Recent studies have identified various mutations in the FAM20A gene that lead to conditions like amelogenesis imperfecta (AI) and enamel renal syndrome (ERS). These conditions are marked by severe ...

Amelogenesis imperfecta (AI) is a genetic disorder that affects both primary and permanent teeth. It primarily manifests as developmental disorders of enamel. The condition occurs independently of ...

osteogenesis imperfecta, CREB3L1-related, domestic cat (MONDO:1012921) Parkinson disease, PINK1-related, rhesus monkey (MONDO:1012876) XX difference of sexual development, goat (MONDO:1012638) ...

The cone dystrophies are a heterogeneous group of inherited disorders that result in dysfunction of the cone photoreceptors and sometimes their post-receptoral pathways. The major clinical ...

All organisms have various circadian, behavioral, and physiological 24-h periodic rhythms, which are controlled by the circadian clock. The circadian clock controls various behavioral and ...

The volumes of a cell [cell volume (CV)] and its organelles are adjusted by osmoregulatory processes. During pinocytosis, extracellular fluid volume equivalent to its CV is incorporated within an hour ...