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Science (New York, N.Y.)|December 18, 2010
Spin transfer torques in MnSi at ultralow current densitiesF Jonietz, S Mühlbauer, C Pfleiderer, et al.Molecular and Cellular Biology|October 1, 1991
axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinaseJ P O'Bryan, R A Frye, P C Cogswell, et al.The British Journal of Dermatology|June 3, 1999
The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two casesM Mempel, D Abeck, I Lange, et al.American Journal of Medical Genetics. Part A|March 23, 2017
Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndromeThushiha Logeswaran, Christoph Friedburg, Karoline Hofmann, et al.Neurology|July 16, 2008
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromesB A Neubauer, S Waldegger, J Heinzinger, et al.Oncogene|May 3, 2006
siRNA-mediated AML1/MTG8 depletion affects differentiation and proliferation-associated gene expression in t(8;21)-positive cell lines and primary AML blastsJ Dunne, C Cullmann, M Ritter, et al.Journal of Oncology Practice|March 17, 2018
Three-Year Results of a Medicare Advantage Cancer Management ProgramJ Russell Hoverman, Marcus A Neubauer, Melissa Jameson, et al.Blood|March 15, 1994
Prognostic importance of mutations in the ras proto-oncogenes in de novo acute myeloid leukemiaA Neubauer, R K Dodge, S L George, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 9, 2020
Fully percutaneous fetoscopic repair of myelomeningocele: 30-month follow-up dataD Diehl, F Belke, T Kohl, et al.Journal of Oncology Practice|January 3, 2012
Benchmarks for value in cancer care: an analysis of a large commercial populationMichael Kolodziej, J Russell Hoverman, Jody S Garey, et al.Pageof 49