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An early study indicated that the ATP7A transcript lacking exon 10 encodes a partially functional protein, and this residual function is associated with a milder form of occipital horn syndrome (OHS), which is caused by mutations at the ATP7A splicing site

Lower gut surface area (48), thin villi (48), prolonged cell cycle time (49), and impaired peristalsis (50)were observed in germ-free (GF) mice

Fish Sci (Dalian) 29(9):505509 Maeda M, Shibata A, Biswas G, Korenaga H, Kono T, Itami T, Sakai M (2014) Isolation of lactic acid bacteria from kuruma shrimp ( Marsupenaeus japonicus ) intestine and assessment of immunomodulatory role of a selected strain as probiotic

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Therapeutic applications of genetic code expansion