Regen Drouin
Affiliations: | Université de Sherbrooke, Sherbrooke, Québec, Canada |
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BiochemistryGoogle:
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Children
Sign in to add traineeMacoura Gadji | grad student | 2010 | Université de Sherbrooke |
Oumar Samassekou | grad student | 2011 | Université de Sherbrooke |
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Publications
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Gadji M, Mathur S, Bélanger B, et al. (2020) Three-Dimensional Nuclear Telomere Profiling as a Biomarker for Recurrence in Oligodendrogliomas: A Pilot Study. International Journal of Molecular Sciences. 21 |
Samassekou O, Bastien N, Yan J, et al. (2018) Expression of Genes Associated with Telomere Homeostasis in TP53 Mutant LoVo Cell Lines as a Model for Genomic Instability. Methods in Molecular Biology (Clifton, N.J.). 1769: 253-262 |
Samassekou O, Bastien N, Yan J, et al. (2018) Study of Telomere Dysfunction in TP53 Mutant LoVo Cell Lines as a Model for Genomic Instability. Methods in Molecular Biology (Clifton, N.J.). 1769: 209-230 |
Ayub S, Gadji M, Krabchi K, et al. (2016) Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations. American Journal of Medical Genetics. Part A. 170: 896-907 |
Emad A, Lamoureux J, Ouellet A, et al. (2015) Rapid Aneuploidy Detection of Chromosomes 13, 18, 21, X and Y Using Quantitative Fluorescent Polymerase Chain Reaction with Few Microdissected Fetal Cells. Fetal Diagnosis and Therapy. 38: 65-76 |
Samassekou O, Bastien N, Lichtensztejn D, et al. (2014) Different TP53 mutations are associated with specific chromosomal rearrangements, telomere length changes, and remodeling of the nuclear architecture of telomeres. Genes, Chromosomes & Cancer. 53: 934-50 |
Emad A, Bouchard EF, Lamoureux J, et al. (2014) Validation of automatic scanning of microscope slides in recovering rare cellular events: application for detection of fetal cells in maternal blood. Prenatal Diagnosis. 34: 538-46 |
Gadji M, Crous-Tsanaclis AM, Mathieu D, et al. (2014) A new der(1;7)(q10;p10) leading to a singular 1p loss in a case of glioblastoma with oligodendroglioma component. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 34: 170-8 |
Emad A, Ayub S, Samassékou O, et al. (2012) Efficiency of manual scanning in recovering rare cellular events identified by fluorescence in situ hybridization: simulation of the detection of fetal cells in maternal blood. Journal of Biomedicine & Biotechnology. 2012: 610856 |
Gadji M, Krabchi K, Langis P, et al. (2011) Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22. American Journal of Medical Genetics. Part A. 155: 430-3 |