Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Athanasios Vachtsevanos"'
Autor:
Georgia Perganta, Alun R Barnard, Christiana Katti, Athanasios Vachtsevanos, Ron H Douglas, Robert E MacLaren, Marcela Votruba, Sumathi Sekaran
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56350 (2013)
Autosomal dominant optic atrophy (ADOA) is a slowly progressive optic neuropathy that has been associated with mutations of the OPA1 gene. In patients, the disease primarily affects the retinal ganglion cells (RGCs) and causes optic nerve atrophy and
Externí odkaz:
https://doaj.org/article/14f80289780343f1b4994e58db16d710
Autor:
Stavrenia Koukoula, Georgia Perganta, Solon Asteriadis, Ilias Georgalas, Paris Tranos, Athanasios Vachtsevanos, Athanasios Vacalis
Publikováno v:
Drug Design, Development and Therapy
Age-related macular degeneration (AMD) is the main cause of visual impairment and blindness in people aged over 65 years in developed countries. Vascular endothelial growth factor (VEGF) is a positive regulator of angiogenesis and its proven role in
Autor:
Alun R. Barnard, Marcela Votruba, Robert E MacLaren, Sumathi Sekaran, Christiana Katti, Georgia Perganta, Ronald H. Douglas, Athanasios Vachtsevanos
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 2, p e56350 (2013)
PLoS ONE, Vol 8, Iss 2, p e56350 (2013)
Autosomal dominant optic atrophy (ADOA) is a slowly progressive optic neuropathy that has been associated with mutations of the OPA1 gene. In patients, the disease primarily affects the retinal ganglion cells (RGCs) and causes optic nerve atrophy and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f2555393b8a473d17de9f659b99601b
https://ora.ox.ac.uk/objects/uuid:75f014ec-dcf4-43ea-8a85-e4e72c571aa5
https://ora.ox.ac.uk/objects/uuid:75f014ec-dcf4-43ea-8a85-e4e72c571aa5