메뉴 건너뛰기




Volumn 45, Issue 6, 2004, Pages 2005-2012

Photoreceptor degeneration and loss of retinal function in the C57BL/6-C2J mouse

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FIBROBLAST GROWTH FACTOR 2; GLIAL FIBRILLARY ACIDIC PROTEIN; LEUCINE; METHIONINE; RHODOPSIN;

EID: 3042584839     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.03-0842     Document Type: Article
Times cited : (21)

References (38)
  • 1
    • 0023356308 scopus 로고
    • Strain differences in sensitivity to light-induced photoreceptor degeneration albino mice
    • LaVail M, Gorrin G, Repaci M, Yasumura D. Strain differences in sensitivity to light-induced photoreceptor degeneration albino mice. Curr Eye Res. 1987;6:825-834.
    • (1987) Curr Eye Res , vol.6 , pp. 825-834
    • LaVail, M.1    Gorrin, G.2    Repaci, M.3    Yasumura, D.4
  • 2
    • 0034125911 scopus 로고    scopus 로고
    • A QTL on distal chromosome 3 that influences the severity of light-induced damage to mouse photoreceptors
    • Danciger M, Matthes MT, Yasamura D, et al. A QTL on distal chromosome 3 that influences the severity of light-induced damage to mouse photoreceptors. Mamm Genome. 2000;11:422-427.
    • (2000) Mamm Genome , vol.11 , pp. 422-427
    • Danciger, M.1    Matthes, M.T.2    Yasamura, D.3
  • 3
    • 17344366357 scopus 로고    scopus 로고
    • Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle
    • Redmond TM, Yu S, Lee E, et al. Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle. Nat Genet. 1998;20: 344-351.
    • (1998) Nat Genet , vol.20 , pp. 344-351
    • Redmond, T.M.1    Yu, S.2    Lee, E.3
  • 4
    • 0034105724 scopus 로고    scopus 로고
    • Protection of Rpe65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degeneration
    • Grimm C, Wenzel A, Hafezi F, Yu S, Redmond TM, Reme CE. Protection of Rpe65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degeneration. Nat Genet. 2000;25:63-66.
    • (2000) Nat Genet , vol.25 , pp. 63-66
    • Grimm, C.1    Wenzel, A.2    Hafezi, F.3    Yu, S.4    Redmond, T.M.5    Reme, C.E.6
  • 5
    • 0035144779 scopus 로고    scopus 로고
    • The Rpe65 Leu450Met variation increases retinal resistance against light-induced degeneration by slowing rhodopsin regeneration
    • Wenzel A, Reme CE, Williams TP, Hafezi F, Grimm C. The Rpe65 Leu450Met variation increases retinal resistance against light-induced degeneration by slowing rhodopsin regeneration. J Neurosci. 2001;21:53-58.
    • (2001) J Neurosci , vol.21 , pp. 53-58
    • Wenzel, A.1    Reme, C.E.2    Williams, T.P.3    Hafezi, F.4    Grimm, C.5
  • 6
    • 0141756370 scopus 로고    scopus 로고
    • Electroretinographic evidence for altered phototransduction gain and slowed recovery from photobleaches in albino mice with a MET450 variant in RPE65
    • Nusinowitz S, Nguyen L, Radu R, Kashani Z, Farber D, Danciger M. Electroretinographic evidence for altered phototransduction gain and slowed recovery from photobleaches in albino mice with a MET450 variant in RPE65. Exp Eye Res. 2003;77:627-638.
    • (2003) Exp Eye Res , vol.77 , pp. 627-638
    • Nusinowitz, S.1    Nguyen, L.2    Radu, R.3    Kashani, Z.4    Farber, D.5    Danciger, M.6
  • 7
    • 0030588070 scopus 로고    scopus 로고
    • Base substitution at different alternative splice donor sites of the tyrosinase gene in murine albinism
    • Le Fur N, Kelsall SR, Mintz B. Base substitution at different alternative splice donor sites of the tyrosinase gene in murine albinism. Genomics. 1996;37:245-248.
    • (1996) Genomics , vol.37 , pp. 245-248
    • Le Fur, N.1    Kelsall, S.R.2    Mintz, B.3
  • 8
    • 0036921854 scopus 로고    scopus 로고
    • Developmental death of photoreceptors in the C57BL/6J mouse: Association with retinal function and self-protection
    • Mervin K, Stone J. Developmental death of photoreceptors in the C57BL/6J mouse: association with retinal function and self-protection. Exp Eye Res. 2002;75:703-713.
    • (2002) Exp Eye Res , vol.75 , pp. 703-713
    • Mervin, K.1    Stone, J.2
  • 9
    • 0030826430 scopus 로고    scopus 로고
    • Tissue oxygen during a critical developmental period controls the death and survival of photoreceptors
    • Maslim J, Valter K, Egensperger R, Hollander H, Stone J. Tissue oxygen during a critical developmental period controls the death and survival of photoreceptors. Invest Ophthalmol Vis Sci. 1997; 38:1667-1677.
    • (1997) Invest Ophthalmol Vis Sci , vol.38 , pp. 1667-1677
    • Maslim, J.1    Valter, K.2    Egensperger, R.3    Hollander, H.4    Stone, J.5
  • 10
    • 0026648674 scopus 로고
    • Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation
    • Gavrieli Y, Sherman Y, Ben-Sasson SA. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol. 1992;119:493-501.
    • (1992) J Cell Biol , vol.119 , pp. 493-501
    • Gavrieli, Y.1    Sherman, Y.2    Ben-Sasson, S.A.3
  • 11
    • 0014296712 scopus 로고
    • An electron microscopic study of synapse formation, receptor outer segment development, and other aspects of developing mouse retina
    • Olney JW. An electron microscopic study of synapse formation, receptor outer segment development, and other aspects of developing mouse retina. Invest Ophthalmol Vis Sci. 1968;7:250-267.
    • (1968) Invest Ophthalmol Vis Sci , vol.7 , pp. 250-267
    • Olney, J.W.1
  • 12
    • 0030665993 scopus 로고    scopus 로고
    • Migration and synaptogenesis of cone photoreceptors in the developing mouse retina
    • Rich K, Zhan Y, Blanks J. Migration and synaptogenesis of cone photoreceptors in the developing mouse retina. J Comp Neurol. 1997;388:47-63.
    • (1997) J Comp Neurol , vol.388 , pp. 47-63
    • Rich, K.1    Zhan, Y.2    Blanks, J.3
  • 13
    • 0021679078 scopus 로고
    • Cell death during differentiation of the retina in the mouse
    • Young RW. Cell death during differentiation of the retina in the mouse. J Comp Neurol. 1984;229:362-373.
    • (1984) J Comp Neurol , vol.229 , pp. 362-373
    • Young, R.W.1
  • 14
    • 3042809941 scopus 로고    scopus 로고
    • Photoreceptor death, trophic factor expression, retinal oxygen status and photoreceptor function in the P23H rat: Stress and protection in a slow degeneration
    • In press
    • Yu D, Cringle S, Valter K, Walsh N, Lee D, Stone J. Photoreceptor death, trophic factor expression, retinal oxygen status and photoreceptor function In the P23H rat: stress and protection in a slow degeneration. Invest Ophthalmol Vis Sci. In press.
    • Invest Ophthalmol Vis Sci
    • Yu, D.1    Cringle, S.2    Valter, K.3    Walsh, N.4    Lee, D.5    Stone, J.6
  • 15
    • 0031762302 scopus 로고    scopus 로고
    • Photoreceptor dystrophy in the RCS rat: Roles of oxygen, debris and bFGF
    • Valter K, Maslim J, Bowers F, Stone J. Photoreceptor dystrophy in the RCS rat: Roles of oxygen, debris and bFGF. Invest Ophthalmol Vis Sci. 1998;39:2427-2442.
    • (1998) Invest Ophthalmol Vis Sci , vol.39 , pp. 2427-2442
    • Valter, K.1    Maslim, J.2    Bowers, F.3    Stone, J.4
  • 16
    • 0036925939 scopus 로고    scopus 로고
    • Regulation by oxygen of photoreceptor death in the developing and adult C57BL/6J mouse
    • Mervin K, Stone J. Regulation by oxygen of photoreceptor death in the developing and adult C57BL/6J mouse. Exp Eye Res. 2002;75: 715-722.
    • (2002) Exp Eye Res , vol.75 , pp. 715-722
    • Mervin, K.1    Stone, J.2
  • 17
    • 0023356308 scopus 로고
    • Strain differences in sensitivity to light-induced photoreceptor degeneration in albino mice
    • LaVail MM, Gorrin GM, Repaci MA. Strain differences in sensitivity to light-induced photoreceptor degeneration in albino mice. Curr Eye Res. 1987;6:825-834.
    • (1987) Curr Eye Res , vol.6 , pp. 825-834
    • LaVail, M.M.1    Gorrin, G.M.2    Repaci, M.A.3
  • 18
    • 0034781731 scopus 로고    scopus 로고
    • Cellular and subcellular patterns of expression of bFGF and CNTF in the normal and light stressed adult rat retina
    • Walsh N, Valter K, Stone J. Cellular and subcellular patterns of expression of bFGF and CNTF in the normal and light stressed adult rat retina. Exp Eye Res. 2001;72:495-501.
    • (2001) Exp Eye Res , vol.72 , pp. 495-501
    • Walsh, N.1    Valter, K.2    Stone, J.3
  • 19
    • 17744371655 scopus 로고    scopus 로고
    • A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
    • Boycott KM, Maybaum TA, Naylor MJ, et al. A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants. Hum Genet. 2001;108:91-97.
    • (2001) Hum Genet , vol.108 , pp. 91-97
    • Boycott, K.M.1    Maybaum, T.A.2    Naylor, M.J.3
  • 20
    • 3543100236 scopus 로고    scopus 로고
    • Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23
    • Bech-Hansen NT, Boycott KM, Gratton KJ, Ross DA, Field LL, Pearce WG. Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23. Hum Genet. 1998;103: 124-130.
    • (1998) Hum Genet , vol.103 , pp. 124-130
    • Bech-Hansen, N.T.1    Boycott, K.M.2    Gratton, K.J.3    Ross, D.A.4    Field, L.L.5    Pearce, W.G.6
  • 21
    • 17344366487 scopus 로고    scopus 로고
    • An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
    • Strom TM, Nyakatura G, Apfelstedt-Sylla E, et al. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nature Genet. 1998;19:260-263.
    • (1998) Nature Genet , vol.19 , pp. 260-263
    • Strom, T.M.1    Nyakatura, G.2    Apfelstedt-Sylla, E.3
  • 22
    • 0037215387 scopus 로고    scopus 로고
    • Molecular identity, synaptic localization, and physiology of calcium channels in retinal bipolar cells
    • Berntson A, Taylor WR, Morgans CW. Molecular identity, synaptic localization, and physiology of calcium channels in retinal bipolar cells. J Neurosci Res. 2003;71:146-51.
    • (2003) J Neurosci Res , vol.71 , pp. 146-151
    • Berntson, A.1    Taylor, W.R.2    Morgans, C.W.3
  • 23
    • 0034799576 scopus 로고    scopus 로고
    • Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene
    • Scholl HP, Langrova H, Pusch CM, Wissinger B, Zrenner E, Apfelstedt-Sylla E. Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene. Invest Ophthalmol Vis Sci. 2001;42:2728-2736.
    • (2001) Invest Ophthalmol Vis Sci , vol.42 , pp. 2728-2736
    • Scholl, H.P.1    Langrova, H.2    Pusch, C.M.3    Wissinger, B.4    Zrenner, E.5    Apfelstedt-Sylla, E.6
  • 24
    • 0033762779 scopus 로고    scopus 로고
    • The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
    • Pusch CM, Zeitz C, Brandau O, et al. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. Nat Genet. 2000;26:324-327.
    • (2000) Nat Genet , vol.26 , pp. 324-327
    • Pusch, C.M.1    Zeitz, C.2    Brandau, O.3
  • 26
    • 0037246889 scopus 로고    scopus 로고
    • Identification of the gene and the mutation responsible for the mouse nob phenotype
    • Gregg RG, Mukhopadhyay S, Candille SI, et al. Identification of the gene and the mutation responsible for the mouse nob phenotype. Invest Ophthalmol Vis Sci. 2003;44:378-384.
    • (2003) Invest Ophthalmol Vis Sci , vol.44 , pp. 378-384
    • Gregg, R.G.1    Mukhopadhyay, S.2    Candille, S.I.3
  • 27
    • 0028128535 scopus 로고
    • Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness
    • Gal A, Orth U, Baehr W, Schwinger E, Rosenberg T. Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness. Nature Genet. 1994;7:64-68.
    • (1994) Nature Genet , vol.7 , pp. 64-68
    • Gal, A.1    Orth, U.2    Baehr, W.3    Schwinger, E.4    Rosenberg, T.5
  • 28
    • 0029902034 scopus 로고    scopus 로고
    • Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness
    • Dryja TP, Hahn LB, Reboul T, Arnaud B. Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness. Nature Genet. 1996; 13:358-360.
    • (1996) Nature Genet , vol.13 , pp. 358-360
    • Dryja, T.P.1    Hahn, L.B.2    Reboul, T.3    Arnaud, B.4
  • 29
    • 0032943572 scopus 로고    scopus 로고
    • A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness
    • al-Jandal N, Farrar GJ, Kiang AS, et al. A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. Hum Mutat. 1999;13:75-81.
    • (1999) Hum Mutat , vol.13 , pp. 75-81
    • Al-Jandal, N.1    Farrar, G.J.2    Kiang, A.S.3
  • 30
    • 0027248024 scopus 로고
    • Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
    • Dryja TP, Berson EL, Rao VR, Oprian DD. Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. Nat Genet. 1993;4:280-283.
    • (1993) Nat Genet , vol.4 , pp. 280-283
    • Dryja, T.P.1    Berson, E.L.2    Rao, V.R.3    Oprian, D.D.4
  • 33
    • 0032753090 scopus 로고    scopus 로고
    • Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness)
    • Chen J, Simon MI, Matthes MT, Yasumura D, LaVail MM. Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness). Invest Ophthalmol Vis Sci. 1999;40:2978-2982.
    • (1999) Invest Ophthalmol Vis Sci , vol.40 , pp. 2978-2982
    • Chen, J.1    Simon, M.I.2    Matthes, M.T.3    Yasumura, D.4    LaVail, M.M.5
  • 34
    • 0035425947 scopus 로고    scopus 로고
    • Constitutive "light" adaptation in rods from G90D rhodopsin: A mechanism for human congenital nightblindness without rod cell loss
    • Sieving PA, Fowler ML, Bush RA, et al. Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss. J Neurosci. 2001; 21:5449-5460.
    • (2001) J Neurosci , vol.21 , pp. 5449-5460
    • Sieving, P.A.1    Fowler, M.L.2    Bush, R.A.3
  • 35
    • 0028125886 scopus 로고
    • Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness
    • Rao VR, Cohen GB, Oprian DD. Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. Nature. 1994;367:639-642.
    • (1994) Nature , vol.367 , pp. 639-642
    • Rao, V.R.1    Cohen, G.B.2    Oprian, D.D.3
  • 36
    • 0141918537 scopus 로고    scopus 로고
    • Structure-function analysis of rods and cones in juvenile, adult, and aged C57b1/6 and Balb/c mice
    • Gresh J, Goletz PW, Crouch RK, Rohrer B. Structure-function analysis of rods and cones in juvenile, adult, and aged C57b1/6 and Balb/c mice. Vis Neurosci. 2003;20:211-220.
    • (2003) Vis Neurosci , vol.20 , pp. 211-220
    • Gresh, J.1    Goletz, P.W.2    Crouch, R.K.3    Rohrer, B.4
  • 37
    • 0038823838 scopus 로고    scopus 로고
    • A strong and highly significant QTL on chromosome 6 that protects the mouse from age-related retinal degeneration
    • Danciger M, Lyon J, Worrill D, LaVail MM, Yang H. A strong and highly significant QTL on chromosome 6 that protects the mouse from age-related retinal degeneration. Invest Ophthalmol Vis Sci. 2003;44:2442-2449.
    • (2003) Invest Ophthalmol Vis Sci , vol.44 , pp. 2442-2449
    • Danciger, M.1    Lyon, J.2    Worrill, D.3    LaVail, M.M.4    Yang, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.