Cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-regulated Cl - channel functional in neonatal rat spinal motoneurons. The present study investigated the developmental (P1-P8) expression of CFTR, its impact on motoneuron excitability and Cl - homeostasis in relation to canonical Cl - transporters.
Cystic fibrosis transmembrane conductance regulator modulates synaptic chloride homeostasis in motoneurons of the rat spinal cored during neonatal development / A., Ostroumov; M., Simonetti; Nistri, Andrea. - In: DEVELOPMENTAL NEUROBIOLOGY. - ISSN 1932-8451. - 71:3(2011), pp. 253-268. [10.1002/dneu.20855]
Cystic fibrosis transmembrane conductance regulator modulates synaptic chloride homeostasis in motoneurons of the rat spinal cored during neonatal development
Nistri, Andrea
2011-01-01
Abstract
Cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-regulated Cl - channel functional in neonatal rat spinal motoneurons. The present study investigated the developmental (P1-P8) expression of CFTR, its impact on motoneuron excitability and Cl - homeostasis in relation to canonical Cl - transporters.File in questo prodotto:
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