Search filters

List of works by Maria Cristina D'Adamo

5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates.

scientific article published on 24 May 2013

A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release

scientific article

A method to identify tissue cell subpopulations with distinct multi-molecular profiles from data on co-localization of two markers at a time: the case of sensory ganglia.

scientific article

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1

scientific article

Altered functional properties of a missense variant in the TRESK K+ channel (KCNK18) associated with migraine and intellectual disability

scientific article published on 12 May 2020

Amiloride inhibits tissue-type plasminogen activator (t-PA) release from vascular endothelium

scientific article published on 01 August 1995

Antithrombotic activity of dermatan sulphates, heparins and their combination in an animal model of arterial thrombosis

scientific article published on 01 December 1996

Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.

scientific article published on 31 March 2011

Contribution of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties

scientific article

De novo point mutations in patients diagnosed with ataxic cerebral palsy.

scientific article

Different response of vascular fibrinolysis to adrenergic stimulation in young and aged rats

Effects of dyslipidemia on t-PA release in rats

scientific article published on 01 October 2000

Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker

scientific article published on 23 June 2020

Enhanced vascular plasminogen activator (t-PA) release by epinephrine in aged rats

scientific article published on 01 May 1995

Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvbeta1.1.

scientific article published on 6 September 2006

Episodic ataxia type 1 mutations affect fast inactivation of K+ channels by a reduction in either subunit surface expression or affinity for inactivation domain.

scientific article published on 9 February 2011

Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.

scientific article published in December 2006

Episodic ataxia type-1 mutations in the hKv1.1 cytoplasmic pore region alter the gating properties of the channel

scientific article published on March 2, 1998

Erratum: K+ channelepsy: progress in the neurobiology of potassium channels and epilepsy.

scientific article published on 30 January 2014

Experimental arterial thrombosis in genetically or diet induced hyperlipidemia in rats--role of vitamin K-dependent clotting factors and prevention by low-intensity oral anticoagulation

scientific journal article

Expression and function of a CP339,818-sensitive K⁺ current in a subpopulation of putative nociceptive neurons from adult mouse trigeminal ganglia.

scientific article published on 4 February 2015

Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion protein.

scientific article published in July 2002

Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels

scientific article (publication date: June 2003)

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.

scientific article

Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity

scientific article published on November 3, 2010

Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.

scientific article published on 2 May 2014

K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy

scientific article

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability

scientific article published on 31 August 2016

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches

scientific article published on 22 April 2020

Morphological and hemostatic changes in rats with abdominal arterial prosthesis

scientific article published on 01 April 1996

Neutrophil derived cathepsin G induces potentially thrombogenic changes in human endothelial cells: a scanning electron microscopy study in static and dynamic conditions.

scientific article published in July 1994

New insights into the pathogenesis and therapeutics of episodic ataxia type 1

scientific article

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene

scientific article

Prostacyclin is required for t-PA release after venous occlusion

scientific article published on 01 February 1994

Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration

scientific article published on 20 April 2015

Role of receptor protein tyrosine phosphatase alpha (RPTPalpha) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels

scientific article published in December 2000

The adrenergic mechanisms of acute t-PA release in normal and diseased animals

The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma.

scientific article published on January 2014

Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder

scientific article published on 02 March 2015