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Stephanie Halford

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Experimental Eye Research|July 13, 2011
Focus on molecules: cytochrome P450 family 4, subfamily V, polypeptide 2 (CYP4V2)Donna S Mackay, Stephanie Halford
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|September 2, 2009
The evolution of irradiance detection: melanopsin and the non-visual opsinsStuart N Peirson, Stephanie Halford, Russell G Foster
Acta Ophthalmologica|April 24, 2018
Diabetic macular oedema: under-represented in the genetic analysis of diabetic retinopathySuzanne Broadgate, Christine Kiire, Stephanie Halford, et al.
Progress in Retinal and Eye Research|April 2, 2017
Unravelling the genetics of inherited retinal dystrophies: Past, present and futureSuzanne Broadgate, Jing Yu, Susan M Downes, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 13, 2012
Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophyStephanie Halford, Richard Holt, Andrea H Németh, et al.
Scientific Reports|May 10, 2016
Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapyMandeep S Singh, Suzanne Broadgate, Ranjana Mathur, et al.
Human Molecular Genetics|November 17, 2018
Targeted deletion of an NRL- and CRX-regulated alternative promoter specifically silences FERM and PDZ domain containing 1 (Frmpd1) in rod photoreceptorsChristie K Campla, Hannah Mast, Lijin Dong, et al.
Vision (Basel, Switzerland)|March 28, 2023
Intraretinal Microvascular Abnormalities and Venous Beading Have Different Genetic Profiles in Caucasian Patients with Non-Proliferative Diabetic RetinopathyElizabeth Pearce, Sobha Sivaprasad, Suzanne Broadgate, et al.
Experimental Eye Research|November 30, 2002
Genomic organization of human CDS2 and evaluation as a candidate gene for corneal hereditary endothelial dystrophy 2 on chromosome 20p13Stephanie Halford, Suzanne Inglis, Rhian Gwilliam, et al.
Experimental Eye Research|January 13, 2015
Identification of rod- and cone-specific expression signatures to identify candidate genes for retinal diseaseRichard Holt, Laurence Brown, Suzanne Broadgate, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Experimental Eye Research|July 13, 2011
Focus on molecules: cytochrome P450 family 4, subfamily V, polypeptide 2 (CYP4V2)Donna S Mackay, Stephanie Halford
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|September 2, 2009
The evolution of irradiance detection: melanopsin and the non-visual opsinsStuart N Peirson, Stephanie Halford, Russell G Foster
Acta Ophthalmologica|April 24, 2018
Diabetic macular oedema: under-represented in the genetic analysis of diabetic retinopathySuzanne Broadgate, Christine Kiire, Stephanie Halford, et al.
Progress in Retinal and Eye Research|April 2, 2017
Unravelling the genetics of inherited retinal dystrophies: Past, present and futureSuzanne Broadgate, Jing Yu, Susan M Downes, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 13, 2012
Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophyStephanie Halford, Richard Holt, Andrea H Németh, et al.
Scientific Reports|May 10, 2016
Hypotrichosis and juvenile macular dystrophy caused by CDH3 mutation: A candidate disease for retinal gene therapyMandeep S Singh, Suzanne Broadgate, Ranjana Mathur, et al.
Human Molecular Genetics|November 17, 2018
Targeted deletion of an NRL- and CRX-regulated alternative promoter specifically silences FERM and PDZ domain containing 1 (Frmpd1) in rod photoreceptorsChristie K Campla, Hannah Mast, Lijin Dong, et al.
Vision (Basel, Switzerland)|March 28, 2023
Intraretinal Microvascular Abnormalities and Venous Beading Have Different Genetic Profiles in Caucasian Patients with Non-Proliferative Diabetic RetinopathyElizabeth Pearce, Sobha Sivaprasad, Suzanne Broadgate, et al.
Experimental Eye Research|November 30, 2002
Genomic organization of human CDS2 and evaluation as a candidate gene for corneal hereditary endothelial dystrophy 2 on chromosome 20p13Stephanie Halford, Suzanne Inglis, Rhian Gwilliam, et al.
Experimental Eye Research|January 13, 2015
Identification of rod- and cone-specific expression signatures to identify candidate genes for retinal diseaseRichard Holt, Laurence Brown, Suzanne Broadgate, et al.
Pageof 5