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Novartis Foundation Symposium|January 31, 2004
Identifying retinal disease genes: how far have we come, how far do we have to go?Stephen P DaigerAdvances in Experimental Medicine and Biology|October 3, 2015
The Role of X-Chromosome Inactivation in Retinal Development and DiseaseAbigail T Fahim, Stephen P DaigerArchives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Perspective on genes and mutations causing retinitis pigmentosaStephen P Daiger, Sara J Bowne, Lori S SullivanCold Spring Harbor Perspectives in Medicine|October 12, 2014
Genes and Mutations Causing Autosomal Dominant Retinitis PigmentosaStephen P Daiger, Sara J Bowne, Lori S SullivanCold Spring Harbor Perspectives in Medicine|October 3, 2023
History of Finding Genes and Mutations Causing Inherited Retinal DiseasesStephen P Daiger, Lori S Sullivan, Elizabeth L Cadena, et al.Healthcare (Amsterdam, Netherlands)|December 14, 2017
Innovating patient care delivery: DSRIP's interrupted time series analysis paradigmAmrita G Shenoy, Charles E Begley, Lee Revere, et al.Archives of Biochemistry and Biophysics|February 26, 2008
Retinal isoforms of inosine 5'-monophosphate dehydrogenase type 1 are poor nucleic acid binding proteinsDong Xu, Garrett Cobb, Catherine J Spellicy, et al.Advances in Experimental Medicine and Biology|March 19, 2010
Investigating the mechanism of disease in the RP10 form of retinitis pigmentosaCatherine J Spellicy, Dong Xu, Garrett Cobb, et al.Investigative Ophthalmology & Visual Science|January 7, 2018
Molecular Defects of the Disease-Causing Human Arrestin-1 C147F MutantSergey A Vishnivetskiy, Lori S Sullivan, Sara J Bowne, et al.American Journal of Ophthalmology|December 25, 2018
Time Course of Disease Progression of PRPF31-mediated Retinitis PigmentosaKelly Kiser, Kaylie D Webb-Jones, Sara J Bowne, et al.Pageof 8