CRIS Current Research Information System

RUGOLO, MICHELA
 Distribuzione geografica
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Continente #
NA - Nord America 5.320
AS - Asia 3.933
EU - Europa 3.867
AF - Africa 337
Continente sconosciuto - Info sul continente non disponibili 246
SA - Sud America 185
OC - Oceania 19
Totale 13.907
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Nazione #
US - Stati Uniti d'America 5.253
CN - Cina 1.106
SG - Singapore 1.039
VN - Vietnam 906
GB - Regno Unito 866
IT - Italia 812
DE - Germania 459
SE - Svezia 447
UA - Ucraina 265
HK - Hong Kong 262
FR - Francia 220
IN - India 210
RU - Federazione Russa 202
BR - Brasile 134
CI - Costa d'Avorio 125
IE - Irlanda 115
FI - Finlandia 102
JP - Giappone 85
ZA - Sudafrica 83
NL - Olanda 79
TG - Togo 72
CH - Svizzera 65
KR - Corea 65
BD - Bangladesh 63
EE - Estonia 56
JO - Giordania 52
SC - Seychelles 39
CA - Canada 37
BG - Bulgaria 31
AR - Argentina 25
ES - Italia 23
PH - Filippine 20
MX - Messico 19
PL - Polonia 19
AU - Australia 18
BE - Belgio 18
AT - Austria 17
ID - Indonesia 17
IQ - Iraq 16
PK - Pakistan 16
BY - Bielorussia 11
TW - Taiwan 11
GR - Grecia 10
IR - Iran 10
SA - Arabia Saudita 9
TR - Turchia 9
CZ - Repubblica Ceca 8
EC - Ecuador 8
TH - Thailandia 8
HR - Croazia 7
LB - Libano 7
JM - Giamaica 6
NG - Nigeria 6
RO - Romania 6
SK - Slovacchia (Repubblica Slovacca) 6
AE - Emirati Arabi Uniti 5
CO - Colombia 5
DK - Danimarca 5
LT - Lituania 5
UZ - Uzbekistan 5
CL - Cile 4
PT - Portogallo 4
DZ - Algeria 3
MA - Marocco 3
PE - Perù 3
SI - Slovenia 3
VE - Venezuela 3
XK - ???statistics.table.value.countryCode.XK??? 3
DO - Repubblica Dominicana 2
EG - Egitto 2
EU - Europa 2
KG - Kirghizistan 2
MY - Malesia 2
NO - Norvegia 2
NP - Nepal 2
PY - Paraguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BO - Bolivia 1
CR - Costa Rica 1
GE - Georgia 1
GN - Guinea 1
GT - Guatemala 1
IL - Israele 1
KE - Kenya 1
LU - Lussemburgo 1
MD - Moldavia 1
MM - Myanmar 1
MN - Mongolia 1
MT - Malta 1
PG - Papua Nuova Guinea 1
PS - Palestinian Territory 1
RS - Serbia 1
SN - Senegal 1
TJ - Tagikistan 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
Totale 13.667
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Città #
Singapore 706
Southend 700
Ashburn 506
Fairfield 440
Chandler 435
Santa Clara 256
San Jose 255
Hong Kong 249
Ann Arbor 242
Wilmington 221
Bologna 216
Woodbridge 206
Houston 200
Seattle 190
Jacksonville 178
Ho Chi Minh City 164
Princeton 160
Cambridge 144
Hefei 143
Beijing 127
Abidjan 125
Council Bluffs 121
Dong Ket 118
Hanoi 118
Dublin 113
Boardman 107
New York 96
Helsinki 91
Los Angeles 90
Padova 74
Lomé 72
Westminster 72
Tokyo 71
Lauterbourg 66
Nanjing 59
Bern 57
Berlin 55
Amman 52
Jinan 46
Seoul 46
Milan 44
Dallas 43
Saint Petersburg 43
Redmond 41
Turin 41
Buffalo 34
Changsha 34
Mülheim 32
Guangzhou 31
Medford 31
San Diego 29
Shanghai 29
Sofia 29
Tianjin 28
Hebei 27
Rome 26
Shenyang 24
Florence 22
Haiphong 22
Johannesburg 22
Nanchang 21
Redondo Beach 21
Parma 20
Phoenix 20
Falls Church 19
Mahé 19
Redwood City 19
Glasgow 18
São Paulo 18
Brussels 17
Dearborn 17
Frankfurt am Main 17
Ningbo 17
Bengaluru 16
Da Nang 16
Jiaxing 16
Taizhou 16
Zhengzhou 16
Amsterdam 15
London 14
Munich 14
Norwalk 14
Shenzhen 14
Des Moines 13
Orem 13
Taiyuan 13
Verona 13
Atlanta 12
Chicago 12
Kuban 12
Modena 12
San Francisco 12
Yubileyny 12
Chennai 11
Dongjak-gu 11
Falkenstein 11
Fuzhou 11
Haikou 11
Hangzhou 11
Jakarta 11
Totale 8.614
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Nome #
Eight human OPA1 isoforms, long and short: What are they for? 391
'Behr syndrome' with OPA1 compound heterozygote mutations 382
Coenzyme Q biosynthesis inhibition induces HIF-1α stabilization and metabolic switch toward glycolysis 325
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 291
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 274
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment 273
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells 264
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 244
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 241
The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. 237
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance 230
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. 224
Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder 223
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 219
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 215
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein mutant 212
Reactive Oxygen Species Produced by Mutated Mitochondrial Respiratory Chains of Entire Cells Monitored Using Modified Microelectrodes 211
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. 210
Metabolomics hallmarks OPA1 variants correlating with their in-vitro phenotype and predicting clinical severity 208
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 204
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 200
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 200
Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G. 197
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes 195
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function 195
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III 194
ATP depletion and caspase independent death of cybrids bearing Leber's Hereditary Optic neuropathy MTDNA mutations incubated in galactose medium. A model for endonuclease G-mediated apoptosis 188
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. 187
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 186
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 185
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations 183
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 183
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 182
GLUCOSE TRANSPORT ACTIVATION IN HUMAN HEMATOPOIETIC CELLS M07e IS MODULATED BY CYTOSOLIC CALCIUM AND CALMODULIN 181
OPA1: how much do we know to approach therapy? 180
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 177
Green Tea Modulates Alpha-1-Adrenergic Stimulated Glucose Transport in Cultured Rat Cardiomyocytes 177
Green tea modulates a-1-adrenergic stimulated glucose transport in cultured cardiomyocytes via protein kinase C beta and delta isoforms 177
A cellular model for cancer progression: Role of mitochondrial mutations and metabolism 172
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). 166
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization 163
Biochimica 162
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation 160
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. 160
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels 159
Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration 159
OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes 156
OPA3, a new regulator of mitochondrial fission? 154
OPA1 Links Human Mitochondrial Genome Maintenance to mtDNA Replication and Distribution 153
Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics 151
Mitochondrial DNA mutations in relation to cancer: the model of thyroid oncocytoma 151
Why mitochondria must fuse to maintain their genome integrity 150
AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations 149
Learning from oncocytic tumors: why choose inefficient mitochondria? 148
Cellular and mitochondrial determination of low molecular mass organic acids by LC-MS/MS 146
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 143
The energetic failure caused by severe mutations in the mitochondrial genome is not rescued by Bcl-2 overexpression 143
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. 143
The effects of idebenone on mitochondrial bioenergetics 141
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. 137
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III 136
Modelling ND subunits of complex I: Leber’s Hereditary Optic Neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype-phenotype correlation 135
Functional investigation of the mitochondrial protein OPA3 132
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 129
OPA1 directly interacts with respiratory complexes and AIF. 128
Effect of bcl-2 on the oxidative phosphorylation efficiency of cells with defective respiratory complex I. 127
Cybrids with mtDNA mutations causing Leber’s hereditary optic neuropathy are sensitized to apoptotic death induced by a mitochondrial oxidative stress 127
Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations. 125
Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration 124
Functional genomics of thyroid oncocytoma 124
Organization of the respiratory supercomplexes in cells with defective complex III: Structural features and metabolic consequences 123
Mitochondrial Respiratory Supercomplexes in Physiology and Diseases 121
Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies. 111
Molecular mechanisms of superoxide production by complex III: A bacterial versus human mitochondrial comparative case study. 110
null 109
null 109
Respiratory Chain Function and Mitochondrial Dynamics in Leber's Hereditary Optic Neuropathy (LHON) and OPA1-Related Dominant Optic Atrophy (DOA) Fibroblasts. 97
Histamine activates phospholipase C in human airway epithelial cells via a phorbol ester-sensitive pathway 29
Totale 13.907
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Categoria #
all - tutte 36.667
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 36.667
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.504 0 55 97 88 137 85 56 113 57 208 358 250
2022/20231.825 199 306 101 222 91 131 53 107 301 48 150 116
2023/2024507 23 61 17 38 47 128 26 29 9 88 16 25
2024/20251.511 43 219 141 105 334 94 127 48 10 56 58 276
2025/20263.970 222 369 350 319 485 278 500 157 686 282 151 171
2026/2027161 95 66 0 0 0 0 0 0 0 0 0 0
Totale 13.907