The nonapeptide oxytocin (OT) is a master regulator of the social brain in early infancy,
adolescence, and adult life. Here, we review the postnatal dynamic development of OT …

Oxytocin (OT) is a neurohormone involved early in neurodevelopment and is implicated in
multiple functions, including sensory modulation. Evidence of such modulation has been …

Introduction A microdeletion including the SNORD116 gene (SNORD116 MD) has been
shown to drive the Prader-Willi syndrome (PWS) features. PWS is a neurodevelopmental …

According to classic neuroendocrinology, hypothalamic oxytocin cells can be categorized
into parvo‐and magnocellular neurons. However, research in the last decade provided …

Prader–Willi syndrome (PWS) is a neurodevelopmental disorder characterized by
hyperphagia, obesity, developmental delay and intellectual disability. Studies suggest …

Abstract Background and aims Prader-Willi Syndrome (PWS) is a rare genetic disease.
Oxytocin is a neuropeptide hormone that impacts fear, and social recognition. Intranasal …

Oxytocin is a hormone secreted from definite neuroendocrine neurons located in specific
nuclei in the hypothalamus (mainly from paraventricular and supraoptic nuclei), and its main …

Prader-Willi syndrome (PWS) is a rare neurodevelopmental disorder, commonly linked to
hyperphagia and related behavioral and metabolic disturbances, such as food obsession …

Oxytocin (Oxt) regulates thermogenesis, and altered thermoregulation results in Prader-Willi
syndrome (PWS), Schaaf-Yang syndrome (SYS), and Autism spectrum disorder (ASD). PWS …

Methods Using Magel2 knockout mice, an animal model of Prader Willi Syndrome (PWS)
and Schaaf-Yang Syndrome (SYS), we tested memory of social fear and safety after a …