메뉴 건너뛰기




Volumn 107, Issue 1, 2003, Pages 79-86

Gene transfer in the RPE65 null mutation dog: Relationship between construct volume, visual behavior and electroretinographic (ERG) results

Author keywords

Dystrophy; ERG; Gene; Retina; RPE65; Vision

Indexed keywords

ADENOVIRUS VECTOR; ATROPINE; COMPLEMENTARY DNA; GREEN FLUORESCENT PROTEIN; ISOFLURANE; PHENYLEPHRINE; PROPOFOL; RETINAL PIGMENT EPITHELIUM PROTEIN 65; RNA; UNCLASSIFIED DRUG; VIRUS PROTEIN;

EID: 0041312614     PISSN: 00124486     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1024431827812     Document Type: Conference Paper
Times cited : (30)

References (11)
  • 1
    • 0027535377 scopus 로고
    • A developmentally regulated microsomal protein specific for the pigment epithelium of the vertebrate retina
    • Hamel CP, Tsilou E, Harris E, Pfeffer BA, Hooks JJ, Detrick B, Redmond TM. A developmentally regulated microsomal protein specific for the pigment epithelium of the vertebrate retina. J Neurosci Res 1993; 34: 414-25.
    • (1993) J Neurosci Res , vol.34 , pp. 414-425
    • Hamel, C.P.1    Tsilou, E.2    Harris, E.3    Pfeffer, B.A.4    Hooks, J.J.5    Detrick, B.6    Redmond, T.M.7
  • 2
    • 0027242119 scopus 로고
    • Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitro
    • Hamel CP, Tsilou E, Pfeffer BA, Hooks JJ, Detrick B, Redmond TM. Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitro. J Biol Chem 1993; 268: 15751-7.
    • (1993) J Biol Chem , vol.268 , pp. 15751-15757
    • Hamel, C.P.1    Tsilou, E.2    Pfeffer, B.A.3    Hooks, J.J.4    Detrick, B.5    Redmond, T.M.6
  • 6
    • 0032582425 scopus 로고    scopus 로고
    • Congenital stationary night blindness in the dog: Common mutation in the RPE65 gene indicates founder effect
    • Aguirre G, Baldwin V, Pearce-Kelling S, Narfström K, Ray K, Acland GM. Congenital stationary night blindness in the dog: Common mutation in the RPE65 gene indicates founder effect. Mol Vis 1998; 4: 23.
    • (1998) Mol Vis , vol.4 , pp. 23
    • Aguirre, G.1    Baldwin, V.2    Pearce-Kelling, S.3    Narfström, K.4    Ray, K.5    Acland, G.M.6
  • 7
    • 0033118884 scopus 로고    scopus 로고
    • Retinal dystrophy of Swedish/Beagle dogs is due to a 4-bp deletion in RPE65
    • Veske A, Nilsson SEG, Narfström K, Gal A. Retinal dystrophy of Swedish/Beagle dogs is due to a 4-bp deletion in RPE65. Genomics 1999; 57: 57-61.
    • (1999) Genomics , vol.57 , pp. 57-61
    • Veske, A.1    Nilsson, S.E.G.2    Narfström, K.3    Gal, A.4
  • 8
    • 0024417892 scopus 로고
    • The Briard dog: A new animal model of congenital stationary night blindness
    • Narfström K, Wrigstad A, Nilsson SEG. The Briard dog: A new animal model of congenital stationary night blindness. Br J Ophthalmol 1988; 73: 750-6.
    • (1988) Br J Ophthalmol , vol.73 , pp. 750-756
    • Narfström, K.1    Wrigstad, A.2    Nilsson, S.E.G.3
  • 9
    • 0002656817 scopus 로고
    • Hereditary retinal dystrophy in the Briard dog: Clinical and hereditary characteristics
    • Narfström K, Wrigstad A, Ekesten B, Nilsson SE. Hereditary retinal dystrophy in the Briard dog: Clinical and hereditary characteristics. Prog Vet Comp Ophthalmol 1994; 4: 85-92.
    • (1994) Prog Vet Comp Ophthalmol , vol.4 , pp. 85-92
    • Narfström, K.1    Wrigstad, A.2    Ekesten, B.3    Nilsson, S.E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.