Zobrazeno 1 - 10
of 114
pro vyhledávání: '"J. Jason McAnany"'
Autor:
Dhavamani Sugasini, Jason C. Park, J. Jason McAnany, Tae-Hoon Kim, Guangying Ma, Xincheng Yao, Babu Antharavally, Anil Oroskar, Asha A. Oroskar, Brian T. Layden, Papasani V. Subbaiah
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-13 (2023)
Abstract Alzheimer disease (AD) is the most prevalent cause of dementia in the elderly. Although impaired cognition and memory are the most prominent features of AD, abnormalities in visual functions often precede them, and are increasingly being use
Externí odkaz:
https://doaj.org/article/b0f8746686a34e1289bf3e014810371d
Autor:
Jason C. Park, Oksana Persidina, Giri Balasubramanian, Tara Nguyen, Anubhav Pradeep, John R. Hetling, J. Jason McAnany
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Changes in the full-field flash and flicker electroretinogram (ERG) that accompany normal aging were evaluated in mice. ERGs were recorded from a single cohort of C57BL/6J mice from 5 to 70 weeks of age using conventional techniques. Dark-ad
Externí odkaz:
https://doaj.org/article/1e6665774ffb448ba76ae4f89061990f
Autor:
Yanliang Li, Basma Baccouche, Norma Del-Risco, Jason Park, Amy Song, J. Jason McAnany, Andrius Kazlauskas
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 10869 (2023)
The purpose of this study was to investigate the reason that diabetic retinopathy (DR) is delayed from the onset of diabetes (DM) in diabetic mice. To this end, we tested the hypothesis that the deleterious effects of DM are initially tolerated becau
Externí odkaz:
https://doaj.org/article/b0a879ecd99241869fafd71888955e7b
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract To characterize rod- and cone-pathway function in the 5xFAD mouse model of Alzheimer’s disease (AD) using the full-field electroretinogram (ERG). Dark-adapted (DA; rod-pathway) and light-adapted (LA; cone-pathway) ERGs were recorded from t
Externí odkaz:
https://doaj.org/article/9f3da13689e44b65bc357740fe0f6c9a
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Purpose: To assess the nature and extent of non-linear processes in pupil responses using rod- and cone-isolating visual beat stimuli.Methods: A four-primary photostimulating method based on the principle of silent substitution was implemented to gen
Externí odkaz:
https://doaj.org/article/64a0555040984e10925a7ef8807732ef
Autor:
LakshmiPriya Rangaraju, Xuejuan Jiang, J. Jason McAnany, Michael R. Tan, Justin Wanek, Norman P. Blair, Jennifer I. Lim, Mahnaz Shahidi
Publikováno v:
Journal of Ophthalmology, Vol 2018 (2018)
Purpose. Diabetes is known to cause alterations in retinal microvasculature and tissue that progressively lead to visual impairment. Optical coherence tomography (OCT) is useful for assessment of total retinal thickening due to diabetic macular edema
Externí odkaz:
https://doaj.org/article/291bde03123148e9814486c5130df86c
Publikováno v:
Documenta Ophthalmologica. 146:191-197
Autor:
Kazlauskas, Yanliang Li, Basma Baccouche, Norma Del-Risco, Jason Park, Amy Song, J. Jason McAnany, Andrius
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 13; Pages: 10869
The purpose of this study was to investigate the reason that diabetic retinopathy (DR) is delayed from the onset of diabetes (DM) in diabetic mice. To this end, we tested the hypothesis that the deleterious effects of DM are initially tolerated becau
Autor:
Cyril G. Eleftheriou, Carlo Corona, Shireen Khattak, Nazia M. Alam, Elena Ivanova, Paola Bianchimano, Yang Liu, Duo Sun, Rupesh Singh, Julia C. Batoki, Glen T. Prusky, J. Jason McAnany, Neal S. Peachey, Carmelo Romano, Botir T. Sagdullaev
Publikováno v:
J Neurosci
Genetic disorders that present during development make treatment strategies particularly challenging because there is a need to disentangle primary pathophysiology from downstream dysfunction caused at key developmental stages. To provide a deeper in
Publikováno v:
Ophthalmic Genet
PURPOSE: To evaluate retinal function in a family presenting with Jalili syndrome due to a previously unreported variant in CNNM4. METHODS: A family of three sisters with a novel CNNM4 variant, c.482T>C p.(Leu161Pro), and ten visually normal, age-sim