113 research outputs found
The calcium-sensing receptor in physiology and in calcitropic and noncalcitropic diseases
The Ca2+-sensing receptor (CaSR) is a dimeric family C G protein-coupled receptor that is expressed in calcitropic tissues such as the parathyroid glands and the kidneys and signals via G proteins and β-arrestin. The CaSR has a pivotal role in bone and mineral metabolism, as it regulates parathyroid hormone secretion, urinary Ca2+ excretion, skeletal development and lactation. The importance of the CaSR for these calcitropic processes is highlighted by loss-of-function and gain-of-function CaSR mutations that cause familial hypocalciuric hypercalcaemia and autosomal dominant hypocalcaemia, respectively, and also by the fact that alterations in parathyroid CaSR expression contribute to the pathogenesis of primary and secondary hyperparathyroidism. Moreover, the CaSR is an established therapeutic target for hyperparathyroid disorders. The CaSR is also expressed in organs not involved in Ca2+ homeostasis: it has noncalcitropic roles in lung and neuronal development, vascular tone, gastrointestinal nutrient sensing, wound healing and secretion of insulin and enteroendocrine hormones. Furthermore, the abnormal expression or function of the CaSR is implicated in cardiovascular and neurological diseases, as well as in asthma, and the CaSR is reported to protect against colorectal cancer and neuroblastoma but increase the malignant potential of prostate and breast cancers
1388 Human Milk Fortification with Different Amounts of Fortifier and Its Association with Growth and Metabolic Responses of Preterm Infants
The relationship between trough drug concentrations and ductal closure in preterm infants treated with three-dose-oral ibuprofen
1185 Neutrophile Volume, Conductivity and Scatter Parameters and Better Results with Emma Statistical Programme in Neonatal Sepsis
1836 Inflammatory Responses to Hepatitis B Virus Vaccine among Healty Term Infants at Birth
Management of serious isolated gingival synechia in a newborn: case report and review of the literature
Congenital synechia of the gums is a rare malformation. The fusion may be partial or complete and may be associated with other facial dysmorphologic malformations. The synechia can be fibrous or bony and may develop between the upper and lower alveolar ridges. The authors report a newborn with partial, but broad and continuous, synechia of the gums and discuss its management during the first days of life
Total Antioxidant Capacity and Total Oxidant Status in Perinatal Asphyxia in Relation to Neurological Outcome
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