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Oncotarget|September 18, 2018
Absence of correlation between radiation-induced CD8 T-lymphocyte apoptosis and sequelae in patients with prostate cancer accidentally overexposed to radiationGuillaume Vogin, Jean-Louis Merlin, Alexandra Rousseau, et al.Cancer Medicine|October 18, 2013
Optimization of routine KRAS mutation PCR-based testing procedure for rational individualized first-line-targeted therapy selection in metastatic colorectal cancerAnne-Sophie Chretien, Alexandre Harlé, Magali Meyer-Lefebvre, et al.Cell Death Discovery|September 27, 2024
DDB2 expression lights the way for precision radiotherapy response in PDAC cells, with or without olaparibJulie Dardare, Andréa Witz, Margaux Betz, et al.European Journal of Human Genetics : EJHG|July 5, 2007
A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophyMyriam Vezain, Pascale Saugier-Veber, Judith Melki, et al.Neuropediatrics|March 7, 2020
Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIAChloé Angelini, Marie Thibaud, Nathalie Aladjidi, et al.Frontiers in Oncology|December 26, 2022
DDB2 represses epithelial-to-mesenchymal transition and sensitizes pancreatic ductal adenocarcinoma cells to chemotherapyJulie Dardare, Andréa Witz, Margaux Betz, et al.Plos One|January 16, 2020
Evaluation of KRAS, NRAS and BRAF mutations detection in plasma using an automated system for patients with metastatic colorectal cancerClaire Franczak, Andréa Witz, Karen Geoffroy, et al.Journal of Medical Genetics|January 12, 2020
Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndromeChaker Aloui, Stéphanie Guey, Eva Pipiras, et al.Oncology Letters|November 14, 2025
Sensitive cell-free DNA assay for accurate detection of RAS and BRAF mutations in liquid biopsies of patients with metastatic colorectal cancer: Final results of the multicentric ColoBEAM studyAlexandre Harlé, Céline Gavoille, Olivier Bouché, et al.Human Mutation|June 29, 2010
LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhoodCaroline Michot, Laurence Hubert, Michèle Brivet, et al.Pageof 4