Identification of a major pathogenic epitope in the human IRBP molecule recognized by mice of the H-2r haplotype

Autor: Pb, Silver, Lv, Rizzo, Cc, Chan, La, Donoso, Wiggert B, Rachel Caspi

Publikováno v: Europe PubMed Central

Mice of the H-2b, H-2k, and H-2r haplotypes develop experimental autoimmune uveoretinitis (EAU) after immunization with interphotoreceptor retinoid-binding protein (IRBP) of bovine or monkey origin. The purpose of this study was to identify putative

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2045035033af1015c99bfbcf1703a887
https://pubmed.ncbi.nlm.nih.gov/7706044

Role of complement cascade in abdominal aortic aneurysms.

Autor: Hinterseher I; Sigfried and Janet Weis Center for Research, Geisinger Health System, Danville, PA 17822-2610, USA., Erdman R, Donoso LA, Vrabec TR, Schworer CM, Lillvis JH, Boddy AM, Derr K, Golden A, Bowen WD, Gatalica Z, Tapinos N, Elmore JR, Franklin DP, Gray JL, Garvin RP, Gerhard GS, Carey DJ, Tromp G, Kuivaniemi H

Publikováno v: Arteriosclerosis, thrombosis, and vascular biology [Arterioscler Thromb Vasc Biol] 2011 Jul; Vol. 31 (7), pp. 1653-60. Date of Electronic Publication: 2011 Apr 14.

Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26.

Autor: Hadley D; Scheie Eye Institute, Department of Ophthalmology, and., Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D

Publikováno v: Investigative ophthalmology & visual science [Invest Ophthalmol Vis Sci] 2010 Apr; Vol. 51 (4), pp. 2191-6. Date of Electronic Publication: 2009 Nov 20.

X-linked retinoschisis: novel mutation in the initiation codon of the XLRS1 gene in a large family.

Autor: Kim DY; Henry and Corinne Bower Laboratory, Wills Eye Hospital and the Eye Research Institute, 211 South 9th Street, Room 402, Philadelphia, PA 19107, USA., Neely KA, Sassani JW, Vrabec TR, Tantri A, Frost A, Donoso LA

Publikováno v: Retina (Philadelphia, Pa.) [Retina] 2006 Oct; Vol. 26 (8), pp. 940-6.

Autosomal dominant pattern dystrophy: identification of a novel splice site mutation in the peripherin/RDS gene.

Autor: Khoubian FJ; Henry and Corinne Bower Laboratory, the Eye Research Institute, the International Retinal Research Foundation, and Wills Eye Hospital, Philadelphia, PA 19107, USA., Shakin EP, Tantri A, Kim DY, Edwards AO, Donoso LA

Publikováno v: Retina (Philadelphia, Pa.) [Retina] 2005 Dec; Vol. 25 (8), pp. 999-1004.