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International Journal of Cancer|December 11, 2023
BRAF and MEK inhibitor combinations induce potent molecular and immunological effects in NRAS-mutant melanoma cells: Insights into mode of action and resistance mechanismsLisa Dinter, Paula C Karitzky, Alexander Schulz, et al.Nature Plants|June 2, 2016
Identification of the transporter responsible for sucrose accumulation in sugar beet taprootsBenjamin Jung, Frank Ludewig, Alexander Schulz, et al.International Journal of Molecular Sciences|May 24, 2020
C-Fiber Loss as a Possible Cause of Neuropathic Pain in SchwannomatosisSaid C Farschtschi, Tina Mainka, Markus Glatzel, et al.Journal of Hematology & Oncology|April 24, 2025
PFS24 as a prognostic milestone in patients with newly diagnosed primary CNS lymphomaVanja Zeremski, Tobias R Haage, Hanno M Witte, et al.Nature Neuroscience|March 5, 2013
Merlin isoform 2 in neurofibromatosis type 2-associated polyneuropathyAlexander Schulz, Stephan L Baader, Michiko Niwa-Kawakita, et al.Circulation. Cardiovascular Imaging|June 30, 2021
Analysis of 3-Dimensional Arch Anatomy, Vascular Flow, and Postnatal Outcome in Cases of Suspected Coarctation of the Aorta Using Fetal Cardiac Magnetic Resonance ImagingDavid F A Lloyd, Milou P M van Poppel, Kuberan Pushparajah, et al.Lancet (London, England)|March 27, 2019
Three-dimensional visualisation of the fetal heart using prenatal MRI with motion-corrected slice-volume registration: a prospective, single-centre cohort studyDavid F A Lloyd, Kuberan Pushparajah, John M Simpson, et al.The Journal of Investigative Dermatology|January 30, 2023
Identification of Epigenetically Regulated Genes Distinguishing Intracranial from Extracranial Melanoma MetastasesDana Westphal, Matthias Meinhardt, Konrad Grützmann, et al.Neurology. Genetics|July 22, 2024
Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related EncephalopathyAngela Clara-Hwang, Stefani Stefani, Tracy Lau, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2024
RORA-neurodevelopmental disorder: A unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizuresMariagrazia Talarico, Julitta de Bellescize, Matthias De Wachter, et al.Pageof 19