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Nonetheless, a more comprehensive understanding of gap junctions concerning the BBB in neurodegenerative diseases is still required
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They help stabilize cell membranes by interacting with lipid bilayers and minimizing lipid peroxidation
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)
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