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Albert O Edwards

Showing results (31-40 of 57) with videos related to

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Retina (Philadelphia, Pa.)|December 13, 2005
Autosomal dominant pattern dystrophy: identification of a novel splice site mutation in the peripherin/RDS geneFarzad J Khoubian, Eric P Shakin, Avinash Tantri, et al.
Retina (Philadelphia, Pa.)|April 10, 2009
Infectious endophthalmitis after intravitreal injection of antiangiogenic agentsTeresa Diago, Colin A McCannel, Sophie J Bakri, et al.
American Journal of Ophthalmology|November 14, 2002
Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome familyLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Plos One|December 2, 2008
Evaluation of clustering and genotype distribution for replication in genome wide association studies: the age-related eye disease studyAlbert O Edwards, Brooke L Fridley, Katherine M James, et al.
Plos One|November 28, 2012
A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophyEric D Wieben, Ross A Aleff, Nirubol Tosakulwong, et al.
Survey of Ophthalmology|April 11, 2003
Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 geneLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Plos One|August 27, 2013
Snowflake vitreoretinal degeneration (SVD) mutation R162W provides new insights into Kir7.1 ion channel structure and functionBikash R Pattnaik, Sara Tokarz, Matti P Asuma, et al.
Molecular Vision|March 16, 2007
Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4Anne McMahon, Igor A Butovich, Nathan L Mata, et al.
Investigative Ophthalmology & Visual Science|June 26, 2009
Contribution of copy number variation in the regulation of complement activation locus to development of age-related macular degenerationKatharina E Schmid-Kubista, Nirubol Tosakulwong, Yanhong Wu, et al.
American Journal of Human Genetics|January 9, 2008
Mutations in KCNJ13 cause autosomal-dominant snowflake vitreoretinal degenerationJ Fielding Hejtmancik, Xiaodong Jiao, Anren Li, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Retina (Philadelphia, Pa.)|December 13, 2005
Autosomal dominant pattern dystrophy: identification of a novel splice site mutation in the peripherin/RDS geneFarzad J Khoubian, Eric P Shakin, Avinash Tantri, et al.
Retina (Philadelphia, Pa.)|April 10, 2009
Infectious endophthalmitis after intravitreal injection of antiangiogenic agentsTeresa Diago, Colin A McCannel, Sophie J Bakri, et al.
American Journal of Ophthalmology|November 14, 2002
Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome familyLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Plos One|December 2, 2008
Evaluation of clustering and genotype distribution for replication in genome wide association studies: the age-related eye disease studyAlbert O Edwards, Brooke L Fridley, Katherine M James, et al.
Plos One|November 28, 2012
A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophyEric D Wieben, Ross A Aleff, Nirubol Tosakulwong, et al.
Survey of Ophthalmology|April 11, 2003
Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 geneLarry A Donoso, Albert O Edwards, Arcilee T Frost, et al.
Plos One|August 27, 2013
Snowflake vitreoretinal degeneration (SVD) mutation R162W provides new insights into Kir7.1 ion channel structure and functionBikash R Pattnaik, Sara Tokarz, Matti P Asuma, et al.
Molecular Vision|March 16, 2007
Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4Anne McMahon, Igor A Butovich, Nathan L Mata, et al.
Investigative Ophthalmology & Visual Science|June 26, 2009
Contribution of copy number variation in the regulation of complement activation locus to development of age-related macular degenerationKatharina E Schmid-Kubista, Nirubol Tosakulwong, Yanhong Wu, et al.
American Journal of Human Genetics|January 9, 2008
Mutations in KCNJ13 cause autosomal-dominant snowflake vitreoretinal degenerationJ Fielding Hejtmancik, Xiaodong Jiao, Anren Li, et al.
Pageof 6