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

PESSIA, Mauro
 Distribuzione geografica
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Continente #
NA - Nord America 3.772
EU - Europa 3.276
AS - Asia 2.675
SA - Sud America 489
AF - Africa 75
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 4
Totale 10.299
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Nazione #
US - Stati Uniti d'America 3.689
SG - Singapore 1.343
IE - Irlanda 573
UA - Ucraina 561
FR - Francia 461
RU - Federazione Russa 404
BR - Brasile 365
IT - Italia 363
CN - Cina 361
HK - Hong Kong 330
SE - Svezia 248
DE - Germania 223
VN - Vietnam 205
FI - Finlandia 152
KR - Corea 93
GB - Regno Unito 92
IN - India 66
TR - Turchia 48
AR - Argentina 45
RO - Romania 37
CA - Canada 36
BD - Bangladesh 33
IQ - Iraq 32
MX - Messico 31
BE - Belgio 25
NL - Olanda 25
PL - Polonia 25
EC - Ecuador 24
CH - Svizzera 22
ZA - Sudafrica 22
AE - Emirati Arabi Uniti 21
AT - Austria 20
SA - Arabia Saudita 18
JP - Giappone 17
CO - Colombia 16
PK - Pakistan 16
VE - Venezuela 14
UZ - Uzbekistan 13
ID - Indonesia 12
MA - Marocco 10
PH - Filippine 10
TN - Tunisia 10
EG - Egitto 9
LT - Lituania 9
CL - Cile 8
ES - Italia 8
KE - Kenya 8
CZ - Repubblica Ceca 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
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
JM - Giamaica 2
NI - Nicaragua 2
OM - Oman 2
PT - Portogallo 2
TW - Taiwan 2
AM - Armenia 1
DZ - Algeria 1
EE - Estonia 1
GH - Ghana 1
GP - Guadalupe 1
HN - Honduras 1
HU - Ungheria 1
IR - Iran 1
KH - Cambogia 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
MZ - Mozambico 1
NO - Norvegia 1
NR - Nauru 1
PG - Papua Nuova Guinea 1
PS - Palestinian Territory 1
Totale 10.290
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Città #
Singapore 893
Dublin 571
Chandler 554
Hong Kong 330
Jacksonville 288
San Mateo 262
San Jose 256
Ashburn 215
Boardman 178
Santa Clara 160
Moscow 131
Perugia 131
Ann Arbor 130
Medford 130
Princeton 128
Lauterbourg 116
Wilmington 105
Beijing 104
Seoul 88
Andover 75
Dong Ket 66
Des Moines 63
Munich 62
Altamura 58
Ho Chi Minh City 52
Los Angeles 46
Lawrence 43
Saint Petersburg 39
New York 38
São Paulo 36
The Dalles 35
Bucharest 34
Piscataway 32
Izmir 31
Norwalk 31
Hanoi 27
Brussels 25
Helsinki 24
Rome 19
Brooklyn 18
Falls Church 18
Johannesburg 18
Warsaw 18
Woodbridge 18
Chennai 17
Tokyo 16
Orem 14
Turku 14
Al Ain City 13
Baghdad 13
Chicago 13
Frankfurt am Main 13
Quito 13
Rio de Janeiro 13
Amsterdam 11
Dallas 11
Shanghai 11
Den Haag 10
Auburn Hills 9
Da Nang 9
Manchester 9
Montreal 9
Nuremberg 9
San Paolo di Civitate 9
Stockholm 9
Toronto 9
Atlanta 8
Belo Horizonte 8
Council Bluffs 8
Denver 8
Falkenstein 8
Redwood City 8
Tashkent 8
Cairo 7
Dearborn 7
Dhaka 7
Mexico City 7
Poplar 7
Riyadh 7
Haiphong 6
Houston 6
London 6
Medellín 6
Nairobi 6
New Delhi 6
Redmond 6
Amman 5
Ankara 5
Boston 5
Brescia 5
Buenos Aires 5
Calgary 5
Civitanova Marche 5
Hefei 5
Miami 5
Mumbai 5
Salvador 5
Santiago 5
Shijiazhuang 5
Abidjan 4
Totale 6.159
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Nome #
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy 136
The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma 134
Voltage-gated calcium channels modulate synaptic transmission at vestibular neurons. 130
Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies 126
Fisiologia Medica 118
An Episodic Ataxia Type-1 (EA1) mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+ 117
A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release 117
Fotorecettori ed Epitelio Pigmentato della Retina; Meccanismi di Trasduzione e Rinnovamento. 114
Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1. 111
Episodic Ataxias as Ion Channel Diseases. 111
Modulation of hKv 1.1 and hKv 1.2 voltage gating and C-type inactivation by 5-HT2C receptors. 110
Effects of Episodic Ataxia-Associated Mutations on hKv1.4-1.1/Kvbeta1 channels 104
ERG channels modulate the medial vestibular neurons processing of temporal information 104
Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration 104
The emerging role of the inwardly rectifying K+channels in autism spectrum disorders andepilepsy 103
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 103
Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia 102
Hypoxia Modulates the Swelling-Activated Cl Current in Human Glioblastoma Cells: Role in Volume Regulation and Cell Survival 102
Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 102
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 101
Actions of 5-hydroxytryptamine on ventral tegmental area neurons of the rat in vitro. 101
ERG voltage-gated K+ channels regulate excitability and discharge dynamics of the medial vestibular nucleus neurons 100
Role(s) of the 5-HT2C receptor in the development of maximal dentate activation in the hippocampus of anesthetized rats. 99
Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents. 99
ERG voltage-gated K+ channels regulate excitability and discharege dynamics of the medial vestibular nucleus neurones 99
Role of inwardly-rectifying potassium channels Kir5.1 in learning and memory processes in a mouse knock-out model. 98
Episodic Ataxia Type 1 Mutations Affect Fast Inactivation of K+ Channels by a Reduction in Either Subunit Surface Expression or Affinity for Inactivation Domain 97
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 97
5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates 97
All atom molecular dynamics simulation of the K+ Channel Chimera Kv1.2/2.1 96
Episodic Ataxia Type 1 Mutation F184C Alters Zn2+-Induced Modulation of the Human Potassium Channel Kv1.4-Kv1.1/Kvbeta1.1 94
Voltage gated calcium channels modulation of glutamate synaptic transmission to medial vestibular nucleus neurons 94
Kir4.1 gain-of-function and gut dysbiosis appear as risk factors for autism-epilepsy phenotype in a new mouse model of autism 94
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties 93
Episodic ataxia type 1 mutations cause loss-of-function impairments of heteromeric channels formed by the Kv1.4 and Kv1.1 subunits. 93
Reply to ‘F508del-CFTR is not corrected by thymosin α1’ 93
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties. 92
Controllo locale del flusso ematico da parte dei tessuti e regolazione umorale 92
K+ channelepsy: progress in the neurobiology of potassium channels and epilepsy 92
CIC-1 chloride channels: State-of-the-art research and future challenges 91
Structure, gating and basic functions of the Ca2+-activated K channel of intermediate conductance 91
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker 91
Inward Rectifier Potassium Channels: Cloning, Expression and Structure-Function Studies. 90
Genetically-induced abnormalities of Kir2.1 channels: implications for short QT3 syndrome and autism/epilepsy phenotype. 90
Tavola Rotonda Telethon 88
Episodic Ataxia Type 1 87
Expression and function of a CP339,818-sensitive K+ current in a subpopulation of putative nociceptive neurons from adult mouse trigeminal ganglia 87
Lethal digenic mutations in the K+channels kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay 87
Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder 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) 85
Animal Models of Episodic Ataxia Type 1 (EA1). 84
Cloning and expression of a family of inward rectifier potassium channels. 84
Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I 84
Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature 83
The Episodic Ataxia Type 1 Mutation F184C Alters the Zn2+ Modulation of the Human Kv1.4-Kv1.1/Kvbeta1 Channel 82
Identification and functional characterization of a novel mutation in the KCNA1 gene of a Sicilian family affected by 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
Contributions of the C-terminal domain to gating properties of inward rectifier potassium channels. 81
Mutations in KCNA1 affect stoichiometry and fast inactivation of heteromeric K+ channels 79
Trace amines depress D2-autoreceptor-mediated responses on midbrain dopaminergic cells. 78
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. 78
Functional Characterization of an Episodic Ataxia Type-1 Mutation Occurring in the S1 Segment of hKv1.1 Channels. 78
EA-1 mutations alter the fast inactivation properties of Kv1.1 channels conferred by Kv1.4 and Kvbeta1.1 subunits 77
Il Sistema Endocrino: le ghiandole endocrine e le azioni ormonali. 77
Fisiologia medica, 13° Edizione 77
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene 77
Localization and Age Dependent Expression of the Inward Rectifier K+ Channel Kir 5.1 in a Mammalian Reproductive System. 76
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 76
Gating properties of human heteromeric voltage-gated potassium channels and effects of episodic ataxia type-1 mutations. 76
Episodic Ataxia Type-1 Mutations in the hKv1.1 Cytoplasmic Pore Region Alter the Gating Properties of the Channel. 75
Role of the S1 segment in the voltage-dependent gating of Kv1.1 channels revealed by naturally occurring pathogenic mutations. 75
Mutations in KCNA1 gene associated with episodic ataxia type-1 sindrome impair heteromeric voltage-gated K+ channel function. 75
In Vivo Microdialysis to Study Striatal Dopaminergic Neurodegeneration 75
A Novel KCNA1 Mutation Identified in an Italian Family Affected by Episodic Ataxia Type 1 75
Identification of a heteromeric interaction which influences the rectification, gating and pH-sensitivity of Kir4.1/Kir5.1 potassium channels. 75
Neurotensin excitation of rat ventral tegmental neurones. 74
Differential pH-sensitivity of Kir4.1 and Kir4.2 and Modulation by Heteropolymerisation with Kir5.1. 74
Copertina della rivista scientifica: Neuroscience 74
Il ruolo delle alterazioni genetiche dei canali ionici nelle cefalee e nella vertigine. 74
Copertina della rivista The Journal of Physiology 73
Genetic investigation of children with ataxia using exome sequencing 73
The CaMKII/MLC1 Axis Confers Ca2+-Dependence to Volume-Regulated Anion Channels (VRAC) in Astrocytes 72
Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 72
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia 72
De novo point mutations in patients diagnosed with ataxic cerebral palsy 72
Heteromeric Channel Formation and Ca2+-free Media Reduce the Toxic Effect of the weaver Kir 3.2 Allele. 71
THE ROLE OF THE SEROTONERGIC SYSTEM AT THE INTERFACE OF AGGRESSION AND SUICIDE 71
The Kir5.1 Potassium Channel is an Important Determinant of Neuronal PCO2/pH Sensitivity 70
Il sistema endocrino: regolazione del metabolismo energetico e della crescita 69
Role of Potassium Channels of the Nervous System in Health and Disease. 68
Copertina della rivista FEBS Letters 68
Publisher Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis 68
Mutations in the KCNA1 Gene Associated with Episodic Ataxia Type-1 Syndrome Impair Heteromeric Voltage-Gated K+ Channel Function 67
Modulation of delayed rectifier K+ channels by 5HT2c receptors. 67
ERG channels regulate the excitability of medial vestibular neurons 67
Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 Contributes to Autism with Seizures and Intellectual Disability. 67
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions 67
Inhibitory Interactions Between Two Inward Rectifier K+ Channel Subunits Mediated by Transmembrane Domains. 66
Il sistema endocrino: regolazione del metabolismo energetico e della crescita. 66
Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity 66
Totale 8.751
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Categoria #
all - tutte 45.482
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 45.482
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021201 0 0 0 0 0 0 0 0 0 30 95 76
2021/20221.068 17 174 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
2025/20263.145 246 221 155 416 446 296 598 171 333 263 0 0
Totale 10.569