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Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K+ channel function 1-gen-1998 M., Pessia; Imbrici, Paola; F., Sponcichetti; M. C., D’Adamo
Human voltage-dependent potassium channel heteropolymerization results in episodic ataxia type-1 myokymia syndrome. 1-gen-1998 M. C., D’Adamo; Imbrici, Paola; F., Sponcichetti; M., Pessia
Modification by aging of the TTX-sensitive sodium channel in rat skeletal muscle fibres 1-gen-1998 Desaphy, Jean Francois; A., DE LUCA; Imbrici, Paola; AND D., CONTE CAMERINO
Partial recovery of skeletal muscle sodium channel properties in aged rats chronically treated with growth hormone or the GH-secretagogue hexarelin 1-gen-1998 Desaphy, Jean Francois; DE LUCA, Annamaria; Pierno, Sabata; Imbrici, Paola; Conte, Diana
Modification by ageing of the tetrodotoxin-sensitive sodium channels in rat skeletal muscle fibres 1-gen-1998 Desaphy, Jean Francois; DE LUCA, Annamaria; Imbrici, Paola; Conte, Diana
Gating properties of human heteromeric voltage-gated potassium channels and effects of episodic ataxia type-1 mutations 1-gen-1999 D’Adamo, Mc; Imbrici, Paola; Sponcichetti, F; Pessia, M.
Mutations in KCNA1 gene associated with episodic ataxia type-1 sindrome impair heteromeric voltage-gated K+ channel function 1-gen-1999 D’Adamo, Mc; Imbrici, Paola; Sponcichetti, F; Pessia, M.
Episodic ataxia type-1 mutations alter the open state stability of voltage-gated K+ channels and the cell resting potential. 1-gen-1999 M., Pessia; Imbrici, Paola; M. C., D’Adamo
Modulation of delayed rectifier K+ channels by 5HT2c receptors 1-gen-1999 Imbrici, Paola; D’Adamo, Mc; Sponcichetti, F; Pessia, M.
Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K+ channel function 1-gen-1999 M. C., Dadamo; Imbrici, Paola; F., Sponcichetti; M., Pessia
Modulation of hKv 1.1 and hKv 1.2 voltage gating and C-type inactivation by 5-HT2C receptors 1-gen-2000 Imbrici, Paola; Tucker, Sj; D’Adamo, Mc; Sponcichetti, F; Pessia, M.
Role of receptor protein tyrosine phosphatase α (RPTPα) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels 1-gen-2000 Imbrici, Paola; S. J., Tucker; M. C., D'Adamo; M., Pessia
pH Dependence of the inwardly rectifying potassium channel, Kir5.1, and localization in renal tubular epithelia 1-gen-2000 S. J., Tucker; Imbrici, Paola; L., Salvatore; M. C., D'Adamo; M., Pessia
Role of the S1 segment in the voltage-dependent gating of Kv1.1 channels revealed by naturally occurring pathogenic mutations 1-gen-2001 Imbrici, Paola; D’Adamo, Mc; Pessia, M.
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 1-gen-2001 Pessia, M; Imbrici, Paola; D'Adamo, Mc; Salvatore, L; Tucker, Sj
Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents 1-gen-2001 Cusimano, A; Imbrici, Paola; D’Adamo, Mc; Pessia, M.
Copertina della rivista The Journal of Physiology 1-gen-2001 Pessia, M.; Imbrici, Paola; D'Adamo, M. C.; Salvatore, L.; Tucker, S. J.
Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1 1-gen-2001 M., Pessia; Imbrici, Paola; M. C., D'Adamo; L., Salvatore; S. J., Tucker
Episodic Ataxias as Ion Channel Diseases. 1-gen-2001 D'Adamo, Mc; Imbrici, Paola; Pessia, M.
Novel mutations of Kir2.1 underlying Andersen’s syndrome are non-functional and have a dominant negative effect on the wild –type allele 1-gen-2002 Imbrici, Paola; L., Bilsland; N. P., Davies; M. G. HANNA AND D. M., Kullmann
Mostrati risultati da 1 a 20 di 123
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