Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Kristina, Narfström"'
Autor:
Suvi Mäkeläinen, Marta Gòdia, Minas Hellsand, Agnese Viluma, Daniela Hahn, Karim Makdoumi, Caroline J Zeiss, Cathryn Mellersh, Sally L Ricketts, Kristina Narfström, Finn Hallböök, Björn Ekesten, Göran Andersson, Tomas F Bergström
Publikováno v:
PLoS Genetics, Vol 15, Iss 3, p e1007873 (2019)
Autosomal recessive retinal degenerative diseases cause visual impairment and blindness in both humans and dogs. Currently, no standard treatment is available, but pioneering gene therapy-based canine models have been instrumental for clinical trials
Externí odkaz:
https://doaj.org/article/440e2dd2ef7541c0a70a7c12f3d6f9ec
Publikováno v:
Veterinary ophthalmologyREFERENCES.
The rdAc cat has an intronic mutation in the centrosomal 290 kDa (CEP290) gene resulting in a frameshift and a premature stop codon (c.6960 + 9 T G, p.Ile2321AlafsTer3) predicted to truncate the protein by 157 amino acids. CEP290 mutations in human p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8295f52a2b2061a930bed8f4d11407a
https://pubmed.ncbi.nlm.nih.gov/36495011
https://pubmed.ncbi.nlm.nih.gov/36495011
Akademický článek
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Publikováno v:
Journal of Nutritional Science, Vol 5 (2016)
The objective of the study was to examine whether a nutritional antioxidant supplementation could improve visual function in healthy dogs as measured by electroretinography (ERG) and autorefraction. A total of twelve Beagles, 6 to 8 years of age, wit
Externí odkaz:
https://doaj.org/article/5f9c456356d146cfbb1532236fc01cbc
Publikováno v:
Stem Cells International, Vol 2012 (2012)
Intensive breeding and selection on desired traits have produced high rates of inherited diseases in dogs. Hereditary retinal degeneration, often called progressive retinal atrophy (PRA), is prevalent in dogs with disease entities comparable to human
Externí odkaz:
https://doaj.org/article/4fabd093b4bf4ff28d4c8345ce7f9f96
Bilateral retinoschisis in a dog: A veterinary clinical application for optical coherence tomography
Autor:
Elizabeth A. F. Schaefer, Charles W. Hamm, Rebecca E.H. Whiting, Kristina Narfström, Jacqueline W. Pearce, Cecil P. Moore, Bruce H. Grahn
Publikováno v:
Veterinary Ophthalmology. 21:668-674
A 11-year-old neutered male Labrador retriever-cross dog was presented to the University of Missouri-Columbia Veterinary Ophthalmology Service for subtle visual deficits. Indirect ophthalmoscopy revealed a smooth, bullous elevation in the superior-te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d19d0e01b2c0bf822587a9d9a3596fa
https://doi.org/10.1111/vop.12557
https://doi.org/10.1111/vop.12557
Autor:
Manbok Jeong, Kristina Narfström
Publikováno v:
Korean Journal of Veterinary Research. 59:109-111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc4720946170974be392776e07be3e66
https://doi.org/10.14405/kjvr.2019.59.2.109
https://doi.org/10.14405/kjvr.2019.59.2.109
Autor:
Anders R Hellström, Brenda Watt, Shahrzad Shirazi Fard, Danièle Tenza, Paula Mannström, Kristina Narfström, Björn Ekesten, Shosuke Ito, Kazumasa Wakamatsu, Jimmy Larsson, Mats Ulfendahl, Klas Kullander, Graça Raposo, Susanne Kerje, Finn Hallböök, Michael S Marks, Leif Andersson
Publikováno v:
PLoS Genetics, Vol 7, Iss 9, p e1002285 (2011)
PMEL is an amyloidogenic protein that appears to be exclusively expressed in pigment cells and forms intralumenal fibrils within early stage melanosomes upon which eumelanins deposit in later stages. PMEL is well conserved among vertebrates, and alle
Externí odkaz:
https://doaj.org/article/421f79eca213475d87b146fc6194252f
Publikováno v:
Journal of Ophthalmology, Vol 2011 (2011)
Large mammals, including canids and felids, are affected by spontaneously occurring hereditary retinal diseases with similarities to those of humans. The large mammal models may be used for thorough clinical characterization of disease processes, und
Externí odkaz:
https://doaj.org/article/7d9a84c5c59e41b6b1ae78cafdf8813e
Autor:
Grace O. Robinson, Jeffrey T. Student, Joan R. Coates, Eline Rustad, Martin L. Katz, Rebecca E.H. Whiting, Kristina Narfström
Publikováno v:
Neurobiology of Disease, Vol 108, Iss, Pp 277-287 (2017)
The neuronal ceroid lipofuscinoses (NCLs) are devastating inherited progressive neurodegenerative diseases, with most forms having a childhood onset of clinical signs. The NCLs are characterized by progressive cognitive and motor decline, vision loss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f74b8f443a266cb7578cefd23efdfc41
https://doi.org/10.1016/j.nbd.2017.08.017
https://doi.org/10.1016/j.nbd.2017.08.017