메뉴 건너뛰기




Volumn 116, Issue 5, 2009, Pages 971-980

Cellular and Molecular Origin of Circumpapillary Dysgenesis of the Pigment Epithelium

Author keywords

[No Author keywords available]

Indexed keywords

HEPATOCYTE NUCLEAR FACTOR 3BETA; TRANSCRIPTION FACTOR;

EID: 65349106533     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ophtha.2008.10.032     Document Type: Article
Times cited : (6)

References (32)
  • 1
    • 33645437822 scopus 로고
    • Su una particolare anomalia bilaterale e simmetrica dello strato pigmento retinico
    • Rubino A. Su una particolare anomalia bilaterale e simmetrica dello strato pigmento retinico. Boll Ocul 19 (1940) 318-321
    • (1940) Boll Ocul , vol.19 , pp. 318-321
    • Rubino, A.1
  • 2
    • 0002918718 scopus 로고
    • A curious affection of the fundus oculi: helicoid peripapillar chorioretinal degeneration-its relation to pigmentary paravenous chorioretinal degeneration
    • Franceschetti A. A curious affection of the fundus oculi: helicoid peripapillar chorioretinal degeneration-its relation to pigmentary paravenous chorioretinal degeneration. Doc Ophthalmol 16 (1962) 81-110
    • (1962) Doc Ophthalmol , vol.16 , pp. 81-110
    • Franceschetti, A.1
  • 3
    • 0018378439 scopus 로고
    • Helicoidal peripapillary chorioretinal degeneration
    • Sveinsson K. Helicoidal peripapillary chorioretinal degeneration. Acta Ophthalmol (Copenh) 57 (1979) 69-75
    • (1979) Acta Ophthalmol (Copenh) , vol.57 , pp. 69-75
    • Sveinsson, K.1
  • 5
    • 2442603612 scopus 로고    scopus 로고
    • A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)
    • Fossdal R., Jonasson F., Kristjansdottir G.T., et al. A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration). Hum Mol Genet 13 (2004) 975-981
    • (2004) Hum Mol Genet , vol.13 , pp. 975-981
    • Fossdal, R.1    Jonasson, F.2    Kristjansdottir, G.T.3
  • 6
    • 36348985077 scopus 로고    scopus 로고
    • Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junction
    • Jonasson F., Sander B., Eysteinsson T., et al. Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junction. Acta Ophthalmol Scand 85 (2007) 862-867
    • (2007) Acta Ophthalmol Scand , vol.85 , pp. 862-867
    • Jonasson, F.1    Sander, B.2    Eysteinsson, T.3
  • 7
    • 34547230151 scopus 로고    scopus 로고
    • Sveinsson chorioretinal atrophy/helicoid peripapillary chorioretinal degeneration: first histopathology report
    • Jonasson F., Hardarson S., Olafsson B.M., and Klintworth G.K. Sveinsson chorioretinal atrophy/helicoid peripapillary chorioretinal degeneration: first histopathology report. Ophthalmology 114 (2007) 1541-1546
    • (2007) Ophthalmology , vol.114 , pp. 1541-1546
    • Jonasson, F.1    Hardarson, S.2    Olafsson, B.M.3    Klintworth, G.K.4
  • 8
    • 33645224114 scopus 로고    scopus 로고
    • Defects in yolk sac vasculogenesis, chorioallantoic fusion, and embryonic axis elongation in mice with targeted disruption of Yap65
    • Morin-Kensicki E.M., Boone B.N., Howell M., et al. Defects in yolk sac vasculogenesis, chorioallantoic fusion, and embryonic axis elongation in mice with targeted disruption of Yap65. Mol Cell Biol 26 (2006) 77-87
    • (2006) Mol Cell Biol , vol.26 , pp. 77-87
    • Morin-Kensicki, E.M.1    Boone, B.N.2    Howell, M.3
  • 9
    • 34547907131 scopus 로고    scopus 로고
    • A Sveinsson's chorioretinal atrophy-associated missense mutation in mouse TEAD1 affects its interaction with the co-factors YAP and TAZ
    • Kitagawa M. A Sveinsson's chorioretinal atrophy-associated missense mutation in mouse TEAD1 affects its interaction with the co-factors YAP and TAZ. Biochem Biophys Res Commun 361 (2007) 1022-1026
    • (2007) Biochem Biophys Res Commun , vol.361 , pp. 1022-1026
    • Kitagawa, M.1
  • 10
    • 0028997651 scopus 로고
    • Characterization of the mammalian YAP (Yes-associated protein) gene and its role in defining a novel protein module, the WW domain
    • Sudol M., Bork P., Einbond A., et al. Characterization of the mammalian YAP (Yes-associated protein) gene and its role in defining a novel protein module, the WW domain. J Biol Chem 270 (1995) 14733-14741
    • (1995) J Biol Chem , vol.270 , pp. 14733-14741
    • Sudol, M.1    Bork, P.2    Einbond, A.3
  • 11
    • 0037131389 scopus 로고    scopus 로고
    • "Stemness": transcriptional profiling of embryonic and adult stem cells
    • Ramalho-Santos M., Yoon S., Matsuzaki Y., et al. "Stemness": transcriptional profiling of embryonic and adult stem cells. Science 298 (2002) 597-600
    • (2002) Science , vol.298 , pp. 597-600
    • Ramalho-Santos, M.1    Yoon, S.2    Matsuzaki, Y.3
  • 12
    • 28044443871 scopus 로고    scopus 로고
    • TEAD proteins activate the Foxa2 enhancer in the node in cooperation with a second factor
    • Sawada A., Nishizaki Y., Sato H., et al. TEAD proteins activate the Foxa2 enhancer in the node in cooperation with a second factor. Development 132 (2005) 4719-4729
    • (2005) Development , vol.132 , pp. 4719-4729
    • Sawada, A.1    Nishizaki, Y.2    Sato, H.3
  • 13
    • 0037566080 scopus 로고    scopus 로고
    • Elevated hepatocyte levels of the Forkhead box A2 (HNF-3beta) transcription factor cause postnatal steatosis and mitochondrial damage
    • Hughes D.E., Stolz D.B., Yu S., et al. Elevated hepatocyte levels of the Forkhead box A2 (HNF-3beta) transcription factor cause postnatal steatosis and mitochondrial damage. Hepatology 37 (2003) 1414-1424
    • (2003) Hepatology , vol.37 , pp. 1414-1424
    • Hughes, D.E.1    Stolz, D.B.2    Yu, S.3
  • 14
    • 33847176595 scopus 로고    scopus 로고
    • Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness
    • Tsang S.H., Woodruff M.L., Jun L., et al. Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness. Hum Mutat 28 (2007) 243-254
    • (2007) Hum Mutat , vol.28 , pp. 243-254
    • Tsang, S.H.1    Woodruff, M.L.2    Jun, L.3
  • 15
    • 0029022639 scopus 로고
    • Distribution of fundus autofluorescence with a scanning laser ophthalmoscope
    • von Ruckmann A., Fitzke F.W., and Bird A.C. Distribution of fundus autofluorescence with a scanning laser ophthalmoscope. Br J Ophthalmol 79 (1995) 407-412
    • (1995) Br J Ophthalmol , vol.79 , pp. 407-412
    • von Ruckmann, A.1    Fitzke, F.W.2    Bird, A.C.3
  • 16
    • 0347532907 scopus 로고    scopus 로고
    • Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa
    • Robson A.G., Egan C., Holder G.E., et al. Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa. Adv Exp Med Biol 533 (2003) 41-47
    • (2003) Adv Exp Med Biol , vol.533 , pp. 41-47
    • Robson, A.G.1    Egan, C.2    Holder, G.E.3
  • 17
    • 33645292904 scopus 로고    scopus 로고
    • Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity
    • Robson A.G., Saihan Z., Jenkins S.A., et al. Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity. Br J Ophthalmol 90 (2006) 472-479
    • (2006) Br J Ophthalmol , vol.90 , pp. 472-479
    • Robson, A.G.1    Saihan, Z.2    Jenkins, S.A.3
  • 18
    • 33846975451 scopus 로고    scopus 로고
    • Novel phenotypic and genotypic findings in X-linked retinoschisis
    • Tsang S.H., Vaclavik V., Bird A.C., et al. Novel phenotypic and genotypic findings in X-linked retinoschisis. Arch Ophthalmol 125 (2007) 259-267
    • (2007) Arch Ophthalmol , vol.125 , pp. 259-267
    • Tsang, S.H.1    Vaclavik, V.2    Bird, A.C.3
  • 20
    • 0029740113 scopus 로고    scopus 로고
    • Retinal degeneration in mice lacking the gamma subunit of rod cGMP phosphodiesterase
    • Tsang S.H., Gouras P., Yamashita C.K., et al. Retinal degeneration in mice lacking the gamma subunit of rod cGMP phosphodiesterase. Science 272 (1996) 1026-1029
    • (1996) Science , vol.272 , pp. 1026-1029
    • Tsang, S.H.1    Gouras, P.2    Yamashita, C.K.3
  • 21
    • 0032475826 scopus 로고    scopus 로고
    • Role of the target enzyme in deactivation of photoreceptor G protein in vivo
    • Tsang S.H., Burns M.E., Calvert P.D., et al. Role of the target enzyme in deactivation of photoreceptor G protein in vivo. Science 282 (1998) 117-121
    • (1998) Science , vol.282 , pp. 117-121
    • Tsang, S.H.1    Burns, M.E.2    Calvert, P.D.3
  • 22
    • 33646843031 scopus 로고    scopus 로고
    • GAP-independent termination of photoreceptor light response by excess gamma subunit of the cGMP-phosphodiesterase
    • Tsang S.H., Woodruff M.L., Chen C.K., et al. GAP-independent termination of photoreceptor light response by excess gamma subunit of the cGMP-phosphodiesterase. J Neurosci 26 (2006) 4472-4480
    • (2006) J Neurosci , vol.26 , pp. 4472-4480
    • Tsang, S.H.1    Woodruff, M.L.2    Chen, C.K.3
  • 23
    • 33847656947 scopus 로고    scopus 로고
    • Removal of phosphorylation sites of gamma subunit of phosphodiesterase 6 alters rod light response
    • Tsang S.H., Woodruff M.L., Janisch K.M., et al. Removal of phosphorylation sites of gamma subunit of phosphodiesterase 6 alters rod light response. J Physiol 579 (2007) 303-312
    • (2007) J Physiol , vol.579 , pp. 303-312
    • Tsang, S.H.1    Woodruff, M.L.2    Janisch, K.M.3
  • 24
    • 0009482260 scopus 로고
    • Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications
    • Towbin H., Staehelin T., and Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A 76 (1979) 4350-4354
    • (1979) Proc Natl Acad Sci U S A , vol.76 , pp. 4350-4354
    • Towbin, H.1    Staehelin, T.2    Gordon, J.3
  • 25
    • 0026624990 scopus 로고
    • Evolution of age-related macular degeneration with choroidal perfusion abnormality
    • Piguet B., Palmvang I.B., Chisholm I.H., et al. Evolution of age-related macular degeneration with choroidal perfusion abnormality. Am J Ophthalmol 113 (1992) 657-663
    • (1992) Am J Ophthalmol , vol.113 , pp. 657-663
    • Piguet, B.1    Palmvang, I.B.2    Chisholm, I.H.3
  • 26
    • 0033389167 scopus 로고    scopus 로고
    • A fluorescein and indocyanine green angiographic study of choriocapillaris in age-related macular disease
    • Pauleikhoff D., Spital G., Radermacher M., et al. A fluorescein and indocyanine green angiographic study of choriocapillaris in age-related macular disease. Arch Ophthalmol 117 (1999) 1353-1358
    • (1999) Arch Ophthalmol , vol.117 , pp. 1353-1358
    • Pauleikhoff, D.1    Spital, G.2    Radermacher, M.3
  • 27
    • 0036158671 scopus 로고    scopus 로고
    • Choroidal perfusion perturbations in non-neovascular age related macular degeneration
    • Ciulla T.A., Harris A., Kagemann L., et al. Choroidal perfusion perturbations in non-neovascular age related macular degeneration. Br J Ophthalmol 86 (2002) 209-213
    • (2002) Br J Ophthalmol , vol.86 , pp. 209-213
    • Ciulla, T.A.1    Harris, A.2    Kagemann, L.3
  • 28
    • 34250778864 scopus 로고    scopus 로고
    • The relationship between retrobulbar and choroidal hemodynamics in non-neovascular age-related macular degeneration
    • Rechtman E., Harris A., Siesky B., et al. The relationship between retrobulbar and choroidal hemodynamics in non-neovascular age-related macular degeneration. Ophthalmic Surg Lasers Imaging 38 (2007) 219-225
    • (2007) Ophthalmic Surg Lasers Imaging , vol.38 , pp. 219-225
    • Rechtman, E.1    Harris, A.2    Siesky, B.3
  • 29
    • 0035873391 scopus 로고    scopus 로고
    • TEAD/TEF transcription factors utilize the activation domain of YAP65, a Src/Yes-associated protein localized in the cytoplasm
    • Vassilev A., Kaneko K.J., Shu H., et al. TEAD/TEF transcription factors utilize the activation domain of YAP65, a Src/Yes-associated protein localized in the cytoplasm. Genes Dev 15 (2001) 1229-1241
    • (2001) Genes Dev , vol.15 , pp. 1229-1241
    • Vassilev, A.1    Kaneko, K.J.2    Shu, H.3
  • 30
    • 0025181560 scopus 로고
    • Helicoid peripapillary chorioretinal degeneration
    • Brazitikos P.D., and Safran A.B. Helicoid peripapillary chorioretinal degeneration. Am J Ophthalmol 109 (1990) 290-294
    • (1990) Am J Ophthalmol , vol.109 , pp. 290-294
    • Brazitikos, P.D.1    Safran, A.B.2
  • 31
    • 0019419771 scopus 로고
    • Atrophia areata: a variant of peripapillary chorioretinal degeneration
    • Magnusson L. Atrophia areata: a variant of peripapillary chorioretinal degeneration. Acta Ophthalmol (Copenh) 59 (1981) 659-664
    • (1981) Acta Ophthalmol (Copenh) , vol.59 , pp. 659-664
    • Magnusson, L.1
  • 32
    • 0031955729 scopus 로고    scopus 로고
    • Helicoidal peripapillary chorioretinal degeneration: electrophysiology and psychophysics in 17 patients
    • Eysteinsson T., Jonasson F., Jonsson V., and Bird A.C. Helicoidal peripapillary chorioretinal degeneration: electrophysiology and psychophysics in 17 patients. Br J Ophthalmol 82 (1998) 280-285
    • (1998) Br J Ophthalmol , vol.82 , pp. 280-285
    • Eysteinsson, T.1    Jonasson, F.2    Jonsson, V.3    Bird, A.C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.