IRIS  Catalogo Istituzionale della Ricerca dell'Università degli Studi del Molise

TAGLIALATELA, Maurizio
 Distribuzione geografica
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Continente #
NA - Nord America 11.423
EU - Europa 8.747
AS - Asia 2.300
SA - Sud America 581
AF - Africa 262
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 13
AN - Antartide 1
Totale 23.348
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Nazione #
US - Stati Uniti d'America 11.272
RU - Federazione Russa 3.922
IE - Irlanda 1.735
SG - Singapore 981
CN - Cina 580
UA - Ucraina 535
BR - Brasile 480
SE - Svezia 428
FI - Finlandia 388
DE - Germania 372
IT - Italia 365
GB - Regno Unito 324
AT - Austria 229
CI - Costa d'Avorio 201
BE - Belgio 175
HK - Hong Kong 150
VN - Vietnam 126
IN - India 120
CA - Canada 87
JP - Giappone 60
FR - Francia 53
PL - Polonia 53
NL - Olanda 43
MX - Messico 42
BD - Bangladesh 40
ES - Italia 36
TR - Turchia 36
AR - Argentina 34
ZA - Sudafrica 28
IR - Iran 26
ID - Indonesia 25
IQ - Iraq 24
LT - Lituania 18
AU - Australia 14
IL - Israele 14
CL - Cile 13
KR - Corea 13
PK - Pakistan 13
PE - Perù 12
SA - Arabia Saudita 11
JO - Giordania 10
MY - Malesia 10
RO - Romania 10
VE - Venezuela 10
CO - Colombia 9
CZ - Repubblica Ceca 9
EU - Europa 9
PY - Paraguay 9
UZ - Uzbekistan 9
AE - Emirati Arabi Uniti 8
DZ - Algeria 8
EC - Ecuador 8
JM - Giamaica 8
KZ - Kazakistan 8
CH - Svizzera 7
DK - Danimarca 7
NZ - Nuova Zelanda 7
PH - Filippine 7
TN - Tunisia 6
AL - Albania 5
GR - Grecia 5
HU - Ungheria 5
MA - Marocco 5
MD - Moldavia 5
BY - Bielorussia 4
TT - Trinidad e Tobago 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AZ - Azerbaigian 3
BG - Bulgaria 3
HN - Honduras 3
KG - Kirghizistan 3
LB - Libano 3
SN - Senegal 3
SY - Repubblica araba siriana 3
TH - Thailandia 3
UY - Uruguay 3
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
BO - Bolivia 2
EG - Egitto 2
ET - Etiopia 2
KE - Kenya 2
KW - Kuwait 2
LK - Sri Lanka 2
LV - Lettonia 2
NO - Norvegia 2
OM - Oman 2
PA - Panama 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
AO - Angola 1
AQ - Antartide 1
BF - Burkina Faso 1
BS - Bahamas 1
CG - Congo 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
GE - Georgia 1
GM - Gambi 1
GT - Guatemala 1
Totale 23.338
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Città #
Dallas 4.063
Dublin 1.732
Moscow 1.318
Jacksonville 1.233
Chandler 1.176
Singapore 502
Wilmington 420
Ashburn 296
Beijing 285
San Mateo 247
Helsinki 237
Ann Arbor 233
Vienna 220
Houston 217
Abidjan 201
Woodbridge 193
New York 184
Rome 180
Boardman 177
Brussels 174
Princeton 163
The Dalles 150
Los Angeles 149
Hong Kong 134
São Paulo 73
Falls Church 70
Columbus 69
Molise 51
Tokyo 48
Ho Chi Minh City 45
London 43
Council Bluffs 40
Warsaw 40
Santa Clara 38
Toronto 33
Redwood City 32
San Francisco 30
Brooklyn 28
Chennai 28
Dearborn 27
San Jose 27
Stockholm 26
Poplar 25
Montreal 24
Munich 24
Frankfurt am Main 23
Mountain View 23
Phoenix 23
Denver 22
Norwalk 22
Chicago 21
Hanoi 21
Jakarta 21
Orem 21
Amsterdam 18
Boston 18
Johannesburg 18
Jinan 17
Nanjing 17
Ankara 16
Shenyang 16
Atlanta 15
Manchester 15
Da Nang 13
Mexico City 13
Auburn Hills 12
Augusta 12
Falkenstein 12
Naples 12
Seoul 12
Curitiba 11
Kunming 11
Leawood 11
Mumbai 11
Napoli 11
Seattle 11
Tappahannock 11
Clearwater 10
Hefei 10
Charlotte 9
Dhaka 9
Haikou 9
Los Altos 9
Rio de Janeiro 9
Zhengzhou 9
Amman 8
Baghdad 8
Brasília 8
Fortaleza 8
Guangzhou 8
Ottawa 8
Querétaro 8
Tashkent 8
West Jordan 8
Kuala Lumpur 7
Milan 7
Nuremberg 7
Porto Alegre 7
Pune 7
Taiyuan 7
Totale 15.403
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Nome #
109. Involvement of the Na+-H+ antiporter on the effect of protein kinase-C activation on dopamine synthesis in rat corpus striatum 2.881
Activation and Desensitization of Trpv1 Channels in Sensory Neurons by the Peroxisome Proliferator-Activated Receptor α Agonist Palmitoylethanolamide 264
Activation of Kv7 potassium channels inhibits intracellular Ca2+ increases triggered by TRPV1-mediated pain-inducing stimuli in F11 immortalized sensory neurons 246
Consensus group on new-generation antihistamines (CONGA): present status and recommendations 240
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S-4 region of KCNQ2 causing benign familial neonatal convulsions 216
Epilepsy-causing mutations in kv7.2 c-terminus affect binding and functional modulation by calmodulin. 200
BARIUM BLOCKADE OF A CLONAL POTASSIUM CHANNEL AND ITS REGULATION BY A CRITICAL PORE RESIDUE 199
Autism and developmental disability caused by KCNQ3 gain-of-function variants 195
Pharmacological Targeting Of Neuronal Kv7.2/3 Channels: A Focus On Chemotypes And Receptor Sites 192
Adenosine receptors modulate the Na(+)-Ca2+ exchanger in cerebral nerve endings. 191
Characterization of two de novo KCNT1 mutations in children with malignant migrating partial seizures in infancy 187
Molecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channels 186
A y(+)LAT-1 mutant protein interferes with y(+)LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance 185
"Janus face" of nitric oxide action on plasma membrane and intracellular ionic channels 185
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes 185
Activation of pre-synaptic M-type K+ channels inhibits [H-3]d-aspartate release by reducing Ca2+ entry through P/Q-type voltage-gated Ca(2+)channels 184
Epileptic encephalopathy in a patientwith a novel variant in the Kv7.2 S2 transmembrane segment: Clinical, genetic, and functional features 182
Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels 182
Expression and function of Kv7.4 channels in Rat cardiac mitochondria: possible targets for cardioprotection 180
A SINGLE NONPOLAR RESIDUE IN THE DEEP PORE OF RELATED K+ CHANNELS ACTS AS A K+-RB+ CONDUCTANCE SWITCH 179
A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy 178
Early-Onset Epileptic Encephalopathy Caused by Gain-of-Function Mutations in the Voltage Sensor of Kv7.2 and Kv7.3 Potassium Channel Subunits. 177
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation 177
De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy 175
Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphate 173
The occurrence of a Kv7.4 potassium channel in neuronal mitochondria 173
Differential Regulation of PI(4,5)P2Sensitivity of Kv7.2 and Kv7.3 Channels by Calmodulin 170
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. 170
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy 167
AMPA- and P2X7-receptor-mediated facilitation of [H-3]D-aspartate release from nerve terminals isolated from the rat caudal brainstem 162
Cardiotoxic effects of antihistamines: From basics to clinics (... and back) 161
Calcium cytotoxicity sensitizes prostate cancer cells to standard-of-care treatments for locally advanced tumors 161
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant 159
Identification of a Potent Tryptophan-Based TRPM8 Antagonist with in Vivo Analgesic Activity 157
Cell viability studies and operation in cellular culture medium of n-type organic field-effect transistors 155
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha(1) subunit reduces membrane expression and impairs gating by agonists 153
Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels 152
Protective role of Kv7 channels in oxygen and glucose deprivation-induced damage in rat caudate brain slices 145
Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs 144
β-Adrenergic response is counteracted by extremely-low-frequency pulsed electromagnetic fields in beating cardiomyocytes 142
A Novel Kv7.3 Variant in the Voltage-Sensing S4 Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and in vitro Rescue by β-Hydroxybutyrate 142
Neutralization of a unique, negatively-charged residue in the voltage sensor of K(V)7.2 subunits in a sporadic case of benign familial neonatal seizures 140
Critical role of large-conductance calcium- and voltage-activated potassium channels in leptin-induced neuroprotection of N-methyl-d-aspartate-exposed cortical neurons. 140
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions 138
Expression, Localization, and Pharmacological Role of K(v)7 Potassium Channels in Skeletal Muscle Proliferation, Differentiation, and Survival after Myotoxic Insults 136
CORRELATING THE CLINICAL AND GENETIC FEATURES OF BENIGN FAMILIAL NEONATAL SEIZURES (BFNS) WITH THE FUNCTIONAL CONSEQUENCES OF THE UNDERLYING MUTATIONS 136
C-TERMINUS DETERMINANTS FOR MG2+ AND POLYAMINE BLOCK OF THE INWARD RECTIFIER K+ CHANNEL IRK1 134
Retigabine and flupirtine exert neuroprotective actions in organotypic hippocampal cultures 131
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 128
Erratum to: Towards the realization of label-free biosensors through impedance spectroscopy integrated with IDES technology 127
Regulation of the human ether-a-gogo related gene (HERG) K+ channels by reactive oxygen species 126
POSSIBLE INHIBITORY ROLE OF HISTAMINE H-2 RECEPTORS IN THE CONTROL OF BASAL TSH SECRETION IN MALE-RATS - STUDIES WITH DIMAPRIT, A SELECTIVE H-2-RECEPTOR AGONIST 125
Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A 125
Kv7.4 channels regulate potassium permeability in neuronal mitochondria 125
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine 124
EXCHANGE OF CONDUCTION PATHWAYS BETWEEN 2 RELATED K+ CHANNELS 123
CYTOPLASMIC ALKALINIZATION INDUCED BY INSULIN THROUGH AN ACTIVATION OF NA+-H+ ANTIPORTER INHIBITS TYROSINE-HYDROXYLASE ACTIVITY IN STRIATAL SYNAPTOSOMES 122
Driving with no brakes: molecular pathophysiology of kv7 potassium channels 122
Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits 121
The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome 120
H-1-antihistamines: inverse agonism, anti-inflammatory actions and cardiac effects 120
K(V)7 channels regulate muscle tone and nonadrenergic noncholinergic relaxation of the rat gastric fund 119
GATING CURRENTS OF THE CLONED DELAYED-RECTIFIER K+ CHANNEL DRK1 119
SPERMINE AND SPERMIDINE AS GATING MOLECULES FOR INWARD RECTIFIER K+ CHANNELS 118
herg encodes a K+ current highly conserved in tumors of different histogenesis: A selective advantage for cancer cells? 118
Up-regulation and increased activity of K(V)3.4 channels and their accessory subunit MinK-Related peptide 2 induced by amyloid peptide are involved in apoptotic neuronal death 118
COMPARISON OF H-5, S-6, AND H-5-S-6 EXCHANGES ON PORE PROPERTIES OF VOLTAGE-DEPENDENT K+ CHANNELS 118
VOLTAGE-DEPENDENT INHIBITION AND FACILITATION OF CA CHANNEL ACTIVATION BY GTP-GAMMA-S AND CA-AGONISTS IN ADULT-RAT SENSORY NEURONS 117
Pre-synaptic BK channels selectively control glutamate versus GABA release from cortical and hippocampal nerve terminals 117
M channels containing KCNQ2 subunits modulate norepinephrine, aspartate, and GABA release from hippocampal nerve terminals 116
SPECIFICATION OF PORE PROPERTIES BY THE CARBOXYL-TERMINUS OF INWARDLY RECTIFYING K+ CHANNELS 116
Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction 116
De novo variants in KCNA3 cause developmental and epileptic encephalopathy 116
Mutational scanning of potassium, sodium and chloride ion channels in malignant migrating partial seizures in infancy 115
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism 115
DIFFERENCES BETWEEN THE DEEP PORES OF K+ CHANNELS DETERMINED BY AN INTERACTING PAIR OF NONPOLAR AMINO-ACIDS 114
NA+-CA-2+ EXCHANGE ACTIVITY IN CENTRAL NERVE-ENDINGS .1. IONIC CONDITIONS THAT DISCRIMINATE CA-45(2+) UPTAKE THROUGH THE EXCHANGER FROM THAT OCCURRING THROUGH VOLTAGE-OPERATED CA-2+ CHANNELS 114
PLASMA PROLACTIN LEVELS IN THE INFERIOR PETROSAL SINUSES IN VARIOUS PITUITARY DISORDERS DURING PERIHYPOPHYSEAL PHLEBOGRAPHY 113
Specification of skeletal muscle differentiation by repressor element-1 silencing transcription factor (REST)-regulated Kv7.4 potassium channels 113
Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy 113
Functional Characterization of Two Variants at the Intron 6-Exon 7 Boundary of the KCNQ2 Potassium Channel Gene Causing Distinct Epileptic Phenotypes 112
Low expression of Kv7/M channels facilitates intrinsic and network bursting in the developing rat hippocampus 112
THE NA+-CA2+ EXCHANGER ACTIVITY IN CEREBROCORTICAL NERVE-ENDINGS IS REDUCED IN OLD COMPARED TO YOUNG AND MATURE RATS WHEN IT OPERATES AS A CA2+ INFLUX OR EFFLUX PATHWAY 112
PURE UPTAKE BLOCKERS OF DOPAMINE CAN REDUCE PROLACTIN SECRETION - STUDIES WITH DICLOFENSINE 111
STRUCTURAL MOTIFS UNDERLYING VOLTAGE-DEPENDENT K+ CHANNEL FUNCTION 111
Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists. 111
Human neoplastic mesothelial cells express voltage-gated sodium channels involved in cell motility 110
MEMBRANE EVENTS AND IONIC PROCESSES INVOLVED IN DOPAMINE RELEASE FROM TUBEROINFUNDIBULAR NEURONS .2. EFFECT OF THE INHIBITION OF THE NA+-CA++ EXCHANGE BY AMILORIDE 110
Brain distribution of the Na+/Ca2+ exchanger-encoding genes NCX1, NCX2, and NCX3 and their related proteins in the central nervous system 110
Retention in the endoplasmic reticulum as a mechanism of dominant-negative current suppression in human long QT syndrome 109
Effects of manidipine and nitrendipine enantiomers on the plateau phase of K+-induced intracellular Ca2+ increase in GH(3) cells 109
GATING OF INWARDLY RECTIFYING K+ CHANNELS LOCALIZED TO A SINGLE NEGATIVELY CHARGED RESIDUE 109
Gating currents from neuronal K(V)7.4 channels General features and correlation with the ionic conductance 109
PHARMACOLOGICAL CHARACTERIZATION OF SEROTONIN RECEPTORS INVOLVED IN THE CONTROL OF PROLACTIN SECRETION 109
The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants 108
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy 106
INTERNAL AND EXTERNAL TEA BLOCK IN SINGLE CLONED K+ CHANNELS 106
GADOLINIUM AND NEOMYCIN BLOCK VOLTAGE-SENSITIVE CA2+ CHANNELS WITHOUT INTERFERING WITH THE NA+-CA2+ ANTIPORTER IN BRAIN NERVE-ENDINGS 106
EVIDENCE FOR A DIFFERENTIAL INTERACTION OF BUPRENORPHINE WITH OPIATE RECEPTOR SUBTYPES CONTROLLING PROLACTIN SECRETION 106
Cardiotoxic potential and CNS effects of first-generation antihistamines 106
Totale 17.002
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Categoria #
all - tutte 100.176
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 100.176
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021834 0 0 0 0 0 139 187 13 186 14 232 63
2021/20221.112 57 228 8 56 107 93 27 95 200 100 55 86
2022/20234.704 531 171 111 396 371 485 21 221 2.116 126 78 77
2023/2024786 173 85 47 15 17 150 27 100 14 51 14 93
2024/20252.553 242 93 237 106 452 121 99 217 191 71 324 400
2025/20269.990 429 1.519 2.971 539 2.706 1.826 0 0 0 0 0 0
Totale 23.579