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[1] It is suggested that delayed processing of secreted lipids in the interfollicular epidermis and between the corneocytes in the upper parts of the hair follicles may be the cause of an impairment in the permeability of the epithelial barrier/Lipid Lamellae

Oxidative damage in human gingival fibroblasts exposed to cigarette smoke

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May include mild injection site discomfort, nausea, headache, flushing, or temporary fatigue

5-Oxoprolinase deficiency Disease name 5-Oxoprolinase deficiency (OMIM 260005) Definition and diagnostic criteria 5-Oxoprolinase deficiency is a very rare autosomal recessive disease characterized by 5-oxoprolinuria and very heterogeneous clinical presentation (renal stone formation, enterocolitis, mental retardation, neonatal hypoglycemia, microcytic anemia and microcephaly)