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Experimental Eye Research|March 28, 2025
A biometric survey of known and prospective murine models of posterior microphthalmia-nanophthalmiaNavdeep Gogna, Jai Pinkney, Lisa Stone, et al.Human Molecular Genetics|April 18, 2003
Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor)Sakae Ikeda, Leslie A Cunningham, Dawnalyn Boggess, et al.Proceedings of the National Academy of Sciences of the United States of America|August 15, 1995
Lith1, a major gene affecting cholesterol gallstone formation among inbred strains of miceB Khanuja, Y C Cheah, M Hunt, et al.Cell Death & Disease|October 30, 2021
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axisYeming Yang, Xiao Li, Jieping Wang, et al.Human Genetics|December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13G B Collin, J D Marshall, C F Boerkoel, et al.Nature Genetics|June 1, 1995
Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activityJ K Naggert, L D Fricker, O Varlamov, et al.Cells|April 16, 2020
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell LossGayle B Collin, Navdeep Gogna, Bo Chang, et al.Plos One|October 31, 2014
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAsRamani Soundararajan, Jungyeon Won, Timothy M Stearns, et al.Molecular and Cellular Neurosciences|August 23, 2005
Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseasesYongsuk Lee, Shuhei Kameya, Gregory A Cox, et al.Human Molecular Genetics|November 17, 2010
NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm developmentJungyeon Won, Caralina Marín de Evsikova, Richard S Smith, et al.Pageof 17