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Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|May 22, 2023
Synthetic Epigenetic Reprogramming of Mesenchymal to Epithelial States Using the CRISPR/dCas9 Platform in Triple Negative Breast CancerCharlene Waryah, Joseph Cursons, Momeneh Foroutan, et al.
Acta Neuropathologica|October 24, 2015
Gliomatosis cerebri: no evidence for a separate brain tumor entityUlrich Herrlinger, David T W Jones, Martin Glas, et al.
International Journal of Cancer|September 2, 2022
A novel serum extracellular vesicle protein signature to monitor glioblastoma tumor progressionTheophilos Tzaridis, Johannes Weller, Daniel Bachurski, et al.
Blood|September 4, 2004
Gene expression profiling in follicular lymphoma to assess clinical aggressiveness and to guide the choice of treatmentAnnuska M Glas, Marie José Kersten, Leonie J M J Delahaye, et al.
Journal of Neuro-Oncology|January 27, 2021
Machine learning-based differentiation between multiple sclerosis and glioma WHO II°-IV° using O-(2-[18F] fluoroethyl)-L-tyrosine positron emission tomographySied Kebir, Laurèl Rauschenbach, Manuel Weber, et al.
The Journal of Thoracic and Cardiovascular Surgery|April 17, 2003
Off-pump coronary artery bypass grafting provides complete revascularization with reduced myocardial injury, transfusion requirements, and length of stay: a prospective randomized comparison of two hundred unselected patients undergoing off-pump versus conventional coronary artery bypass graftingJ D Puskas, W H Williams, P G Duke, et al.
Neuro-Oncology|June 19, 2023
Individual glioblastoma cells harbor both proliferative and invasive capabilities during tumor progressionMiriam Ratliff, Kianush Karimian-Jazi, Dirk C Hoffmann, et al.
Frontiers in Oncology|July 3, 2026
Caregiver satisfaction with early integrated palliative care in oncology: secondary outcomes from the PALLiON cluster-RCTKristin Vassbotn Guldhav, Andrew Athan McAleavey, Nina Aass, et al.
Genes & Development|March 21, 2018
An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethalityChristina M Ferrer, Marielle Alders, Alex V Postma, et al.
The American Journal of Gastroenterology|March 6, 2009
rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German populationJürgen Glas, Julia Seiderer, Giulia Pasciuto, et al.
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