CRIS Current Research Information System

GHELLI, ANNA MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 4.924
AS - Asia 4.729
EU - Europa 4.223
AF - Africa 399
SA - Sud America 205
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 4
Totale 14.494
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Nazione #
US - Stati Uniti d'America 4.861
CN - Cina 1.346
SG - Singapore 1.288
IT - Italia 1.243
VN - Vietnam 1.049
GB - Regno Unito 757
DE - Germania 455
SE - Svezia 386
HK - Hong Kong 314
FR - Francia 235
UA - Ucraina 234
IN - India 199
RU - Federazione Russa 186
CI - Costa d'Avorio 155
BR - Brasile 154
KR - Corea 139
IE - Irlanda 127
NL - Olanda 115
FI - Finlandia 100
JP - Giappone 100
ZA - Sudafrica 79
TG - Togo 74
CH - Svizzera 68
SC - Seychelles 64
EE - Estonia 51
JO - Giordania 46
ES - Italia 42
AT - Austria 33
BG - Bulgaria 32
CA - Canada 32
ID - Indonesia 32
PL - Polonia 30
BE - Belgio 29
TR - Turchia 29
BD - Bangladesh 28
CZ - Repubblica Ceca 27
PK - Pakistan 27
AR - Argentina 24
MX - Messico 24
PH - Filippine 24
TH - Thailandia 20
IQ - Iraq 17
TW - Taiwan 15
GR - Grecia 12
AE - Emirati Arabi Uniti 10
IR - Iran 10
SA - Arabia Saudita 10
CL - Cile 9
DK - Danimarca 9
HR - Croazia 9
SK - Slovacchia (Repubblica Slovacca) 9
AU - Australia 8
PT - Portogallo 8
RO - Romania 7
SN - Senegal 7
LT - Lituania 6
CO - Colombia 5
DZ - Algeria 5
EC - Ecuador 5
LB - Libano 5
MA - Marocco 5
NG - Nigeria 5
SI - Slovenia 4
UZ - Uzbekistan 4
MT - Malta 3
MY - Malesia 3
PE - Perù 3
XK - ???statistics.table.value.countryCode.XK??? 3
DO - Repubblica Dominicana 2
ET - Etiopia 2
KZ - Kazakistan 2
NO - Norvegia 2
NP - Nepal 2
PY - Paraguay 2
VE - Venezuela 2
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CY - Cipro 1
EG - Egitto 1
EU - Europa 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
JM - Giamaica 1
KE - Kenya 1
KW - Kuwait 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
MM - Myanmar 1
MN - Mongolia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PG - Papua Nuova Guinea 1
PS - Palestinian Territory 1
QA - Qatar 1
TJ - Tagikistan 1
TN - Tunisia 1
Totale 14.493
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Città #
Singapore 873
Southend 623
Ashburn 523
Bologna 436
Chandler 376
Fairfield 376
Hefei 351
Hong Kong 291
Santa Clara 244
Ann Arbor 233
Ho Chi Minh City 233
San Jose 226
Woodbridge 192
Hanoi 188
Houston 173
Seattle 169
Wilmington 160
Jacksonville 158
Abidjan 155
Princeton 149
Dallas 136
Beijing 125
Dublin 125
Seoul 125
Cambridge 123
Dong Ket 120
Boardman 108
New York 88
Tokyo 85
Los Angeles 81
Helsinki 76
Lauterbourg 75
Lomé 74
Padova 73
Milan 71
Westminster 64
Council Bluffs 54
Bern 53
Nanjing 51
Berlin 49
Amman 46
Redmond 41
Saint Petersburg 37
Jinan 36
Turin 36
Bengaluru 35
Buffalo 35
Mülheim 31
Sofia 30
Changsha 29
Modena 29
Da Nang 28
Medford 28
Brussels 27
Haiphong 27
San Diego 27
Jakarta 26
Guangzhou 25
São Paulo 25
Frankfurt am Main 24
Hebei 24
Johannesburg 24
Munich 24
Rome 24
Shanghai 24
Vienna 24
Redondo Beach 23
Amsterdam 22
Florence 22
Nanchang 22
Parma 22
Redwood City 22
Shenyang 22
Tianjin 21
Shenzhen 20
Taizhou 18
Mahé 17
Warsaw 17
Prague 16
Dhaka 15
London 15
Orem 15
Stockholm 15
Chennai 14
Falkenstein 14
Phoenix 14
Valladolid 14
Biên Hòa 13
Des Moines 13
Jiaxing 13
Miami 13
Naples 13
Norwalk 13
Turku 13
Zhengzhou 13
Kuban 12
Montreal 12
Paris 12
Ankara 11
Haikou 11
Totale 9.193
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Nome #
Inducing respiratory complex I impairment elicits an increase in PGC1α in ovarian cancer 309
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy 304
Respiratory complex I deficiency triggers OMA1-mediated integrated stress response and affects lipid homeostasis during glucose restriction 297
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment 265
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells 257
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome b (MT-CYB) Gene 244
MicroRNA and Metabolic Profiling of a Primary Ovarian Neuroendocrine Carcinoma Pulmonary-Type Reveals a High Degree of Similarity with Small Cell Lung Cancer 243
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 242
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 238
NDUFS3 knockout cancer cells and molecular docking reveal specificity and mode of action of anti-cancer respiratory complex I inhibitors 234
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance 225
The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. 225
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways 223
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. 220
Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases 220
Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder 217
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 217
Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization 216
Respiratory complex I null cancer cells and molecular docking reveal specificity and mode of action inhibitors with anticancer activity 214
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 214
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy. 213
Mitochondrial chaperonin DNAJC15 promotes vulnerability to ferroptosis of chemoresistant ovarian cancer cells 209
Metabolomics hallmarks OPA1 variants correlating with their in-vitro phenotype and predicting clinical severity 206
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein mutant 204
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 202
Reactive Oxygen Species Produced by Mutated Mitochondrial Respiratory Chains of Entire Cells Monitored Using Modified Microelectrodes 202
Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene 199
A computational study to assess the pathogenicity of single or combinations of missense variants on respiratory complex I 197
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 195
New Insights on Rotenone Resistance of Complex I Induced by the m.11778G>A/MT-ND4 Mutation Associated with Leber’s Hereditary Optic Neuropathy 195
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 194
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes 192
Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G. 192
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function 190
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III 190
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 185
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 182
Mitochondrial Chaperonin MCJ Promotes Vulnerability to Ferroptosis of Chemoresistant Ovarian Cancer Cells – Dataset 178
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 177
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations 176
Impaired plasma membrane calcium ATPase activity and mitochondrial dysfunction contribute to calcium dysregulation in Fabry disease-related painful neuropathy 175
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 172
Green tea modulates a-1-adrenergic stimulated glucose transport in cultured cardiomyocytes via protein kinase C beta and delta isoforms 172
Green Tea Modulates Alpha-1-Adrenergic Stimulated Glucose Transport in Cultured Rat Cardiomyocytes 171
Mitochondrial metabolism and energy sensing in tumor progression 163
Use of bacterial photosynthetic vesicles to evaluate the effect of ionic liquids on the permeability of biological membranes 160
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). 160
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization 157
Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration 157
Manipulation of Mitochondria Dynamics Reveals Separate Roles for Form and Function in Mitochondria Distribution 157
Dominant Optic Atrophy (DOA) and Sensorineural Hearing Loss: Clinical, Biochemical, Spectroscopic and Molecular Genetic Study of a Large Italian Pedigree Linked to a New Locus on Chromosome 16 156
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation 155
Biochemical and computational approaches to dissect the effect of MT-CYB pathogenic mutations on respiratory chain activity and assembly 153
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. 153
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels 153
MCJ/DNAJC15 mitochondrial chaperone as a metabolic “balance needle” in ovarian cancer chemoresistance 149
AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations 149
Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics 148
Mitochondrial DNA mutations in relation to cancer: the model of thyroid oncocytoma 146
Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy. 143
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. 140
The effects of idebenone on mitochondrial bioenergetics 138
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 137
The energetic failure caused by severe mutations in the mitochondrial genome is not rescued by Bcl-2 overexpression 137
Modelling ND subunits of complex I: Leber’s Hereditary Optic Neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype-phenotype correlation 131
Mitochondrial complex I and cell death: a semi-automatic shogun model 131
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. 130
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III 127
Effect of bcl-2 on the oxidative phosphorylation efficiency of cells with defective respiratory complex I. 125
OPA1 directly interacts with respiratory complexes and AIF. 124
Cybrids with mtDNA mutations causing Leber’s hereditary optic neuropathy are sensitized to apoptotic death induced by a mitochondrial oxidative stress 123
Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration 120
Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations. 120
Mitochondrial Respiratory Supercomplexes in Physiology and Diseases 120
Organization of the respiratory supercomplexes in cells with defective complex III: Structural features and metabolic consequences 120
Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not always 119
Exogenous peptides are able to penetrate human cell and mitochondrial membranes, stabilize mitochondrial tRNA structures, and rescue severe mitochondrial defects 113
Molecular mechanisms of superoxide production by complex III: A bacterial versus human mitochondrial comparative case study. 109
null 109
Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies. 106
Respiratory Chain Function and Mitochondrial Dynamics in Leber's Hereditary Optic Neuropathy (LHON) and OPA1-Related Dominant Optic Atrophy (DOA) Fibroblasts. 96
Duplexing complexome profiling with SILAC to study human respiratory chain assembly defects 87
null 83
Formation of I2+III2 supercomplex rescues respiratory chain defects 78
Methods and models for functional studies on mtDNA mutations 72
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy 53
Totale 14.799
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Categoria #
all - tutte 37.078
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 37.078
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021435 0 0 0 0 0 0 0 0 0 66 57 312
2021/20221.483 101 48 89 79 108 68 52 106 64 168 354 246
2022/20231.785 176 254 92 234 101 130 61 101 317 48 153 118
2023/2024646 35 69 37 46 49 118 31 47 30 105 41 38
2024/20252.223 102 218 170 136 374 152 141 86 69 149 171 455
2025/20264.915 411 704 598 465 615 294 580 138 803 307 0 0
Totale 14.799