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Nitric Oxide : Biology and Chemistry|February 7, 2002
Interleukin-10 inhibition of nitric oxide biosynthesis involves suppression of CAT-2 transcriptionChun-Jen Huang, Bruce R Stevens, R Barton Nielsen, et al.Scientific Reports|August 23, 2020
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophyDavid W Hammers, Cora C Hart, Michael K Matheny, et al.Cancer Biology & Therapy|June 30, 2020
Silencing the intestinal GUCY2C tumor suppressor axis requires APC loss of heterozygosityAmanda M Pattison, Joshua R Barton, Ariana A Entezari, et al.European Journal of Immunology|September 10, 2022
Super-killer CTLs are generated by single gene deletion of Bach2Philippa R Barton, Alexander J Davenport, Jens Hukelmann, et al.The Journal of Cell Biology|April 20, 2016
Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotypeJoana Capote, Irina Kramerova, Leonel Martinez, et al.The Pediatric Infectious Disease Journal|November 19, 2011
Anti-N-methyl D-aspartate receptor encephalitis mimics viral encephalitisMustafa R Bseikri, Jubilee R Barton, Julie A Kulhanjian, et al.Biorxiv : the Preprint Server for Biology|January 27, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.Nucleic Acids Research|February 28, 2014
FineSplice, enhanced splice junction detection and quantification: a novel pipeline based on the assessment of diverse RNA-Seq alignment solutionsAlberto Gatto, Carlos Torroja-Fungairiño, Francesco Mazzarotto, et al.Skeletal Muscle|October 29, 2024
Spiny mice are primed but fail to regenerate volumetric skeletal muscle loss injuriesMackenzie L Davenport, Amaya Fong, Kaela N Albury, et al.Science (New York, N.Y.)|September 23, 2021
Protein-coding repeat polymorphisms strongly shape diverse human phenotypesRonen E Mukamel, Robert E Handsaker, Maxwell A Sherman, et al.Pageof 61