Found: 102
Select item for more details and to access through your institution.
High-Resolution Adaptive Optics Retinal Image Analysis at Early Stage Central Areolar Choroidal Dystrophy With PRPH2 Mutation.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Spontaneous Resolution of Large Macular Retinoschisis in Enhanced S-Cone Syndrome.
- Published in:
- 2016
- By:
- Publication type:
- journal article
The importance of gene order in expression of the red and green visual pigment genes and in color vision.
- Published in:
- Color Research & Application, 2001, v. 26, n. S1, p. S79, doi. 10.1002/1520-6378(2001)26:1+<::AID-COL18>3.0.CO;2-4
- By:
- Publication type:
- Article
Number and arrangement of the red and green visual pigment genes in color-normal Japanese males.
- Published in:
- Color Research & Application, 2001, v. 26, n. S1, p. S84, doi. 10.1002/1520-6378(2001)26:1+<::AID-COL19>3.0.CO;2-1
- By:
- Publication type:
- Article
Increased Iron and Free Radical Generation in Preclinical Alzheimer Disease and Mild Cognitive Impairment.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 19, n. 1, p. 363, doi. 10.3233/JAD-2010-1239
- By:
- Publication type:
- Article
Reexamining Alzheimer's disease: evidence for a protective role for amyloid-beta protein precursor and amyloid-beta.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Reexamining Alzheimer's Disease: Evidence for a Protective Role for Amyloid-β Protein Precursor and Amyloid-β.
- Published in:
- Journal of Alzheimer's Disease, 2009, v. 18, n. 2, p. 447, doi. 10.3233/JAD-2009-1151
- By:
- Publication type:
- Article
Longitudinal follow-up of two patients with isolated paracentral acute middle maculopathy.
- Published in:
- International Medical Case Reports Journal, 2019, v. 12, p. 143, doi. 10.2147/IMCRJ.S196047
- By:
- Publication type:
- Article
Choroidal thickening and macular serous retinal detachment in pregnancy-induced hypertension.
- Published in:
- International Medical Case Reports Journal, 2015, v. 8, p. 291, doi. 10.2147/IMCRJ.S95442
- By:
- Publication type:
- Article
Chemical constituents of an Uzbek medicinal plant, Perovskia scrophularifolia.
- Published in:
- Journal of Natural Medicines, 2007, v. 61, n. 1, p. 84, doi. 10.1007/s11418-006-0023-9
- By:
- Publication type:
- Article
Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35152-6
- By:
- Publication type:
- Article
Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29891-9
- By:
- Publication type:
- Article
ABCC6 Gene Analysis in 20 Japanese Patients with Angioid Streaks Revealing Four Frequent and Two Novel Variants and Pseudodominant Inheritance.
- Published in:
- Journal of Ophthalmology, 2017, p. 1, doi. 10.1155/2017/1079687
- By:
- Publication type:
- Article
The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1 -Related Retinal Dystrophy in Japanese Patients.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 18, p. 13678, doi. 10.3390/ijms241813678
- By:
- Publication type:
- Article
Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1331, doi. 10.3390/ijms21041331
- By:
- Publication type:
- Article
X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 6, p. 1518, doi. 10.3390/ijms20061518
- By:
- Publication type:
- Article
A novel mutation (Cys83Tyr) in the second zinc finger of NR2E3 in enhanced S-cone syndrome.
- Published in:
- Graefe's Archive of Clinical & Experimental Ophthalmology, 2011, v. 249, n. 2, p. 201, doi. 10.1007/s00417-010-1482-y
- By:
- Publication type:
- Article
Genetic Analyses of Elys Mutations in Drosophila Show Maternal-Effect Lethality and Interactions with Nucleoporin Genes.
- Published in:
- G3: Genes | Genomes | Genetics, 2018, v. 8, n. 7, p. 2421, doi. 10.1534/g3.118.200361
- By:
- Publication type:
- Article
Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia.
- Published in:
- Genes, 2023, v. 14, n. 7, p. 1483, doi. 10.3390/genes14071483
- By:
- Publication type:
- Article
Genetic and Phenotypic Landscape of PRPH2 -Associated Retinal Dystrophy in Japan.
- Published in:
- Genes, 2021, v. 12, n. 11, p. 1817, doi. 10.3390/genes12111817
- By:
- Publication type:
- Article
High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation.
- Published in:
- Journal of Ophthalmology, 2014, p. 1, doi. 10.1155/2014/283603
- By:
- Publication type:
- Article
RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa.
- Published in:
- Journal of Ophthalmology, 2014, p. 1, doi. 10.1155/2014/210947
- By:
- Publication type:
- Article
Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.
- Published in:
- Molecular Vision, 2019, v. 25, p. 559
- By:
- Publication type:
- Article
Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants.
- Published in:
- Molecular Vision, 2018, v. 24, p. 286
- By:
- Publication type:
- Article
Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and NitroalkenesWe thank Prof. K. Saigo and Dr. Y. Ishida (The University of Tokyo) for the use of a high-pressure mercury lamp. This work was partially supported by a Grand-in-Aid for Scientific Research on Priority Area (A): “Creation of Biologically Functional Molecules”, from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.
- Published in:
- Angewandte Chemie, 2005, v. 117, n. 27, p. 4284, doi. 10.1002/ange.200500599
- By:
- Publication type:
- Article
Arsenic-containing ribofuranosides and dimethylarsinic acid in green seaweed, Codium fragile.
- Published in:
- Applied Organometallic Chemistry, 1988, v. 2, n. 4, p. 365, doi. 10.1002/aoc.590020414
- By:
- Publication type:
- Article
Nationwide epidemiologic survey on incidence of macular dystrophy in Japan.
- Published in:
- Japanese Journal of Ophthalmology, 2024, v. 68, n. 3, p. 167, doi. 10.1007/s10384-024-01060-8
- By:
- Publication type:
- Article
Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy.
- Published in:
- Japanese Journal of Ophthalmology, 2017, v. 61, n. 5, p. 395, doi. 10.1007/s10384-017-0522-0
- By:
- Publication type:
- Article
In vivo imaging of a cone mosaic in a patient with achromatopsia associated with a GNAT2 variant.
- Published in:
- Japanese Journal of Ophthalmology, 2017, v. 61, n. 1, p. 92, doi. 10.1007/s10384-016-0484-7
- By:
- Publication type:
- Article
New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome.
- Published in:
- Japanese Journal of Ophthalmology, 2016, v. 60, n. 6, p. 476, doi. 10.1007/s10384-016-0470-0
- By:
- Publication type:
- Article
Clinical heterogeneity between two Japanese siblings with congenital achromatopsia.
- Published in:
- Visual Neuroscience, 2004, v. 21, n. 3, p. 413, doi. 10.1017/s0952523804213396
- By:
- Publication type:
- Article
High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Clinical and genetic characteristics of 10 Japanese patients with PROM1‐associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 3, p. 656, doi. 10.1002/ajmg.c.31826
- By:
- Publication type:
- Article
Paraquat- and Diquat-Induced Oxygen Radical Generation and Lipid Peroxidation in Rat Brain Microsomes.
- Published in:
- Journal of Biochemistry, 2002, v. 131, n. 4, p. 565, doi. 10.1093/oxfordjournals.jbchem.a003135
- By:
- Publication type:
- Article
Configuration of the neoaortic root after chimney reconstruction in the Norwood procedure.
- Published in:
- European Journal of Cardio-Thoracic Surgery, 2024, v. 65, n. 4, p. 1, doi. 10.1093/ejcts/ezae103
- By:
- Publication type:
- Article
Elective neck dissection for T3–T4N0 laryngeal carcinoma: evidence from Japan's National Head and Neck Cancer Registry.
- Published in:
- International Journal of Clinical Oncology, 2023, v. 28, n. 2, p. 209, doi. 10.1007/s10147-022-02275-w
- By:
- Publication type:
- Article
Clinical findings in eyes with BEST1-related retinopathy complicated by choroidal neovascularization.
- Published in:
- Graefe's Archive of Clinical & Experimental Ophthalmology, 2022, v. 260, n. 4, p. 1125, doi. 10.1007/s00417-021-05447-y
- By:
- Publication type:
- Article
One-year results of reduced fluence photodynamic therapy for central serous chorioretinopathy: the outer nuclear layer thickness is associated with visual prognosis.
- Published in:
- Graefe's Archive of Clinical & Experimental Ophthalmology, 2013, v. 251, n. 8, p. 1909, doi. 10.1007/s00417-013-2289-4
- By:
- Publication type:
- Article
Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65737-z
- By:
- Publication type:
- Article
Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-62119-3
- By:
- Publication type:
- Article
Efficacy of reduced-fluence photodynamic therapy for serous retinal pigment epithelial detachment with choroidal hyperpermeability.
- Published in:
- 2013
- By:
- Publication type:
- Case Study
Choroidal neovascularization after blunt ocular trauma in angioid streaks.
- Published in:
- Clinical Ophthalmology, 2013, v. 7, p. 1347, doi. 10.2147/OPTH.S45818
- By:
- Publication type:
- Article
Whole Exome Analysis Identifies Frequent CNGA1 Mutations in Japanese Population with Autosomal Recessive Retinitis Pigmentosa.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0108721
- By:
- Publication type:
- Article
Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.
- Published in:
- Nature Genetics, 1999, v. 22, n. 1, p. 90, doi. 10.1038/8798
- By:
- Publication type:
- Article
Genome mining of the sordarin biosynthetic gene cluster from Sordaria araneosa Cain ATCC 36386: characterization of cycloaraneosene synthase and GDP-6-deoxyaltrose transferase.
- Published in:
- Journal of Antibiotics, 2016, v. 69, n. 7, p. 541, doi. 10.1038/ja.2016.40
- By:
- Publication type:
- Article
Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy.
- Published in:
- Documenta Ophthalmologica, 2024, v. 148, n. 3, p. 173, doi. 10.1007/s10633-024-09971-0
- By:
- Publication type:
- Article
A mild form of POC1B-associated retinal dystrophy with relatively preserved cone system function.
- Published in:
- Documenta Ophthalmologica, 2023, v. 147, n. 1, p. 59, doi. 10.1007/s10633-023-09936-9
- By:
- Publication type:
- Article
Electroretinographic abnormalities in Alport syndrome with a novel COL4A5 truncated variant (p.Try20GlyfsTer19).
- Published in:
- Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 281, doi. 10.1007/s10633-023-09935-w
- By:
- Publication type:
- Article