IRIS - Res&Arch Institutional Research Information System - Research & Archive

PESSIA, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 4.020
EU - Europa 3.336
AS - Asia 2.733
SA - Sud America 502
Continente sconosciuto - Info sul continente non disponibili 274
AF - Africa 75
OC - Oceania 8
Totale 10.948
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Nazione #
US - Stati Uniti d'America 3.908
SG - Singapore 1.354
IE - Irlanda 573
UA - Ucraina 561
FR - Francia 461
IT - Italia 417
RU - Federazione Russa 404
BR - Brasile 371
CN - Cina 371
HK - Hong Kong 330
SE - Svezia 248
DE - Germania 223
VN - Vietnam 206
FI - Finlandia 152
KR - Corea 93
GB - Regno Unito 92
IN - India 68
BD - Bangladesh 67
CA - Canada 50
AR - Argentina 48
TR - Turchia 48
RO - Romania 38
MX - Messico 33
IQ - Iraq 32
NL - Olanda 27
BE - Belgio 26
PL - Polonia 26
EC - Ecuador 25
CH - Svizzera 22
ZA - Sudafrica 22
AE - Emirati Arabi Uniti 21
AT - Austria 20
CO - Colombia 18
SA - Arabia Saudita 18
JP - Giappone 17
PK - Pakistan 16
VE - Venezuela 14
UZ - Uzbekistan 13
ID - Indonesia 12
MA - Marocco 10
PH - Filippine 10
TN - Tunisia 10
CL - Cile 9
EG - Egitto 9
LT - Lituania 9
ES - Italia 8
KE - Kenya 8
CZ - Repubblica Ceca 7
JM - Giamaica 7
JO - Giordania 6
LB - Libano 6
MT - Malta 6
PY - Paraguay 6
DO - Repubblica Dominicana 5
KZ - Kazakistan 5
MY - Malesia 5
NP - Nepal 5
CI - Costa d'Avorio 4
GR - Grecia 4
KW - Kuwait 4
PE - Perù 4
UY - Uruguay 4
AZ - Azerbaigian 3
BO - Bolivia 3
EU - Europa 3
IL - Israele 3
KG - Kirghizistan 3
NG - Nigeria 3
NI - Nicaragua 3
NZ - Nuova Zelanda 3
RS - Serbia 3
SY - Repubblica araba siriana 3
AO - Angola 2
AU - Australia 2
CR - Costa Rica 2
GE - Georgia 2
HN - Honduras 2
HU - Ungheria 2
OM - Oman 2
PT - Portogallo 2
SV - El Salvador 2
TW - Taiwan 2
AM - Armenia 1
BB - Barbados 1
DZ - Algeria 1
EE - Estonia 1
GH - Ghana 1
GP - Guadalupe 1
GT - Guatemala 1
IR - Iran 1
KH - Cambogia 1
KN - Saint Kitts e Nevis 1
KY - Cayman, isole 1
LA - Repubblica Popolare Democratica del Laos 1
LC - Santa Lucia 1
LK - Sri Lanka 1
LU - Lussemburgo 1
LY - Libia 1
MD - Moldavia 1
MR - Mauritania 1
Totale 10.664
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Città #
Singapore 895
Dublin 571
Chandler 554
Hong Kong 330
San Jose 311
Jacksonville 288
San Mateo 262
Ashburn 230
Boardman 178
Santa Clara 168
Moscow 131
Perugia 131
Ann Arbor 130
Medford 130
Princeton 128
Lauterbourg 116
Wilmington 107
Beijing 106
Seoul 88
Andover 75
Dong Ket 66
Des Moines 63
Munich 62
Los Angeles 60
Altamura 58
Ho Chi Minh City 52
New York 45
Lawrence 43
Piscataway 39
Saint Petersburg 39
São Paulo 37
The Dalles 35
Bucharest 34
Izmir 31
Norwalk 31
Hanoi 28
Brussels 26
Rome 25
Helsinki 24
Brooklyn 19
Falls Church 18
Johannesburg 18
Warsaw 18
Woodbridge 18
Chennai 17
Montreal 16
Tokyo 16
Dallas 15
Orem 15
Chicago 14
Turku 14
Al Ain City 13
Baghdad 13
Frankfurt am Main 13
Quito 13
Rio de Janeiro 13
Amsterdam 11
Shanghai 11
Den Haag 10
Toronto 10
Atlanta 9
Auburn Hills 9
Da Nang 9
Manchester 9
Milan 9
Nuremberg 9
San Paolo di Civitate 9
Stockholm 9
Belo Horizonte 8
Council Bluffs 8
Denver 8
Falkenstein 8
New Delhi 8
Redwood City 8
Tashkent 8
Cairo 7
Dearborn 7
Dhaka 7
Mexico City 7
Poplar 7
Riyadh 7
Buffalo 6
Haiphong 6
Houston 6
London 6
Medellín 6
Miami 6
Nairobi 6
Redmond 6
Santiago 6
Amman 5
Ankara 5
Boston 5
Brescia 5
Buenos Aires 5
Calgary 5
Civitanova Marche 5
Curitiba 5
Goiânia 5
Hefei 5
Totale 6.306
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Nome #
Fisiologia Medica 140
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy 140
The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma 135
Voltage-gated calcium channels modulate synaptic transmission at vestibular neurons. 131
Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies 130
An Episodic Ataxia Type-1 (EA1) mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+ 119
Fotorecettori ed Epitelio Pigmentato della Retina; Meccanismi di Trasduzione e Rinnovamento. 117
A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release 117
Episodic Ataxias as Ion Channel Diseases. 115
Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1. 114
Modulation of hKv 1.1 and hKv 1.2 voltage gating and C-type inactivation by 5-HT2C receptors. 113
Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration 110
Effects of Episodic Ataxia-Associated Mutations on hKv1.4-1.1/Kvbeta1 channels 107
ERG channels modulate the medial vestibular neurons processing of temporal information 107
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions 106
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 105
Hypoxia Modulates the Swelling-Activated Cl Current in Human Glioblastoma Cells: Role in Volume Regulation and Cell Survival 105
Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 105
The emerging role of the inwardly rectifying K+channels in autism spectrum disorders andepilepsy 104
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 103
Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 103
Actions of 5-hydroxytryptamine on ventral tegmental area neurons of the rat in vitro. 102
Role of inwardly-rectifying potassium channels Kir5.1 in learning and memory processes in a mouse knock-out model. 102
CIC-1 chloride channels: State-of-the-art research and future challenges 102
Role(s) of the 5-HT2C receptor in the development of maximal dentate activation in the hippocampus of anesthetized rats. 101
ERG voltage-gated K+ channels regulate excitability and discharge dynamics of the medial vestibular nucleus neurons 101
ERG voltage-gated K+ channels regulate excitability and discharege dynamics of the medial vestibular nucleus neurones 101
Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents. 100
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 100
Episodic Ataxia Type 1 Mutations Affect Fast Inactivation of K+ Channels by a Reduction in Either Subunit Surface Expression or Affinity for Inactivation Domain 99
5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates 99
Voltage gated calcium channels modulation of glutamate synaptic transmission to medial vestibular nucleus neurons 98
All atom molecular dynamics simulation of the K+ Channel Chimera Kv1.2/2.1 97
Episodic Ataxia Type 1 Mutation F184C Alters Zn2+-Induced Modulation of the Human Potassium Channel Kv1.4-Kv1.1/Kvbeta1.1 96
Reply to ‘F508del-CFTR is not corrected by thymosin α1’ 96
Kir4.1 gain-of-function and gut dysbiosis appear as risk factors for autism-epilepsy phenotype in a new mouse model of autism 96
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 96
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties 95
Structure, gating and basic functions of the Ca2+-activated K channel of intermediate conductance 95
Inward Rectifier Potassium Channels: Cloning, Expression and Structure-Function Studies. 93
Episodic ataxia type 1 mutations cause loss-of-function impairments of heteromeric channels formed by the Kv1.4 and Kv1.1 subunits. 93
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties. 93
Controllo locale del flusso ematico da parte dei tessuti e regolazione umorale 93
K+ channelepsy: progress in the neurobiology of potassium channels and epilepsy 93
Expression and function of a CP339,818-sensitive K+ current in a subpopulation of putative nociceptive neurons from adult mouse trigeminal ganglia 92
Genetically-induced abnormalities of Kir2.1 channels: implications for short QT3 syndrome and autism/epilepsy phenotype. 91
Episodic Ataxia Type 1 89
Tavola Rotonda Telethon 89
Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder 89
Cloning and expression of a family of inward rectifier potassium channels. 89
Lethal digenic mutations in the K+channels kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay 88
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 86
Episodic Ataxia Type 1 Mutations in the KCNA1 Gene Impair the Fast Inactivation Properties of the Human K+ Channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2. 86
Inducible pluripotent stem (iPS) cell-derived human astrocytes as a new disease model to shed light into the molecular pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts (MLC) 86
Trace amines depress D2-autoreceptor-mediated responses on midbrain dopaminergic cells. 85
Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I 85
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature 84
Animal Models of Episodic Ataxia Type 1 (EA1). 84
Contributions of the C-terminal domain to gating properties of inward rectifier potassium channels. 83
Identification and functional characterization of a novel mutation in the KCNA1 gene of a Sicilian family affected by episodic ataxia type 1 83
An activator of voltage-gated K + channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1 82
Il Microcircolo ed il Sistema Linfatico: Lo Scambio dei Liquidi nei Capillari, il Liquido Interstiziale ed il Flusso Linfatico. 82
Functional Characterization of an Episodic Ataxia Type-1 Mutation Occurring in the S1 Segment of hKv1.1 Channels. 80
Mutations in KCNA1 affect stoichiometry and fast inactivation of heteromeric K+ channels 80
Fisiologia medica, 13° Edizione 79
Genetic investigation of children with ataxia using exome sequencing 79
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene 79
Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 78
Localization and Age Dependent Expression of the Inward Rectifier K+ Channel Kir 5.1 in a Mammalian Reproductive System. 78
EA-1 mutations alter the fast inactivation properties of Kv1.1 channels conferred by Kv1.4 and Kvbeta1.1 subunits 78
In Vivo Microdialysis to Study Striatal Dopaminergic Neurodegeneration 78
Neurotensin excitation of rat ventral tegmental neurones. 77
Il Sistema Endocrino: le ghiandole endocrine e le azioni ormonali. 77
Role of the S1 segment in the voltage-dependent gating of Kv1.1 channels revealed by naturally occurring pathogenic mutations. 77
Mutations in KCNA1 gene associated with episodic ataxia type-1 sindrome impair heteromeric voltage-gated K+ channel function. 77
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 77
A Novel KCNA1 Mutation Identified in an Italian Family Affected by Episodic Ataxia Type 1 77
Identification of a heteromeric interaction which influences the rectification, gating and pH-sensitivity of Kir4.1/Kir5.1 potassium channels. 77
Episodic Ataxia Type-1 Mutations in the hKv1.1 Cytoplasmic Pore Region Alter the Gating Properties of the Channel. 76
Gating properties of human heteromeric voltage-gated potassium channels and effects of episodic ataxia type-1 mutations. 76
Copertina della rivista The Journal of Physiology 76
The CaMKII/MLC1 Axis Confers Ca2+-Dependence to Volume-Regulated Anion Channels (VRAC) in Astrocytes 75
Differential pH-sensitivity of Kir4.1 and Kir4.2 and Modulation by Heteropolymerisation with Kir5.1. 75
Copertina della rivista scientifica: Neuroscience 75
Heteromeric Channel Formation and Ca2+-free Media Reduce the Toxic Effect of the weaver Kir 3.2 Allele. 74
Il ruolo delle alterazioni genetiche dei canali ionici nelle cefalee e nella vertigine. 74
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia 74
De novo point mutations in patients diagnosed with ataxic cerebral palsy 74
THE ROLE OF THE SEROTONERGIC SYSTEM AT THE INTERFACE OF AGGRESSION AND SUICIDE 73
Copertina della rivista FEBS Letters 72
Il sistema endocrino: regolazione del metabolismo energetico e della crescita 71
The Kir5.1 Potassium Channel is an Important Determinant of Neuronal PCO2/pH Sensitivity 71
Publisher Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 71
ERG channels regulate the excitability of medial vestibular neurons 70
Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 Contributes to Autism with Seizures and Intellectual Disability. 70
Role of Potassium Channels of the Nervous System in Health and Disease. 69
Inhibitory Interactions Between Two Inward Rectifier K+ Channel Subunits Mediated by Transmembrane Domains. 68
pH-Dependence of the Inwardly Rectifying Potassium Channel Kir5.1 and Localisation in Renal Tubular Epithelia 68
Modulation of delayed rectifier K+ channels by 5HT2c receptors. 68
Il sistema endocrino: regolazione del metabolismo energetico e della crescita. 68
Totale 9.056
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Categoria #
all - tutte 50.421
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 50.421
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.051 0 174 34 54 23 10 26 344 22 37 110 217
2022/20231.778 141 181 38 151 156 218 1 71 726 14 56 25
2023/2024637 50 79 33 7 17 1 126 1 84 25 125 89
2024/20251.633 15 178 66 79 222 67 44 136 341 106 249 130
2025/20263.359 246 221 155 416 446 296 598 171 333 279 87 111
2026/2027165 69 96 0 0 0 0 0 0 0 0 0 0
Totale 10.948