TP53-mutant AML with ribosomal gene loss exhibits impaired protein translation and sensitivity to HSP90 inhibition
Jean-François Spinella, Jalila Chagraoui, Isabel Boivin…·Guy Sauvageau
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Centre Hospitalier Universitaire Sainte-JustineORCID 0000-0001-9095-0066Unclaimed ORCID profile · follow to get notified of new preprints
9 papers
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Jean-François Spinella, Jalila Chagraoui, Isabel Boivin…·Guy Sauvageau
Virgile Raufaste-Cazavieille, Stéphanie Bianco, Lara Herrmann…·Raoul Santiago
This study examines the dynamic changes in the immune microenvironment of paediatric solid tumours over time, revealing a shift toward immunosuppressive and tolerogenic states.
Eric Olivier Audemard, Jean-François Spinella, Vincent‐Philippe Lavallée…·Sébastien Lemieux
EPCY ranks genes by predictive power using cross-validated classifiers and density estimation, outperforming DEG-based methods in selecting robust candidate genes.
Achille Nazaret, Joy Linyue Fan, Vincent‐Philippe Lavallée…·Elham Azizi
Decipher is a deep generative model that integrates single-cell RNA-seq data to visualize and characterize transitions between normal and perturbed cell states across different diseases.
Fadimana Kaya, Findlay Bewicke‐Copley, Juho Jalmari Miettinen…·Ana Rio‐Machín
This study identifies DEK::NUP214 as an XPO1-dependent transcriptional activator of leukemia genes, showing selective response to XPO1 inhibitors in t(6;9) AML cases.
Rose Laflamme, Véronique Lisi, Josée Hébert…·Guillaume Lettre
The paper replicates a GWAS signal near HLA-DQA2 associated with AML risk using a disease-only cohort and external population-based controls, finding a stronger effect in patients with NPM1 mutations.
Mélanie Sagniez, Shawn M. Simpson, Maxime Caron…·Martin A. Smith
This study demonstrates real-time transcriptomic profiling using nanopore sequencing and a neural network classifier to classify childhood acute lymphoblastic leukemia subtypes efficiently.
Eric Olivier Audemard, Patrick Gendron, Vincent‐Philippe Lavallée…·Sébastien Lemieux
This paper introduces km, a method for detecting targeted mutations in AML using unaligned RNA-Seq reads, showing it is fast, accurate, and limited by sequencing depth.