Zobrazeno 1 - 10
of 152
pro vyhledávání: '"G, Inana"'
Publikováno v:
Japanese Journal of Ophthalmology. 46:419-425
Purpose: To determine whether measurements of the a-wave latency of the electroretinogram (ERG) can be made as reliably as that of the implicit time (IT) in rats. In addition, to determine the relationship between the potential level selected for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afdf5fcb748924146e14b0bec8bd87e1
https://doi.org/10.1016/s0021-5155(02)00506-3
https://doi.org/10.1016/s0021-5155(02)00506-3
Autor:
Graeme Wistow, J. F. Hejtmancik, John M. Nickerson, Joram Piatigorsky, Toshimichi Shinohara, G Inana, Barbara Norman, J W Hawkins, Teresa Borrás, Charles R. King
Publikováno v:
Ciba Foundation Symposium 106-Human Cataract Formation
Analysis of recombinant DNAs provides new information on the basis of crystallin evolution and diversity. All crystallin genes contain introns. Two similar, tandemly linked chicken delta-crystallin genes, which probably arose by gene duplication, con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2e1c2d9209fc5d7507723201d522ba3
https://doi.org/10.1002/9780470720875.ch11
https://doi.org/10.1002/9780470720875.ch11
Autor:
Carmelann B. Zintz, G Inana
Publikováno v:
Experimental Eye Research. 50:759-770
Ornithine aminotransferase is a mitochondrial matrix enzyme that is deficient in patients with gyrate atrophy, an autosomal recessive disease of the eye. Southern blots of human DNA probed with a previously characterized OAT cDNA showed a complex pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9b309704810632221151fcf7bf54f03
https://doi.org/10.1016/0014-4835(90)90126-f
https://doi.org/10.1016/0014-4835(90)90126-f
HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model
Autor:
A, Kobayashi, T, Higashide, D, Hamasaki, S, Kubota, H, Sakuma, W, An, T, Fujimaki, M J, McLaren, R G, Weleber, G, Inana
Publikováno v:
Investigative ophthalmologyvisual science. 41(11)
To investigate the function and pathogenicity of HRG4, a photoreceptor synaptic protein homologous to the Caenorhabditis elegans neuroprotein UNC119.HRG4 was screened for mutations in patients with various retinopathies, and a transgenic mouse model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::285d3aad27ae5210ee1243eb4eeaa8c4
https://pubmed.ncbi.nlm.nih.gov/11006213
https://pubmed.ncbi.nlm.nih.gov/11006213
Publikováno v:
Investigative ophthalmologyvisual science. 39(5)
To characterize further HRG4, a novel photoreceptor protein recently identified by subtractive cDNA cloning, by sequence analysis and immunolocalization.The rat homolog of HRG4, RRG4 was expressed and used to prepare an antibody. The antibody was use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d3fe2a2692a12fb7c1b41401a3c475e
https://pubmed.ncbi.nlm.nih.gov/9538874
https://pubmed.ncbi.nlm.nih.gov/9538874
Publikováno v:
Investigative ophthalmologyvisual science. 38(3)
To determine whether defects in the human recoverin gene cause retinitis pigmentosa (RP) or an allied disease such as Usher syndrome, Leber congenital amaurosis, or the Bardet-Biedl syndrome.Single-strand conformation polymorphism analysis and direct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf8253fa36f1d9c51e48f116c0cb20bb
https://pubmed.ncbi.nlm.nih.gov/9071225
https://pubmed.ncbi.nlm.nih.gov/9071225
Publikováno v:
Biochemistry and cell biology = Biochimie et biologie cellulaire. 75(2)
We examined whether primary cultures of rat retinal pigment epithelial (RPE) cells and RPE cells of an immortalized rat cell line, BPEI-1, would be responsive to the neurokines ciliary neurotrophic factor (CNTF) and leukemia inhibitory factor (LIF),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e35e44002c1ab6cf971ab0e304f717d5
https://pubmed.ncbi.nlm.nih.gov/9250359
https://pubmed.ncbi.nlm.nih.gov/9250359
Publikováno v:
Investigative ophthalmologyvisual science. 35(3)
A generalized biochemical deficiency of the mitochondrial matrix enzyme ornithine aminotransferase (OAT) is the inborn error in gyrate atrophy (GA), an autosomal recessive blinding disease of the retina and choroid of the eye. Because mutations in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::456e9332199e5786e82089e9e325d7b4
https://pubmed.ncbi.nlm.nih.gov/8125717
https://pubmed.ncbi.nlm.nih.gov/8125717
Publikováno v:
Investigative ophthalmologyvisual science. 34(2)
The goal of this study was to develop the first vital assay system for in vitro analysis of phagocytosis of rod outer segments (ROS) by normal retinal pigment epithelial (RPE) cells and for study of the phagocytic defect in RPE of the Royal College o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52a693e6d4a7f8fb21ad6bcc09fe2f0b
https://pubmed.ncbi.nlm.nih.gov/7680023
https://pubmed.ncbi.nlm.nih.gov/7680023
Autor:
J B, Bateman, T L, Kojis, R M, Cantor, C, Heinzmann, J T, Ngo, M A, Spence, G, Inana, J D, Kivlin, D, Curtis, R S, Sparkes
Publikováno v:
Transactions of the American Ophthalmological Society. 91
Norrie disease is a rare disease of newborn males caused by prenatal or perinatal retinal detachment, which may be associated with mental retardation, psychosis, and/or hearing loss. DXS7 (L1.28) and MAO A and B loci have been linked to the ND locus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b2af64b0c7993c8056b216f63b68e5e
https://pubmed.ncbi.nlm.nih.gov/7908152
https://pubmed.ncbi.nlm.nih.gov/7908152