IRIS
LANNI, Antonia
 Distribuzione geografica
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Continente #
EU - Europa 3.625
NA - Nord America 3.391
AS - Asia 969
AF - Africa 10
SA - Sud America 8
OC - Oceania 3
Totale 8.006
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Nazione #
US - Stati Uniti d'America 3.382
IE - Irlanda 1.124
UA - Ucraina 564
CN - Cina 557
DE - Germania 532
IT - Italia 517
GB - Regno Unito 420
SG - Singapore 249
FI - Finlandia 143
GR - Grecia 99
SE - Svezia 90
FR - Francia 73
TR - Turchia 69
KR - Corea 34
PK - Pakistan 20
BE - Belgio 15
NL - Olanda 11
DK - Danimarca 9
HK - Hong Kong 8
IR - Iran 6
CA - Canada 5
CH - Svizzera 5
CZ - Repubblica Ceca 5
EG - Egitto 5
RU - Federazione Russa 5
AT - Austria 4
IN - India 4
JP - Giappone 4
BR - Brasile 3
DZ - Algeria 3
MX - Messico 3
QA - Qatar 3
VN - Vietnam 3
AE - Emirati Arabi Uniti 2
AR - Argentina 2
BD - Bangladesh 2
CL - Cile 2
MA - Marocco 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PT - Portogallo 2
RO - Romania 2
RS - Serbia 2
TH - Thailandia 2
AU - Australia 1
BG - Bulgaria 1
EC - Ecuador 1
HN - Honduras 1
ID - Indonesia 1
IL - Israele 1
IQ - Iraq 1
PL - Polonia 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
Totale 8.006
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Città #
Dublin 1.124
Jacksonville 873
Chandler 540
Shenzhen 380
Santa Clara 321
Grafing 199
Princeton 164
Singapore 164
Medford 133
Bremen 131
Boardman 116
Roxbury 105
Ann Arbor 83
New York 79
Wilmington 76
San Mateo 68
Beijing 55
Woodbridge 45
Cambridge 37
Des Moines 35
Mountain View 34
Naples 34
Seoul 28
Los Angeles 27
Nanjing 26
Düsseldorf 24
Caserta 23
Napoli 23
Schio 18
Aversa 16
Brussels 15
Rome 15
Jinan 14
Norwalk 14
Falls Church 9
Gujranwala 9
Houston 9
Redwood City 9
Ashburn 8
Lubbock 8
Palermo 8
Kunming 7
Auburn Hills 6
Karachi 6
Macerata Campania 6
Mugnano del Cardinale 6
Portici 6
San Martino Sannita 6
Tianjin 6
Brno 5
Changsha 5
Copenhagen 5
Giugliano in Campania 5
Hangzhou 5
Nanchang 5
Rotondella 5
San Potito Sannitico 5
Shanghai 5
Bagheria 4
Benevento 4
Central 4
Helsinki 4
Lappeenranta 4
Milan 4
Munich 4
Salerno 4
San Marco Evangelista 4
Venice 4
Atlanta 3
Bisceglie 3
Capodrise 3
Casoria 3
Champaign 3
Cicciano 3
Doha 3
Groningen 3
Lausanne 3
Limatola 3
London 3
Orta di Atella 3
Providence 3
San Giorgio Del Sannio 3
San Prisco 3
San Remo 3
Seattle 3
Shenyang 3
Taiyuan 3
Tokyo 3
Torre Del Greco 3
Vienna 3
Afragola 2
Altavilla Silentina 2
Amsterdam 2
Athens 2
Auckland 2
Bangkok 2
Bridgwater 2
Castellarano 2
Changchun 2
Ciudad Nezahualcoyotl 2
Totale 5.319
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Nome #
3,5-Diiodo-L-Thyronine Activates Brown Adipose Tissue Thermogenesis in Hypothyroid Rats 460
Ruolo della proteina disaccoppiante 3 (UCP3) nella sensibilità all’insulina del muscolo scheletrico 201
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 111
3,5 Diiodo-L-Thyronine (T2) Targets Different Pathways To Induce White Adipose Tissue Browning. 88
3,5-DIIODO-L-THYRONINE INCREASES RESTING METABOLIC RATE AND REDUCES BODY WEIGHT WITHOUT UNDESIRABLE SIDE EFFECTS 80
TRC150094, a novel functional analog of iodothyronines, reduces adiposity by increasing energy expenditure and fatty acid oxidation in rats receiving a high-fat diet 77
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 76
3,5-diiodo-L-thyronine influences fatty acid metabolism in higt-fat diet-fed rats through organ-specific regulation of AMP-activated proteine kinase. 72
Responses of skeletal muscle lipid metabolism in rat gastrocnemius to hypothyroidism and iodothyronine administration: a putative role for FAT/CD36 71
3,5-diiodo-l-thyronine, by modulating mitochondrial functions, reverses hepatic fat accumulation in rats fed a high-fat diet 68
3,5-Diiodo-L-Thyronine Exerts Metabolically Favorable Effects on Visceral Adipose Tissue of Rats Receiving a High-Fat Diet 68
Effect of thyroid status on the oxidative capacity of Sertoli cells isolated from immature rat testis 67
Metabolomic analysis shows differential hepatic effects of T-2 and T-3 in rats after short-term feeding with high fat diet 66
3,5-Diiodo-L-thyronine regulates glucose-6-phosphate dehydrogenase activity in the rat 63
3,5-Diiodo-L-thyronine modulates the expression of genes of lipid metabolism in a rat model of fatty liver 62
Composizioni comprendenti la 3,5-diiodotironina e uso farmaceutico di esse 62
Both 3,3′,5-triiodothyronine and 3,5-diodo-L-thyronine are able to repair mitochondrial DNA damage but by different mechanisms 62
Metabolic effects of thyroid hormone derivatives 61
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 61
Defining the transcriptomic and proteomic profiles of rat ageing skeletal muscle by the use of a cDNA array, 2D-and Blue native-PAGE approach 60
3,5-diiodo-L-thyronine improves glucose tolerance in high fat fed rats 60
3,5-Diiodothyronine: A Novel Thyroid Hormone Metabolite and Potent Modulator of Energy Metabolism 60
A proteomics approach to identify protein expression changes in rat liver following administration of 3,5,3′-triiodo-L-thyronine 59
3,5-Diiodo-L-thyronine powerfully reduces adiposity in rats by increasing the burning of fats 59
3, 5-diiodothyronine: Biological actions and therapeutic perspectives 59
RAPID STIMULATION IN-VITRO OF RAT-LIVER CYTOCHROME-OXIDASE ACTIVITY BY 3,5-DIIODO-L-THYRONINE AND BY 3,3'-DIIODO-L-THYRONINE 55
EFFECT OF 3,3'-DIIODOTHYRONINE AND 3,5-DIIODOTHYRONINE ON RAT-LIVER OXIDATIVE CAPACITY 55
Tissue specific modulation of AMPK phosphorylation in high-fat diet-fed rats treated with 3,5-diiodothyronine (T2) is related to fatty acid demand 55
Thyroid-state influence on protein-expression profile of rat skeletal muscle 54
Effect of 3,5-diiodo-L-thyronine on the mitochondrial energy trasduction apparatus 54
Nonshivering thermogenesis in king penguin chicks. I. Role of skeletal muscle 54
PPARs: Nuclear receptors controlled by, and controlling, nutrient handling through nuclear and cytosolic signaling 54
Pathways affected by 3,5-diiodo-l-thyronine in liver of high fat-fed rats: Evidence from two-dimensional electrophoresis, blue-native PAGE, and mass spectrometry 53
3,5-diiodo-L-thyronine-induced proteomic changes in liver mitochondria from high fat-fed rats: Evidences from two-dimensional electrophoresis 53
3,5-diiodothyronine: biological actions and therapeutic perspctives 53
3,5-Diiodo-L-Thyronine improves mitochondrial function in nonalcoholic steatosis through the stimulation of SIRT3 mitochondrial targets 53
3,5-Diiodo-L-thyronine prevents high-fat-diet-induced insulin resistance in rat skeletal muscle through metabolic and structural adaptations 53
UCP3 Translocates Lipid Hydroperoxide and Mediates Lipid Hydroperoxide-dependent Mitochondrial Uncoupling 52
Dimorphic expression of uncoupling protein-3 in golden hamster harderian gland: Effects of castration and testosterone administration 52
Mitochondrial DNA, RNA and protein synthesis in normal, hypothyroid and mildly hyperthyroid rat liver during cold exposure 52
Differential 3,5,3′-triiodothyronine-mediated regulation of uncoupling protein 3 transcription: Role of fatty acids 51
IN-VITRO BINDING OF 3,5-DI-IODO-L-THYRONINE TO RAT-LIVER MITOCHONDRIA 51
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. 51
Effect of 3,5-diiodo-L-thyronine on thyroid stimulating hormone and growth hormone serum levels in hypothyroid rats 50
Effects of 3,5,3'-triiodothyronine (T3) on rat liver peroxisomal compartment during cold exposure 50
T3 coordinately affects expression of genes related to uncoupling protein 3 (UCP3) activity and lipid handling in rat gastrocnemius muscle. 50
Exercise and metabolic health 50
Uncoupling protein-3 is a molecular determinant for the regulation of resting metabolic rate by thyroid hormone 49
3,5-diiodo-L-thyronine and 3,5,3 '-triiodo-L-thyronine both improve the cold tolerance of hypothyroid rats, but possibly via different mechanisms 49
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 49
Absence of uncoupling protein 3 at thermoneutrality influences brown adipose tissue mitochondrial functionality in mice 49
Thyroid hormone affects secretory activity and uncoupling protein-3 expression in rat Harderian gland 48
Absence of Uncoupling Protein-3 at Thermoneutrality Impacts Lipid Handling and Energy Homeostasis in Mice 48
Ablation of uncoupling protein 3 affects interrelated factors leading to lipolysis and insulin resistance in visceral white adipose tissue 48
Skeletal muscle mitochondrial free-fatty-acid content and membrane potential sensitivity in different thyroid states: Involvement of uncoupling protein-3 and adenine nucleotide translocase 47
De novo expression of uncoupling protein 3 is associated to enhanced mitochondrial thioesterase-1 expression and fatty acid metabolism in liver of fenofibrate-treated rats 47
Calorigenic effect of diiodothyronines in the rat 47
Temporal relationship between organ responses to 3,5-diiodo-L-thyronine in high-fat diet-fed rats role of AMPK 47
Uncoupling proteins: A complex journey to function discovery 46
Thyroid-hormone effects on putative biochemical pathways involved in UCP3 activation in rat skeletal muscle mitochondria 46
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 46
Thyroid hormone and uncoupling proteins 45
Tri-iodothyronine enhances the formation of light mitochondria during cold exposure 45
3,5-Diiodo-L-thyronine rapidly enhances mitochondrial fatty acid oxidation rate and thermogenesis in rat skeletal muscle: AMP-activated protein kinase involvement 45
ROLE OF THYROID HORMONES IN THE CONTROL OF ENERGY BALANCE 45
The Degree Of Fatty Acid Saturation Influences The Effects Of T3 And 3,5-T2 On Insulin Sensitivity In Muscle Cell. 45
3,5-Diiodo-L-Thyronine (T2) Administration Affects Visceral Adipose Tissue Inflammatory State in Rats Receiving Long-Lasting High-Fat Diet 45
3,5-DIIODO-L-THYRONINE (T2) ADMINISTRATION AFFECTS VISCERAL ADIPOSE TISSUE INFLAMMATORY STATE IN RAT RECEIVING LONG-LASTING HIGH-FAT DIET 44
Fenofibrate activates the biochemical pathways and the de novo expression of genes related to lipid handling and uncoupling protein-3 functions in liver of normal rats 44
Inefficienza mitocondriale mediata da UCP3: induzione da parte dell’acido arachidonico e coinvolgimento della perossidazione lipidica 44
Exercise, fasting, and mimetics: Toward beneficial combinations? 44
Effect of age and cold exposure on morphofunctional characteristics of skeletal muscle in neonatal pigs 43
RELATIONSHIP BETWEEN DOSE, MODE OF ADMINISTRATION AND EFFECTS OF TRIIODOTHYRONINE ON 2 HEPATIC RESPONSIVE ENZYMES 43
Light mitochondria and cellular thermogenesis 43
Control of energy metabolism by iodothyronines 43
Liver and brown fat mitochondrial response to cold in the garden dormouse (Eliomys quercinus) 43
Ruolo dell’AMPK nella risposta organo specifica alla somministrazione di 3,5-diiodo-L-tironina (T2) a ratti alimentati con dieta iperlipidica 43
A contributing role for hepatic Sirtuins in the prevention of diet-induced adiposity by 3,5-Diiodo-L-Thyronine (T2) 43
(Healthy) Ageing: Focus on Iodothyronines 43
Fasting, lipid metabolism, and triiodothyronine in rat gastrocnemius muscle: interrelated roles of uncoupling protein 3, mitochondrial thioesterase, and coenzyme Q 42
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 42
3,5diiodoLthyronine (T2) and not 3,5,3’ triiodoLthyronine (T3) reduces lipogenic signaling pathways in rats receiving a high-fat-diet. 42
Altered Mitochondrial Quality Control in Rats with Metabolic Dysfunction-Associated Fatty Liver Disease (MAFLD) Induced by High-Fat Feeding 42
Interrelated influence of superoxides and free fatty acids over mitochondrial uncoupling in skeletal muscle 41
Alteration in hepatic mitochondrial compartment of cold acclimated rats. Association with enhanced triiodothyronine serum levels. A morphometric/stereologic study by electron microscopy 41
Morphological and biochemical changes in the Harderian gland of hypothyroid rats 41
Induction of UCP2 mRNA by thyroid hormones in rat heart 41
Influence of 3,5-diiodo-L-thyronine on skeletal muscle lipid metabolism 41
Prevention of diet-induced insulin resistance by 3,5-Diiodo-L-Thyronine in rats involves SIRT1 41
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 41
miR-22-3p is involved in gluconeogenic pathway modulated by 3,5-diiodo-L-thyronine (T2) 41
Thyroid hormone metabolites and analogues 41
Effect of CB1 Receptor Deficiency on Mitochondrial Quality Control Pathways in Gastrocnemius Muscle 40
Metabolic action of thyroid hormones: Insights from functional and proteomic studies 40
Fructose-Rich Diet Affects Mitochondrial DNA Damage and Repair in Rats 40
Actin remodeling driven by circLIMA1: sperm cell as an intriguing cellular model 39
Combined cDNA array/RT-PCR analysis of gene expression profile in rat gastrocnemius muscle: relation to its adaptive function in energy metabolism during fasting. 39
Thyroid: biological actions of 'nonclassical' thyroid hormones 39
Effect of cold acclimation on oxidative capacity and respiratory properties of liver and muscle mitochondria in ducklings, Cairina moschata 39
3,5-diiodothyronine (T2) induces calcium oscillations and NO release in GH3 cells 39
Totale 5.696
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Categoria #
all - tutte 36.202
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 36.202
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020534 0 0 0 0 170 7 171 38 62 29 44 13
2020/20211.117 120 6 148 40 174 11 167 141 16 155 115 24
2021/20221.137 82 4 8 12 338 228 12 31 38 26 70 288
2022/20232.166 214 71 16 176 269 142 5 105 1.028 17 62 61
2023/20241.318 92 36 412 80 270 101 25 43 10 6 63 180
2024/2025551 17 55 39 42 398 0 0 0 0 0 0 0
Totale 8.172