IRIS
GOGLIA, Fernando
 Distribuzione geografica
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Continente #
NA - Nord America 3.018
EU - Europa 1.643
AS - Asia 1.001
AF - Africa 41
SA - Sud America 30
Continente sconosciuto - Info sul continente non disponibili 21
OC - Oceania 3
Totale 5.757
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Nazione #
US - Stati Uniti d'America 2.715
UA - Ucraina 784
CN - Cina 672
DE - Germania 370
CA - Canada 302
IT - Italia 173
SE - Svezia 161
SG - Singapore 134
TR - Turchia 103
IN - India 52
FI - Finlandia 51
FR - Francia 33
CI - Costa d'Avorio 31
BR - Brasile 27
EU - Europa 21
BE - Belgio 16
GB - Regno Unito 16
IR - Iran 14
HK - Hong Kong 11
NL - Olanda 11
RU - Federazione Russa 6
PT - Portogallo 5
BD - Bangladesh 4
CH - Svizzera 4
ZA - Sudafrica 4
EG - Egitto 3
PL - Polonia 3
AR - Argentina 2
AZ - Azerbaigian 2
LT - Lituania 2
NP - Nepal 2
NZ - Nuova Zelanda 2
PK - Pakistan 2
AU - Australia 1
BG - Bulgaria 1
BZ - Belize 1
CO - Colombia 1
DK - Danimarca 1
DZ - Algeria 1
EE - Estonia 1
GR - Grecia 1
IE - Irlanda 1
JO - Giordania 1
JP - Giappone 1
KH - Cambogia 1
KR - Corea 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
NG - Nigeria 1
RS - Serbia 1
TN - Tunisia 1
Totale 5.757
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Città #
Jacksonville 515
Chandler 513
Toronto 294
Boardman 204
Nanjing 117
Bremen 108
Princeton 107
Istanbul 101
Wilmington 99
Singapore 76
Ashburn 66
Shenyang 65
Ann Arbor 63
Dearborn 62
Ogden 55
Boydton 49
Helsinki 48
Guangzhou 40
Jiaxing 40
Nanchang 33
Shanghai 32
Abidjan 31
Changsha 29
Tianjin 26
Hebei 25
Leawood 24
Strasbourg 24
Ningbo 23
Los Angeles 21
Jinan 19
Beijing 18
Augusta 16
Brussels 16
Norwalk 16
Zhengzhou 16
Pune 15
San Mateo 15
Taizhou 13
Naples 12
Shenzhen 11
Ardabil 10
Dallas 10
Falls Church 10
Hangzhou 9
Monmouth Junction 9
Munich 9
San Giorgio Del Sannio 9
Frankfurt am Main 8
Capua 7
Mumbai 7
Meppel 6
Ottawa 6
Qingdao 6
Isola del Liri 5
London 5
Rome 5
Wuhan 5
Wuxi 5
Hanover 4
Hong Kong 4
Marano Equo 4
Piedimonte d'Alife 4
Tappahannock 4
Verona 4
West Jordan 4
Xi'an 4
Altavilla Irpina 3
Ariano Irpino 3
Bangalore 3
Benevento 3
Berlin 3
Calitri 3
Central 3
Coimbra 3
Espoo 3
Fairfield 3
Fargo 3
Fort Wayne 3
Hyannis 3
Neuchâtel 3
Portland 3
Redmond 3
Rui'an 3
Sabz 3
Seattle 3
Wolverhampton 3
Woodbridge 3
Xuzhou 3
Acerra 2
Amsterdam 2
Avellino 2
Baku 2
Bronx 2
Cagliari 2
Dinami 2
Durban 2
Guarulhos 2
Houston 2
Islamabad 2
Jaipur 2
Totale 3.310
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Nome #
3,5-diiodo-L-thyronine increases resting metabolic rate and reduces body weight without undesirable side effects 93
Peroxisome Proliferator-Activated Receptor Delta: A Conserved Director of Lipid Homeostasis through Regulation of the Oxidative Capacity of Muscle 86
Mitochondrial Actions of Thyroid Hormone 84
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 83
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 78
3,5-diiodo-L-thyronine: a possible pharmacological agent? 75
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. 75
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 75
3,5-Diiodo-L-thyronine powerfully reduces adiposity in rats by increasing the burning of fats 75
3,5-Diiodo-L-thyronine rapidly enhances mitochondrial fatty acid oxidation rate and thermogenesis in rat skeletal muscle: AMP-activated protein kinase involvement 75
Induction of UCP2 mRNA by thyroid hormones in rat heart 73
Fructose-Rich Diet Affects Mitochondrial DNA Damage and Repair in Rats. 71
Sequential changes in the signal transduction responses of skeletal muscle following food deprivation 70
Both 3,3',5-triiodothyronine and 3,5-diodo-L-thyronine Are Able to Repair Mitochondrial DNA Damage but by Different Mechanisms 70
Action of thyroid hormones at the cellular level: the mitochondrial target 69
Alterations of brain and cerebellar proteomes linked to Aβ and tau pathology in a female triple-transgenic murine model of Alzheimer's disease. 69
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 69
3,5,3'-Triiodo-L-Thyronine- and 3,5-Diiodo-L-Thyronine- Affected Metabolic Pathways in Liver of LDL Receptor Deficient Mice 68
3,5-diiodo-L-thyronine prevents high fat diet-induced skeletal muscle mitochondrial dysfunctions: an integrated approach 68
3,5-diiodothyronine (T2) induces calcium oscillations and NO release in GH3 cells 68
3, 5-diiodothyronine: Biological actions and therapeutic perspectives 68
Changes in the functional proteomic profiles of rat skeletal muscles after caloric restriction and catch-up fat upon refeeding 67
Are the effects of triiodothyronine (T3) on resting metabolism in euthyroid rats entirely due to T3 itself ? 66
(Healthy) ageing: Focus on iodothyronines 65
Activation and inactivation of thyroid hormone by type I iodothyronine deiodinase 64
Characterization of specific mitochondrial binding sites for 3,3'-diiodo-L-thyronine 64
Defining the transcriptomic profile of rat ageing skeletal muscle using cDNA array, 2D- and Blue Native-PAGE 64
Fenofibrate prevents and reduces body weight gain and adiposity in diet-induced obese rats 63
3,5-Diiodo-L-Thyronine Exerts Metabolically Favorable Effects on Visceral Adipose Tissue of Rats Receiving a High-Fat Diet 63
Cold exposure induces different uncoupling protein thermogenin masking-unmasking processes in brown adipose tissue depending on mitochondrial subtypes 62
Fasting, lipid metabolism and triiodothyronine in rat gastrocnemius muscle: interrelated roles of uncoupling protein 3, mitochondrial thioesterase and coenzyme Q 61
BN-PAGE-based approach to study thyroid hormones and mitochondrial function. 61
Proteomic approaches for the study of tissue specific effects of 3,5,3'-triiodo-L-thyronine and 3,5-diiodo-L-thyronine in conditions of altered energy metabolism. 61
3,5-Diiodo-L-thyronine prevents high-fat-diet-induced insulin resistance in rat skeletal muscle through metabolic and structural adaptations 61
Indentification by photoaffinity labeling of 3,5-diiodo-L-thyronine-binding proteins in rat liver cytosol 59
Relationship between dose, mode of administration and effects of triiodothyronine on two hepatic responsive enzymes 58
Direct and rapid effects of 3,5-diiodo-L-thyronine (T2) 58
Absence of Uncoupling Protein-3 at Thermoneutrality Impacts Lipid Handling and Energy Homeostasis in Mice 58
3,5-Diiodothyronine: A Novel Thyroid Hormone Metabolite and Potent Modulator of Energy Metabolism 58
Insights into sarcopenia: interrelation between protein profiles and mitochondrial functionality in rat ageing skeletal muscle 57
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 56
Thyroid-state influence on protein-expression profile of rat skeletal muscle 56
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 56
THE DEGREE OF FATTY ACID SATURATION INFLUENCES THE EFFECTS OF T3 AND 3,5-T2 ON INSULIN SENSITIVITY IN MUSCLE CELLS 56
Calorigenic effect of diiodothyronines 56
Age-related changes in renal and hepatic cellular mechanisms associated with variations in rat serum thyroid hormone levels 56
Ablation of uncoupling protein 3 affects interrelated factors leading to lipolysis and insulin resistance in visceral white adipose tissue 56
3,5-diiodo-L-thyronine, by modulatine mitochondrial functions, reverses hepatic fat accumulation in rats fed a high-fat diet 55
3,5-Diiodo-L-thyronine regulates glucose-6-phosphate dehydrogenase activity in the rat 55
Acute administration of 3,5-diiodo-L-thyronine to hypothyroid rats affects bioenergetic parameters in rat skeletal muscle mitochondria 55
Dietary zinc supplementation of 3xTg-AD mice increases BDNF levels and prevents cognitive deficits as well as mitochondrial dysfunction 54
Control of energy metabolism by iodothyronines 54
15TH INTERNATIONAL THYROID CONGRESS PROGRAM AND MEETING ABSTRACTS 53
ORGAN-SPECIFIC RESPONSE TO HIGH-FAT DIET AND 3,5-DIIODOTHYRONINE (T2) TREATMENT; A POSSIBLE INVOLVEMENT OF THE AMP-ACTIVATED PROTEIN KINASE (AMPK)., 53
PPARs: Nuclear Receptors Controlled by, and Controlling, Nutrient Handling through Nuclear and Cytosolic Signaling. 53
Interrelated influence of superoxides and free fatty acids over mitochondrial uncoupling in skeletal muscle 53
Metabolic action of thyroid hormones: insights from functional and proteomic studies 52
Differential effects of 3,5-Diiodo-L-Thyronine and 3,5,3'-Triiodo-L-Thyronine on mitochondrial respiratory pathways in liver from hypothyroid rats 52
Effect of 3,3’-diiodo-L-thyronine and 3,5-diiodo-L-thyronine on rat liver oxidative capacity 51
Metabolic effects of thyroid hormone derivatives 51
Uncoupling proteins 2 and 3 influence obesità and inflammation in transgenic mice 51
In vitro binding of 3,5-diiodo-L-thyronine to rat liver mitochondria 51
High expression of thyroid hormone receptors and mitochondrial glycerol-3-phosphate dehydrogenase in the liver is linked to enhanced fatty acid oxidation in Lou/C rat strain resistant to obesity 51
Thyroid hormone analogues and derivatives: Actions in fatty liver 51
Combined cDNA array/RT-PCR analysis of gene expression profile in rat gastrocnemius muscle: relation to its adaptive function in energy metabolism during fasting 51
“A Proteomics Approach to Identify Protein Expression Changes in Rat Liver Following Administration of 3,5,3'-Triiodo-l-thyronine.” 50
Effect of 3,5-diiodo-L-thyronine on thyroid stimulating hormone and growth hormone serum levels in hypothyroid rats. 50
Combined effect of gender and caloric restriction on liver proteomic expression profile 50
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
Expression of uncoupling protein-3 and mitochondrial activity in the transition from hypothyroid to hyperthyroid state in rat skeletal muscle 49
Biochemical and functional differences in rat liver mitochondrial subpopulations obtained at different gravitational forces 49
Temporal relationship between organ responses to 3,5-diiodo-L-thyronine in high-fat diet-fed rats role of AMPK 48
Role of AMPK in the organ-specific responses to 3,5-diiodo-L-thyronine in high-fat diet-fed rats 48
The thyroid hormone metabolite 3,5-diiodo-l-thyronine prevents hepatic fat accumulation and systemic insulin resistance through direct activation of sirtuin 1 (SIRT1) 47
3,5-Diiodo-L-Thyronine (T2) Administration Affects Visceral Adipose Tissue Inflammatory State in Rats Receiving Long-Lasting High-Fat Diet 47
Composition including 3,5-diiodothyronine and pharmacological use of them 46
Studies of Complex Biological Systems with Applications to Molecular Medicine: the Need to Integrate Transcriptomic and Proteomic Approaches 45
Differential 3,5,3'-triiodothyronine-mediated regulation of uncoupling protein 3 transcription: role of Fatty acids 45
Responses of skeletal muscle lipid metabolism in rat gastrocnemius to hypothyroidism and iodothyronine administration: a putative role for FAT/CD36 44
Effect of 3,3’-diiodo-L-thyronine and 3,5-diiodo-L-thyronine on rat liver mitochondria 43
Regulation of skeletal muscle mitochondrial activity by thyroid hormones: focus on the "old" triiodothyronine and the "emerging" 3,5-diiodothyronine. 43
Absence of uncoupling protein 3 at thermoneutrality influences brown adipose tissue mitochondrial functionality in mice 42
TRC150094, a novel functional analogue of iodothyronines, reduces adiposity by increasing energy expenditure and fatty acid oxidation in rats receiving a high-fat diet 41
Mammalian mitochondrial proteome and its functions: current investigative techniques and future perspectives on ageing and diabetes 40
Exercise with food withdrawal at thermoneutrality impacts fuel use, the microbiome, AMPK phosphorylation, muscle fibers, and thyroid hormone levels in rats 40
Nonthyrotoxic prevention of diet-induced insulin resistance by 3,5-diiodo-L-thyronine in rats. 39
Thyroid-hormone effects on putative biochemical pathways involved in UCP3 activation in rat skeletal muscle mitochondria 39
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 39
Influence of 3,5-diiodo-L-thyronine on skeletal muscle lipid metabolism 38
Uncoupling protein 3 expression levels influence insulin sensitivity, fatty acid oxidation, and related signaling pathways. 38
The effect of 3,5 diiodo-L-thyronine on mitochondrial energetic transduction apparatus 37
Thyroid hormones and uncoupling proteins 37
Uncoupling protein-3 is a molecular determinant for the regulation of resting metabolic rate by thyroid hormone 37
Intracellular and plasma membrane-initiated pathways involved in the [Ca2+]i elevations induced by iodothyronines (T3 and T2) in pituitary GH3 cells 37
Rapid stimulation in vitro of rat liver cytochrome oxidase activity by 3,5-diiodo-L-thyronine and by 3,3'-diiodo-L-thyronine 37
Mitochondrial function and thyroid hormones 37
BN-PAGE-Based Approach to Study Thyroid Hormones and Mitochondrial Function 37
How thyroid controls metabolism: a different role for triiodothyronine and for diiodothyronines 36
Specific binding sites for 3,3'-diiodo-L-thyronine (3,3'-T2) in rat liver mitochondria 36
Fuel economy in food-deprived skeletal muscle: signaling pathways and regulatory mechanisms 36
Totale 5.546
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Categoria #
all - tutte 38.289
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 38.289
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020446 0 0 0 0 0 104 19 155 8 120 32 8
2020/20211.075 109 104 14 103 8 247 7 103 33 117 216 14
2021/2022541 16 6 297 23 10 17 18 74 41 3 17 19
2022/20231.600 236 56 42 193 150 290 7 149 308 41 86 42
2023/2024631 44 158 91 23 28 33 3 42 113 32 5 59
2024/2025714 127 41 109 70 322 45 0 0 0 0 0 0
Totale 5.923