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Gene Therapy|May 31, 2013
An armed oncolytic measles vaccine virus eliminates human hepatoma cells independently of apoptosisJ Lampe, S Bossow, T Weiland, et al.Human Molecular Genetics|April 10, 1999
Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivityS Colella, T Nardo, D Mallery, et al.British Journal of Pharmacology|December 1, 2018
Xeroderma pigmentosum: overview of pharmacology and novel therapeutic strategies for neurological symptomsRosella Abeti, Anna Zeitlberger, Colm Peelo, et al.Acta Oto-Laryngologica|June 27, 2001
A post-processing protocol for three-dimensional visualization of the inner ear using the volume-rendering technique based on a standard magnetic resonance imaging protocolR Klingebiel, N Thieme, J F Werner, et al.Journal of Cataract and Refractive Surgery|September 1, 1995
Clinical comparison of Provisc and Healon in cataract surgeryR Lehmann, S Brint, R Stewart, et al.Journal of Chromatography. A|July 1, 1998
Capillary electrophoresis in biochemical and clinical laboratoriesp selected attractive examplesW Voelter, J Schütz, O E Tsitsiloni, et al.Molecular Biology of the Cell|February 1, 1994
Identification and characterization of new elements involved in checkpoint and feedback controls in fission yeastF al-Khodairy, E Fotou, K S Sheldrick, et al.Annals of Clinical and Translational Neurology|January 30, 2018
Xeroderma pigmentosum is a definite cause of Huntington's disease-like syndromeHector Garcia-Moreno, Hiva Fassihi, Robert P E Sarkany, et al.International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|April 1, 1986
A derivative of an ataxia-telangiectasia (A-T) cell line with normal radiosensitivity but A-T-like inhibition of DNA synthesisA R Lehmann, C F Arlett, J F Burke, et al.Nucleic Acids Research|March 25, 1993
Evolutionary conservation of excision repair in Schizosaccharomyces pombe: evidence for a family of sequences related to the Saccharomyces cerevisiae RAD2 geneA M Carr, K S Sheldrick, J M Murray, et al.Pageof 67