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Frontiers in Molecular Neuroscience|February 13, 2024
Methods to extract and analyze fluid from human pluripotent stem cell-derived choroid plexus organoidsLeon H Chew, Eloi Mercier, Jason C Rogalski, et al.Molecular Human Reproduction|June 14, 2015
Genomic characteristics of miscarriage copy number variantsHani Bagheri, Eloi Mercier, Ying Qiao, et al.Plos One|March 2, 2011
An integrated pipeline for the genome-wide analysis of transcription factor binding sites from ChIP-SeqEloi Mercier, Arnaud Droit, Leping Li, et al.BMC Genomics|August 14, 2013
miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disabilityYing Qiao, Chansonette Badduke, Eloi Mercier, et al.Marine Genomics|May 2, 2021
RNA-seq analysis of the mantle transcriptome from Mytilus edulis during a seasonal spawning event in deep and shallow water culture sites on the northeast coast of Newfoundland, CanadaDaria Gallardi, Xi Xue, Eloi Mercier, et al.BMC Medical Genetics|July 18, 2014
Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID)Ying Qiao, Eloi Mercier, Jila Dastan, et al.The Journal of Biological Chemistry|July 21, 2022
The amino acid sensor GCN2 suppresses terminal oligopyrimidine (TOP) mRNA translation via La-related protein 1 (LARP1)Zeenat Farooq, Fedho Kusuma, Phillip Burke, et al.Orphanet Journal of Rare Diseases|August 10, 2011
Understanding the impact of 1q21.1 copy number variantChansonette Harvard, Emma Strong, Eloi Mercier, et al.Gigascience|June 12, 2019
GenPipes: an open-source framework for distributed and scalable genomic analysesMathieu Bourgey, Rola Dali, Robert Eveleigh, et al.Nature Immunology|July 17, 2019
Altered differentiation is central to HIV-specific CD4+ T cell dysfunction in progressive diseaseAntigoni Morou, Elsa Brunet-Ratnasingham, Mathieu Dubé, et al.Pageof 2