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A peer-reviewed clinical paper confirmed that ADH released during dehydration can bind to uterine oxytocin receptors and stimulate contractions

The discovery of sodium-channel block as the major mechanism underlying antiarrhythmic effects of quinidine led to the development of class I antiarrhythmic agents such as flecainide and propafenone

These compounds enhance the liver and gallbladders role by decreasing fat deposits and speeding up the metabolism of fat and its removal

Inhibition of the RNase activity of IRE1 by drugs reduces viral protein levels and viral titers produced by JEV-infected mouse neuroblastoma cells (Neuro2a), which suggests that the activation of the RIDD pathway may have a direct benefit on JEV replication (Bhattacharyya et al., 2014)

A., Baehner, R

Esta propiedad est directamente relacionada con su origen gstrico: resiste la degradacin enzimtica en el estmago, lo que abre la va a una administracin oral una ventaja considerable frente a otros pptidos que requieren imperativamente una inyeccin