CAMERINO, GIULIA MARIA
 Distribuzione geografica
Continente #
NA - Nord America 6.040
AS - Asia 2.407
EU - Europa 1.836
SA - Sud America 655
AF - Africa 115
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 11.069
Nazione #
US - Stati Uniti d'America 5.945
SG - Singapore 927
CN - Cina 603
BR - Brasile 522
IT - Italia 473
SE - Svezia 273
HK - Hong Kong 264
RU - Federazione Russa 253
VN - Vietnam 188
DE - Germania 179
FR - Francia 152
FI - Finlandia 137
GB - Regno Unito 130
IN - India 86
UA - Ucraina 74
BD - Bangladesh 55
AR - Argentina 52
CA - Canada 51
ID - Indonesia 50
IQ - Iraq 34
BE - Belgio 32
CI - Costa d'Avorio 32
MX - Messico 31
PK - Pakistan 27
ZA - Sudafrica 26
JP - Giappone 25
NL - Olanda 25
EC - Ecuador 23
ES - Italia 21
TR - Turchia 20
SA - Arabia Saudita 19
VE - Venezuela 18
PL - Polonia 15
CO - Colombia 13
AT - Austria 12
AU - Australia 12
PH - Filippine 12
CZ - Repubblica Ceca 10
EG - Egitto 10
UZ - Uzbekistan 10
IE - Irlanda 9
MA - Marocco 9
MY - Malesia 9
CL - Cile 8
DZ - Algeria 8
LT - Lituania 8
TN - Tunisia 8
PE - Perù 7
IR - Iran 6
JO - Giordania 6
KE - Kenya 6
OM - Oman 6
AZ - Azerbaigian 5
CH - Svizzera 5
KG - Kirghizistan 5
NP - Nepal 5
PS - Palestinian Territory 5
UY - Uruguay 5
AE - Emirati Arabi Uniti 4
AL - Albania 4
ET - Etiopia 4
KR - Corea 4
KZ - Kazakistan 4
RO - Romania 4
SN - Senegal 4
TW - Taiwan 4
AM - Armenia 3
BH - Bahrain 3
BO - Bolivia 3
IL - Israele 3
PA - Panama 3
PY - Paraguay 3
RS - Serbia 3
A1 - Anonimo 2
BY - Bielorussia 2
CR - Costa Rica 2
EE - Estonia 2
HR - Croazia 2
HU - Ungheria 2
MN - Mongolia 2
MU - Mauritius 2
NO - Norvegia 2
TH - Thailandia 2
AO - Angola 1
BW - Botswana 1
CY - Cipro 1
DK - Danimarca 1
DM - Dominica 1
DO - Repubblica Dominicana 1
GD - Grenada 1
GM - Gambi 1
GR - Grecia 1
GY - Guiana 1
HT - Haiti 1
KH - Cambogia 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LK - Sri Lanka 1
LY - Libia 1
Totale 11.051
Città #
Ashburn 648
Fairfield 631
Woodbridge 495
Singapore 488
Chandler 439
Houston 349
Cambridge 278
Dallas 270
Hong Kong 263
San Jose 250
Nyköping 235
Seattle 235
Ann Arbor 213
Beijing 209
Wilmington 205
Jacksonville 171
Bari 161
New York 93
Los Angeles 88
Roxbury 81
Lawrence 77
Lauterbourg 72
Nanjing 70
Helsinki 61
Inglewood 55
Des Moines 52
Ho Chi Minh City 49
São Paulo 41
Bitetto 40
Princeton 40
Jakarta 37
Dong Ket 36
Santa Clara 36
Bitonto 34
Abidjan 32
Brussels 32
Council Bluffs 32
San Diego 32
Hanoi 31
Brooklyn 30
London 30
Boardman 27
Munich 27
Chicago 26
Shenyang 24
Nanchang 22
Buffalo 20
Rio de Janeiro 19
Turku 19
Jiaxing 18
Nuremberg 18
Shanghai 18
Toronto 18
Orem 17
Tokyo 17
Frankfurt am Main 16
Falkenstein 15
Guangzhou 15
Baghdad 14
Brasília 14
Dearborn 14
Hebei 14
Johannesburg 14
Montreal 14
Belo Horizonte 13
Mexico City 13
Moscow 13
Pune 12
Redwood City 12
Chennai 11
Washington 11
Atlanta 10
Denver 10
Dhaka 10
Paris 10
Stockholm 10
The Dalles 10
Warsaw 10
Campinas 9
Changsha 9
Dublin 9
Guayaquil 9
Lahore 9
Milan 9
Phoenix 9
San Francisco 9
Tianjin 9
Biên Hòa 8
Düsseldorf 8
Haiphong 8
Jeddah 8
Jinan 8
Poplar 8
Salvador 8
San Mateo 8
Tashkent 8
Brno 7
City of London 7
Columbus 7
Hefei 7
Totale 7.477
Nome #
Proof-of-concept validation of the mechanism of action of Src tyrosine kinase inhibitors in dystrophic mdx mouse muscle: in vivo and in vitro studies 286
Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat 235
Effects of Nandrolone in the counteraction of skeletal muscle atrophy in a mouse model of muscle disuse: molecular biology and functional evaluation 234
Effect of a long-term treatment with metformin in dystrophic mdx mice: A reconsideration of its potential clinical interest in Duchenne muscular dystrophy 226
ATP Sensitive Potassium Channels in the Skeletal Muscle Function: Involvement of the KCNJ11(Kir6.2) Gene in the Determination of Mechanical Warner Bratzer Shear Force 225
Assessment of resveratrol, apocynin and taurine on mechanical-metabolic uncoupling and oxidative stress in a mouse model of Duchenne muscular dystrophy: a comparison with the gold standard, α-methyl prednisolone. 224
Contractile efficiency of dystrophic mdx mouse muscle: In vivo and ex vivo assessment of adaptation to exercise of functional end points 216
A long-term treatment with taurine prevents cardiac dysfunction in mdx mice 215
Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies 209
Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat 203
Antioxidant treatment of hindlimb-unloaded mouse counteracts fiber type transition but not atrophy of disused muscles 197
Elucidating the Contribution of Skeletal Muscle Ion Channels to Amyotrophic Lateral Sclerosis in search of new therapeutic options 196
Statin-induced myotoxicity is exacerbated by aging: A biophysical and molecular biology study in rats treated with atorvastatin 191
Growth hormone secretagogues hexarelin and JMV2894 protect skeletal muscle from mitochondrial damages in a rat model of cisplatin-induced cachexia 191
Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita 188
In vivo longitudinal study of rodent skeletal muscle atrophy using ultrasonography 188
Growth hormone secretagogues prevent dysregulation of skeletal muscle calcium homeostasis in a rat model of cisplatin-induced cachexia 187
Ryanodine channel complex stabilizer compound S48168/ARM210 as a disease modifier in dystrophin-deficient mdx mice: proof-of-concept study and independent validation of efficacy. 185
Adaptation of mouse skeletal muscle to long-term microgravity in the MDS mission 179
Risk of myopathy in patients in therapy with statins: Identification of biological markers in a pilot study 160
GLPG0492, a novel selective androgen receptor modulator, improves muscle performance in the exercised-mdx mouse model of muscular dystrophy 156
Ergogenic effect of bcaas and l-alanine supplementation: Proof-of-concept study in a murine model of physiological exercise 148
BCAAs and Di-Alanine supplementation in the prevention of skeletal muscle atrophy: preclinical evaluation in a murine model of hind limb unloading 145
Aberrant mechanical-metabolic coupling in muscular dystrophy: gene expression and functional studies in mdx mouse muscle in relation to age and exercise 141
Changes in Expression and Cellular Localization of Rat Skeletal Muscle ClC-1 Chloride Channel in Relation to Age, Myofiber Phenotype and PKC Modulation 141
Calcium-Activated K Channel Regulates Cell Viability in Hyperkalemic and Hypokalemic Conditions: Implication in the Neuromuscular Disoders 139
The large conductance Ca2+ -activated K+ (BKCa) channel regulates cell proliferation in SH-SY5Y neuroblastoma cells by activating the staurosporine-sensitive protein kinases 138
Antioxidant treatment of hindlimb-unloaded mouse in vivo counteracts fiber type transition but not atrophy of disused skeletal muscles 135
Therapeutic approaches to genetic ion channelopathies and perspectives in drug discovery 132
Paracrine Effects of IGF-1 Overexpression on the Functional Decline Due to Skeletal Muscle Disuse: Molecular and Functional Evaluation in Hindlimb Unloaded MLC/mIgf-1 Transgenic Mice 132
Alteration of stim1/orai1-mediated soce in skeletal muscle: Impact in genetic muscle diseases and beyond 131
Atrophy and phenotype transition signaling exert opposite actions on the KATP channels of disused rat soleus muscle 129
Staurosporine Blocks the ATP-Sensitive K+ Channels and Induces Atrophy in Rodent Skeletal Muscles 127
Single-dose extended-toxicity preclinical study on novel radiotracer formulations for use in the diagnosis of neuroendocrine tumor and neurodegenerative disorders 127
Calcium homeostasis is altered in skeletal muscle of spontaneously hypertensive rats cytofluorimetric and gene expression analysis 123
Splicing of the rSlo gene affects the molecular composition and drug response of Ca2+-activated K+ channels in skeletal muscle 123
Peptidic and Nonpeptidic Growth Hormone Secretagogues exert a protective effect on mitochondrial parameters analysed in a rat model of cachexia 122
Statins and fenofibrate affect skeletal muscle chloride conductance in rats by different impairing ClC-1 channel regulation and expression 121
Molecular determinants for the activating/blocking actions of the 2H-1,4-benzoxazine derivatives, a class of potassium channel modulators targeting the skeletal muscle KATP channels 120
Protein kinase C theta (PKCθ) modulates the ClC-1 chloride channel activity and skeletal muscle phenotype: a biophysical and gene expression study in mouse models lacking the PKCθ 119
Dual response of the KATP channels to staurosporine: a novel role of SUR2B, SUR1 and Kir6.2 subunits in the regulation of the atrophy in different skeletal muscle phenotypes 118
Chaperone activity of niflumic acid on ClC-1 chloride channel mutants causing myotonia congenita 115
Gentamicin treatment in exercised mdx mice: Identification of dystrophin-sensitive pathways and evaluation of efficacy in work-loaded dystrophic muscle 114
Visceral fat dysfunctions in the rat social isolation model of psychosis 110
In-vivo administration of CLC-K kidney chloride channels inhibitors increases water diuresis in rats: A new drug target for hypertension? 110
Functional Study of Novel Bartter's Syndrome Mutations in ClC-Kb and Rescue by the Accessory Subunit Barttin Toward Personalized Medicine 106
Kidney CLC-K chloride channels inhibitors: structure-based studies and efficacy in hypertension and associated CLC-K polymorphisms. 105
An olive oil-derived antioxidant mixture ameliorates the age-related decline of skeletal muscle function 104
Ion channels gene expression analysis in myotonia congenita patients carrying ClC-1 chloride channel mutations 103
Effects of Pleiotrophin Overexpression on Mouse Skeletal Muscles in Normal Loading and in Actual and Simulated Microgravity 103
CLC-K kidney chloride channels as drug target for hypertension: effects of acute in vivo administration to rats of newly synthesized inhibitors 102
Statin or fibrate chronic treatment modifies the proteomic profile of rat skeletal muscle 100
null 100
Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia 100
Gain-of-Function STIM1 L96V Mutation Causes Myogenesis Alteration in Muscle Cells From a Patient Affected by Tubular Aggregate Myopathy 99
Statin‐induced myopathy: Translational studies from preclinical to clinical evidence 98
Protein Kinase C-Theta Controls the CLC-1 Chloride Channel Function and Skeletal Muscle Phenotype: A Biophysical and Gene Expression Study in Pkc-Theta Null Mice 96
The KATP channel is a molecular sensor of atrophy in skeletal muscle 96
Pathophysiological Consequences of KATP Channel Overactivity and Pharmacological Response to Glibenclamide in Skeletal Muscle of a Murine Model of Cantù Syndrome 96
Consequences of SUR2[A478V] Mutation in Skeletal Muscle of Murine Model of Cantu Syndrome 95
Therapeutic Targets in Amyotrophic Lateral Sclerosis: Focus on Ion Channels and Skeletal Muscle 95
Dapagliflozin protects the kidney in a non-diabetic model of cardiorenal syndrome 94
Potential benefits of taurine in the prevention of skeletal muscle impairment induced by disuse in the hindlimb-unloaded rat 94
null 93
Comparison of the effects of chronic treatments with drugs targeting different disease-related pathways in dystrophic mdx mice 91
null 90
null 87
Molecular mechanisms responsible for fluvastatin and fenofibrateinduced reduction of resting membrane chloride conductance in rat skeletal muscle 84
Angiotensin II modulates mouse skeletal muscle resting conductance to chloride and potassium ions and calcium homeostasis via the AT1 receptor and NADPH oxidase. 83
Expression of sarcolemmal ion channels in slow and fast-twitch muscles of rodents in simulated and actual microgravity 76
null 75
Multiple pathological events in exercised dystrophic mdx mice are targeted by pentoxifylline: Outcome of a large array of in vivo and ex vivo tests 75
Gentamicin-induced enhancement of dystrophinglycoprotein complex modulates biophysical markers of dystrophic progression in mdx mouse muscles 71
On ground preflight studies on skeletal muscle from mice kept in the Mouse Drawer System (MDS) 70
null 70
Protein kinase C theta (PKCθ) modulates the ClC-1 chloride channel activity and skeletal muscle phenotype: a biophysical and gene expression study in mouse models lacking the PKCθ. 70
EVALUATION OF THE RESTING CHLORIDE CONDUCTANCE, SARCOLEMMA EXCITABILITY AND CALCIUM HOMEOSTASIS IN SKELETAL MUSCLE OF A SOD-1 RELATED AMYOTROPHIC LATERAL SCLEROSIS (ALS) MOUSE MODEL 69
null 68
null 68
Skeletal muscle impairment during microgravity-induced disuse: Beneficial effects of different pharmacological countermeasures 67
Pharmacological evaluation of NADPH oxidase involvement in pathophysiology of mdx mouse, an animal model of muscular dystrophy 65
KIDNEY CLC-K CHLORIDE CHANNELS AS NEW TARGETS FOR ANTIHYPERTENSIVE AND DIURETIC DRUGS: EFFECT OF ACUTE IN VIVO ADMINISTRATION OF CLC-K BLOCKERS IN RATS 64
The Functional Interaction of KATP and BK Channels with Aquaporin-4 in the U87 Glioblastoma Cell 62
Evaluation of time-dependent effects of statins and fibrate 'in vivo' treatment on ClC-1 chloride channel expression and function and on proteomic profile of rat skeletal muscle 62
Immune checkpoint inhibitors and neurotoxicity: a focus on diagnosis and management for a multidisciplinary approach 61
null 61
Effect of pleiotrophin overexpression on ion channel function/expression in mouse soleus muscle after hindlimb unloading 60
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation 60
Gene expression in mdx mouse muscle in relation to age and exercise: aberrant mechanical-metabolic coupling and implications for pre-clinical studies in duchenne muscular dystrophy 60
MuRF-1 gene deletion prevents atrophy of disused muscle in the hindlimb-unloaded mice 57
Emerging role of calcium-activated potassium channel in the regulation of cell viability following potassium ions challenge in HEK293 cell and pharmacological modulation 54
Toward the identification of druggable pathways involved in disease-related fatigue in Duchenne muscular dystrophy: In vivo and ex vivo studies in dystrophic mdx mice 51
null 49
In vivo silencing of aquaporin-1 by RNA interference inhibits angiogenesis in the chick embryo chorioallantoic membrane assay 48
Disease-Related Modification of Chloride Conductance in Skeletal Muscle of Dystrophic Mice: Expression of CLC-1 Channel and Role of Inflammation and Oxidative Stress-Related Signaling 48
null 45
Functional performance and muscle gene expression in dystrophic mdx mouse in relation to age and exercise: defects in mechanical-metabolic coupling 41
null 29
null 23
Fluvastatin and atorvastatin affect calcium homeostasis of rat skeletal muscle fibers in vivo and in vitro by impairing the sarcoplasmic reticulum/mitochondria Ca2+-release system 21
Totale 11.465
Categoria #
all - tutte 45.362
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 45.362


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021378 0 0 0 0 0 0 0 0 0 193 102 83
2021/2022700 42 78 11 22 18 52 36 25 60 61 113 182
2022/20231.156 132 145 95 90 112 154 11 134 179 21 37 46
2023/2024454 27 59 25 43 53 116 32 23 4 12 5 55
2024/20251.830 83 40 120 65 81 176 231 195 87 86 213 453
2025/20263.552 616 224 402 345 463 173 434 115 458 322 0 0
Totale 11.465