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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2018, Volume 115, Issue 15, pp. 3936 - 3941
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 03/2019, Volume 60, Issue 4, pp. 1044 - 1049
PURPOSE. We investigate whether choriocapillaris deficits can be visualized in patients with retinitis pigmentosa (RP) using wide-angle swept-source optical... 
swept-source OCT | BIETTI CRYSTALLINE DYSTROPHY | optical coherence tomography angiography | SPECTRAL-DOMAIN | choriocapillaris | retinitis pigmentosa | OPHTHALMOLOGY | MACULAR DEGENERATION | CYP4V2 MUTATIONS | retinal pigment epithelium | NEOVASCULARIZATION
Journal Article
Toxicology and Applied Pharmacology, ISSN 0041-008X, 09/2017, Volume 330, pp. 100 - 106
Because macrophages respond to a variety of pathological and pharmacological reagents, understanding the role of P450s in macrophages is important for... 
THP1 | CYP | Fatty acid metabolism | PPAR gamma | CYP4V2 | Macrophage | CYTOCHROME-P450 | MESSENGER-RNA EXPRESSION | PROSTAGLANDIN-H | BLOOD MONONUCLEAR-CELLS | BRONCHOALVEOLAR MACROPHAGES | GENE | METABOLISM | MONOCYTE-DERIVED MACROPHAGES | PPAR-GAMMA | PHARMACOLOGY & PHARMACY | TOXICOLOGY | INFLAMMATORY MEDIATORS | Tetradecanoylphorbol Acetate | 12-hydroxydodecanoic acid | Fatty Acids | Humans | PPAR alpha | Macrophages | Anilides | Lauric Acids | Liver X Receptors | Cytochrome P450 Family 4 | Transcription, Genetic | CYP4V2 protein, human | lauric acid | Cell Line | Index Medicus | Gene Expression Regulation, Enzymologic | Hydroxycholesterols | RNA, Small Interfering | 22-hydroxycholesterol | 2-chloro-5-nitrobenzanilide | RNA, Messenger | PPAR alpha - pharmacology | Gene Expression Regulation, Enzymologic - drug effects | RNA, Small Interfering - genetics | PPAR alpha - antagonists & inhibitors | Tetradecanoylphorbol Acetate - pharmacology | Liver X Receptors - antagonists & inhibitors | RNA, Messenger - genetics | PPAR alpha - genetics | Lauric Acids - metabolism | Cytochrome P450 Family 4 - biosynthesis | Hydroxycholesterols - pharmacology | Macrophages - enzymology | RNA, Messenger - biosynthesis | Anilides - pharmacology | Macrophages - drug effects | Fatty Acids - metabolism | Cytochrome P450 Family 4 - genetics | Metabolites | RNA | Atherosclerosis | Cytochrome P-450 | Genetic aspects | Genetic transcription | Fatty acids | Medical colleges | Pharmacogenetics | Liver | Physiological aspects | DNA polymerases
Journal Article
Zhonghua Shiyan Yanke Zazhi/Chinese Journal of Experimental Ophthalmology, ISSN 2095-0160, 07/2018, Volume 36, Issue 7, pp. 559 - 563
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2015, Volume 8, Issue 3, pp. 465 - 469
AIM: To analyze the CYP4V2 mutations in five unrelated Chinese patients with Bietti crystalline corneoretinal dystrophy(BCD) and to provide clinical features... 
corneoretinal | mutation | dystrophy | gene | CYP4V2 | Bietti’s | Bietti’s dystrophy | Corneoretinal dystrophy | Mutation | CYP4V2 gene | GENE | FAMILIES | OPHTHALMOLOGY | RETINOPATHY | CHOROIDAL NEOVASCULARIZATION | IDENTIFICATION | comeoretinal dystrophy | Bietti's dystrophy | corneoretinal dystrophy
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 04/2018, Volume 115, Issue 15, pp. 3936 - 3941
Bietti’s crystalline dystrophy (BCD) is an intractable and progressive chorioretinal degenerative disease caused by mutations in the CYP4V2 gene, resulting in... 
Animal models | Lipids | Retina | Cyclodextrins | Autophagy | Muscular dystrophy | Accumulation | Retinal pigment epithelium | Genotype & phenotype | Reduction | Autopsy | Crystal structure | Phenotypes | Crystallinity | Epithelium | Patients | Cholesterol | Studies | Cyclodextrin | Cell death | Blindness | Stem cells | Dystrophy | Mutation | Tocopherol | Phagocytosis | Cytoplasm | Pluripotency | Inhibitory postsynaptic potentials
Journal Article
Journal Article
Journal of Ophthalmology, ISSN 2090-004X, 2019, Volume 2019, pp. 2097087 - 7
Purpose. Several studies have indicated morphological changes in the choroid in amblyopia cases. This study investigates whether choroidal vasculature was... 
MEDICINE, RESEARCH & EXPERIMENTAL | BIETTI CRYSTALLINE DYSTROPHY | CHILDRENS EYES | OPHTHALMOLOGY | CYP4V2 MUTATIONS | LUTEIN | RETINITIS-PIGMENTOSA | THICKNESS | FEATURES
Journal Article
JAPANESE JOURNAL OF OPHTHALMOLOGY, ISSN 0021-5155, 09/2006, Volume 50, Issue 5, pp. 426 - 431
Purpose: To identify CYP4V2 mutations in three unrelated Japanese patients with Bietti crystalline corneoretinal dystrophy (BCD). Methods: The three cases were... 
Bietti crystalline corneoretinal dystrophy | CYP4V2 | gene mutation | OPHTHALMOLOGY | MUTATIONS | CYP4V2 GENE | CORNEO-RETINAL DYSTROPHY
Journal Article
International Ophthalmology, ISSN 0165-5701, 6/2013, Volume 33, Issue 3, pp. 269 - 276
Bietti crystalline corneoretinal dystrophy (BCD, MIM 210370) is a type of hereditary retinal disorder which commonly occurs in China. It is known that... 
Ophthalmology | Medicine & Public Health | Bietti crystalline dystrophy | CYP4V2 gene
Journal Article
Ophthalmology, ISSN 0161-6420, 2014, Volume 121, Issue 6, pp. 1174 - 1184
Journal Article
The British journal of ophthalmology, ISSN 0007-1161, 02/2018, Volume 102, Issue 2, pp. 187 - 194
Journal Article
Journal Article