Showing results (521-530 of 562) with videos related to

Sort By:
Pageof 57
Frontiers in Endocrinology|May 10, 2017
Evaluation of Salivary Cytokines for Diagnosis of both Trauma-Induced and Genetic Heterotopic OssificationHsiao Hsin Sung Hsieh, Michael T Chung, Ronald M Allen, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 13, 2020
Tuning Macrophage Phenotype to Mitigate Skeletal Muscle FibrosisDavid M Stepien, Charles Hwang, Simone Marini, et al.
Stem Cells (Dayton, Ohio)|November 19, 2016
Scleraxis-Lineage Cells Contribute to Ectopic Bone Formation in Muscle and TendonShailesh Agarwal, Shawn J Loder, David Cholok, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 2, 2016
Inhibition of Hif1α prevents both trauma-induced and genetic heterotopic ossificationShailesh Agarwal, Shawn Loder, Cameron Brownley, et al.
Applied and Environmental Microbiology|February 25, 2018
Genus-Wide Assessment of Lignocellulose Utilization in the Extremely Thermophilic Genus Caldicellulosiruptor by Genomic, Pangenomic, and Metagenomic AnalysesLaura L Lee, Sara E Blumer-Schuette, Javier A Izquierdo, et al.
Frontiers in Immunology|November 12, 2019
Disruption of Neutrophil Extracellular Traps (NETs) Links Mechanical Strain to Post-traumatic InflammationShailesh Agarwal, Shawn J Loder, David Cholok, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 31, 2022
Amelioration of pathologic α-synuclein-induced Parkinson's disease by irisinTae-In Kam, Hyejin Park, Shih-Ching Chou, et al.
The American Journal of Pathology|August 25, 2018
Characterizing the Circulating Cell Populations in Traumatic Heterotopic OssificationShawn J Loder, Shailesh Agarwal, Michael T Chung, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 19, 2017
Strategic Targeting of Multiple BMP Receptors Prevents Trauma-Induced Heterotopic OssificationShailesh Agarwal, Shawn J Loder, Christopher Breuler, et al.
Nature Genetics|April 24, 2012
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndromeTobias Willer, Hane Lee, Mark Lommel, et al.
Pageof 57