JK McBee, K Palczewski, W Baehr… - Progress in retinal and …, 2001 - Elsevier
Absorption of light by rhodopsin or cone pigments in photoreceptors triggers photoisomerization of their universal chromophore, 11-cis-retinal, to all-trans-retinal. This …
EN Pugh Jr, TD Lamb - Handbook of biological physics, 2000 - Elsevier
Publisher Summary This chapter discusses the research that has characterized the G- protein cascade of transduction in vertebrate photoreceptors, with particular emphasis on …
A Bonnomet, L Syne, A Brysse, E Feyereisen… - Oncogene, 2012 - nature.com
Epithelial-to-mesenchymal transition (EMT) processes endow epithelial cells with enhanced migratory/invasive properties and are therefore likely to contribute to tumor invasion and …
SM Saszik, JG Robson… - The Journal of physiology, 2002 - Wiley Online Library
The most sensitive response in the dark‐adapted electroretinogram (ERG), the scotopic threshold response (STR) which originates from the proximal retina, has been identified in …
Under twenty-first-century metropolitan conditions, almost all of our vision is mediated by cones and the photopic system, yet cones make up barely 5% of our retinal photoreceptors …
SF Stasheff - Journal of neurophysiology, 2008 - journals.physiology.org
Complex alterations in the anatomy of outer retinal pathways accompany photoreceptor degeneration in the rd1 mouse model of retinitis pigmentosa, whereas inner retinal neurons …
BV Bui, B Fortune - The Journal of physiology, 2004 - Wiley Online Library
The purpose of this study was to determine what contributions are made to the rat full‐field electroretinogram (ERG) by ganglion cells (GCs). To that end, the ERG was assessed …
A Tantri, TR Vrabec, A Cu-Unjieng, A Frost… - Survey of …, 2004 - Elsevier
X-linked retinoschisis is a leading cause of macular degeneration in male children. It is characterized by a high degree of clinical variability. Clinical features include a stellate …
BHF Weber, H Schrewe, LL Molday… - Proceedings of the …, 2002 - National Acad Sciences
Deleterious mutations in RS1 encoding retinoschisin are associated with X-linked juvenile retinoschisis (RS), a common form of macular degeneration in males. The disorder is …