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Mutations in fetal genes involved in innate immunity and host defense against microbes increase risk of preterm premature rupture of membranes (PPROM)
MAOA rs1137070 and heroin addiction interactively alter gray matter volume of the salience network
N370S-GBA1 mutation causes lysosomal cholesterol accumulation in Parkinson’s disease
Mass spectrometry-based assay for the molecular diagnosis of glioma: concomitant detection of chromosome 1p/19q codeletion, and IDH1, IDH2, and TERT mutation status
Neuropeptide S (NPS) variants modify the signaling and risk effects of NPS Receptor 1 (NPSR1) variants in asthma
Maternal Methyl Donor Supplementation during Gestation Counteracts the Bisphenol A-Induced Impairment of Intestinal Morphology, Disaccharidase Activity, and Nutrient Transporters Gene Expression in Newborn and Weaning Pigs
Maternal nutrient restriction in mid-to-late gestation influences fetal mRNA expression in muscle tissues in beef cattle
MET exon 14 mutations as targets in routine molecular analysis of primary sarcomatoid carcinoma of the lung
Metastatic thyroid carcinoma without identifiable primary tumor within the thyroid gland: a retrospective study of a rare phenomenon
Methylated +322-327 CpG site decreases hOGG1 mRNA expression in non-small cell lung cancer