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Genesis (New York, N.Y. : 2000)|February 8, 2008
Efficient, inducible Cre-recombinase activation in vascular endotheliumSuzanne Claxton, Vassiliki Kostourou, Shalini Jadeja, et al.Nature Protocols|May 12, 2012
Visualization of gene expression in whole mouse retina by in situ hybridizationMichael B Powner, Kristis Vevis, Jenny A G McKenzie, et al.Nature Genetics|January 20, 2004
A direct functional link between the multi-PDZ domain protein GRIP1 and the Fraser syndrome protein Fras1Kogo Takamiya, Vassiliki Kostourou, Susanne Adams, et al.Investigative Ophthalmology & Visual Science|May 2, 2013
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathyShalini Jadeja, Richard L Mort, Margaret Keighren, et al.EMBO Molecular Medicine|December 15, 2010
Endothelial FAK is required for tumour angiogenesisBernardo Tavora, Silvia Batista, Louise E Reynolds, et al.Investigative Ophthalmology & Visual Science|March 5, 2015
Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunctionShalini Jadeja, Alun R Barnard, Lisa McKie, et al.Plos Genetics|October 31, 2014
Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing lossJing Chen, Neil Ingham, John Kelly, et al.Nature Genetics|April 20, 2005
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebsShalini Jadeja, Ian Smyth, Jolanta E Pitera, et al.Plos Genetics|May 10, 2014
A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected]Sally H Cross, Danilo G Macalinao, Lisa McKie, et al.Nature Genetics|May 27, 2003
Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix proteinLesley McGregor, Ville Makela, Susan M Darling, et al.Pageof 1