Zobrazeno 1 - 10
of 26
pro vyhledávání: '"J R, Heckenlively"'
Autor:
A R, Webster, E, Héon, A J, Lotery, K, Vandenburgh, T L, Casavant, K T, Oh, G, Beck, G A, Fishman, B L, Lam, A, Levin, J R, Heckenlively, S G, Jacobson, R G, Weleber, V C, Sheffield, E M, Stone
Publikováno v:
Investigative ophthalmologyvisual science. 42(6)
To assess the allelic variation of the ATP-binding transporter protein (ABCA4).A combination of single-strand conformation polymorphism (SSCP) and automated DNA sequencing was used to systematically screen this gene for sequence variations in 374 unr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8aa4d27da7c2460609ea06913e20233
https://pubmed.ncbi.nlm.nih.gov/11328725
https://pubmed.ncbi.nlm.nih.gov/11328725
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 118(11)
To investigate whether antirecoverin antibodies are present in patients with retinitis pigmentosa (RP). Recoverin, a retinal protein, has been implicated as a cause of cancer-associated retinopathy (CAR), which manifests as an RP-like retinal degener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c617478da0cedea7e6a712d1ce3c899
https://pubmed.ncbi.nlm.nih.gov/11074806
https://pubmed.ncbi.nlm.nih.gov/11074806
Autor:
N L, Hawes, B, Chang, G S, Hageman, S, Nusinowitz, P M, Nishina, B S, Schneider, R S, Smith, T H, Roderick, M T, Davisson, J R, Heckenlively
Publikováno v:
Investigative ophthalmologyvisual science. 41(10)
To characterize the genetics and phenotype of a new mouse mutant with retinal degeneration, rd6, that is associated with extensive, scattered, small white retinal dots seen ophthalmoscopically.The phenotype was characterized using ophthalmoscopy, fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::471698085d4b73d0ba8dd84d8f0e4055
https://pubmed.ncbi.nlm.nih.gov/10967077
https://pubmed.ncbi.nlm.nih.gov/10967077
Publikováno v:
Investigative ophthalmologyvisual science. 40(12)
To test the feasibility of recording rod multifocal electroretinograms (ERGs) from the mouse eye.Multifocal ERGs were recorded from normal mice (C57BL/6J) using an array of equal-sized hexagons. Local stimuli were blue (W47A), and the number of blank
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b69a9af7bcd7d4184373a484b459b656
https://pubmed.ncbi.nlm.nih.gov/10549645
https://pubmed.ncbi.nlm.nih.gov/10549645
Publikováno v:
Molecular vision. 5
Mice are an increasingly important tool in ophthalmic research. As a result of studying spontaneous and induced mutations, many new ocular diseases have been described in mice in recent years, including several degenerative retinal diseases that demo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8b72f55b5ac69fca45e9a1433c5c16e
https://pubmed.ncbi.nlm.nih.gov/10493779
https://pubmed.ncbi.nlm.nih.gov/10493779
Autor:
B, Chang, N L, Hawes, T H, Roderick, R S, Smith, J R, Heckenlively, J, Horwitz, M T, Davisson
Publikováno v:
Molecular vision. 5
The mouse lop18 (lens opacity 18) mutation causes a white cataract obvious at weaning age. It soon progresses to a large white nuclear cataract with mild cortical changes. The mutation maps to mouse Chromosome 17 in close linkage to the alphaA-crysta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9acfef6e4dc5100fd6e114073367156
https://pubmed.ncbi.nlm.nih.gov/10493778
https://pubmed.ncbi.nlm.nih.gov/10493778
Autor:
Y Q, Gao, M, Danciger, R, Longmuir, N I, Piriev, D Y, Zhao, J R, Heckenlively, G A, Fishman, R G, Weleber, S G, Jacobson, E M, Stone, D B, Farber
Publikováno v:
Investigative ophthalmologyvisual science. 40(8)
To screen the exons of the gene encoding the alpha'-subunit of cone cyclic guanosine monophosphate (cGMPphosphodiesterase (PDE6C) for mutations in a group of 456 unrelated patients with various forms of inherited retinal disease, including cone dystr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::79b998ccc7a6509a7e7b9bcee41b6661
https://pubmed.ncbi.nlm.nih.gov/10393054
https://pubmed.ncbi.nlm.nih.gov/10393054
Autor:
Y Q, Gao, M, Danciger, N B, Akhmedov, D Y, Zhao, J R, Heckenlively, G A, Fishman, R G, Weleber, S G, Jacobson, D B, Farber
Publikováno v:
Molecular vision. 4
To screen the exons of the genes encoding the beta3-subunit (GNB3) and gammac-subunit (GNGT2) of cone transducin for mutations in a large number of unrelated patients with various forms of inherited retinal disease including cone dystrophy, cone-rod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f527b4a0ce421dd1430669b30a295ad7
https://pubmed.ncbi.nlm.nih.gov/9743540
https://pubmed.ncbi.nlm.nih.gov/9743540
Autor:
S W, John, R S, Smith, O V, Savinova, N L, Hawes, B, Chang, D, Turnbull, M, Davisson, T H, Roderick, J R, Heckenlively
Publikováno v:
Investigative ophthalmologyvisual science. 39(6)
To characterize ocular abnormalities associated with iris atrophy in DBA/2J mice and to determine whether mice of this strain develop elevated intraocular pressure (IOP) and glaucoma.Different approaches, including slit-lamp biomicroscopy, ophthalmos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::be1237af98a2f4e184fa0b39eb134a46
https://pubmed.ncbi.nlm.nih.gov/9579474
https://pubmed.ncbi.nlm.nih.gov/9579474
Autor:
Rachel E. McGuire, Lori S. Sullivan, Susan H. Blanton, M. W. Church, J. R. Heckenlively, S.P. Daiger
Publikováno v:
Angiología. 57:87-88
Retinitis pigmentosa is the name given to a heterogeneous group of hereditary retinal degenerations characterized by progressive visual field loss, pigmentary changes of the retina, abnormal electroretinograms, and, frequently, night blindness. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b7b1d73b417c6831728fe825a60bb73
https://doi.org/10.1016/s0003-3170(05)74922-1
https://doi.org/10.1016/s0003-3170(05)74922-1