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Minimally Invasive Therapy & Allied Technologies : MITAT : Official Journal of the Society for Minimally Invasive Therapy|February 17, 2010
The medical engineering program of Forschungszentrum KarlsruheH Fischer, M Selig, J Vagner, et al.
Nature Communications|January 8, 2024
Compartments in medulloblastoma with extensive nodularity are connected through differentiation along the granular precursor lineageDavid R Ghasemi, Konstantin Okonechnikov, Anne Rademacher, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
Comprehensive investigation of DNA damage repair genes in children with cancer identifies <i>SMARCAL1</i> as novel osteosarcoma predisposition geneNinad Oak, Wenan Chen, Alise Blake, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 10, 2020
Temporal patterns and short-term progression of paroxysmal atrial fibrillation: data from RACE VRuben R De With, Ömer Erküner, Michiel Rienstra, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|June 2, 2017
Planning benchmark study for SBRT of early stage NSCLC : Results of the DEGRO Working Group Stereotactic RadiotherapyChristos Moustakis, Oliver Blanck, Fatemeh Ebrahimi Tazehmahalleh, et al.
Journal of Community Genetics|March 31, 2019
Linking pre-existing biorepositories for medical research: the PopGen 2.0 NetworkWolfgang Lieb, Gunnar Jacobs, Andreas Wolf, et al.
Biological Research|February 17, 2023
DNA sequencing in the classroom: complete genome sequence of two earwig (Dermaptera; Insecta) speciesSanae Kobayashi, Jonathan E Maldonado, Alexis Gaete, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 9, 2025
Investigation of DNA Damage Response Genes Validates the Role of DNA Repair in Pediatric Cancer Risk and Identifies <i>SMARCAL1</i> as a Novel Osteosarcoma Predisposition GeneNinad Oak, Wenan Chen, Alise Blake, et al.
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