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American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 15, 2014
Dose-intensive response-based chemotherapy and radiation therapy for children and adolescents with newly diagnosed intermediate-risk hodgkin lymphoma: a report from the Children's Oncology Group Study AHOD0031Debra L Friedman, Lu Chen, Suzanne Wolden, et al.Experimental Eye Research|January 14, 2021
Intravitreal melphalan hydrochloride vs propylene glycol-free melphalan for retinoblastoma vitreous seeds: Efficacy, toxicity and stability in rabbits models and patientsCarley M Bogan, Janene M Pierce, Stephanie D Doss, et al.Experimental and Molecular Pathology|September 21, 2011
Human hepatic stellate cell line (LX-2) exhibits characteristics of bone marrow-derived mesenchymal stem cellsAndrielle Castilho-Fernandes, Danilo Candido de Almeida, Aparecida Maria Fontes, et al.Hepatology (Baltimore, Md.)|August 5, 2010
Acute liver failure is associated with elevated liver stiffness and hepatic stellate cell activationAlexander Dechêne, Jan-Peter Sowa, Robert K Gieseler, et al.Prehospital Emergency Care|October 25, 2000
A comparison of biphasic and monophasic shocks for external defibrillation. Physio-Control Biphasic InvestigatorsS L Higgins, J M Herre, A E Epstein, et al.The New England Journal of Medicine|October 13, 2006
Chronic health conditions in adult survivors of childhood cancerKevin C Oeffinger, Ann C Mertens, Charles A Sklar, et al.Plos Pathogens|December 29, 2010
Mycobacterium tuberculosis eis regulates autophagy, inflammation, and cell death through redox-dependent signalingDong-Min Shin, Bo-Young Jeon, Hye-Mi Lee, et al.JAMA|January 30, 2009
Breast cancer surveillance practices among women previously treated with chest radiation for a childhood cancerKevin C Oeffinger, Jennifer S Ford, Chaya S Moskowitz, et al.Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.Pageof 149