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Gene mutations and clinical manifestations of alpha-1 antitrypsin deficiency in Czech patients – a pilot study
Effects of dietary PUFA patterns and FADS genotype on breast milk PUFAs in Chinese lactating mothers
Genetic polymorphisms of GGT1 gene (rs8135987, rs5751901 and rs2017869) are associated with neoadjuvant chemotherapy efficacy and toxicities in breast cancer patients
Loss of fragile WWOX gene leads to senescence escape and genome instability
Hyper-Methylation of CpG Island in 5′ UTR of the HLA-G Gene Reduces Its Expression in Individuals with Immune Thrombocytopenia
Contrast Enhanced CT Radiogenomics in a Retrospective NSCLC Cohort: Models, Attempted Validation of a Published Model and the Relevance of the Clinical Context
Genetic mapping identifies SNP mutations in MITF-M promoter associated with melanin formation in Putian black duck
Haplotype phasing of CYP2D6: an allelic ratio method using Agena MassARRAY data
Associations between the proliferation of palatal mesenchymal cells, Tgfβ2 promoter methylation, Meg3 expression, and Smad signaling in atRA-induced cleft palate
Associations of IL6R and IL10 Gene Polymorphisms with Susceptibility to Ankylosing Spondylitis with or without Acute Anterior Uveitis