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Clinical Journal of the American Society of Nephrology : CJASN|March 31, 2015
Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1Anja Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow, et al.
Genome Medicine|May 9, 2025
Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumorJenny Wegert, Silke Appenzeller, Taryn D Treger, et al.
Genes & Development|August 22, 2020
Functional loss of a noncanonical BCOR-PRC1.1 complex accelerates SHH-driven medulloblastoma formationLena M Kutscher, Konstantin Okonechnikov, Nadja V Batora, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 9, 2020
Influence of Surgical Excision on the Survival of Patients With Stage 4 High-Risk Neuroblastoma: A Report From the HR-NBL1/SIOPEN StudyKeith Holmes, Ulrike Pötschger, Andrew D J Pearson, et al.
European Journal of Cancer (Oxford, England : 1990)|November 29, 2020
Clinical and genetic risk factors define two risk groups of extracranial malignant rhabdoid tumours (eMRT/RTK)Karolina Nemes, Susanne Bens, Denis Kachanov, et al.
Nature Reviews. Urology|October 17, 2023
Hallmark discoveries in the biology of Wilms tumourDaniela Perotti, Richard D Williams, Jenny Wegert, et al.
Journal of Magnetic Resonance Imaging : JMRI|August 7, 2021
MRI Characteristics of Pediatric Renal Tumors: A SIOP-RTSG Radiology Panel Delphi StudyJustine N van der Beek, Tom A Watson, Rutger A J Nievelstein, et al.
Cancer Discovery|December 12, 2024
Predisposition Footprints in the Somatic Genome of Wilms TumorsTaryn D Treger, Jenny Wegert, Anna Wenger, et al.
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