Literature DB >> 3496233

Retinal degenerations in the dog: IV. Early retinal degeneration (erd) in Norwegian elkhounds.

G M Acland, G D Aguirre.   

Abstract

A new early onset hereditary retinal degeneration is characterized in Norwegian elkhound dogs. This disease, termed early retinal degeneration (erd), was studied in 10 affected dogs, from 30 days- to 7 years old, clinically, by electroretinography, and by light- and electron-microscopic morphology. Control studies were performed on 49 non-affected dogs. Affected dogs are initially nightblind, and become totally blind between 12- and 18 months of age. The postnatal development of their rod and cone photoreceptors is abnormal both structurally and functionally. Morphologically, rod and cone inner- and outer-segment growth occurs but appears uncoordinated. Adjacent rods become very disparate in the size and proportions of their inner- and outer segments. Prominent villiform processes extend from the inner segments of rods and, to a lesser extent, cones. Synaptic terminals of rods and cones fail to develop properly. The b-wave of the electroretinogram fails to develop and the electroretinogram (ERG) remains a-wave-dominated. Subsequent to these abnormalities of development, the rods and cones degenerate, rapidly at first and later more gradually. In normal dogs, development of the ERG a- and b-waves is shown to follow, respectively, morphologic development of the photoreceptor outer segments and synaptic terminals. Similarly the abnormal development and subsequent degeneration of photoreceptor outer segments and synaptic terminals in affected dogs, correspond in time course to development and degeneration of the ERG a- and b-waves.

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Year:  1987        PMID: 3496233     DOI: 10.1016/s0014-4835(87)80160-4

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


  42 in total

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2.  Transcriptional profile analysis of RPGRORF15 frameshift mutation identifies novel genes associated with retinal degeneration.

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Review 3.  Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies.

Authors:  Keiko Miyadera; Gregory M Acland; Gustavo D Aguirre
Journal:  Mamm Genome       Date:  2011-11-08       Impact factor: 2.957

4.  Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration.

Authors:  Matthew M LaVail; Shimpei Nishikawa; Roy H Steinberg; Muna I Naash; Jacque L Duncan; Nikolaus Trautmann; Michael T Matthes; Douglas Yasumura; Cathy Lau-Villacorta; Jeannie Chen; Ward M Peterson; Haidong Yang; John G Flannery
Journal:  Exp Eye Res       Date:  2017-11-06       Impact factor: 3.467

5.  Steroids do not prevent photoreceptor degeneration in the light-exposed T4R rhodopsin mutant dog retina irrespective of AP-1 inhibition.

Authors:  Danian Gu; William A Beltran; Sue Pearce-Kelling; Zexiao Li; Gregory M Acland; Gustavo D Aguirre
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-02-21       Impact factor: 4.799

Review 6.  Underdeveloped RPE Apical Domain Underlies Lesion Formation in Canine Bestrophinopathies.

Authors:  Karina E Guziewicz; Emily McTish; Valerie L Dufour; Kathryn Zorych; Anuradha Dhingra; Kathleen Boesze-Battaglia; Gustavo D Aguirre
Journal:  Adv Exp Med Biol       Date:  2018       Impact factor: 2.622

7.  IQCB1 and PDE6B mutations cause similar early onset retinal degenerations in two closely related terrier dog breeds.

Authors:  Orly Goldstein; Jason G Mezey; Peter A Schweitzer; Adam R Boyko; Chuan Gao; Carlos D Bustamante; Julie Ann Jordan; Gustavo D Aguirre; Gregory M Acland
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-10-25       Impact factor: 4.799

8.  Clinical electroretinography in the dog with ganzfeld stimulation: a practical method of examining rod and cone function.

Authors:  K Narfström; B E Andersson; S Andreasson; P Gouras
Journal:  Doc Ophthalmol       Date:  1995       Impact factor: 2.379

9.  A naturally occurring mutation of the opsin gene (T4R) in dogs affects glycosylation and stability of the G protein-coupled receptor.

Authors:  Li Zhu; Geeng-Fu Jang; Beata Jastrzebska; Slawomir Filipek; Susan E Pearce-Kelling; Gustavo D Aguirre; Ronald E Stenkamp; Gregory M Acland; Krzysztof Palczewski
Journal:  J Biol Chem       Date:  2004-09-30       Impact factor: 5.157

10.  Analysis of six candidate genes as potential modifiers of disease expression in canine XLPRA1, a model for human X-linked retinitis pigmentosa 3.

Authors:  Richard Guyon; Susan E Pearce-Kelling; Caroline J Zeiss; Gregory M Acland; Gustavo D Aguirre
Journal:  Mol Vis       Date:  2007-07-11       Impact factor: 2.367

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