CRIS Current Research Information System

ZANNA, CLAUDIA
 Distribuzione geografica
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Continente #
NA - Nord America 3.434
EU - Europa 2.861
AS - Asia 2.813
AF - Africa 232
SA - Sud America 122
OC - Oceania 7
Totale 9.469
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Nazione #
US - Stati Uniti d'America 3.394
CN - Cina 919
SG - Singapore 783
IT - Italia 719
GB - Regno Unito 591
VN - Vietnam 496
DE - Germania 345
SE - Svezia 334
HK - Hong Kong 195
UA - Ucraina 177
RU - Federazione Russa 158
IN - India 148
FR - Francia 124
CI - Costa d'Avorio 94
IE - Irlanda 92
BR - Brasile 91
KR - Corea 89
NL - Olanda 66
JP - Giappone 60
JO - Giordania 47
TG - Togo 47
ZA - Sudafrica 47
EE - Estonia 41
CH - Svizzera 36
SC - Seychelles 35
FI - Finlandia 31
CA - Canada 25
BG - Bulgaria 23
AT - Austria 21
BE - Belgio 17
PL - Polonia 17
ID - Indonesia 15
PK - Pakistan 12
CZ - Repubblica Ceca 11
IR - Iran 11
MX - Messico 11
AR - Argentina 10
BY - Bielorussia 10
ES - Italia 10
BD - Bangladesh 9
GR - Grecia 9
EC - Ecuador 8
AU - Australia 6
HR - Croazia 6
RO - Romania 5
TR - Turchia 5
DK - Danimarca 4
LB - Libano 4
CL - Cile 3
CO - Colombia 3
LT - Lituania 3
NG - Nigeria 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
TH - Thailandia 3
TW - Taiwan 3
AE - Emirati Arabi Uniti 2
DO - Repubblica Dominicana 2
NO - Norvegia 2
PH - Filippine 2
PT - Portogallo 2
PY - Paraguay 2
SI - Slovenia 2
UZ - Uzbekistan 2
BB - Barbados 1
BO - Bolivia 1
DZ - Algeria 1
EG - Egitto 1
GN - Guinea 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
IQ - Iraq 1
KE - Kenya 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MA - Marocco 1
MN - Mongolia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
SA - Arabia Saudita 1
SN - Senegal 1
VE - Venezuela 1
Totale 9.469
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Città #
Singapore 529
Southend 503
Ashburn 338
Chandler 312
Fairfield 298
Hefei 235
Bologna 219
Hong Kong 194
Ann Arbor 171
Santa Clara 167
Wilmington 147
Seattle 145
Woodbridge 142
Houston 128
Jacksonville 118
Dong Ket 115
Princeton 115
Beijing 101
Abidjan 94
Cambridge 94
Dublin 90
Seoul 88
Boardman 87
Ho Chi Minh City 80
Los Angeles 58
Padova 52
Westminster 52
Tokyo 50
Hanoi 48
Amman 47
Lomé 47
New York 47
Milan 44
Dallas 42
Turin 42
Nanjing 40
Redmond 40
Berlin 38
Redwood City 37
Jinan 35
Bern 32
Saint Petersburg 29
Shanghai 26
Buffalo 24
Changsha 24
Parma 24
Medford 23
Bengaluru 22
Mülheim 22
Sofia 22
Doylestown 21
Warrington 21
Rome 19
Guangzhou 18
Redondo Beach 18
Brussels 17
Shenyang 17
Tianjin 17
Florence 16
Hebei 16
Dearborn 15
San Diego 15
Helsinki 14
Mahé 14
Munich 14
São Paulo 14
Frankfurt am Main 13
Jakarta 13
Kuban 13
London 13
Nanchang 13
Phoenix 13
Haikou 12
Vienna 12
Zhengzhou 12
Hangzhou 11
Taiyuan 11
Amsterdam 10
Des Moines 10
Minsk 10
Olalla 10
Brooklyn 9
Modena 9
Naples 9
Norwalk 9
Nuremberg 9
Taizhou 9
Lappeenranta 8
Verona 8
Ancona 7
Boston 7
Falls Church 7
Jiaxing 7
San Francisco 7
Shenzhen 7
Toronto 7
Turku 7
Warsaw 7
Yubileyny 7
Boydton 6
Totale 6.065
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Nome #
'Behr syndrome' with OPA1 compound heterozygote mutations 287
Coenzyme Q biosynthesis inhibition induces HIF-1α stabilization and metabolic switch toward glycolysis 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
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 227
Eight human OPA1 isoforms, long and short: What are they for? 226
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 224
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 223
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance 218
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. 207
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. 198
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 198
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein mutant 192
Genetic Basis of Mitochondrial Optic Neuropathies. 191
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
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations 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
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations 168
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 167
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 166
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 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
Metabolomics hallmarks OPA1 variants correlating with their in-vitro phenotype and predicting clinical severity 161
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 160
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 158
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 158
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 155
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). 154
OPA1: how much do we know to approach therapy? 153
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
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. 145
The Pro-Oncogenic Protein IF1 Promotes Proliferation of Anoxic Cancer Cells during Re-Oxygenation 144
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation 143
OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes 139
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 136
OPA3, a new regulator of mitochondrial fission? 136
AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations 136
Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics 134
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 133
Why mitochondria must fuse to maintain their genome integrity 129
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. 129
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? 126
OPA1 Links Human Mitochondrial Genome Maintenance to mtDNA Replication and Distribution 126
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. 120
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. 113
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 109
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
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 105
Organization of the respiratory supercomplexes in cells with defective complex III: Structural features and metabolic consequences 103
Functional investigation of the mitochondrial protein OPA3 102
OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes 100
Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies. 99
Respiratory Chain Function and Mitochondrial Dynamics in Leber's Hereditary Optic Neuropathy (LHON) and OPA1-Related Dominant Optic Atrophy (DOA) Fibroblasts. 84
Totale 9.671
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Categoria #
all - tutte 25.243
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 25.243
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021653 0 0 0 0 0 60 29 69 62 58 53 322
2021/20221.257 90 52 77 77 108 50 52 91 50 152 258 200
2022/20231.382 140 221 81 161 72 104 48 85 237 33 121 79
2023/2024467 21 55 13 35 29 91 22 35 24 77 35 30
2024/20251.471 67 167 118 102 256 100 124 50 21 69 99 298
2025/20262.067 274 491 339 321 446 196 0 0 0 0 0 0
Totale 9.671