Maria Cristina D'Adamo
Maria Cristina D'Adamo
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TitleCited byYear
Differential pH sensitivity of Kir4. 1 and Kir4. 2 potassium channels and their modulation by heteropolymerisation with Kir5. 1
M Pessia, P Imbrici, MC D'Adamo, L Salvatore, SJ Tucker
The Journal of Physiology 532 (2), 359-367, 2001
pH dependence of the inwardly rectifying potassium channel, Kir5. 1, and localization in renal tubular epithelia
SJ Tucker, P Imbrici, L Salvatore, MC D'Adamo, M Pessia
Journal of Biological Chemistry 275 (22), 16404-16407, 2000
Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4. 1
F Sicca, P Imbrici, MC D'Adamo, F Moro, F Bonatti, P Brovedani, ...
Neurobiology of disease 43 (1), 239-247, 2011
De novo point mutations in patients diagnosed with ataxic cerebral palsy
R Parolin Schnekenberg, EM Perkins, JW Miller, WIL Davies, ...
Brain 138 (7), 1817-1832, 2015
Episodic ataxia type‐1 mutations in the hKv1. 1 cytoplasmic pore region alter the gating properties of the channel
MC D'Adamo, Z Liu, JP Adelman, J Maylie, M Pessia
The EMBO journal 17 (5), 1200-1207, 1998
Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K+ channel function
MC D’Adamo, P Imbrici, F Sponcichetti, M Pessia
The FASEB Journal 13 (11), 1335-1345, 1999
Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis
L Romani, V Oikonomou, S Moretti, RG Iannitti, MC D'Adamo, VR Villella, ...
Nature medicine 23 (5), 590, 2017
K+ channelepsy: progress in the neurobiology of potassium channels and epilepsy
MC D'Adamo, L Catacuzzeno, G Di Giovanni, F Franciolini, M Pessia
Frontiers in cellular neuroscience 7, 134, 2013
Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4‐1.1/Kvβ1.1 and Kv1.4‐1.1/Kvβ1.2
P Imbrici, MC D'Adamo, DM Kullmann, M Pessia
European Journal of Neuroscience 24 (11), 3073-3083, 2006
Update on the implication of potassium channels in autism: K+ channelautism spectrum disorder
L Guglielmi, I Servettini, M Caramia, L Catacuzzeno, F Franciolini, ...
Frontiers in cellular neuroscience 9, 34, 2015
Genetically induced dysfunctions of Kir2. 1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype
E Ambrosini, F Sicca, MS Brignone, MC D'adamo, C Napolitano, ...
Human molecular genetics 23 (18), 4875-4886, 2014
Localization and age‐dependent expression of the inward rectifier K+ channel subunit Kir 5.1 in a mammalian reproductive system
L Salvatore, MC D'Adamo, R Polishchuk, M Salmona, M Pessia
FEBS letters 449 (2-3), 146-152, 1999
Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4. 1/Kir5. 1 potassium channels
M Casamassima, MC D'Adamo, M Pessia, SJ Tucker
Journal of Biological Chemistry 278 (44), 43533-43540, 2003
Genetic inactivation of Kcnj16 identifies Kir5. 1 as an important determinant of neuronal PCO2/pH sensitivity
MC D'Adamo, L Shang, P Imbrici, SDM Brown, M Pessia, SJ Tucker
Journal of Biological Chemistry 286 (1), 192-198, 2011
Antithrombotic activity of dermatan sulphates, heparins and their combination in an animal model of arterial thrombosis
L Iacoviello, MC D'Adamo, K Pawlak, R Polishchuck, T Wollny, W Buczko, ...
Thrombosis and haemostasis 76 (06), 1102-1107, 1996
Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion protein
A Corsaro, S Thellung, C Russo, V Villa, S Arena, MC D’Adamo, D Paludi, ...
Neurochemistry international 41 (1), 55-63, 2002
Role of receptor protein tyrosine phosphatase α (RPTPα) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels
P Imbrici, SJ Tucker, MC D'adamo, M Pessia
Pflügers Archiv 441 (2-3), 257-262, 2000
Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1. 1 channels
P Imbrici, A Cusimano, M D'adamo, A De Curtis, M Pessia
Pflügers Archiv 446 (3), 373-379, 2003
New insights into the pathogenesis and therapeutics of episodic ataxia type 1
MC D’Adamo, S Hasan, L Guglielmi, I Servettini, M Cenciarini, ...
Frontiers in cellular neuroscience 9, 317, 2015
Episodic ataxia type 1 mutations affect fast inactivation of K+ channels by a reduction in either subunit surface expression or affinity for inactivation domain
P Imbrici, MC D'Adamo, A Grottesi, A Biscarini, M Pessia
American Journal of Physiology-Cell Physiology 300 (6), C1314-C1322, 2011
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