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Human Molecular Genetics|May 23, 2002
Protein localization in the human eye and genetic screen of opticinJames S Friedman, Mathieu Faucher, Paul Hiscott, et al.Plos One|April 18, 2018
Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithmsMorteza Seifi, Michael A WalterOphthalmic Genetics|April 13, 2016
Prostaglandins in the eye: Function, expression, and roles in glaucomaLance P Doucette, Michael A WalterClinical & Experimental Ophthalmology|January 18, 2014
Genomics and anterior segment dysgenesis: a reviewYoko A Ito, Michael A WalterExperimental Eye Research|September 28, 2019
Aniridia and Axenfeld-Rieger Syndrome: Clinical presentations, molecular genetics and current/emerging therapiesPaul W Chrystal, Michael A WalterHuman Mutation|March 6, 2007
Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activityAtsuhiro Kanda, James S Friedman, Koji M Nishiguchi, et al.Journal of Ophthalmology|May 22, 2018
Molecular Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma: New Insights into MechanismsAdrian A Lahola-Chomiak, Michael A WalterInvestigative Ophthalmology & Visual Science|January 2, 2007
Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutationsM Hermina Strungaru, Irina Dinu, Michael A WalterThe Journal of Biological Chemistry|February 24, 2006
Regulation of FOXC1 stability and transcriptional activity by an epidermal growth factor-activated mitogen-activated protein kinase signaling cascadeFred B Berry, Farideh Mirzayans, Michael A WalterOncotarget|March 1, 2018
FOXC1, the new player in the cancer sandboxFahed A Elian, Elizabeth Yan, Michael A WalterPageof 7