France (FR)

Sorafenib promotes graft-versus-leukemia activity in mice and humans through IL-15 production in FLT3-ITD-mutant leukemia cells (2018) Mathew NR, Baumgartner F, Braun L, O'Sullivan D, Thomas S, Waterhouse M, Mueller TA, et al. Journal article Strategies for radiation dose reduction in nuclear cardiology and cardiac computed tomography imaging: a report from the European Association of Cardiovascular Imaging (EACVI), the Cardiovascular Committee of European Association of Nuclear Medicine (EANM), and the European Society of Cardiovascular Radiology (ESCR) (2018) Gimelli A, Achenbach S, Buechel RR, Edvardsen T, Francone M, Gaemperli O, Hacker M, et al. Journal article Pharmacology and pharmacokinetics of imatinib in pediatric patients (2018) Suttorp M, Bornhaeuser M, Metzler M, Schleyer E, Millot F Journal article The role of uranium-arene bonding in H2O reduction catalysis (2018) Halter D, Heinemann FW, Maron L, Meyer K Journal article Stereo Rectification for X-ray Data Consistency Conditions (2018) Aichert A, Jérôme L, Würfl T, Clackdoyle R, Desbat L, Maier A Conference contribution, Original article Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT). (2018) Neirijnck Y, Reginensi A, Renkema KY, Massa F, Kozlov VM, Dhib H, Bongers EMHF, et al. Journal article, Original article Embedded Fluorescence Lifetime Determination for High-Throughput, Low-Photon-Number Applications (2018) Lieske T, Uhring W, Dumas N, Skilitsi AI, Leonard J, Fey D Journal article, Original article Commonalities in epileptogenic processes from different acute brain insults: Do they translate? (2018) Klein P, Dingledine R, Aronica E, Bernard C, Blümcke I, Boison D, Brodie MJ, et al. Journal article A multinational clinical approach to assessing the effectiveness of catheter-based ultrasound renal denervation: The RADIANCE-HTN and REQUIRE clinical study designs (2018) Mauri L, Kario K, Basile J, Daemen J, Davies J, Kirtane AJ, Mahfoud F, et al. Journal article Genetic and molecular insights into genotype-phenotype relationships in osteopathia striata with cranial sclerosis (OSCS) through the analysis of novel mouse Wtx mutant alleles (2018) Comai G, Boutet A, Tanneberger K, Massa F, Rocha AS, Charlet A, Panzolini C, et al. Journal article