Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Diana eConte Camerino"'
Autor:
Roberta eCarbonara, Alessia eCarocci, Julien eRoussel, Giuseppe eCrescenzo, Canio eBuonavoglia, Carlo eFranchini, Giovanni eLentini, Diana eConte Camerino, Jean-François eDesaphy
Publikováno v:
Frontiers in Pharmacology, Vol 6 (2015)
Voltage-gated sodium channels are known to play a pivotal role in perception and transmission of pain sensations. Gain-of-function mutations in the genes encoding the peripheral neuronal sodium channels, hNav1.7-1.9, cause human painful diseases. Thu
Externí odkaz:
https://doaj.org/article/adaf1e51d697482db3307fd55b0a919d
Autor:
Paola eImbrici, Concetta eAltamura, Mauro ePessia, Renato eMantegazza, Jean-Francois eDesaphy, Diana eConte Camerino
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2015)
The voltage-dependent ClC-1 chloride channel belongs to the CLC channel/transporter family. It is a homodimer comprising two individual pores which can operate independently or simultaneously according to two gating modes, the fast and the slow gate
Externí odkaz:
https://doaj.org/article/2f761434904043819c885cf5eda09f6a
Publikováno v:
Frontiers in Genetics, Vol 4 (2013)
Voltage-gated ion channels are important mediators of physiological functions in the central nervous system. The cyclic activation of these channels influences neurotransmitter release, neuron excitability, gene transcription and plasticity, providin
Externí odkaz:
https://doaj.org/article/15cfb72fd8ac4eaf9b809d74b43cb147
Autor:
Jean-François eDesaphy, Antonella eDipalma, Teresa eCostanza, Roberta eCarbonara, Maria Maddalena eDinardo, Alessia eCatalano, Alessia eCarocci, Giovanni eLentini, Carlo eFranchini, Diana eConte Camerino
Publikováno v:
Frontiers in Pharmacology, Vol 3 (2012)
We previously showed that the β-adrenoceptor modulators, clenbuterol and propranolol, directly blocked voltage-gated sodium channels, whereas salbutamol and nadolol did not (Desaphy et al., 2003), suggesting the presence of two hydroxyl groups on th
Externí odkaz:
https://doaj.org/article/17242d9f29a4411aa34163d05448951e
Publikováno v:
Frontiers in Pharmacology, Vol 2 (2011)
The periodic paralysis(PP) are rare autosomal-dominant disorders associated to mutations in the skeletal muscle sodium, calcium and potassium channel genes characterized by muscle fiber depolarization with un-excitability, episodes of weakness with v
Externí odkaz:
https://doaj.org/article/0a7115fdb59e4667b2f681afd7a1097c
Publikováno v:
Frontiers in Pharmacology, Vol 1 (2010)
Externí odkaz:
https://doaj.org/article/5c1ff253fec64846af62b6b095626506