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Frontiers in Microbiology|June 9, 2020
SMRT Sequencing of Paramecium Bursaria Chlorella Virus-1 Reveals Diverse Methylation Stability in Adenines Targeted by Restriction Modification SystemsSamantha R Coy, Eric R Gann, Spiridon E Papoulis, et al.Investigative Ophthalmology & Visual Science|August 29, 2007
Pathological and electrophysiological features of a canine cone-rod dystrophy in the miniature longhaired dachshundClare Turney, N H Victor Chong, Robert A Alexander, et al.Brain : a Journal of Neurology|February 27, 2016
CCDC88A mutations cause PEHO-like syndrome in humans and mouseMichael S Nahorski, Masato Asai, Emma Wakeling, et al.Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.Molecular Neurobiology|January 1, 1991
Evidence for plasticity of the dopaminergic system in parkinsonismG A Donnan, D G Woodhouse, S J Kaczmarczyk, et al.Ophthalmology|June 18, 2013
The clinical effect of homozygous ABCA4 alleles in 18 patientsKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.The British Journal of Ophthalmology|November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathyM Michaelides, L L Chen, M A Brantley, et al.Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.American Journal of Ophthalmology|February 18, 2014
A randomized trial to assess functional and structural effects of ranibizumab versus laser in diabetic macular edema (the LUCIDATE study)Oliver Comyn, Sobha Sivaprasad, Tunde Peto, et al.Retina (Philadelphia, Pa.)|April 14, 2011
Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing lossZubin Saihan, Polona Le Quesne Stabej, Anthony G Robson, et al.Pageof 36