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Combinatorial Chemistry & High Throughput Screening|July 16, 2009
Inkjet printing of growth factor concentration gradients and combinatorial arrays immobilized on biologically-relevant substratesEric D Miller, Julie A Phillippi, Gregory W Fisher, et al.Medical Physics|April 10, 2012
A method to evaluate dose errors introduced by dose mapping processes for mass conserving deformationsC Yan, G Hugo, F J Salguero, et al.The New England Journal of Medicine|April 6, 1989
Association of protamine IgE and IgG antibodies with life-threatening reactions to intravenous protamineM E Weiss, D Nyhan, Z K Peng, et al.Nature Nanotechnology|April 22, 2020
Three-dimensional localization microscopy in live flowing cellsLucien E Weiss, Yael Shalev Ezra, Sarah Goldberg, et al.Biomaterials Research|October 24, 2019
Mineral deposition and vascular invasion of hydroxyapatite reinforced collagen scaffolds seeded with human adipose-derived stem cellsHolly E Weiss-Bilka, Matthew J Meagher, Joshua A Gargac, et al.Journal of Biomedical Materials Research. Part A|April 27, 2016
Acellular hydroxyapatite-collagen scaffolds support angiogenesis and osteogenic gene expression in an ectopic murine model: Effects of hydroxyapatite volume fractionMatthew J Meagher, Holly E Weiss-Bilka, Margaret E Best, et al.Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|March 19, 2010
Health state preferences are equivalent in the United States and Trinidad and TobagoRichard D Hector, John P Anderson, Rosemarie C P Paul, et al.Endocrinology|April 23, 2005
Temperature homeostasis in transgenic mice lacking thyroid hormone receptor-alpha gene productsHusnia Marrif, Aria Schifman, Zaruhi Stepanyan, et al.The Journal of Clinical Endocrinology and Metabolism|June 1, 1994
Low intelligence but not attention deficit hyperactivity disorder is associated with resistance to thyroid hormone caused by mutation R316H in the thyroid hormone receptor beta geneR E Weiss, M A Stein, S C Duck, et al.Thyroid : Official Journal of the American Thyroid Association|February 6, 2014
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extractionSolomon Maximo Greenberg, Alfonso Massimiliano Ferrara, Everton S Nicholas, et al.Pageof 114