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Volumn 39, Issue 6, 1998, Pages 951-962

Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice

Author keywords

[No Author keywords available]

Indexed keywords

ADHESION; ADOLESCENT; AGED; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL DEATH; FEMALE; GLAUCOMA; INTRAOCULAR PRESSURE; IRIS ATROPHY; MALE; MOUSE; MOUSE STRAIN; NONHUMAN; OPTIC NERVE ATROPHY; PIGMENTATION; PRIORITY JOURNAL; RETINA GANGLION CELL;

EID: 0031968397     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (490)

References (32)
  • 2
    • 0020955893 scopus 로고
    • The epidemiology of open-angle glaucoma: A review
    • Leske MC. The epidemiology of open-angle glaucoma: a review. Am J Epidemiol. 1983;118:166-191.
    • (1983) Am J Epidemiol. , vol.118 , pp. 166-191
    • Leske, M.C.1
  • 4
    • 0004257968 scopus 로고
    • Primary open-angle glaucoma
    • Baltimore: Williams & Wilkins
    • Shields MB. Primary open-angle glaucoma. In: Textbook of Glaucoma. Baltimore: Williams & Wilkins; 1992:172-197.
    • (1992) Textbook of Glaucoma , pp. 172-197
    • Shields, M.B.1
  • 6
    • 0030874913 scopus 로고    scopus 로고
    • Recent advances in molecular genetics of glaucomas
    • Sarfarazi M. Recent advances in molecular genetics of glaucomas. Hum Mol Genet. 1997;6:1667-1677.
    • (1997) Hum Mol Genet. , vol.6 , pp. 1667-1677
    • Sarfarazi, M.1
  • 7
    • 14444283397 scopus 로고    scopus 로고
    • Identification of a gene that causes primary open angle glaucoma
    • Stone EM, Fingert JH, Alward WLM, et al. Identification of a gene that causes primary open angle glaucoma. Science. 1997;275:668-678.
    • (1997) Science , vol.275 , pp. 668-678
    • Stone, E.M.1    Fingert, J.H.2    Alward, W.L.M.3
  • 8
    • 0030942553 scopus 로고    scopus 로고
    • Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21
    • Stoilov I, Akarsu AN, Sarfarazi M. Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. Hum Mol Genet. 1997;6:641-647.
    • (1997) Hum Mol Genet. , vol.6 , pp. 641-647
    • Stoilov, I.1    Akarsu, A.N.2    Sarfarazi, M.3
  • 9
    • 0028945864 scopus 로고
    • A miracle enough: The power of mice
    • Paigen K. A miracle enough: the power of mice. Nat Med. 1995; 1:215-220.
    • (1995) Nat Med. , vol.1 , pp. 215-220
    • Paigen, K.1
  • 10
    • 0029019464 scopus 로고
    • Gene targeting approaches to complex genetic diseases: Atherosclerosis and essential hypertension
    • Smithies O, Maeda N. Gene targeting approaches to complex genetic diseases: atherosclerosis and essential hypertension. Proc Natl Acad Sci USA. 1995;92:5266-5272.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 5266-5272
    • Smithies, O.1    Maeda, N.2
  • 11
    • 0024571803 scopus 로고
    • Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)
    • Travis GH, Brennan MB, Danielson PE, Kozak CA, Sutcliffe JG. Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds). Nature. 1989;338:70-73.
    • (1989) Nature , vol.338 , pp. 70-73
    • Travis, G.H.1    Brennan, M.B.2    Danielson, P.E.3    Kozak, C.A.4    Sutcliffe, J.G.5
  • 12
    • 0027500565 scopus 로고
    • Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase
    • Bowes C, Li T, Frankel WN, et al. Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase. Proc Natl Acad Sci USA. 1993;90:2955-2959.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 2955-2959
    • Bowes, C.1    Li, T.2    Frankel, W.N.3
  • 13
    • 0026072333 scopus 로고
    • Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse
    • Pittler SJ, Baehr W. Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse. Proc Natl Acad Sci USA. 1991;88:8322-8326.
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 8322-8326
    • Pittler, S.J.1    Baehr, W.2
  • 14
    • 0028815440 scopus 로고
    • Defective myosin VIIA gene responsible for Usher syndrome type 1B
    • Weil D, Blanchard S, Kaplan J, et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature. 1995;374:60-61.
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1    Blanchard, S.2    Kaplan, J.3
  • 15
    • 0028860302 scopus 로고
    • A type VII myosin encoded by the mouse deafness gene shaker-1
    • Gibson F, Walsh J, Mburu P, et al. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature. 1995;374:62-64.
    • (1995) Nature , vol.374 , pp. 62-64
    • Gibson, F.1    Walsh, J.2    Mburu, P.3
  • 16
    • 0025720710 scopus 로고
    • Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
    • Kajiwara K, Hahn LB, Mukai S, et al. Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. Nature. 1991;354:480-483.
    • (1991) Nature , vol.354 , pp. 480-483
    • Kajiwara, K.1    Hahn, L.B.2    Mukai, S.3
  • 17
    • 0027270053 scopus 로고
    • Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa
    • McLaughlin MF, Sandberg MA, Berson EL, Dryja TP. Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa. Nat Genet. 1993;4:130-134.
    • (1993) Nat Genet. , vol.4 , pp. 130-134
    • McLaughlin, M.F.1    Sandberg, M.A.2    Berson, E.L.3    Dryja, T.P.4
  • 18
    • 0027521914 scopus 로고
    • Apoptosis: Final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice
    • Chang GQ, Hao Y, Wong F. Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice. Neuron. 1993;11:595-605.
    • (1993) Neuron , vol.11 , pp. 595-605
    • Chang, G.Q.1    Hao, Y.2    Wong, F.3
  • 19
    • 0004257968 scopus 로고
    • Glaucomas associated with disorders of the iris
    • Baltimore: Williams & Wilkins
    • Shields MB. Glaucomas associated with disorders of the iris. In: Textbook of Glaucoma. Baltimore: Williams & Wilkins; 1992:276-286.
    • (1992) Textbook of Glaucoma , pp. 276-286
    • Shields, M.B.1
  • 20
    • 12344262459 scopus 로고
    • Glaucomas associated with disorders of the corneal endothelium
    • Baltimore: Williams & Wilkins
    • Shields MB. Glaucomas associated with disorders of the corneal endothelium. In: Textbook of Glaucoma. Baltimore: Williams & Wilkins; 1992:258-275.
    • (1992) Textbook of Glaucoma , pp. 258-275
    • Shields, M.B.1
  • 21
    • 0015755298 scopus 로고
    • Ultrastructural studies of the blood-aqueous barrier 2: The barrier to horseradish peroxidase in primates
    • Smith RS, Rudt LA. Ultrastructural studies of the blood-aqueous barrier 2: the barrier to horseradish peroxidase in primates. Am J Ophthalmol. 1973;76:937-947.
    • (1973) Am J Ophthalmol. , vol.76 , pp. 937-947
    • Smith, R.S.1    Rudt, L.A.2
  • 23
    • 0028896445 scopus 로고
    • A 40-100 MHz B-scan ultrasound backscatter microscope for skin imaging
    • Turnbull DH, Starkoski BG, Harasiewicz KA, et al. A 40-100 MHz B-scan ultrasound backscatter microscope for skin imaging. Ultrasound Med Biol. 1995;21:79-88.
    • (1995) Ultrasound Med Biol. , vol.21 , pp. 79-88
    • Turnbull, D.H.1    Starkoski, B.G.2    Harasiewicz, K.A.3
  • 26
    • 0023007243 scopus 로고
    • Corneal opacities and anterior segment anomalies in DBA/2 mice: Possible models for corneal elastosis and the iridocorneal endothelial (ICE) syndrome
    • Epstein RJ, Halkias A, Stulting DR, Rodrigues MM. Corneal opacities and anterior segment anomalies in DBA/2 mice: possible models for corneal elastosis and the iridocorneal endothelial (ICE) syndrome. Cornea. 1986;5:95-105.
    • (1986) Cornea , vol.5 , pp. 95-105
    • Epstein, R.J.1    Halkias, A.2    Stulting, D.R.3    Rodrigues, M.M.4
  • 27
    • 0025841730 scopus 로고
    • Reduction in rate of occurrence of age related lesions in dietary restricted laboratory mice
    • Bronson RT, Lipman RD. Reduction in rate of occurrence of age related lesions in dietary restricted laboratory mice. Growth Dev Aging. 1991;55:169-184.
    • (1991) Growth Dev Aging , vol.55 , pp. 169-184
    • Bronson, R.T.1    Lipman, R.D.2
  • 29
    • 0019495089 scopus 로고
    • Pigment dispersion syndrome: A clinical study
    • Scheie HG, Cameron JD. Pigment dispersion syndrome: a clinical study. Br J Ophthalmol. 1981;65:264-269.
    • (1981) Br J Ophthalmol. , vol.65 , pp. 264-269
    • Scheie, H.G.1    Cameron, J.D.2
  • 30
    • 0017938702 scopus 로고
    • The spectrum of Chandler's syndrome: An often overlooked cause of unilateral glaucoma
    • Lichter PR. The spectrum of Chandler's syndrome: an often overlooked cause of unilateral glaucoma. Ophthalmology. 1978;85:245-251.
    • (1978) Ophthalmology , vol.85 , pp. 245-251
    • Lichter, P.R.1
  • 31
    • 0018724520 scopus 로고
    • Progressive essential iris atrophy, Chandler's syndrome, and the iris nevus (Cogan-Reese) syndrome: A spectrum of disease
    • Shields MB. Progressive essential iris atrophy, Chandler's syndrome, and the iris nevus (Cogan-Reese) syndrome: a spectrum of disease. Surv Ophthalmol. 1979;24:3-20.
    • (1979) Surv Ophthalmol. , vol.24 , pp. 3-20
    • Shields, M.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.