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Frontiers in Cell and Developmental Biology|September 29, 2022
Eyes on CHARGE syndrome: Roles of CHD7 in ocular developmentLaura A Krueger, Ann C MorrisBiochemical and Biophysical Research Communications|April 4, 2022
Generation of a zebrafish knock-in line expressing MYC-tagged Sox11a using CRISPR/Cas9 genome editingLaura A Krueger, Ann C MorrisGenes|March 25, 2022
Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1Mariya R Ahmed, Saumil Sethna, Laura A Krueger, et al.Investigative Ophthalmology & Visual Science|November 4, 2015
Nucleoside Reverse Transcriptase Inhibitors Suppress Laser-Induced Choroidal Neovascularization in MiceTakeshi Mizutani, Benjamin J Fowler, Younghee Kim, et al.American Journal of Medical Genetics. Part A|November 20, 2015
A new frontonasal dysplasia syndrome associated with deletion of the SIX2 geneRobert B Hufnagel, Sarah L Zimmerman, Laura A Krueger, et al.Experimental Eye Research|November 7, 2022
Chromatin remodeler Chd7 regulates photoreceptor development and outer segment lengthLaura A Krueger, Jessica D Bills, Zun Yi Lim, et al.Scientific Reports|September 5, 2020
Author Correction: Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survivalCagney E Coomer, Stephen G Wilson, Kayla F Titialii-Torres, et al.Scientific Reports|July 11, 2020
Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survivalCagney E Coomer, Stephen G Wilson, Kayla F Titialii-Torres, et al.Journal of Medical Genetics|December 7, 2014
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromesRobert B Hufnagel, Gavin Arno, Nichole D Hein, et al.Nature Genetics|July 14, 2015
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorderAlexander J Abrams, Robert B Hufnagel, Adriana Rebelo, et al.Pageof 1