Direct mutation analysis by high-throughput sequencing: From germline to low-abundant, somatic variants - ScienceDirect
Thèse de doctorat NNT : 202
Direct mutation analysis by high-throughput sequencing: From germline to low-abundant, somatic variants - ScienceDirect
Potential of transposon-mediated cellular reprogramming towards cell-based therapies
S&TR Past Issues
Epigenetic Regulation of a Murine Retrotransposon by a Dual Histone Modification Mark | PLOS Genetics
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization | BMC Genomics | Full Text
Epigenetic Regulation of a Murine Retrotransposon by a Dual Histone Modification Mark | PLOS Genetics
Five months of voluntary wheel running downregulates skeletal muscle LINE-1 gene expression in rats
Preferential Epigenetic Suppression of the Autonomous MusD over the Nonautonomous ETn Mouse Retrotransposons | Molecular and Cellular Biology
Preferential Epigenetic Suppression of the Autonomous MusD over the Nonautonomous ETn Mouse Retrotransposons | Molecular and Cellular Biology
Diseases and Comorbid Conditions Predisposing Children to Kidney Stones | SpringerLink
MicroRNAs: Tools of Mechanistic Insights and Biological Therapeutics Discovery for the Rare Neurogenetic Syndrome Lesch–Nyhan Disease (LND) - ScienceDirect
S&TR Past Issues
Preferential Epigenetic Suppression of the Autonomous MusD over the Nonautonomous ETn Mouse Retrotransposons | Molecular and Cellular Biology
Potential of transposon-mediated cellular reprogramming towards cell-based therapies
Five months of voluntary wheel running downregulates skeletal muscle LINE-1 gene expression in rats | American Journal of Physiology-Cell Physiology
Frontiers | Nephrolithiasis and Nephrocalcinosis in Childhood—Risk Factor-Related Current and Future Treatment Options
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization | BMC Genomics | Full Text
MicroRNAs: Tools of Mechanistic Insights and Biological Therapeutics Discovery for the Rare Neurogenetic Syndrome Lesch–Nyhan Disease (LND) - ScienceDirect
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