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ESMO Open|April 13, 2023
Natural history and treatment efficacy in an ambispective case series of NTRK-rearranged mesenchymal tumorsA Dufresne, D Pissaloux, C Ngo, et al.NPJ Genomic Medicine|March 14, 2025
Unraveling MECP2 structural variants in previously elusive Rett syndrome cases through IGV interpretationTomer Poleg, Noam Hadar, Gali Heimer, et al.The New England Journal of Medicine|November 23, 2012
Long-term comparison of endovascular and open repair of abdominal aortic aneurysmFrank A Lederle, Julie A Freischlag, Tassos C Kyriakides, et al.European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|July 25, 2021
Microbubbles and Ultrasound Accelerated Thrombolysis for Peripheral Arterial Occlusions: The Outcomes of a Single Arm Phase II TrialSabrina A N Doelare, Dayanara M Jean Pierre, Johanna H Nederhoed, et al.Journal of Environmental Radioactivity|February 24, 2005
Automated radioxenon monitoring for the comprehensive nuclear-test-ban treaty in two distinctive locations: Ottawa and TahitiT J Stocki, X Blanchard, R D'Amours, et al.Elife|April 26, 2022
A bidirectional switch in the Shank3 phosphorylation state biases synapses toward up- or downscalingChi-Hong Wu, Vedakumar Tatavarty, Pierre M Jean Beltran, et al.Bioorganic & Medicinal Chemistry Letters|December 3, 2014
Synthesis of new bioisosteric hemiasterlin analogues with extremely high cytotoxicityThi Tuyet Anh Dang, The Chinh Pham, Quoc Anh Ngo, et al.Infection and Immunity|October 24, 2003
Critical role of the complement system in group B streptococcus-induced tumor necrosis factor alpha releaseOfer Levy, Rochelle M Jean-Jacques, Colette Cywes, et al.Bioinformatics (Oxford, England)|January 31, 2025
Relative quantification of proteins and post-translational modifications in proteomic experiments with shared peptides: a weight-based approachMateusz Staniak, Ting Huang, Amanda M Figueroa-Navedo, et al.Journal of Inherited Metabolic Disease|January 25, 2023
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutationAmit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz, et al.Pageof 23