Blättern Fakultät für Biologie und Psychologie (inkl. GAUSS) nach "Mironov, Sergej Dr." Betreuer
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Calcium and cAMP homeostasis determine network organisation of respiratory pre-Bötzinger neurons in Mecp2 null mice in vitro.
(2013-07-03)Rett Syndrome (RS) is a neurodevelopmental disorder caused primarily by mutations in a Mecp2 gene on the X chromosome that encodes methyl-cytosine binding protein (MeCP2). MeCP2 acts as a transcriptional repressor and an ... -
Glutamate receptors potentiate single K-ATP channels through intracellular ATP changes
(2013-12-20)Rett Syndrome (RTT) is a neurodevelopmental disorder caused primarily by mutations in a Mecp2 gene and exclusively affects females. RTT is one of the prevalent developmental disorders with a high frequency of occurrence ...