CRIS Current Research Information System

GHELLI, ANNA MARIA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 4.416
EU - Europa 3.948
AS - Asia 3.718
AF - Africa 368
SA - Sud America 182
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 4
Totale 12.646
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.365
CN - Cina 1.212
IT - Italia 1.180
SG - Singapore 1.141
GB - Regno Unito 736
VN - Vietnam 535
DE - Germania 434
SE - Svezia 384
HK - Hong Kong 282
UA - Ucraina 230
RU - Federazione Russa 186
IN - India 176
CI - Costa d'Avorio 155
FR - Francia 152
BR - Brasile 140
IE - Irlanda 127
KR - Corea 127
NL - Olanda 109
TG - Togo 74
JP - Giappone 73
CH - Svizzera 68
SC - Seychelles 63
ZA - Sudafrica 58
FI - Finlandia 57
EE - Estonia 50
JO - Giordania 44
ES - Italia 36
AT - Austria 31
BG - Bulgaria 31
CA - Canada 29
ID - Indonesia 29
CZ - Repubblica Ceca 27
BE - Belgio 26
PL - Polonia 24
AR - Argentina 20
PK - Pakistan 19
BD - Bangladesh 18
MX - Messico 18
TR - Turchia 17
GR - Grecia 10
IR - Iran 10
AE - Emirati Arabi Uniti 9
DK - Danimarca 9
AU - Australia 8
HR - Croazia 8
PT - Portogallo 8
SK - Slovacchia (Repubblica Slovacca) 8
CL - Cile 7
RO - Romania 6
DZ - Algeria 5
EC - Ecuador 5
LB - Libano 5
NG - Nigeria 5
CO - Colombia 4
LT - Lituania 4
TW - Taiwan 4
MA - Marocco 3
PE - Perù 3
SN - Senegal 3
XK - ???statistics.table.value.countryCode.XK??? 3
DO - Repubblica Dominicana 2
IQ - Iraq 2
KZ - Kazakistan 2
MY - Malesia 2
PH - Filippine 2
SI - Slovenia 2
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
EG - Egitto 1
EU - Europa 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
KW - Kuwait 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
MN - Mongolia 1
NO - Norvegia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PG - Papua Nuova Guinea 1
PY - Paraguay 1
SA - Arabia Saudita 1
TH - Thailandia 1
TN - Tunisia 1
UZ - Uzbekistan 1
VC - Saint Vincent e Grenadine 1
VE - Venezuela 1
Totale 12.646
Salva come PNG Salva come JPEG
Città #
Singapore 745
Southend 623
Ashburn 480
Bologna 414
Chandler 376
Fairfield 376
Hefei 349
Hong Kong 271
Santa Clara 237
Ann Arbor 233
Woodbridge 192
Houston 171
Seattle 169
Wilmington 160
Jacksonville 157
Abidjan 155
Princeton 149
Dallas 133
Dublin 125
Seoul 125
Cambridge 123
Beijing 121
Dong Ket 120
Boardman 107
Ho Chi Minh City 101
New York 78
Lomé 74
Padova 73
Los Angeles 70
Milan 70
Tokyo 67
Hanoi 65
Westminster 64
Bern 53
Nanjing 51
Berlin 49
Amman 44
Redmond 41
Saint Petersburg 37
Jinan 36
Turin 36
Bengaluru 35
Helsinki 34
Buffalo 32
Mülheim 31
Sofia 30
Changsha 29
Medford 28
Modena 27
Jakarta 26
San Diego 26
Brussels 24
Hebei 24
Munich 24
Redondo Beach 23
Rome 23
Vienna 23
Parma 22
Redwood City 22
Shenyang 22
São Paulo 22
Florence 21
Nanchang 21
Guangzhou 19
Tianjin 19
Amsterdam 17
Mahé 17
Shanghai 17
Taizhou 17
Prague 16
Falkenstein 14
Phoenix 14
Valladolid 14
Dhaka 13
Jiaxing 13
Naples 13
Norwalk 13
Stockholm 13
Turku 13
Des Moines 12
Frankfurt am Main 12
Kuban 12
Shenzhen 12
Warsaw 12
Zhengzhou 12
Haikou 11
Montreal 11
Mountain View 11
Ningbo 11
Verona 11
Miami 10
Brooklyn 9
Caravaggio 9
Castel Maggiore 9
Chennai 9
Falls Church 9
Hangzhou 9
Hyderabad 9
Nuremberg 9
Xi'an 9
Totale 8.149
Salva come PNG Salva come JPEG
Nome #
Inducing respiratory complex I impairment elicits an increase in PGC1α in ovarian cancer 270
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy 260
Respiratory complex I deficiency triggers OMA1-mediated integrated stress response and affects lipid homeostasis during glucose restriction 250
Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment 240
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 227
Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells 223
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance 218
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. 214
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. 207
NDUFS3 knockout cancer cells and molecular docking reveal specificity and mode of action of anti-cancer respiratory complex I inhibitors 206
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome b (MT-CYB) Gene 204
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways 201
MicroRNA and Metabolic Profiling of a Primary Ovarian Neuroendocrine Carcinoma Pulmonary-Type Reveals a High Degree of Similarity with Small Cell Lung Cancer 200
Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder 200
The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. 197
Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization 197
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III 195
Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases 194
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein mutant 192
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy. 183
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 180
Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G. 180
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 179
Reactive Oxygen Species Produced by Mutated Mitochondrial Respiratory Chains of Entire Cells Monitored Using Modified Microelectrodes 179
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 174
Mild phenotypes and proper supercomplex assembly in human cells carrying the homoplasmic m.15557G > A mutation in cytochrome b gene 174
Respiratory complex I null cancer cells and molecular docking reveal specificity and mode of action inhibitors with anticancer activity 173
Mitochondrial chaperonin DNAJC15 promotes vulnerability to ferroptosis of chemoresistant ovarian cancer cells 173
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations 168
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. 168
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 166
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes 165
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 165
A computational study to assess the pathogenicity of single or combinations of missense variants on respiratory complex I 162
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function 162
Metabolomics hallmarks OPA1 variants correlating with their in-vitro phenotype and predicting clinical severity 161
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 158
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). 154
Green tea modulates a-1-adrenergic stimulated glucose transport in cultured cardiomyocytes via protein kinase C beta and delta isoforms 153
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance. 152
New Insights on Rotenone Resistance of Complex I Induced by the m.11778G>A/MT-ND4 Mutation Associated with Leber’s Hereditary Optic Neuropathy 149
Green Tea Modulates Alpha-1-Adrenergic Stimulated Glucose Transport in Cultured Rat Cardiomyocytes 148
Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration 147
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III 147
Mitochondrial Chaperonin MCJ Promotes Vulnerability to Ferroptosis of Chemoresistant Ovarian Cancer Cells – Dataset 145
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. 145
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization 144
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation 143
Mitochondrial metabolism and energy sensing in tumor progression 142
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 16 141
Manipulation of Mitochondria Dynamics Reveals Separate Roles for Form and Function in Mitochondria Distribution 138
AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations 136
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels 135
Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics 134
Mitochondrial DNA mutations in relation to cancer: the model of thyroid oncocytoma 134
Use of bacterial photosynthetic vesicles to evaluate the effect of ionic liquids on the permeability of biological membranes 129
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. 129
Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy. 127
The energetic failure caused by severe mutations in the mitochondrial genome is not rescued by Bcl-2 overexpression 125
MCJ/DNAJC15 mitochondrial chaperone as a metabolic “balance needle” in ovarian cancer chemoresistance 123
The effects of idebenone on mitochondrial bioenergetics 122
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. 120
Novel mutations in mitochondrial respiratory complexes and their functional relevance in thyroid oncocytoma. 118
Biochemical and computational approaches to dissect the effect of MT-CYB pathogenic mutations on respiratory chain activity and assembly 117
Modelling ND subunits of complex I: Leber’s Hereditary Optic Neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype-phenotype correlation 117
Impaired plasma membrane calcium ATPase activity and mitochondrial dysfunction contribute to calcium dysregulation in Fabry disease-related painful neuropathy 116
Mitochondrial complex I and cell death: a semi-automatic shogun model 114
Cybrids with mtDNA mutations causing Leber’s hereditary optic neuropathy are sensitized to apoptotic death induced by a mitochondrial oxidative stress 114
OPA1 directly interacts with respiratory complexes and AIF. 112
null 109
Effect of bcl-2 on the oxidative phosphorylation efficiency of cells with defective respiratory complex I. 108
Melanopsin-expressing retinal ganglion cells are resistant to cell injury, but not always 108
Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations. 107
Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration 106
Mitochondrial Respiratory Supercomplexes in Physiology and Diseases 105
Organization of the respiratory supercomplexes in cells with defective complex III: Structural features and metabolic consequences 103
Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies. 99
Molecular mechanisms of superoxide production by complex III: A bacterial versus human mitochondrial comparative case study. 98
Exogenous peptides are able to penetrate human cell and mitochondrial membranes, stabilize mitochondrial tRNA structures, and rescue severe mitochondrial defects 98
Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III 92
Respiratory Chain Function and Mitochondrial Dynamics in Leber's Hereditary Optic Neuropathy (LHON) and OPA1-Related Dominant Optic Atrophy (DOA) Fibroblasts. 84
null 83
Methods and models for functional studies on mtDNA mutations 60
Duplexing complexome profiling with SILAC to study human respiratory chain assembly defects 59
Targeting estrogen receptor β as preventive therapeutic strategy for Leber's hereditary optic neuropathy 40
Formation of I2+III2 supercomplex rescues respiratory chain defects 38
Totale 12.932
Salva come PNG Salva come JPEG
Categoria #
all - tutte 33.924
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 33.924
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021702 0 0 0 0 0 73 23 81 90 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
2025/20263.048 411 704 598 465 615 255 0 0 0 0 0 0
Totale 12.932