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Frontiers in Pediatrics|February 24, 2023
Resolving inherited and <i>de novo</i> germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignanciesTriantafyllia Brozou, Layal Yasin, Danielle Brandes, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|July 5, 2011
New insights into the molecular pathology of radiation-induced pneumopathyFederica Cappuccini, Therese Eldh, Dunja Bruder, et al.
Plos One|March 20, 2014
Mycoplasma salivarium as a dominant coloniser of Fanconi anaemia associated oral carcinomaBirgit Henrich, Madis Rumming, Alexander Sczyrba, et al.
Journal of Pediatric Hematology/Oncology|May 10, 2022
Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their ParentsRabea Wagener, Carolin Walter, Harald M Surowy, et al.
Hepatology (Baltimore, Md.)|August 21, 2007
Increased hepatotoxicity of tumor necrosis factor-related apoptosis-inducing ligand in diseased human liverXandra Volkmann, Ute Fischer, Matthias J Bahr, et al.
Elife|August 22, 2014
A RanGTP-independent mechanism allows ribosomal protein nuclear import for ribosome assemblySabina Schütz, Ute Fischer, Martin Altvater, et al.
Clinical Immunology (Orlando, Fla.)|November 4, 2015
De novo PIK3R1 gain-of-function with recurrent sinopulmonary infections, long-lasting chronic CMV-lymphadenitis and microcephalyMichaela Kuhlen, Andrea Hönscheid, Loizos Loizou, et al.
Cellular Microbiology|July 13, 2005
Multiple virulence factors are required for Staphylococcus aureus-induced apoptosis in endothelial cellsBettina Haslinger-Löffler, Barbara C Kahl, Matthias Grundmeier, et al.
International Journal of Cancer|September 30, 2023
Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patientsRabea Wagener, Danielle Brandes, Marie Jung, et al.
Frontiers in Immunology|November 3, 2018
EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 DeficiencyCyrill Schipp, David Schlütermann, Andrea Hönscheid, et al.
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