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Bio-Protocol|August 1, 2017
Assaying the Effects of Splice Site Variants by Exon Trapping in a Mammalian Cell LineStuart W Tompson, Terri L Young
Biorxiv : the Preprint Server for Biology|September 5, 2025
Leveraging Single-Cell Transcriptomics of Developing Rat Ocular Outflow Tissues for Prioritization of Congenital Glaucoma Candidate GenesSean M Martin, Kristina N Whisenhunt, Stuart W Tompson
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 20, 2014
Mice expressing mutant Trpv4 recapitulate the human TRPV4 disordersMichael M Weinstein, Stuart W Tompson, Yuqing Chen, et al.
Ophthalmology. Glaucoma|July 17, 2020
Comparative Intraoperative Anterior Segment OCT Findings in Pediatric Patients with and without GlaucomaYasmin Bradfield, Thaisa Barbosa, Barbara Blodi, et al.
Investigative Ophthalmology & Visual Science|June 24, 2022
Sonic Hedgehog Intron Variant Associated With an Unusual Pediatric Cortical CataractTerri L Young, Kristina N Whisenhunt, Sarah M LaMartina, et al.
Investigative Ophthalmology & Visual Science|April 7, 2017
Exome Sequence Analysis of 14 Families With High MyopiaBethany A Kloss, Stuart W Tompson, Kristina N Whisenhunt, et al.
American Journal of Human Genetics|April 3, 2012
Exome sequencing identifies PDE4D mutations in acrodysostosisHane Lee, John M Graham, David L Rimoin, et al.
Nature Communications|October 19, 2021
Cellular crosstalk regulates the aqueous humor outflow pathway and provides new targets for glaucoma therapiesBenjamin R Thomson, Pan Liu, Tuncer Onay, et al.
Scientific Reports|July 1, 2026
Assessment of anti-VEGF intravitreal injection effects on murine neonatal Schlemm's canal morphologyGabriella D Hartman, Amirhesam Afsharpour, Sean M Martin, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2Stuart W Tompson, Eissa Ali Faqeih, Leena Ala-Kokko, et al.
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