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Journal of Proteomics|May 28, 2011
Proteome profiling of wild type and lumican-deficient mouse corneasHanjuan Shao, Raghothama Chaerkady, Shoujun Chen, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|October 15, 2011
Sudden death after pediatric heart transplantation: analysis of data from the Pediatric Heart Transplant Study GroupKevin P Daly, Sujata B Chakravarti, Margaret Tresler, et al.
Cardiology in the Young|February 24, 2022
Aortic migration of Amplatzer Piccolo™ ductal OccluderPrashant K Minocha, Nicole Sutton, Maya T Crawford, et al.
Journal of Pediatric Surgery|May 19, 2021
Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjectsAshish Kapoor, Priyanka Nandakumar, Dallas R Auer, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2000
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locusS Bolk, A Pelet, R M Hofstra, et al.
Translational Oncogenomics|May 4, 2013
A STAT3 Gene Expression Signature in Gliomas is Associated with a Poor PrognosisJames V Alvarez, Neelanjan Mukherjee, Arnab Chakravarti, et al.
Investigative Ophthalmology & Visual Science|June 27, 2007
Cryopreservation and lentiviral-mediated genetic modification of human primary cultured corneal endothelial cellsLeejee H Suh, Cheng Zhang, Roy S Chuck, et al.
World Journal for Pediatric & Congenital Heart Surgery|June 28, 2018
Ubiquitin C-Terminal Hydrolase 1 and Phosphorylated Axonal Neurofilament Heavy Chain in Infants Undergoing Cardiac Surgery: Preliminary Assessment as Potential Biomarkers of Brain InjuryTimothy Lee, Sathish M Chikkabyrappa, Diane Reformina, et al.
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