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Plos Computational Biology|November 5, 2019
Network-based analysis of prostate cancer cell lines reveals novel marker gene candidates associated with radioresistance and patient relapseMichael Seifert, Claudia Peitzsch, Ielizaveta Gorodetska, et al.
Bioinformatics (Oxford, England)|April 22, 2023
Digital PCR cluster predictor: a universal R-package and shiny app for the automated analysis of multiplex digital PCR dataAlfonso De Falco, Christophe M Olinger, Barbara Klink, et al.
Clinical Neurology and Neurosurgery|January 12, 2010
Cordectomy as final treatment option for diffuse intramedullary malignant glioma using 5-ALA fluorescence-guided resectionChristian Ewelt, Walter Stummer, Barbara Klink, et al.
Cellular Oncology (Dordrecht, Netherlands)|May 4, 2011
Glioblastomas with oligodendroglial component-common origin of the different histological parts and genetic subclassificationBarbara Klink, Ben Schlingelhof, Martin Klink, et al.
Analytical Cellular Pathology (Amsterdam)|October 23, 2010
Glioblastomas with oligodendroglial component - common origin of the different histological parts and genetic subclassificationBarbara Klink, Ben Schlingelhof, Martin Klink, et al.
BMC Cancer|December 29, 2017
Chromosomal instability induced by increased BIRC5/Survivin levels affects tumorigenicity of glioma cellsMarina Conde, Susanne Michen, Ralf Wiedemuth, et al.
Molecular Cancer|June 3, 2014
Survivin safeguards chromosome numbers and protects from aneuploidy independently from p53Ralf Wiedemuth, Barbara Klink, Katrin Töpfer, et al.
Carcinogenesis|August 13, 2016
Janus face-like effects of Aurora B inhibition: antitumoral mode of action versus induction of aneuploid progenyRalf Wiedemuth, Barbara Klink, Mamoru Fujiwara, et al.
American Journal of Medical Genetics. Part A|June 4, 2016
Interstitial 1q23.3q24.1 deletion in a patient with renal malformation, congenital heart disease, and mild intellectual disabilityLuisa Mackenroth, Karl Hackmann, Barbara Klink, et al.
European Journal of Human Genetics : EJHG|March 11, 2026
Validation structures for sequence variants of uncertain significance in hereditary cancerMorghan C Lucas, Thomas Keßler, Anna Benet-Pagès, et al.
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