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Generation and characterization of a murine model of Bietti crystalline dystrophy

Generation and characterization of a murine model of Bietti crystalline dystrophy

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The Crystal Structure of Cytochrome P450 4B1 (CYP4B1) Monooxygenase Complexed with Octane Discloses Several Structural Adaptations for ω-Hydroxylation.A Novel, Real-Time, In Vivo Mouse Retinal Imaging System Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy.Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularization.Specific regulation of thermosensitive lipid droplet fusion by a nuclear hormone receptor pathway.Reduction of lipid accumulation rescues Bietti's crystalline dystrophy phenotypes.

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P2860

Generation and characterization of a murine model of Bietti crystalline dystrophy

http://www.wikidata.org/entity/Q34159536

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Generation and characterization of a murine model of Bietti crystalline dystrophy

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Generation and characterization of a murine model of Bietti crystalline dystrophy

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Generation and characterization of a murine model of Bietti crystalline dystrophy

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type

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Generation and characterization of a murine model of Bietti crystalline dystrophy

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Generation and characterization of a murine model of Bietti crystalline dystrophy

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Generation and characterization of a murine model of Bietti crystalline dystrophy

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prefLabel

Generation and characterization of a murine model of Bietti crystalline dystrophy

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Generation and characterization of a murine model of Bietti crystalline dystrophy

@en

Generation and characterization of a murine model of Bietti crystalline dystrophy

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Investigative Ophthalmology & Visual Science

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Generation and characterization of a murine model of Bietti crystalline dystrophy

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P2093

Allan E Rettie

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Catherine M Lockhart

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Edward J Kelly

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Mariko Nakano

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P2860

Exome sequencing identifies compound heterozygous mutations in CYP4V2 in a pedigree with retinitis pigmentosa.

Expression and characterization of CYP4V2 as a fatty acid omega-hydroxylase

Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2

Evolution of Cellular Inclusions in Bietti's Crystalline Dystrophy

Retinitis pigmentosa

Molecular analysis and phenotypic study in 14 Chinese families with Bietti crystalline dystrophy

Apolipoprotein B-containing lipoproteins in retinal aging and age-related macular degeneration.

Expression of the CYP4F3 gene. tissue-specific splicing and alternative promoters generate high and low K(m) forms of leukotriene B(4) omega-hydroxylase.

Omega-3 fatty acids and their lipid mediators: towards an understanding of resolvin and protectin formation.

Screening for mutations in CYP4V2 gene in Japanese patients with Bietti's crystalline corneoretinal dystrophy.

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5572-5581

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scholarly article

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10.1167/IOVS.13-13717

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9

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