Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alan F Wright

Showing results (21-30 of 239) with videos related to

Pageof 24
Sort By:
Annual Review of Neuroscience|June 25, 2010
The genomic, biochemical, and cellular responses of the retina in inherited photoreceptor degenerations and prospects for the treatment of these disordersAlexa N Bramall, Alan F Wright, Samuel G Jacobson, et al.
The British Journal of Ophthalmology|May 21, 2013
Papillorenal syndrome in a family with unusual complicationsRoly D Megaw, Anne Lampe, Baljean Dhillon, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 geneRuth Riise, Kristina Tornqvist, Alan F Wright, et al.
Genetic Epidemiology|October 19, 2011
Identity-by-descent-based phasing and imputation in founder populations using graphical modelsKimmo Palin, Harry Campbell, Alan F Wright, et al.
Human Molecular Genetics|September 22, 2011
The role of RPGR in cilia formation and actin stabilityMilica Gakovic, Xinhua Shu, Ioannis Kasioulis, et al.
Retina (Philadelphia, Pa.)|November 10, 2010
Pathogenesis of rhegmatogenous retinal detachment: predisposing anatomy and cell biologyDanny Mitry, Brian W Fleck, Alan F Wright, et al.
Investigative Ophthalmology & Visual Science|October 3, 2015
Evolutionary Characterization of the Retinitis Pigmentosa GTPase Regulator GeneRakesh Kotapati Raghupathy, Philippe Gautier, Dinesh C Soares, et al.
Nature Genetics|October 31, 2006
Contribution of consanguinuity to polygenic and multifactorial diseasesIgor Rudan, Harry Campbell, Andrew D Carothers, et al.
JAMA Ophthalmology|July 11, 2014
Late-onset retinal degeneration caused by C1QTNF5 mutation: sub-retinal pigment epithelium deposits and visual consequencesSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Nature Reviews. Genetics|March 10, 2010
Photoreceptor degeneration: genetic and mechanistic dissection of a complex traitAlan F Wright, Christina F Chakarova, Mai M Abd El-Aziz, et al.
Pageof 24

Showing results (21-30 of 239) with videos related to

Sort By:
Pageof 24
Annual Review of Neuroscience|June 25, 2010
The genomic, biochemical, and cellular responses of the retina in inherited photoreceptor degenerations and prospects for the treatment of these disordersAlexa N Bramall, Alan F Wright, Samuel G Jacobson, et al.
The British Journal of Ophthalmology|May 21, 2013
Papillorenal syndrome in a family with unusual complicationsRoly D Megaw, Anne Lampe, Baljean Dhillon, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 geneRuth Riise, Kristina Tornqvist, Alan F Wright, et al.
Genetic Epidemiology|October 19, 2011
Identity-by-descent-based phasing and imputation in founder populations using graphical modelsKimmo Palin, Harry Campbell, Alan F Wright, et al.
Human Molecular Genetics|September 22, 2011
The role of RPGR in cilia formation and actin stabilityMilica Gakovic, Xinhua Shu, Ioannis Kasioulis, et al.
Retina (Philadelphia, Pa.)|November 10, 2010
Pathogenesis of rhegmatogenous retinal detachment: predisposing anatomy and cell biologyDanny Mitry, Brian W Fleck, Alan F Wright, et al.
Investigative Ophthalmology & Visual Science|October 3, 2015
Evolutionary Characterization of the Retinitis Pigmentosa GTPase Regulator GeneRakesh Kotapati Raghupathy, Philippe Gautier, Dinesh C Soares, et al.
Nature Genetics|October 31, 2006
Contribution of consanguinuity to polygenic and multifactorial diseasesIgor Rudan, Harry Campbell, Andrew D Carothers, et al.
JAMA Ophthalmology|July 11, 2014
Late-onset retinal degeneration caused by C1QTNF5 mutation: sub-retinal pigment epithelium deposits and visual consequencesSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Nature Reviews. Genetics|March 10, 2010
Photoreceptor degeneration: genetic and mechanistic dissection of a complex traitAlan F Wright, Christina F Chakarova, Mai M Abd El-Aziz, et al.
Pageof 24