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Journal of Neurovirology|April 25, 2007
Reactivation phenotype in rabbits of a herpes simplex virus type 1 mutant containing an unrelated antiapoptosis gene in place of latency-associated transcriptLing Jin, Guey-Chuen Perng, Dale Carpenter, et al.Journal of Virology|September 15, 2005
A herpes simplex virus type 1 mutant expressing a baculovirus inhibitor of apoptosis gene in place of latency-associated transcript has a wild-type reactivation phenotype in the mouseLing Jin, Guey-Chuen Perng, Kevin R Mott, et al.The Journal of General Virology|October 24, 2003
The bovine herpesvirus-1 LR ORF2 is critical for this gene's ability to restore the high wild-type reactivation phenotype to a herpes simplex virus-1 LAT null mutantKevin R Mott, Nelson Osorio, Ling Jin, et al.Human Mutation|September 17, 2014
Identification of fragile X syndrome specific molecular markers in human fibroblasts: a useful model to test the efficacy of therapeutic drugsDaman Kumari, Aditi Bhattacharya, Jeffrey Nadel, et al.Stem Cells Translational Medicine|October 3, 2014
The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug DiscoveryDavid J Brick, Hubert E Nethercott, Samantha Montesano, et al.Molecular Therapy. Methods & Clinical Development|June 9, 2015
A novel, long-lived, and highly engraftable immunodeficient mouse model of mucopolysaccharidosis type IDaniel C Mendez, Alexander E Stover, Anthony D Rangel, et al.Pageof 2