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  • Baseline and treatment-related changes in thrombin generation in patients with multiple myeloma
  • Integrated analysis of genome-wide DNA methylation and gene expression data provide a regulatory network in intrauterine growth restriction
  • EGFR T790M mutation testing within the osimertinib AURA Phase I study
  • Association of TGF-β3 and ANXA11 With Pulmonary Sarcoidosis in Greek Population
  • MiRNA155HG polymorphisms influenced the risk of liver cancer among the Han Chinese population
  • Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses
  • The Impact of the Genetic Polymorphism in DNA Repair Pathways on Increased Risk of Glioblastoma Multiforme in the Arab Jordanian Population: A Case–Control Study
  • Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population
  • Genetic analysis of nucleotide-binding leucine-rich repeat (NLR) receptors in multiple sclerosis
  • TRPV1 polymorphisms and risk of interferon β-induced flu-like syndrome in patients with relapsing-remitting multiple sclerosis
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