Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Ross F Collery"'
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e110699 (2014)
Refractive errors in vision can be caused by aberrant axial length of the eye, irregular corneal shape, or lens abnormalities. Causes of eye length overgrowth include multiple genetic loci, and visual parameters. We evaluate zebrafish as a potential
Externí odkaz:
https://doaj.org/article/a12d8af3e97340bc9c4e0b3312620da3
Autor:
Kerry N Veth, Jason R Willer, Ross F Collery, Matthew P Gray, Gregory B Willer, Daniel S Wagner, Mary C Mullins, Ava J Udvadia, Richard S Smith, Simon W M John, Ronald G Gregg, Brian A Link
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001310 (2011)
The glaucomas comprise a genetically complex group of retinal neuropathies that typically occur late in life and are characterized by progressive pathology of the optic nerve head and degeneration of retinal ganglion cells. In addition to age and fam
Externí odkaz:
https://doaj.org/article/38ba329e10954c9f95fdf5132f63c35f
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2021)
Interkinetic nuclear migration (IKNM) is the process in which pseudostratified epithelial nuclei oscillate from the apical to basal surface and in phase with the mitotic cycle. In the zebrafish retina, neuroepithelial retinal progenitor cells (RPCs)
Externí odkaz:
https://doaj.org/article/a82f8ceaff574df8868cff79bec6fc47
Autor:
Shahram Eisa-Beygi, Meng-Ming Hu, Suresh N. Kumar, Brooke E. Jeffery, Ross F. Collery, Nghia (Jack) Vo, Bhawika S. Lamichanne, H. Joseph Yost, Matthew B. Veldman, Brian A. Link
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology.
BACKGROUND: The goal of this study was to identify and characterize cell-cell interactions that facilitate endothelial tip cell fusion downstream of BMP (bone morphogenic protein)-mediated venous plexus formation. METHODS: High resolution and time-la
Autor:
Elena V. Semina, Jesús-José Ferre-Fernández, Joy Lincoln, Ross F Collery, Emily Nordquist, Samuel Thompson, Elena A. Sorokina
Publikováno v:
Hum Mol Genet
The Forkhead Box C1 (FOXC1) gene encodes a forkhead/winged helix transcription factor involved in embryonic development. Mutations in this gene cause dysgenesis of the anterior segment of the eye, most commonly Axenfeld-Rieger syndrome (ARS), often w
Publikováno v:
Investigative Ophthalmology & Visual Science
PURPOSEProper refractive development of the eye, termed emmetropization, is critical for focused vision and impacted by both genetic determinants and several visual environment factors. Improper emmetropization caused by genetic variants can lead to
Autor:
Jonathon B. Young, Khalid Yusuf Al-Kirwi, Niamh Wynne, Amanda Rae Buchberger, Christine M.B. Skumatz, Ross F. Collery, Iris S. Kassem
Publikováno v:
Exp Eye Res
Children that undergo intraocular surgery have an exaggerated postoperative response compared to adults that can result in significant postoperative challenges and reduced post-operative visual acuity. Rabbits were used as an animal model for investi
Autor:
Kenneth P. Allen, Daniel A. Gil, Eric Buckland, Ramin Pashaie, Melissa C. Skala, Mina Gaffney, Joseph Carroll, Dana K. Merriman, Ross F Collery, Alexander E Salmon, Farid Atry, Rex Chin-Hao Chen
Publikováno v:
Translational Vision Science & Technology
Purpose To assess the performance of two spectral-domain optical coherence tomography-angiography systems in a natural model of hypoperfusion: the hibernating thirteen-lined ground squirrel (13-LGS). Methods Using a high-speed (130 kHz) OCT-A system
Autor:
Ross F. Collery, Brian A. Link
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
LRP2 is a large transmembrane receptor expressed on absorptive epithelia where it binds many extracellular ligands to control several signaling pathways. Mutations in LRP2 are associated with buphthalmic eye enlargement, myopia and other non-ocular s
Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant developmental disorder characterized by ocular anterior chamber anomalies with an increased risk of glaucoma and systemic defects. Mutations in the transcription factorPITX2were the first id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ae4a3263b2f3d65fe8e525910144102