CRIS Current Research Information System

RUGOLO, MICHELA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 4.150
EU - Europa 3.252
AS - Asia 1.479
AF - Africa 199
OC - Oceania 6
SA - Sud America 4
Continente sconosciuto - Info sul continente non disponibili 3
Totale 9.093
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.136
GB - Regno Unito 786
IT - Italia 627
CN - Cina 562
SE - Svezia 444
DE - Germania 417
VN - Vietnam 373
SG - Singapore 284
UA - Ucraina 260
RU - Federazione Russa 197
IN - India 157
FR - Francia 130
IE - Irlanda 115
TG - Togo 72
CH - Svizzera 63
EE - Estonia 56
ZA - Sudafrica 55
JO - Giordania 50
CI - Costa d'Avorio 45
BG - Bulgaria 31
FI - Finlandia 23
SC - Seychelles 21
NL - Olanda 19
BE - Belgio 18
CA - Canada 14
JP - Giappone 14
AT - Austria 11
GR - Grecia 10
ID - Indonesia 9
IR - Iran 9
CZ - Repubblica Ceca 8
HK - Hong Kong 7
AU - Australia 6
HR - Croazia 6
SK - Slovacchia (Repubblica Slovacca) 6
DK - Danimarca 5
LB - Libano 5
NG - Nigeria 5
RO - Romania 5
ES - Italia 4
BR - Brasile 3
PK - Pakistan 3
AE - Emirati Arabi Uniti 2
EU - Europa 2
NO - Norvegia 2
PL - Polonia 2
PT - Portogallo 2
SI - Slovenia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BD - Bangladesh 1
DZ - Algeria 1
KR - Corea 1
LT - Lituania 1
LU - Lussemburgo 1
MD - Moldavia 1
MN - Mongolia 1
PE - Perù 1
TR - Turchia 1
Totale 9.093
Salva come PNG Salva come JPEG
Città #
Southend 700
Fairfield 440
Chandler 435
Ashburn 344
Ann Arbor 242
Singapore 236
Santa Clara 234
Wilmington 221
Woodbridge 206
Houston 193
Bologna 192
Seattle 187
Jacksonville 176
Princeton 160
Cambridge 137
Dong Ket 118
Dublin 113
Boardman 98
Padova 74
Lomé 72
Westminster 72
New York 60
Nanjing 59
Bern 57
Berlin 55
Amman 50
Abidjan 45
Jinan 45
Saint Petersburg 43
Redmond 41
Turin 40
Mülheim 32
Medford 31
Changsha 30
Sofia 29
Beijing 27
Hebei 27
Milan 27
San Diego 27
Shenyang 24
Guangzhou 23
Nanchang 21
Tianjin 21
Florence 20
Helsinki 20
Shanghai 20
Falls Church 19
Mahé 19
Redwood City 19
Los Angeles 18
Brussels 17
Dearborn 17
Jiaxing 16
Zhengzhou 15
Norwalk 14
Taizhou 14
Des Moines 13
Tokyo 13
Verona 13
Kuban 12
Yubileyny 12
Fuzhou 11
Haikou 11
Ningbo 11
Rome 11
Taiyuan 11
Argelato 10
Mountain View 10
Jakarta 9
Modena 9
Olalla 9
Pune 9
Shenzhen 9
Hangzhou 8
Falkenstein 7
London 7
Paris 7
Phoenix 7
Bratislava 6
Bremen 6
Hyderabad 6
Lanzhou 6
Abeokuta 5
Amsterdam 5
Bühl 5
Fremont 5
Groningen 5
Hefei 5
Hong Kong 5
Lynchburg 5
Monmouth Junction 5
Munich 5
Vienna 5
Xi'an 5
Chengdu 4
Chicago 4
Costa Mesa 4
Forlì 4
Frankfurt Am Main 4
Kunming 4
Totale 6.019
Salva come PNG Salva come JPEG
Nome #
Coenzyme Q biosynthesis inhibition induces HIF-1α stabilization and metabolic switch toward glycolysis 211
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 202
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment 199
'Behr syndrome' with OPA1 compound heterozygote mutations 198
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 182
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells 180
Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder 174
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. 168
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 166
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance 165
The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. 165
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 157
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells. 156
Eight human OPA1 isoforms, long and short: What are they for? 155
A cellular model for cancer progression: Role of mitochondrial mutations and metabolism 146
Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G. 146
Reactive Oxygen Species Produced by Mutated Mitochondrial Respiratory Chains of Entire Cells Monitored Using Modified Microelectrodes 146
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein mutant 143
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations 139
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 137
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 135
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes 132
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 132
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function 131
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 129
GLUCOSE TRANSPORT ACTIVATION IN HUMAN HEMATOPOIETIC CELLS M07e IS MODULATED BY CYTOSOLIC CALCIUM AND CALMODULIN 129
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α. 128
Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration 124
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 124
Green tea modulates a-1-adrenergic stimulated glucose transport in cultured cardiomyocytes via protein kinase C beta and delta isoforms 124
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization 123
OPA1: how much do we know to approach therapy? 123
AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations 121
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 121
Metabolomics hallmarks OPA1 variants correlating with their in-vitro phenotype and predicting clinical severity 120
Green Tea Modulates Alpha-1-Adrenergic Stimulated Glucose Transport in Cultured Rat Cardiomyocytes 119
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 117
Biochimica 117
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). 116
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. 116
OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes 116
OPA3, a new regulator of mitochondrial fission? 114
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 113
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 113
Learning from oncocytic tumors: why choose inefficient mitochondria? 112
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels 111
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 110
null 109
null 109
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. 108
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation 107
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 106
The effects of idebenone on mitochondrial bioenergetics 102
Why mitochondria must fuse to maintain their genome integrity 102
OPA1 Links Human Mitochondrial Genome Maintenance to mtDNA Replication and Distribution 101
Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics 100
Mitochondrial DNA mutations in relation to cancer: the model of thyroid oncocytoma 99
Cybrids with mtDNA mutations causing Leber’s hereditary optic neuropathy are sensitized to apoptotic death induced by a mitochondrial oxidative stress 98
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III 96
Modelling ND subunits of complex I: Leber’s Hereditary Optic Neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype-phenotype correlation 93
The energetic failure caused by severe mutations in the mitochondrial genome is not rescued by Bcl-2 overexpression 92
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. 92
Functional genomics of thyroid oncocytoma 91
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 88
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 88
OPA1 directly interacts with respiratory complexes and AIF. 85
Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations. 83
Effect of bcl-2 on the oxidative phosphorylation efficiency of cells with defective respiratory complex I. 83
Mitochondrial Respiratory Supercomplexes in Physiology and Diseases 83
Molecular mechanisms of superoxide production by complex III: A bacterial versus human mitochondrial comparative case study. 82
Functional investigation of the mitochondrial protein OPA3 80
Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies. 79
Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration 77
Cellular and mitochondrial determination of low molecular mass organic acids by LC-MS/MS 73
Respiratory Chain Function and Mitochondrial Dynamics in Leber's Hereditary Optic Neuropathy (LHON) and OPA1-Related Dominant Optic Atrophy (DOA) Fibroblasts. 70
Organization of the respiratory supercomplexes in cells with defective complex III: Structural features and metabolic consequences 70
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III 62
Histamine activates phospholipase C in human airway epithelial cells via a phorbol ester-sensitive pathway 7
Totale 9.320
Salva come PNG Salva come JPEG
Categoria #
all - tutte 23.141
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 23.141
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.244 0 0 0 0 0 0 217 297 304 147 107 172
2020/20211.276 243 87 26 61 21 69 27 92 93 82 59 416
2021/20221.632 128 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
2024/20251.055 43 219 141 105 334 94 119 0 0 0 0 0
Totale 9.320