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Human genome variation, ISSN 2054-345X, 2019, Volume 6, Issue 1, pp. 18 - 5
We analyzed two siblings in a Japanese family with delayed onset cone-rod dystrophy (CRD) using whole-exome sequencing. A novel frameshift c.1106dup... 
Journal Article
Japanese Journal of Ophthalmology, ISSN 0021-5155, 3/2018, Volume 62, Issue 2, pp. 186 - 193
Journal Article
Journal of Reproduction and Development, ISSN 0916-8818, 01/2019, Volume 65, Issue 4, pp. 327 - 334
In mammals, ejaculated sperm acquire their fertilizing ability during migration through the female reproductive tract, which secretes several factors that... 
Tyrosine | Frogs | Immunohistochemistry | Glutamic acid | Capacitation | Phosphorylation | Estrus | Immunocytochemistry | Sperm | Central nervous system | Acrosome reaction | mRNA | Glutamate decarboxylase | γ-Aminobutyric acid | Uterus | Oviduct | Reproductive system
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 01/2018, Volume 2018, Issue 2, pp. 170 - 177
A simple, general method for the synthesis of fully substituted 5‐selanyl‐1,2,3‐triazoles is described. In the presence of CuI (10 mol‐%) and... 
Antimony | Multicomponent reactions | Selenium | Copper | Triazoles | Alkynes | ROOM-TEMPERATURE | C-SE | CHEMISTRY, ORGANIC | SE BOND FORMATION | ARYLBORONIC ACIDS | ANTIOXIDANT PROPERTIES | ARYL BORONIC ACIDS | COUPLING REACTIONS | DIPHENYL DISELENIDE | ORGANOSELENIUM CHEMISTRY | SELECTIVE INHIBITORS | Azides (organic) | Selenides | Chemical synthesis | Tellurium
Journal Article
Applied Microbiology and Biotechnology, ISSN 0175-7598, 1/2018, Volume 102, Issue 1, pp. 261 - 268
Japanese cedar pollinosis is a seasonal allergic disease caused by two major pollen allergens: Cry j 1 and Cry j 2 antigens. To develop an oral vaccine to... 
Life Sciences | Biotechnology | Lactococcus lactis | Nisin | Microbiology | Microbial Genetics and Genomics | Japanese cedar pollen allergen | T cell epitope | ORAL VACCINE | ESCHERICHIA-COLI | CRYPTOMERIA-JAPONICA POLLEN | CRY-J-II | POLLINOSIS | SYSTEM NICE | CLONING | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | FUSION PROTEIN | ACID BACTERIA | HELICOBACTER-PYLORI | Adjuvants, Immunologic - administration & dosage | Humans | Nisin - administration & dosage | Epitopes, T-Lymphocyte - genetics | Lactococcus lactis - metabolism | Pollen - immunology | Rhinitis, Allergic, Seasonal - immunology | Rhinitis, Allergic, Seasonal - therapy | Immunoglobulin E - immunology | Allergens - immunology | Epitopes, T-Lymphocyte - drug effects | Epitopes, T-Lymphocyte - immunology | Cryptomeria - immunology | Lactococcus lactis - genetics | Recombinant Proteins - metabolism | Cholera Toxin - administration & dosage | Plant Proteins - immunology | Allergens - genetics | Recombinant Proteins - genetics | Rhinitis, Allergic, Seasonal - prevention & control | Plant Proteins - genetics | Nisin - pharmacology | Bacterial Vaccines - immunology | Cholera Toxin - genetics | Escherichia coli - genetics | Plasmids | Epitopes, T-Lymphocyte - metabolism | Lactococcus lactis - drug effects | Prevention | Allergy | Antigens | Usage | Peptides | Lactococcus | T cells | Health aspects | Allergic reaction | Water-borne diseases | Allergens | Cell culture | Cry j 1 antigen | Escherichia coli | Lymphocytes T | Infections | Vaccines | Cedar | Lymphocytes | Bacteria | Pollen | Cholera toxin | Public health | Recombinant | Cholera toxin B subunit | Toxin b | Cloning vectors | Cloning | C-Terminus | Epitopes | Gene expression | Cholera | Pollinosis | Index Medicus
Journal Article
Case Reports in Ophthalmology, ISSN 1663-2699, 01/2017, Volume 8, Issue 1, pp. 237 - 244
This report describes a 45-year-old man with complete congenital stationary night blindness (CSNB1) who has been followed up for 38 years. The patient first... 
Visual function | Electroretinogram | Long-term observation | Complete congenital stationary night blindness | Hospitals | Tomography | Optics | Retina | Mutation | Ophthalmology | Patients | Age
Journal Article
Journal of Reproduction and Development, ISSN 0916-8818, 2019
Journal Article
Coastal Engineering Journal, ISSN 2166-4250, 03/2012, Volume 54, Issue 1, pp. 1250001-1 - 1250001-27
At 14:46 local time on March 11, 2011, a magnitude 9.0 earthquake occurred off the coast of northeast Japan. This earthquake generated a tsunami that struck... 
inundation height | Tsunami | run-up height | post event survey | ENGINEERING, CIVIL | SRI-LANKA | ENGINEERING, OCEAN | INDIAN-OCEAN TSUNAMI | Surveys | Tsunamis | Earthquakes | Japan | Databases | Earthquake engineering | Satellite navigation systems | Coastal environments | Seismic phenomena | Inundation | Global Positioning System
Journal Article
Molecular Vision, ISSN 1090-0535, 04/2018, Volume 24, pp. 286 - 296
Purpose: To report genetic and clinical features of two unrelated Japanese patients with early onset flecked retinal dystrophy. Methods: Patients underwent... 
TRIAL | LEBER CONGENITAL AMAUROSIS | FUNDUS-ALBIPUNCTATUS | EFFICACY | VISUAL FUNCTION | SAFETY | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECESSIVE RETINITIS-PIGMENTOSA | OPHTHALMOLOGY | GENE-THERAPY | OPEN-LABEL | MUTATIONS | Blindness | Retinal degeneration | Retina | Dystrophy | Nyctalopia | Patients | Acuity | Electroretinograms | Index Medicus
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1661-6596, 03/2019, Volume 20, Issue 6, p. 1518
X-linked retinitis pigmentosa (XLRP) is a type of severe retinal dystrophy, and female carriers of XLRP demonstrate markedly variable clinical severity. In... 
COMPREHENSIVE MOLECULAR DIAGNOSIS | NORTH-AMERICAN COHORT | FUNDUS AUTOFLUORESCENCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | RP2 GENE | IDENTIFICATION | CHEMISTRY, MULTIDISCIPLINARY | X-linked inheritance | RPGR | LEBER CONGENITAL AMAUROSIS | RP2 | FAMILIES | retinitis pigmentosa | MUTATIONS | visual function | genetic findings | Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 8279 - 11
Leber congenital amaurosis (LCA) is a genetically and clinically heterogeneous disease, and represents the most severe form of inherited retinal dystrophy... 
CLINICAL DEFINITION | REFINEMENT | NMNAT1 | ONSET RETINAL DYSTROPHY | RPGRIP1 GENE | MULTIDISCIPLINARY SCIENCES | DISEASE | RECESSIVE RETINITIS-PIGMENTOSA | GENETIC-HETEROGENEITY | COHORT | MUTATIONS | Polymerase chain reaction | Copy number | Blindness | Retinal degeneration | Retina | Diagnosis | Mutation | Dystrophy
Journal Article
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