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CSH Protocols|March 2, 2011
Mouse Mutagenesis Using N-Ethyl-N-Nitrosourea (ENU)Andrew P Salinger, Monica J JusticeDisease Models & Mechanisms|December 3, 2008
Removing the cloak of invisibility: phenotyping the mouseMonica J JusticePlos One|December 5, 2013
A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus)Frank J Probst, Rebecca R Corrigan, Daniela Del Gaudio, et al.Emerging Topics in Life Sciences|February 1, 2021
Model systems inform rare disease diagnosis, therapeutic discovery and pre-clinical efficacyAdebola Enikanolaiye, Monica J JusticeDisease Models & Mechanisms|February 4, 2016
Using the mouse to model human disease: increasing validity and reproducibilityMonica J Justice, Paraminder DhillonDisease Models & Mechanisms|March 2, 2019
From gene to treatment: supporting rare disease translational research through model systemsJulija Hmeljak, Monica J JusticeMammalian Genome : Official Journal of the International Mammalian Genome Society|March 2, 2019
Treating Rett syndrome: from mouse models to human therapiesNeeti Vashi, Monica J JusticeBiochemical and Biophysical Research Communications|April 24, 2007
The kinesin related motor protein, Eg5, is essential for maintenance of pre-implantation embryogenesisAndrew Castillo, Monica J JusticePageof 11