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A significant proportion (up to 62%) of oral squamous cell carcinomas (OSCCs) may arise from oral potential malignant lesions… Expand Disc-related disorders are highly genetic conditions with heritability estimates of up to 75 % and yet, few genomic locations… Expand 3p deletion syndrome is a rare disorder involving developmental delay, dysmorphic physical features, and growth retardation… Expand Objective: To identify of the gene responsible for the onset of spinocerebellar ataxia type 16 (SCA16). Methods: We reanalyzed… Expand 3p deletion syndrome is a rare contiguous-gene disorder involving the loss of the telomeric portion of the short arm of… Expand The oxytocin receptor belongs to the G-protein-coupled seven transmembrane receptor superfamily. Its main physiological role is… Expand 8-Hydroxyguanine (oh8G) is a major base lesion produced by reactive oxygen species. oh8G in DNA causes G:C to T:A transversions… Expand Oxidative damage is implicated in several chronic diseases including cancer. 8‐Hydroxyguanine (8‐oxoG) is one of the major… Expand We report the cloning of a human homolog of the yeast OGG1 gene, which encodes a DNA glycosylase that excises an oxidatively… Expand We isolated and characterized the human oxytocin receptor gene. Southern blots indicated that the human genome has a single copy… Expand