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455 Ferroptosis in Duchenne muscular dystrophy Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder caused by mutations in dystrophin protein encoded by the DMD gene

Estrogen deficiency induces bone loss through the gut microbiota

KIAA0408 is a novel cilium molecule that has never been studied

In some cases, further tests may be required to identify the underlying cause, such as the Schilling test (now rare) or the detection of antibodies against intrinsic factor or gastric parietal cells

Autophagy regulates sex steroid hormone synthesis through lysosomal degradation of lipid droplets in human ovary and testis