of Ophthalmology, Juntendo University School of Medicine
-
IWATA Fumino
Department of Ophthalmology, Juntendo University School of Medicine
-
WATANABE Michifumi
Department of Ophthalmology, Juntendo University School of Medicine
-
Sakuma Hitoshi
Department Of Mechanical Engineering Science University Of Tokyo
-
Nakayasu Kiyoo
Department Of Ophthalmology Juntendo University School Of Medicine
-
Iwata Fumino
Department Of Ophthalmology Juntendo University School Of Medicine
-
Kanai Atsushi
Department Of Ophthalmology Juntendo Tokyo Koto Geriatric Medical Center
-
Ohnuki Hisashi
Department Of Ophthalmology Juntendo University School Of Medicine
-
Kitagawa Hitoshi
Department Of Electronic Science And Engineering Kyoto University
-
Watanabe Michifumi
Department Of Ophthalmology Juntendo University School Of Medicine
-
Watanabe Michifumi
Department Of Ophthalmology Asama Municipal Hospital
関連論文
- A Novel Mutation (967-970+2)delAAAGGT in the Choroideremia Gene Found in a Japanese Family and Related Clinical Findings
- 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
- Seroepidemiological Investigation of Feline Chlamydiosis in Cats and Human in Japan
- 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.
- 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
- Analysis of Peripherin/RDS Gene for Japanese Retinal Dystrophies
- FREQUENCIES OF POLYMORPHISMS IN THE RHODOPSIN GENE OF JAPANESE RETINITIS PIGMENTOSA AND NORMAL INDIVIDUALS
- Incident of congenital malformations in Tokyo Metropolitan Hospitals, 1979-1993
- Mitochondrial DNA Mutations with Leber's Hereditary Optic Neuropathy in Japanese Patients with Open-Angle Glaucoma
- Estimation of the mode of inheritance, the gene frequency and the manifestation rate of genotypes by maximum likelihood method. : II. The case of parents and sibs of propositus.
- Expression and Distribution of Junctional Adhesion Molecule-1 in the Human Cornea
- Green Photoluminescence from GaInN Photonic Crystals
- Trial for New Intraocular Lens Power Calculation Following Phototherapeutic Keratectomy
- Molecular Cloning of ELOVL4 Gene from Cynomolgus Monkey (Masasa fascicularis)
- Studies on Cardiac Ingredients of Plants. XIII : Chemical Modification of Gitoxin to Cardiotonic Compounds without Vascular Contractile Effect
- Heterozygous Ala137Pro Mutation in Keratin 12 Gene Found in Japanese with Meesmann's Corneal Dystrophy
- Computer Tomography Diagnosis of Meningoencephalocele in a Calf
- 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
- Measurement of Activities of Human Serum Sulfotransferases Which Transfer Sulfate to the Galactose Residues of Keratan Sulfate and to the Nonreducing End N-Acetylglucosamine Residues of N-Acetyllactosamine Trisaccharide: Comparison between Normal Controls
- 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
- Central Corneal Thickness in Japanese Children
- DNA Analysis for Diagnosis of X-Linked Juvenile Retinoschisis When Clinical Examination Is Difficult in a Young Child
- CLONING AND HIGH EXPRESSION OF RABBIT FKBP25 IN CORNEA
- Effects of dimethyl amiloride on ionic and metabolic alterations of isoleted rabbit hearts under ischemia-reperfusion : ^P nuclear magnetic resonance study.
- Service Matching and Collaboration for Electronic Commerce(IEICE/IEEE Joint Special Issue on Autonomous Decentralized Systems and Systems' Assurance)
- Case of a Japanese Patient with X-linked Ocular Albinism Associated with the GPR143 Gene Mutation
- Ocular Fundus Lesions in Systemic Lupus Erythematosus Model Mice
- Genetical Analysis of Bronchial Asthma
- Insulin Responses to Administrations of Amino Acids and Fatty Acids in Healthy Cats
- Endogenous Substance P in Corneal Epithelial Cells and Keratocytes
- ASEBOTOXIN-INDUCED CENTROGENIC PULMONARY HEMORRHAGE IN GUINEA PIGS
- Bilateral Multifocal Retinal Pigment Epithelial Detachments Associated with Abnormal Multifocal Electroretinograms
- Clinical Findings in a Choroideremia Patient Who Underwent Vitrectomy for Retinal Detachment Associated with Macular Hole
- Japanese Black Cattle with Ateliosis Showed Lower Insulin Responses during Glucose Tolerance Test
- Estimations of the Mode of Inheritance, the Gene Frequency and the Manifestation Rate of Genotypes by Maximum Likelihood Method on Human Genetics : I. The Case of Random Family Studies
- A Study of Conical Annular Mixed-Flow Diffusers with Guide Fences
- OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophy
- Novel USH2A mutations in Japanese Usher syndrome type 2 patients : marked differences in the mutation spectrum between the Japanese and other populations
- Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1
- Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes
- The Effects of Vitamin A Compounds on Hyaluronic Acid Released from Cultured Rabbit Corneal Epithelial Cells and Keratocytes
- Insulin and Glucagon Secretory Patterns during Propionate and Arginine Tolerance Tests in Japanese Black Cattle with Growth Retardation
- Relationship between the inotropy speeds in guinea-pig myocardium and lipophilic character of cardenolides and ericaceous toxins.
- Expression Analysis of CCL27 and CCL28 mRNA in Lesional and Non-Lesional Skin of Dogs with Atopic Dermatitis
- Influences of Long-term Tolbutamide Administration on Diabetic Syndrome in Alloxan Rabbits
- A Case of Sectorial Benign Flecked Retina