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Faculty of Medicine and Surgery
Department of Physiology and Biochemistry
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Results 1-10 of 49 (Search time: 0.009 seconds).
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Issue Date
Title
Author(s)
2007
Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvβ1.1
Imbrici, Paola
;
D'Adamo, Maria Cristina
;
Cusimano, Antonella
;
Pessia, Mauro
2003
Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4.1/Kir5.1 potassium channels
Casamassima, Maria
;
D'Adamo, Maria Cristina
;
Pessia, Mauro
;
Tucker, Stephen J.
2014
Genetically induced dysfunctions of Kir2.1 channels : implications for short QT3 syndrome and autism-epilepsy phenotype
Ambrosini, Elena
;
Sicca, Federico
;
Brignone, Maria Stefania
;
D'Adamo, Maria Cristina
;
Napolitano, Carlo
;
Servettini, Ilenio
;
Moro, Francesca
;
Ruan, Yanfei
;
Guglielmi, Luca
;
Pieroni, Stefania
;
Servillo, Giuseppe
;
Lanciotti, Angela
;
Valvo, Giulia
;
Catacuzzeno, Luigi
;
Franciolini, Fabio
;
Molinari, Paola
;
Marchese, Maria
;
Grottesi, Alessandro
;
Guerrini, Renzo
;
Santorelli, Filippo Maria
;
Priori, Silvia Giuliana
;
Pessia, Mauro
2000
Role of receptor protein tyrosine phosphatase α (RPTPα) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels
Imbrici, Paola
;
Tucker, Stephen J.
;
D'Adamo, Maria Cristina
;
Pessia, Mauro
2015
De novo point mutations in patients diagnosed with ataxic cerebral palsy
Parolin Schnekenberg, Ricardo
;
Perkins, Emma M.
;
Miller, Jack W.
;
Davies, Wayne L.
;
D'Adamo, Maria Cristina
;
Pessia, Mauro
;
Fawcett, Katherine A.
;
Sims, David
;
Gillard, Elodie
;
Hudspith, Karl A. Z.
;
Skehel, Paul A.
;
Williams, Jonathan
;
O'Regan, Mary E.
;
Jayawant, Sandeep S.
;
Jefferson, Rosalind J.
;
Hughes, Sarah M.
;
Lustenberger, Andrea
;
Ragoussis, Jiannis
;
Jackson, Mandy
;
Tucker, Stephen J.
;
Nemeth, Andrea H.
2015
The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma
Sforna, Luigi
;
Cenciarini, Marta
;
Belia, Silvia
;
D'Adamo, Maria Cristina
;
Pessia, Mauro
;
Franciolini, Fabio
;
Catacuzzeno, Luigi
2015
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene
D'Adamo, Maria Cristina
;
Gallenmuller, Constanze
;
Servettini, Ilenio
;
Hartl, Elisabeth
;
Tucker, Stephen J.
;
Arning, Larissa
;
Biskup, Saskia
;
Grottesi, Alessandro
;
Guglielmi, Luca
;
Imbrici, Paola
;
Bernasconi, Pia
;
Di Giovanni, Giuseppe
;
Franciolini, Fabio
;
Catacuzzeno, Luigi
;
Pessia, Mauro
;
Klopstock, Thomas
2001
Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1
Pessia, Mauro
;
Imbrici, Paola
;
D'Adamo, Maria Cristina
;
Salvatore, Lorena
;
Tucker, Stephen J.
1999
Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K+ channel function
D'Adamo, Maria Cristina
;
Imbrici, Paola
;
Sponcichetti, Fabio
;
Pessia, Mauro
2017
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia
Hasan, Sonia M.
;
Bove, Cecilia
;
Silvestri, Gabriella
;
Mantuano, Elide
;
Modoni, Anna
;
Veneziano, Liana
;
Macchioni, Lara
;
Hunter, Therese
;
Hunter, Gary J.
;
Pessia, Mauro
;
D'Adamo, Maria Cristina
Discover
Author
36
D'Adamo, Maria Cristina
20
Imbrici, Paola
13
Di Giovanni, Giuseppe
10
Tucker, Stephen J.
9
Catacuzzeno, Luigi
8
Grottesi, Alessandro
8
Sforna, Luigi
7
D’Adamo, Maria Cristina
7
Franciolini, Fabio
.
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Subject
25
Potassium channels
19
Ataxia
6
Ion channels
4
Glioblastoma multiforme
3
Electrophysiology
3
Myokymia
3
Temporal lobe epilepsy
2
Autism
2
Confocal microscopy
.
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