SENESE, Rosalba
 Distribuzione geografica
Continente #
EU - Europa 6.691
NA - Nord America 3.979
AS - Asia 3.414
SA - Sud America 436
Continente sconosciuto - Info sul continente non disponibili 189
AF - Africa 34
OC - Oceania 3
Totale 14.746
Nazione #
RU - Federazione Russa 3.984
US - Stati Uniti d'America 3.820
SG - Singapore 1.017
IT - Italia 975
CN - Cina 949
IE - Irlanda 599
BR - Brasile 368
HK - Hong Kong 368
VN - Vietnam 325
DE - Germania 284
UA - Ucraina 240
GB - Regno Unito 239
ID - Indonesia 165
FR - Francia 97
KR - Corea 92
MY - Malesia 92
TH - Thailandia 89
FI - Finlandia 76
IN - India 70
GR - Grecia 51
PH - Filippine 49
CA - Canada 45
TR - Turchia 45
JP - Giappone 37
NL - Olanda 28
AR - Argentina 26
PK - Pakistan 26
CR - Costa Rica 23
MX - Messico 22
BE - Belgio 21
JM - Giamaica 21
SE - Svezia 21
BD - Bangladesh 17
AT - Austria 14
PL - Polonia 13
VE - Venezuela 13
IQ - Iraq 11
DK - Danimarca 10
EC - Ecuador 10
SA - Arabia Saudita 10
SV - El Salvador 9
UZ - Uzbekistan 9
ZA - Sudafrica 9
IR - Iran 8
NI - Nicaragua 8
PR - Porto Rico 8
CZ - Repubblica Ceca 7
EG - Egitto 7
HN - Honduras 7
AE - Emirati Arabi Uniti 6
GT - Guatemala 6
TT - Trinidad e Tobago 6
CO - Colombia 5
ES - Italia 5
MA - Marocco 5
CH - Svizzera 4
CL - Cile 4
KE - Kenya 4
TW - Taiwan 4
BG - Bulgaria 3
HU - Ungheria 3
IL - Israele 3
NO - Norvegia 3
PT - Portogallo 3
PY - Paraguay 3
QA - Qatar 3
RO - Romania 3
TN - Tunisia 3
UY - Uruguay 3
AU - Australia 2
AZ - Azerbaigian 2
BH - Bahrain 2
BO - Bolivia 2
CW - ???statistics.table.value.countryCode.CW??? 2
DZ - Algeria 2
EE - Estonia 2
JO - Giordania 2
KG - Kirghizistan 2
LB - Libano 2
PE - Perù 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
CI - Costa d'Avorio 1
CY - Cipro 1
DM - Dominica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GE - Georgia 1
IM - Isola di Man 1
IS - Islanda 1
KW - Kuwait 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LU - Lussemburgo 1
MN - Mongolia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
Totale 14.555
Città #
Moscow 1.454
Dublin 599
Singapore 476
Jacksonville 384
Shenzhen 383
San Jose 372
Santa Clara 360
Hong Kong 358
Ashburn 305
Chandler 293
Council Bluffs 210
Jakarta 143
Ho Chi Minh City 121
Naples 107
Bangkok 89
Beijing 89
Seoul 86
Grafing 85
Princeton 83
New York 81
Milan 79
Hanoi 74
Ann Arbor 72
Hefei 72
Kuala Selangor 71
Roxbury 71
Bremen 65
Medford 59
Boardman 52
Rome 51
Dallas 49
Los Angeles 46
Manila 45
Wilmington 40
The Dalles 38
Munich 33
Napoli 31
Bengaluru 28
Aversa 27
Nanjing 27
Cambridge 26
Des Moines 26
Caserta 25
São Paulo 25
Woodbridge 23
Atlanta 22
Kuala Lumpur 21
Haiphong 18
Miano 18
Schio 18
Frankfurt am Main 16
San José 16
Da Nang 15
Houston 15
Montreal 14
Orem 14
Rio de Janeiro 14
Tokyo 14
Brussels 13
Falls Church 13
Kingston 13
Turku 13
San Mateo 12
Tianjin 12
Mountain View 11
Nuremberg 11
Bekasi 10
Biên Hòa 10
Brooklyn 10
Curitiba 10
Jinan 10
North Bergen 10
Warsaw 10
Cagliari 9
Chennai 9
Chicago 9
Falkenstein 9
Gujranwala 9
Helsinki 9
Karachi 9
Mexico City 9
Orta di Atella 9
Palermo 9
San Salvador 9
Amsterdam 8
Düsseldorf 8
Managua 8
Nanchang 8
Phoenix 8
Vienna 8
Bologna 7
Changsha 7
Denver 7
Jeddah 7
London 7
Portici 7
Queens 7
Quito 7
San Francisco 7
Tashkent 7
Totale 7.833
Nome #
3,5-Diiodo-L-Thyronine Activates Brown Adipose Tissue Thermogenesis in Hypothyroid Rats 572
3,5-Diiodothyronine (T2) and 3,3’,5-Triiodothyronine (T3) mitigate Brown Adipose Tissue Mitochondrial Dysfunction in mice with obesity: Implications for Therapeutic Strategies in Metabolic Diseases 558
Mechanism linking miR-18a-5p/SREBP1/PERK axis, ER stress and autophagy to the early stages of Nonalcoholic Fatty Liver Disease (NAFLD) induced by high fat diet 270
Ruolo della proteina disaccoppiante 3 (UCP3) nella sensibilità all’insulina del muscolo scheletrico 265
3,3’,5-triiodo-l-thyronine and 3,5-diodo-l-thyronine differentially modulate hepatic mitochondrial quality control in hypothyroid rats 231
D-Aspartate Induces Proliferative Pathways in Spermatogonial GC-1 Cells 222
Mild exercise rescues steroidogenesis and spermatogenesis in rats submitted to food withdrawal 218
3,5-Diiodothyronine: A Novel Thyroid Hormone Metabolite and Potent Modulator of Energy Metabolism 200
3,5 Diiodo-L-Thyronine (T2) Targets Different Pathways To Induce White Adipose Tissue Browning. 200
A landscape of mouse mitochondrial small non-coding RNAs 191
3,5 Diiodo-l-Thyronine (T-2) Promotes the Browning of White Adipose Tissue in High-Fat Diet-Induced Overweight Male Rats Housed at Thermoneutrality 189
Ruolo della proteina disaccoppiante 3 (UCP3) nella modulazione della sensibilità all’insulina 187
Differential effects of 3,5-Diiodo-L-Thyronine and 3,5,3'-Triiodo-L-Thyronine on mitochondrial respiratory pathways in liver from hypothyroid rats 179
The impact of cannabinoid receptor 1 absence on mouse liver mitochondria homeostasis: insight into mitochondrial unfolded protein response 178
Both 3,3′,5-triiodothyronine and 3,5-diodo-L-thyronine are able to repair mitochondrial DNA damage but by different mechanisms 176
Effect of CB1 Receptor Deficiency on Mitochondrial Quality Control Pathways in Gastrocnemius Muscle 173
3,5-DIIODO-L-THYRONINE (T2) ADMINISTRATION AFFECTS VISCERAL ADIPOSE TISSUE INFLAMMATORY STATE IN RAT RECEIVING LONG-LASTING HIGH-FAT DIET 169
3,5-Diiodo-L-thyronine prevents high-fat-diet-induced insulin resistance in rat skeletal muscle through metabolic and structural adaptations 164
Mild Endurance Exercise during Fasting Increases Gastrocnemius Muscle and Prefrontal Cortex Thyroid Hormone Levels through Differential BHB and BCAA-Mediated BDNF-mTOR Signaling in Rats 163
Actin remodeling driven by circLIMA1: sperm cell as an intriguing cellular model 162
3,5-diiodo-L-thyronine influences fatty acid metabolism in higt-fat diet-fed rats through organ-specific regulation of AMP-activated proteine kinase. 158
3,5-Diiodo-L-Thyronine Affects Structural and Metabolic Features of Skeletal Muscle Mitochondria in High-Fat-Diet Fed Rats Producing a Co-adaptation to the Glycolytic Fiber Phenotype 158
3,5-Diiodo-L-Thyronine Exerts Metabolically Favorable Effects on Visceral Adipose Tissue of Rats Receiving a High-Fat Diet 157
Ablation of uncoupling protein 3 affects interrelated factors leading to lipolysis and insulin resistance in visceral white adipose tissue 157
Triiodothyronine induces lipid oxidation and mitochondrial biogenesis in rat Harderian gland 155
Responses of skeletal muscle lipid metabolism in rat gastrocnemius to hypothyroidism and iodothyronine administration: a putative role for FAT/CD36 153
Metabolomic analysis shows differential hepatic effects of T-2 and T-3 in rats after short-term feeding with high fat diet 153
A short-term high-fat diet alters rat testicular activity and blood-testis barrier integrity through the SIRT1/NRF2/MAPKs signaling pathways 150
Altered Mitochondrial Quality Control in Rats with Metabolic Dysfunction-Associated Fatty Liver Disease (MAFLD) Induced by High-Fat Feeding 150
Ruolo di AMPK nell’effetto della 3,5-diiodotironina (T2) sul metabolismo lipidico 147
Acute administration of 3,5-diiodo-l-thyronine to hypothyroid rats affects bioenergetic parameters in rat skeletal muscle mitochondria 146
Absence of uncoupling protein 3 at thermoneutrality influences brown adipose tissue mitochondrial functionality in mice 145
Insulin-Sensitizing Properties of Decoctions from Leaves, Stems, and Roots of Cucumis prophetarum L. 144
TRC150094, a novel functional analog of iodothyronines, reduces adiposity by increasing energy expenditure and fatty acid oxidation in rats receiving a high-fat diet 144
3,5-Diiodo-L-Thyronine improves mitochondrial function in nonalcoholic steatosis through the stimulation of SIRT3 mitochondrial targets 144
The Degree Of Fatty Acid Saturation Influences The Effects Of T3 And 3,5-T2 On Insulin Sensitivity In Muscle Cell. 144
3,5-Diiodo-L-Thyronine (T2) opposes 3,5,3’-Triiodo-L- Thyronine (T3) in regulation of lipogenic signaling in rats receiving a high-fat diet. 142
3,5-Diiodo-L-Thyronine (T2) Administration Affects Visceral Adipose Tissue Inflammatory State in Rats Receiving Long-Lasting High-Fat Diet 142
Fructose-Rich Diet Affects Mitochondrial DNA Damage and Repair in Rats 140
Absence of Uncoupling Protein-3 at Thermoneutrality Impacts Lipid Handling and Energy Homeostasis in Mice 138
Protective Action of 3,5-Diiodo-L-Thyronine on Cigarette Smoke-Induced Mitochondrial Dysfunction in Human Alveolar Epithelial Cells 134
The effect of fructose-rich diet on mtDNA oxidative damage 133
Both 3,5-Diiodo-L-Thyronine and 3,5,3'-Triiodo-L-Thyronine Prevent Short-term Hepatic Lipid Accumulation via Distinct Mechanisms in Rats Being Fed a High-Fat Diet 132
3,5diiodoLthyronine (T2) and not 3,5,3’ triiodoLthyronine (T3) reduces lipogenic signaling pathways in rats receiving a high-fat-diet. 132
High fat diet-induced insulin resistance: effects of 3,5-diiodo-L-thyronine on muscle mitochondrial proteome and function. 131
miR-22-3p is involved in gluconeogenic pathway modulated by 3,5-diiodo-L-thyronine (T2) 131
A contributing role for hepatic Sirtuins in the prevention of diet-induced adiposity by 3,5-Diiodo-L-Thyronine (T2) 127
Thyroid hormone metabolites and analogues 127
Adipose Tissue Remodeling in Obesity: An Overview of the Actions of Thyroid Hormones and Their Derivatives 126
Dysfunctional Mitochondria Characterize Amyotrophic Lateral Sclerosis Patients’ Cells Carrying the p.G376D TARDBP Pathogenetic Substitution 124
Exercise Equals the Mobilization of Visceral versus Subcutaneous Adipose Fatty Acid Molecules in Fasted Rats Associated with the Modulation of the AMPK/ATGL/HSL Axis 123
New avenues for regulation of lipid metabolism by thyroid hormones and analogs 123
Differential 3,5,3′-triiodothyronine-mediated regulation of uncoupling protein 3 transcription: Role of fatty acids 122
Defining the transcriptomic and proteomic profiles of rat ageing skeletal muscle by the use of a cDNA array, 2D-and Blue native-PAGE approach 120
PPARs: Nuclear receptors controlled by, and controlling, nutrient handling through nuclear and cytosolic signaling 120
Tissue specific modulation of AMPK phosphorylation in high-fat diet-fed rats treated with 3,5-diiodothyronine (T2) is related to fatty acid demand 119
Skeletal muscle mitochondrial free-fatty-acid content and membrane potential sensitivity in different thyroid states: Involvement of uncoupling protein-3 and adenine nucleotide translocase 118
Gadolinium impairs male steroidogenesis: In vivo and in vitro evidence 118
Atrogin-1, MuRF1, and FoXo, as well as phosphorylated GSK-3β and 4E-BP1 are reduced in skeletal muscle of chronic spinal cord-injured patients 115
Comparative effects of 3,5-diiodo-L-thyronine and 3,5,3’-triiodo-L-thyronine on mitochondrial damage and cGAS/STING-driven inflammation in liver of hypothyroid rats 114
Risposta organo-specifica alla 3,5 diiodotironina (T2); un possibile coinvolgimento della proteina chinasi attivata dall’AMP (AMPK) 114
Uncoupling proteins: A complex journey to function discovery 113
Thyroid: biological actions of 'nonclassical' thyroid hormones 113
Metabolic effects of the iodothyronine functional analogue TRC150094 on the liver and skeletal muscle of high-fat diet fed overweight rats: An integrated proteomic study 113
Ruolo dell’AMPK nella risposta organo specifica alla somministrazione di 3,5-diiodo-L-tironina (T2) a ratti alimentati con dieta iperlipidica 110
Temporal relationship between organ responses to 3,5-diiodo-L-thyronine in high-fat diet-fed rats role of AMPK 109
Effects of a high‐fat diet on rat epididymis 108
Mammalian mitochondrial proteome and its functions: Current investigative techniques and future perspectives on ageing and diabetes 107
La 3,5-diiodo-L-tironina stimola la lipolisi nel tessuto adiposo bianco mediante una regolazione transiente della fosforilazione dell’AMPK. 106
T3 coordinately affects expression of genes related to uncoupling protein 3 (UCP3) activity and lipid handling in rat gastrocnemius muscle. 106
Nonthyrotoxic Prevention of Diet-Induced Insulin Resistance by 3,5-Diiodo-L-Thyronine in Rats 106
Effetti non genomici della 3,5,3’-L-Triiodotironina: induzione delle vie di segnalazione mediate da AMPK/ACC e AKT/PKB nel muscolo gastrocnemio di ratto 105
Unaltered maximal power and submaximal performance correlates with an oxidative vastus lateralis proteome phenotype during tapering in male cyclists 104
Rapid activation by 3,5,3′-L-triiodothyronine of adenosine 5′-monophosphate-activated protein kinase/acetyl-coenzyme A carboxylase and Akt/protein kinase B signaling pathways: Relation to changes in fuel metabolism and myosin heavy-chain protein content in rat gastrocnemius muscle in vivo 104
Role of AMPK in the organ-specific responses to 3,5-diiodo-L-thyronine in high-fat diet-fed rats 104
Effect of d-aspartate uptake on uncoupling protein-3 and α-tubulin expressions in rat Harderian gland 102
The saturation degree of fatty acids and their derived acylcarnitines determines the direct effect of metabolically active thyroid hormones on insulin sensitivity in skeletal muscle cells 102
Adaptive Thermogenesis Driving Catch-Up Fat Is Associated With Increased Muscle Type 3 and Decreased Hepatic Type 1 Iodothyronine Deiodinase Activities: A Functional and Proteomic Study 102
Absence of uncoupling protein-3 (UCP3) affects mice metabolic parameters and the metabolic adaptation induced by the administration of triiodothyronine to hypothyroid rats 101
Influence of 3,5-diiodo-L-thyronine on skeletal muscle lipid metabolism 100
Effect of 3,5-Diiodo-L-Thyronine on high-fat diet-induced visceral adiposity in the rat 100
Metabolic effects of 3,5-Diiodo-L-Thyronine: focus on Brown Adipose Tissue 100
MicroRNA-18a-5p regulates hepatic lipid accumulation in response to high-fat diet 100
Uncoupling Protein-3 (UCP3) is involved in metabolic adaptation induced by Triiodothyronine 99
Thyroid hormones and mitochondria: With a brief look at derivatives and analogues 99
Uncoupling protein 3 expression levels influence insulin sensitivity, fatty acid oxidation, and related signaling pathways 99
Studies of complex biological systems with applications to molecular medicine: The need to integrate transcriptomic and proteomic approaches 99
Non genomic effects of 3,5,3-L-triiodothyronina through AMPK/ACC and AKT/PKB signaling: relation to changes in fuel metabolism and myosin heavy chain protein content in rat gastrocnemius muscle in vivo 97
Inefficienza mitocondriale mediata da UCP3: induzione da parte dell’acido arachidonico e coinvolgimento della perossidazione lipidica 97
Short-term fructose feeding alters tissue metabolic pathways by modulating microRNAs expression both in young and adult rats 95
The thyroid hormone metabolite 3,5-diiodo-l-thyronine prevents hepatic fat accumulation and systemic insulin resistance through direct activation of sirtuin 1 (SIRT1) 94
Organ-specific response to high-fat diet and 3,5-diiodothyronine (T2) treatment; a possible involvement of the AMP-activated protein kinase (AMPK) 92
Thyroid Hormone and Metabolites: Central Versus Peripheral Effects 92
Ruolo degli acidi grassi nella regolazione mediata dalla 3-5-3’-triiodotironina della trascrizione del gene codificante la proteina disaccoppiante 3 91
Interrelated role between superoxides and polyunsaturated fatty acids in inducing uncoupling protein 3 (UCP3) activity. 91
Prevention of diet-induced insulin resistance by 3,5-Diiodo-L-Thyronine in rats involves SIRT1 91
TRC150094, nuovo analogo funzionale delle iodotironine, riduce l’adiposità in ratti a dieta iperlipidica. 91
Exercise with food withdrawal at thermoneutrality impacts fuel use, the microbiome, AMPK phosphorylation, muscle fibers, and thyroid hormone levels in rats 91
Short-Term, Combined Fasting and Exercise Improves Body Composition in Healthy Males 89
Rapid activation by 3,5,3’-L-triiodothyronine of AMPK/ACC and Akt/PKB signaling pathways in rat gastrocnemius muscle in vivo 88
Totale 14.147
Categoria #
all - tutte 47.564
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 47.564


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022566 0 0 0 7 173 115 8 16 18 20 44 165
2022/20231.223 117 56 15 84 141 71 10 56 558 13 59 43
2023/20241.001 58 25 405 32 158 77 29 34 11 5 56 111
2024/20251.636 16 42 36 36 273 177 249 121 251 182 139 114
2025/20267.159 209 246 321 342 613 3.891 465 261 341 247 138 85
2026/20271.419 162 297 406 554 0 0 0 0 0 0 0 0
Totale 14.746