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Volumn 55, Issue 9, 2014, Pages 5572-5581

Generation and characterization of a murine model of bietti crystalline dystrophy

Author keywords

Bietti crystalline dystrophy; CYP4V2; Preclinical model

Indexed keywords

ATROPINE; FATTY ACID BINDING PROTEIN; POLYUNSATURATED FATTY ACID; LIPID;

EID: 84908108215     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.13-13717     Document Type: Article
Times cited : (37)

References (58)
  • 1
    • 0000390337 scopus 로고
    • Ueber familiaeres vorkommen von “retinitis punctata albescens” (verbunden mit “dystrophia marginalis cristallinea corneae”), glitzern des glaskoerpers und anderen degenerativen augenveraenderungen
    • Bietti G. Ueber familiaeres vorkommen von “retinitis punctata albescens” (verbunden mit “dystrophia marginalis cristallinea corneae”), glitzern des glaskoerpers und anderen degenerativen augenveraenderungen. Klin Monbl Augenheilkd. 1937; 99:21.
    • (1937) Klin Monbl Augenheilkd , vol.99 , pp. 21
    • Bietti, G.1
  • 2
    • 84908112674 scopus 로고    scopus 로고
    • National Eye Institute, National Institutes of Health. Facts about Bietti’s crystalline dystrophy. Available at, Accessed August 7
    • National Eye Institute, National Institutes of Health. Facts about Bietti’s crystalline dystrophy. Available at: http://www. nei.nih.gov/Health/biettis/index.asp. Accessed August 7, 2014.
    • (2014)
  • 3
    • 0028032359 scopus 로고
    • Clinical biochemical and pathologic correlations in Bietti’s crystalline dystrophy
    • Kaiser-Kupfer MI, Chan CC, Markello TC, et al. Clinical biochemical and pathologic correlations in Bietti’s crystalline dystrophy. Am J Ophthalmol. 1994;118:569–582.
    • (1994) Am J Ophthalmol , vol.118 , pp. 569-582
    • Kaiser-Kupfer, M.I.1    Chan, C.C.2    Markello, T.C.3
  • 4
    • 2942670444 scopus 로고    scopus 로고
    • Bietti’s crystalline corneoretinal dystrophy: A cross-sectional study
    • Mataftsi A, Zografos L, Milla E, Secretan M, Munier FL. Bietti’s crystalline corneoretinal dystrophy: a cross-sectional study. Retina. 2004;24:416–426.
    • (2004) Retina , vol.24 , pp. 416-426
    • Mataftsi, A.1    Zografos, L.2    Milla, E.3    Secretan, M.4    Munier, F.L.5
  • 6
    • 2342537802 scopus 로고    scopus 로고
    • Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V 2
    • Li A, Jiao X, Munier FL, et al. Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V 2. Am J Hum Genet. 2004;74:817–826.
    • (2004) Am J Hum Genet , vol.74 , pp. 817-826
    • Li, A.1    Jiao, X.2    Munier, F.L.3
  • 7
    • 72349088917 scopus 로고    scopus 로고
    • Bietti’s crystalline dystrophy in Asians: Clinical, angiographic and electrophysiological characteristics
    • Fong AM, Koh A, Lee K, Ang CL. Bietti’s crystalline dystrophy in Asians: clinical, angiographic and electrophysiological characteristics. Int Ophthalmol. 2008;29:459–470.
    • (2008) Int Ophthalmol , vol.29 , pp. 459-470
    • Fong, A.M.1    Koh, A.2    Lee, K.3    Ang, C.L.4
  • 8
    • 43649099131 scopus 로고    scopus 로고
    • Autofluorescence and OCT features of Bietti’s crystalline dystrophy
    • Ayata A, Tathpinar S, Unal M, Ersanli D, Bilge AH. Autofluorescence and OCT features of Bietti’s crystalline dystrophy. Br J Ophthalmol. 2008;92:718–720.
    • (2008) Br J Ophthalmol , vol.92 , pp. 718-720
    • Ayata, A.1    Tathpinar, S.2    Unal, M.3    Ersanli, D.4    Bilge, A.H.5
  • 9
    • 84884288546 scopus 로고    scopus 로고
    • Optical coherence tomographic findings of crystal deposits in the lens and cornea in Bietti crystalline corneoretinopathy associated with mutation in the CYP4V2 gene
    • Chung JK, Shin JH, Jeon BR, Ki CS, Park TK. Optical coherence tomographic findings of crystal deposits in the lens and cornea in Bietti crystalline corneoretinopathy associated with mutation in the CYP4V2 gene. Jpn J Ophthalmol. 2013;57:447–450.
    • (2013) Jpn J Ophthalmol , vol.57 , pp. 447-450
    • Chung, J.K.1    Shin, J.H.2    Jeon, B.R.3    Ki, C.S.4    Park, T.K.5
  • 11
    • 84872948254 scopus 로고    scopus 로고
    • Clinical and genetic features in Italian Bietti crystalline dystrophy patients
    • Rossi S, Testa F, Li A, et al. Clinical and genetic features in Italian Bietti crystalline dystrophy patients. Br J Ophthalmol. 2012;97:174–179.
    • (2012) Br J Ophthalmol , vol.97 , pp. 174-179
    • Rossi, S.1    Testa, F.2    Li, A.3
  • 12
    • 79955816344 scopus 로고    scopus 로고
    • An atypical form of Bietti crystalline dystrophy
    • Rossi S, Testa F, Li A, et al. An atypical form of Bietti crystalline dystrophy. Ophthalmic Genet. 2011;32:118–121.
    • (2011) Ophthalmic Genet , vol.32 , pp. 118-121
    • Rossi, S.1    Testa, F.2    Li, A.3
  • 13
    • 2342537802 scopus 로고    scopus 로고
    • Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V 2
    • Li A, Jiao X, Munier FL, et al. Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V 2. Am J Hum Genet. 2004;74:817–826.
    • (2004) Am J Hum Genet , vol.74 , pp. 817-826
    • Li, A.1    Jiao, X.2    Munier, F.L.3
  • 14
    • 84866882879 scopus 로고    scopus 로고
    • CYP4V2 in Bietti’s crystalline dystrophy: Ocular localization, metabolism of omega-3-polyunsaturated fatty acids, and functional deficit of the p.H331P variant
    • Nakano M, Kelly EJ, Wiek C, Hanenberg H, Rettie AE. CYP4V2 in Bietti’s crystalline dystrophy: ocular localization, metabolism of omega-3-polyunsaturated fatty acids, and functional deficit of the p.H331P variant. Mol Pharmacol. 2012;82:679–686.
    • (2012) Mol Pharmacol , vol.82 , pp. 679-686
    • Nakano, M.1    Kelly, E.J.2    Wiek, C.3    Hanenberg, H.4    Rettie, A.E.5
  • 15
    • 34548381638 scopus 로고    scopus 로고
    • Characterization of orphan human cytochromes P450
    • Stark K, Guengerich FP. Characterization of orphan human cytochromes P450. Drug Metab Rev. 2007;39:627–637.
    • (2007) Drug Metab Rev , vol.39 , pp. 627-637
    • Stark, K.1    Guengerich, F.P.2
  • 16
    • 79955686815 scopus 로고    scopus 로고
    • Finding homes for orphan cytochrome P450s: CYP4V2 and CYP4F22 in disease states
    • Kelly EJ, Nakano M, Rohatgi P, Yarov-Yarovoy V, Rettie AE. Finding homes for orphan cytochrome P450s: CYP4V2 and CYP4F22 in disease states. Mol Interv. 2011;11:124–132.
    • (2011) Mol Interv , vol.11 , pp. 124-132
    • Kelly, E.J.1    Nakano, M.2    Rohatgi, P.3    Yarov-Yarovoy, V.4    Rettie, A.E.5
  • 17
    • 79957914595 scopus 로고    scopus 로고
    • Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy
    • Xiao X, Mai G, Li S, Guo X, Zhang Q. Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy. Biochem Biophys Res Commun. 2011;409:181–186.
    • (2011) Biochem Biophys Res Commun , vol.409 , pp. 181-186
    • Xiao, X.1    Mai, G.2    Li, S.3    Guo, X.4    Zhang, Q.5
  • 18
    • 84863311657 scopus 로고    scopus 로고
    • Clinical and molecular findings in three Lebanese families with Bietti crystalline dystrophy: Report on a novel mutation
    • Haddad NMN, Waked N, Bejjani R, et al. Clinical and molecular findings in three Lebanese families with Bietti crystalline dystrophy: report on a novel mutation. Mol Vis. 2012;18: 1182–1188.
    • (2012) Mol Vis , vol.18 , pp. 1182-1188
    • Haddad, N.M.N.1    Waked, N.2    Bejjani, R.3
  • 19
    • 33749324466 scopus 로고    scopus 로고
    • Clinical and molecular findings in three Japanese patients with crystalline retinopathy
    • Jin Z-B, Ito S, Saito Y, Inoue Y, Yanagi Y, Nao-i N. Clinical and molecular findings in three Japanese patients with crystalline retinopathy. Jpn J Ophthalmol. 2006;50:426–431.
    • (2006) Jpn J Ophthalmol , vol.50 , pp. 426-431
    • Jin, Z.-B.1    Ito, S.2    Saito, Y.3    Inoue, Y.4    Yanagi, Y.5    Nao-I, N.6
  • 20
    • 38449090105 scopus 로고    scopus 로고
    • Genotype phenotype analysis of Bietti’s crystalline dystrophy in patients with CYP4V2 mutations
    • Lai TYY, Ng TK, Tam POS, et al. Genotype phenotype analysis of Bietti’s crystalline dystrophy in patients with CYP4V2 mutations. Invest Ophthalmol Vis Sci. 2007;48:5212–5220.
    • (2007) Invest Ophthalmol Vis Sci , vol.48 , pp. 5212-5220
    • Lai, T.Y.Y.1    Ng, T.K.2    Tam, P.O.S.3
  • 21
    • 32944468810 scopus 로고    scopus 로고
    • Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations
    • Lee KY, Koh AH, Aung T, et al. Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations. Invest Ophthalmol Vis Sci. 2005;46:3812–3816.
    • (2005) Invest Ophthalmol Vis Sci , vol.46 , pp. 3812-3816
    • Lee, K.Y.1    Koh, A.H.2    Aung, T.3
  • 22
    • 26244466736 scopus 로고    scopus 로고
    • Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy
    • Lin J, Nishiguchi KM, Nakamura M, Dryja TP, Berson EL, Miyake Y. Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy. J Med Genet. 2005;42:e38.
    • (2005) J Med Genet , vol.42 , pp. e38
    • Lin, J.1    Nishiguchi, K.M.2    Nakamura, M.3    Dryja, T.P.4    Berson, E.L.5    Miyake, Y.6
  • 23
    • 84857370151 scopus 로고    scopus 로고
    • The characterization of functional disturbances in Chinese patients with Bietti’s crystalline dystrophy at different fundus stages
    • Liu DN, Liu Y, Meng XH, Yin ZQ. The characterization of functional disturbances in Chinese patients with Bietti’s crystalline dystrophy at different fundus stages. Graefes Arch Clin Exp Ophthalmol. 2011;250:191–200.
    • (2011) Graefes Arch Clin Exp Ophthalmol , vol.250 , pp. 191-200
    • Liu, D.N.1    Liu, Y.2    Meng, X.H.3    Yin, Z.Q.4
  • 24
    • 79960719837 scopus 로고    scopus 로고
    • Molecular screening of the CYP4V2 gene in Bietti crystalline dystrophy that is associated with choroidal neovascularization
    • Mamatha G, Umashankar V, Kasinathan N, et al. Molecular screening of the CYP4V2 gene in Bietti crystalline dystrophy that is associated with choroidal neovascularization. Mol Vis. 2011;17:1970–1977.
    • (2011) Mol Vis , vol.17 , pp. 1970-1977
    • Mamatha, G.1    Umashankar, V.2    Kasinathan, N.3
  • 26
    • 80053629974 scopus 로고    scopus 로고
    • Identification of a novel locus for autosomal dominant primary open angle glaucoma on 4q35.1-q35.2
    • Porter LF, Urquhart JE, O’Donoghue E, et al. Identification of a novel locus for autosomal dominant primary open angle glaucoma on 4q35.1-q35.2. Invest Ophthalmol Vis Sci. 2011; 52:7859–7865.
    • (2011) Invest Ophthalmol Vis Sci , vol.52 , pp. 7859-7865
    • Porter, L.F.1    Urquhart, J.E.2    O’donoghue, E.3
  • 27
    • 26244436316 scopus 로고    scopus 로고
    • Novel mutations in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy
    • Shan M, Dong B, Zhao X, et al. Novel mutations in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy. Mol Vis. 2005;11:738–743.
    • (2005) Mol Vis , vol.11 , pp. 738-743
    • Shan, M.1    Dong, B.2    Zhao, X.3
  • 28
    • 18144381887 scopus 로고    scopus 로고
    • Screening for mutations in CYP4V2 gene in Japanese patients with Bietti’s crystalline corneoretinal dystrophy
    • Wada Y, Itabashi T, Sato H, Kawamura M, Tada A, Tamai M. Screening for mutations in CYP4V2 gene in Japanese patients with Bietti’s crystalline corneoretinal dystrophy. Am J Ophthalmol. 2005;139:894–899.
    • (2005) Am J Ophthalmol , vol.139 , pp. 894-899
    • Wada, Y.1    Itabashi, T.2    Sato, H.3    Kawamura, M.4    Tada, A.5    Tamai, M.6
  • 29
    • 84861708894 scopus 로고    scopus 로고
    • Exome sequencing identifies compound heterozygous mutations in CYP4V2 in a pedigree with retinitis pigmentosa
    • Wang Y, Guo L, Cai S-P, et al. Exome sequencing identifies compound heterozygous mutations in CYP4V2 in a pedigree with retinitis pigmentosa. PLoS One. 2012;7:e33673.
    • (2012) PLoS One , vol.7 , pp. e33673
    • Wang, Y.1    Guo, L.2    Cai, S.-P.3
  • 30
    • 84855283008 scopus 로고    scopus 로고
    • Novel compound heterozygous mutation in the CYP4V2 gene in a Japanese patient with Bietti’s crystalline corneoretinal dystrophy
    • Yokoi Y, Sato K, Aoyagi H, Takahashi Y, Yamagami M, Nakazawa MA. Novel compound heterozygous mutation in the CYP4V2 gene in a Japanese patient with Bietti’s crystalline corneoretinal dystrophy. Case Rep Ophthalmol. 2011;2:296–301.
    • (2011) Case Rep Ophthalmol , vol.2 , pp. 296-301
    • Yokoi, Y.1    Sato, K.2    Aoyagi, H.3    Takahashi, Y.4    Yamagami, M.5    Nakazawa, M.A.6
  • 31
    • 77954633030 scopus 로고    scopus 로고
    • Crystal deposits on the lens capsules in Bietti crystalline corneoretinal dystrophy associated with a mutation in the CYP4V2 gene
    • Yokoi Y, Nakazawa M, Mizukoshi S, Sato K, Usui T, Takeuchi K. Crystal deposits on the lens capsules in Bietti crystalline corneoretinal dystrophy associated with a mutation in the CYP4V2 gene. Acta Ophthalmol. 2009;88:607–609.
    • (2009) Acta Ophthalmol , vol.88 , pp. 607-609
    • Yokoi, Y.1    Nakazawa, M.2    Mizukoshi, S.3    Sato, K.4    Usui, T.5    Takeuchi, K.6
  • 32
    • 41949135860 scopus 로고    scopus 로고
    • Novel CYP4V2 gene mutation in a Mexican patient with Bietti’s crystalline corneoretinal dystrophy
    • Zenteno JC, Ayala-Ramirez R, Graue-Wiechers F. Novel CYP4V2 gene mutation in a Mexican patient with Bietti’s crystalline corneoretinal dystrophy. Curr Eye Res. 2008;33: 313–318.
    • (2008) Curr Eye Res , vol.33 , pp. 313-318
    • Zenteno, J.C.1    Ayala-Ramirez, R.2    Graue-Wiechers, F.3
  • 33
    • 84877919711 scopus 로고    scopus 로고
    • A novel mutation in the CYP4V2 gene in a Chinese patient with Bietti’s crystalline dystrophy
    • Song Y, Mo G, Yin G. A novel mutation in the CYP4V2 gene in a Chinese patient with Bietti’s crystalline dystrophy. Int Ophthalmol. 2013;33:269–276.
    • (2013) Int Ophthalmol , vol.33 , pp. 269-276
    • Song, Y.1    Mo, G.2    Yin, G.3
  • 34
    • 84899742789 scopus 로고    scopus 로고
    • Molecular analysis and phenotypic study in 14 Chinese families with Bietti crystalline dystrophy
    • Yin H, Jin C, Fang X, et al. Molecular analysis and phenotypic study in 14 Chinese families with Bietti crystalline dystrophy. PLoS One. 2014;9:e94960.
    • (2014) PLoS One , vol.9 , pp. e94960
    • Yin, H.1    Jin, C.2    Fang, X.3
  • 35
    • 84901782107 scopus 로고    scopus 로고
    • Detailed phenotypic and genotypic characterization of Bietti crystalline dystrophy
    • Halford S, Liew G, Mackay DS, et al. Detailed phenotypic and genotypic characterization of Bietti crystalline dystrophy. Ophthalmology. 2014;1174–1184.
    • (2014) Ophthalmology , pp. 1174-1184
    • Halford, S.1    Liew, G.2    Mackay, D.S.3
  • 36
    • 40949145685 scopus 로고    scopus 로고
    • Gene variants associated with deep vein thrombosis
    • Bezemer ID, Bare LA, Doggen CJ, et al. Gene variants associated with deep vein thrombosis. JAMA. 2008;299: 1306–1314.
    • (2008) JAMA , vol.299 , pp. 1306-1314
    • Bezemer, I.D.1    Bare, L.A.2    Doggen, C.J.3
  • 37
    • 0032191018 scopus 로고    scopus 로고
    • Identification, isolation, and characterization of a 32-kDa fatty acid-binding protein missing from lymphocytes in humans with Bietti crystalline dystrophy (BCD)
    • Lee J, Jiao X, Hejtmancik JF, Kaiser-Kupfer M, Chader GJ. Identification, isolation, and characterization of a 32-kDa fatty acid-binding protein missing from lymphocytes in humans with Bietti crystalline dystrophy (BCD). Mol Genet Metab. 1998;65:143–154.
    • (1998) Mol Genet Metab , vol.65 , pp. 143-154
    • Lee, J.1    Jiao, X.2    Hejtmancik, J.F.3    Kaiser-Kupfer, M.4    Chader, G.J.5
  • 38
    • 0034946012 scopus 로고    scopus 로고
    • The metabolism of fatty acids in human Bietti crystalline dystrophy
    • Lee J, Jiao X, Hejtmancik JF, et al. The metabolism of fatty acids in human Bietti crystalline dystrophy. Invest Ophthalmol Vis Sci. 2001;42:1707–1714.
    • (2001) Invest Ophthalmol Vis Sci , vol.42 , pp. 1707-1714
    • Lee, J.1    Jiao, X.2    Hejtmancik, J.F.3
  • 39
    • 77449129624 scopus 로고    scopus 로고
    • Alterations in serum fatty acid concentrations and desaturase activities in Bietti crystalline dystrophy unaffected by CYP4V2 genotypes
    • Lai TY, Chu KO, Chan KP, et al. Alterations in serum fatty acid concentrations and desaturase activities in Bietti crystalline dystrophy unaffected by CYP4V2 genotypes. Invest Ophthalmol Vis Sci. 2010;51:1092–1097.
    • (2010) Invest Ophthalmol Vis Sci , vol.51 , pp. 1092-1097
    • Lai, T.Y.1    Chu, K.O.2    Chan, K.P.3
  • 40
    • 0026578295 scopus 로고
    • Bietti’s corneal-retinal dystrophy: A 16- year progression
    • Bernauer W, Daicker B. Bietti’s corneal-retinal dystrophy: a 16- year progression. Retina. 1992;12:18–20.
    • (1992) Retina , vol.12 , pp. 18-20
    • Bernauer, W.1    Daicker, B.2
  • 41
    • 84908092156 scopus 로고    scopus 로고
    • Evolution of cellular inclusions in Bietti’s crystalline dystrophy
    • Furusato E, Cameron JD, Chan C-C. Evolution of cellular inclusions in Bietti’s crystalline dystrophy. Ophthalmol Eye Dis. 2010;2010:9–15.
    • (2010) Ophthalmol Eye Dis. 2010 , pp. 9-15
    • Furusato, E.1    Cameron, J.D.2    Chan, C.-C.3
  • 42
    • 70350332200 scopus 로고    scopus 로고
    • Expression and characterization of CYP4V2 as a fatty acid-hydroxylase
    • Nakano M, Kelly EJ, Rettie AE. Expression and characterization of CYP4V2 as a fatty acid-hydroxylase. Drug Metab Dispos. 2009;37:2119–2122.
    • (2009) Drug Metab Dispos , vol.37 , pp. 2119-2122
    • Nakano, M.1    Kelly, E.J.2    Rettie, A.E.3
  • 43
    • 84865608521 scopus 로고    scopus 로고
    • Focus on molecules: Cytochrome P450 family 4, subfamily V, polypeptide 2 (CYP4V2)
    • Mackay DS, Halford S. Focus on molecules: cytochrome P450 family 4, subfamily V, polypeptide 2 (CYP4V2). Exp Eye Res. 2011;102:111–112.
    • (2011) Exp Eye Res , vol.102 , pp. 111-112
    • Mackay, D.S.1    Halford, S.2
  • 44
    • 84856230669 scopus 로고    scopus 로고
    • Development and characterization of transgenic mouse models for conditional gene knockout in the blood-brain and blood-CSF barriers
    • Crouthamel MH, Kelly EJ, Ho RJ. Development and characterization of transgenic mouse models for conditional gene knockout in the blood-brain and blood-CSF barriers. Transgenic Res. 2012;21:113–130.
    • (2012) Transgenic Res , vol.21 , pp. 113-130
    • Crouthamel, M.H.1    Kelly, E.J.2    Ho, R.J.3
  • 45
    • 84880671989 scopus 로고    scopus 로고
    • Generation and characterization of a Cyp4b1 null mouse and the role of CYP4B1 in the activation and toxicity of Ipomeanol
    • Parkinson OT, Liggitt HD, Rettie AE, Kelly EJ. Generation and characterization of a Cyp4b1 null mouse and the role of CYP4B1 in the activation and toxicity of Ipomeanol. Toxicol Sci. 2013;134:243–250.
    • (2013) Toxicol Sci , vol.134 , pp. 243-250
    • Parkinson, O.T.1    Liggitt, H.D.2    Rettie, A.E.3    Kelly, E.J.4
  • 47
    • 0026076158 scopus 로고
    • Mechanisms of clearance of immune complexes from peritubular capillaries in the rat
    • Alpers CE, Hudkins KL, Pritzl P, Johnson RJ. Mechanisms of clearance of immune complexes from peritubular capillaries in the rat. Am J Pathol. 1991;139:855–867.
    • (1991) Am J Pathol , vol.139 , pp. 855-867
    • Alpers, C.E.1    Hudkins, K.L.2    Pritzl, P.3    Johnson, R.J.4
  • 48
    • 84884453781 scopus 로고    scopus 로고
    • The mouse in aging research
    • In: Fox JG, ed., 2nd ed. Burlington, MA: American College Laboratory Animal Medicine (Elsevier)
    • Flurkey K, Currer JM, Harrison DE. The mouse in aging research. In: Fox JG, ed. The Mouse in Biomedical Research. 2nd ed. Burlington, MA: American College Laboratory Animal Medicine (Elsevier); 2007:637–372.
    • (2007) The Mouse in Biomedical Research , pp. 372-637
    • Flurkey, K.1    Currer, J.M.2    Harrison, D.E.3
  • 50
    • 77950615514 scopus 로고    scopus 로고
    • Apolipoprotein Bcontaining lipoproteins in retinal aging and age-related macular degeneration
    • Curcio CA, Johnson M, Huang JD, Rudolf M. Apolipoprotein Bcontaining lipoproteins in retinal aging and age-related macular degeneration. J Lipid Res. 2010;51:451–467.
    • (2010) J Lipid Res , vol.51 , pp. 451-467
    • Curcio, C.A.1    Johnson, M.2    Huang, J.D.3    Rudolf, M.4
  • 51
    • 0020655183 scopus 로고
    • Chemistry and metabolism of lipids in the vertebrate retina
    • Fliesler SJ, Anderson RE. Chemistry and metabolism of lipids in the vertebrate retina. Prog Lipid Res. 1983;22:79–131.
    • (1983) Prog Lipid Res , vol.22 , pp. 79-131
    • Fliesler, S.J.1    Anderson, R.E.2
  • 53
    • 84891863253 scopus 로고    scopus 로고
    • Resolvins, specialized proresolving lipid mediators, and their potential roles in metabolic diseases
    • Spite M, Claria J, Serhan CN. Resolvins, specialized proresolving lipid mediators, and their potential roles in metabolic diseases. Cell Metab. 2014;19:21–36.
    • (2014) Cell Metab , vol.19 , pp. 21-36
    • Spite, M.1    Claria, J.2    Serhan, C.N.3
  • 54
    • 33745621719 scopus 로고    scopus 로고
    • Resolvin D series and Protectin D1 mitigate acute kidney injury
    • Duffield JS, Hong S, Vaidya VS, et al. Resolvin D series and Protectin D1 mitigate acute kidney injury. J Immunol. 2006; 177:5902–5911.
    • (2006) J Immunol , vol.177 , pp. 5902-5911
    • Duffield, J.S.1    Hong, S.2    Vaidya, V.S.3
  • 55
    • 79951561948 scopus 로고    scopus 로고
    • The role of anti-inflammatory agents in age-related macular degeneration (AMD) treatment
    • Wang Y, Wang VM, Chan CC. The role of anti-inflammatory agents in age-related macular degeneration (AMD) treatment. Eye. 2011;25:127–139.
    • (2011) Eye , vol.25 , pp. 127-139
    • Wang, Y.1    Wang, V.M.2    Chan, C.C.3
  • 56
    • 0014972425 scopus 로고
    • Shedding of discs from rod outer segments in the rhesus monkey
    • Young RW. Shedding of discs from rod outer segments in the rhesus monkey. J Ultrastruct Res. 1971;34:190–203.
    • (1971) J Ultrastruct Res , vol.34 , pp. 190-203
    • Young, R.W.1
  • 57
    • 0033597849 scopus 로고    scopus 로고
    • Expression of the CYP4F3 gene. Tissue-specific splicing and alternative promoters generate high and low K(m) forms of leukotriene B(4) omega-hydroxylase
    • Christmas P, Ursino SR, Fox JW, Soberman RJ. Expression of the CYP4F3 gene. Tissue-specific splicing and alternative promoters generate high and low K(m) forms of leukotriene B(4) omega-hydroxylase. J Biol Chem. 1999;274:21191–21199.
    • (1999) J Biol Chem , vol.274 , pp. 21191-21199
    • Christmas, P.1    Ursino, S.R.2    Fox, J.W.3    Soberman, R.J.4
  • 58
    • 84879336390 scopus 로고    scopus 로고
    • Imaging of neutral lipids by oil red O for analyzing the metabolic status in health and disease
    • Mehlem A, Hagberg CE, Muhl L, Eriksson U, Falkevall A. Imaging of neutral lipids by oil red O for analyzing the metabolic status in health and disease. Nat Protoc. 2013;8: 1149–1154.
    • (2013) Nat Protoc , vol.8 , pp. 1149-1154
    • Mehlem, A.1    Hagberg, C.E.2    Muhl, L.3    Eriksson, U.4    Falkevall, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.