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Volumn 58, Issue 1, 1999, Pages 29-33

Localization of retina/pineal-expressed sequences: Identification of novel candidate genes for inherited retinal disorders

Author keywords

[No Author keywords available]

Indexed keywords

RETINA S ANTIGEN;

EID: 0033563233     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.5810     Document Type: Article
Times cited : (21)

References (18)
  • 2
    • 0030862358 scopus 로고    scopus 로고
    • Developmental expression pattern of phototransduction components in mammalian pineal implies a light-sensing function
    • Blackshaw S., Snyder S. H. Developmental expression pattern of phototransduction components in mammalian pineal implies a light-sensing function. J. Neurosci. 17:1997;8074-8082.
    • (1997) J. Neurosci. , vol.17 , pp. 8074-8082
    • Blackshaw, S.1    Snyder, S.H.2
  • 5
    • 0030669568 scopus 로고    scopus 로고
    • Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
    • Freund C. L., Gregory-Evans C. Y., Furukawa T., Papaioannou M., Looser J., Ploder L., Bellingham J., McInnes R. R. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell. 91:1997;543-553.
    • (1997) Cell , vol.91 , pp. 543-553
    • Freund, C.L.1    Gregory-Evans, C.Y.2    Furukawa, T.3    Papaioannou, M.4    Looser, J.5    Ploder, L.6    Bellingham, J.7    McInnes, R.R.8
  • 7
    • 0029067542 scopus 로고
    • A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese
    • Fuchs S., Nakazawa M., Maw M., Tamai M., Oguchi Y., Gal A. A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese. Nat. Genet. 10:1995;360-362.
    • (1995) Nat. Genet. , vol.10 , pp. 360-362
    • Fuchs, S.1    Nakazawa, M.2    Maw, M.3    Tamai, M.4    Oguchi, Y.5    Gal, A.6
  • 9
    • 0032539806 scopus 로고    scopus 로고
    • Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the Oguchi form of congenital stationary night blindness
    • Khani S. C., Nielsen L., Vogt T. M. Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the Oguchi form of congenital stationary night blindness. Proc. Natl. Acad. Sci. USA. 95:1998;2824-2827.
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 2824-2827
    • Khani, S.C.1    Nielsen, L.2    Vogt, T.M.3
  • 10
    • 0026567557 scopus 로고
    • Photoreceptors of the retina and pinealocytes share common components of signal transduction
    • Lolley R. N., Craft C. M., Lee R. H. Photoreceptors of the retina and pinealocytes share common components of signal transduction. Neurochem. Res. 17:1992;81-89.
    • (1992) Neurochem. Res. , vol.17 , pp. 81-89
    • Lolley, R.N.1    Craft, C.M.2    Lee, R.H.3
  • 12
    • 0031894886 scopus 로고    scopus 로고
    • Arrestin gene mutations in autosomal recessive retinitis pigmentosa
    • Nakazawa M., Wada Y., Tamai M. Arrestin gene mutations in autosomal recessive retinitis pigmentosa. Arch. Ophth. 116:1998;498-501.
    • (1998) Arch. Ophth. , vol.116 , pp. 498-501
    • Nakazawa, M.1    Wada, Y.2    Tamai, M.3
  • 13
    • 0344747555 scopus 로고
    • Isolation and nucleotide sequence of the gene encoding human rhodopsin
    • Nathans J., Hogness D. S. Isolation and nucleotide sequence of the gene encoding human rhodopsin. Science. 232:1984;203-210.
    • (1984) Science , vol.232 , pp. 203-210
    • Nathans, J.1    Hogness, D.S.2
  • 16
    • 0345117571 scopus 로고
    • Mammalian pinealocytes: Ultrastructural aspects and innervation
    • Avon: Pitman. p. 9-17
    • Vollrath L. Mammalian pinealocytes: Ultrastructural aspects and innervation. Photoperiodism, Melatonin and the Pineal, 1985;Pitman, Avon. p. 9-17.
    • (1985) Photoperiodism, Melatonin and the Pineal
    • Vollrath, L.1
  • 17
    • 0344255092 scopus 로고    scopus 로고
    • Phenotypic characteristics of patients with Oguchi's disease associated with frequent 1147delA mutation in the arrestin gene
    • Wada Y., Nakazawa M., Fuchs S., Gal A., Tamai M. Phenotypic characteristics of patients with Oguchi's disease associated with frequent 1147delA mutation in the arrestin gene. Invest. Ophth. Vis. Sci. 37:1996;995.
    • (1996) Invest. Ophth. Vis. Sci. , vol.37 , pp. 995
    • Wada, Y.1    Nakazawa, M.2    Fuchs, S.3    Gal, A.4    Tamai, M.5
  • 18
    • 0031038950 scopus 로고    scopus 로고
    • Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness
    • Yamamoto S., Sippel K. C., Berson E. L., Dryja T. P. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness. Nat. Genet. 15:1997;175-178.
    • (1997) Nat. Genet. , vol.15 , pp. 175-178
    • Yamamoto, S.1    Sippel, K.C.2    Berson, E.L.3    Dryja, T.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.