ZANNA, CLAUDIA
 Distribuzione geografica
Continente #
NA - Nord America 3.985
AS - Asia 3.581
EU - Europa 3.202
AF - Africa 256
SA - Sud America 143
OC - Oceania 18
Totale 11.185
Nazione #
US - Stati Uniti d'America 3.927
CN - Cina 1.049
SG - Singapore 905
IT - Italia 825
VN - Vietnam 804
GB - Regno Unito 639
DE - Germania 357
SE - Svezia 334
HK - Hong Kong 245
FR - Francia 185
UA - Ucraina 179
IN - India 169
RU - Federazione Russa 158
KR - Corea 112
BR - Brasile 105
FI - Finlandia 101
CI - Costa d'Avorio 96
IE - Irlanda 92
JP - Giappone 76
NL - Olanda 75
ZA - Sudafrica 67
JO - Giordania 48
TG - Togo 47
EE - Estonia 41
CH - Svizzera 37
CA - Canada 36
SC - Seychelles 35
BD - Bangladesh 34
ES - Italia 29
BG - Bulgaria 23
AT - Austria 22
PL - Polonia 21
PH - Filippine 18
AU - Australia 17
BE - Belgio 17
ID - Indonesia 16
MX - Messico 14
PK - Pakistan 14
AR - Argentina 13
TW - Taiwan 13
IQ - Iraq 12
TH - Thailandia 12
CZ - Repubblica Ceca 11
IR - Iran 11
BY - Bielorussia 10
GR - Grecia 9
TR - Turchia 9
EC - Ecuador 8
HR - Croazia 7
UZ - Uzbekistan 7
CO - Colombia 5
LB - Libano 5
LT - Lituania 5
RO - Romania 5
SA - Arabia Saudita 5
DK - Danimarca 4
AE - Emirati Arabi Uniti 3
CL - Cile 3
NG - Nigeria 3
NO - Norvegia 3
PE - Perù 3
PY - Paraguay 3
SI - Slovenia 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
BB - Barbados 2
DO - Repubblica Dominicana 2
KG - Kirghizistan 2
KZ - Kazakistan 2
MT - Malta 2
MY - Malesia 2
NP - Nepal 2
PT - Portogallo 2
VE - Venezuela 2
BO - Bolivia 1
CR - Costa Rica 1
CY - Cipro 1
DZ - Algeria 1
EG - Egitto 1
GE - Georgia 1
GN - Guinea 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
JM - Giamaica 1
KE - Kenya 1
LK - Sri Lanka 1
LU - Lussemburgo 1
MA - Marocco 1
MM - Myanmar 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
RS - Serbia 1
TT - Trinidad e Tobago 1
Totale 11.185
Città #
Singapore 638
Southend 503
Ashburn 376
Chandler 312
Fairfield 298
Hefei 238
Hong Kong 236
Bologna 233
San Jose 193
Santa Clara 178
Ann Arbor 171
Ho Chi Minh City 160
Wilmington 147
Seattle 145
Woodbridge 142
Houston 133
Jacksonville 120
Dong Ket 115
Princeton 115
Hanoi 112
Beijing 103
Cambridge 100
Abidjan 96
Seoul 91
Dublin 90
Boardman 88
Council Bluffs 83
Helsinki 83
Los Angeles 70
Tokyo 63
New York 57
Lauterbourg 54
Milan 53
Padova 52
Westminster 52
Amman 48
Dallas 48
Lomé 47
Turin 42
Nanjing 40
Redmond 40
Berlin 38
Redwood City 37
Jinan 36
Bern 32
Saint Petersburg 29
Shanghai 28
Parma 26
Buffalo 25
Changsha 25
Bengaluru 24
Medford 23
Rome 23
Frankfurt am Main 22
Johannesburg 22
Mülheim 22
Sofia 22
Tianjin 22
Doylestown 21
Florence 21
Guangzhou 21
Warrington 21
Haiphong 20
Glasgow 18
Redondo Beach 18
São Paulo 18
Brussels 17
Phoenix 17
Shenyang 17
Hebei 16
Nanchang 16
San Diego 16
Amsterdam 15
Da Nang 15
Dearborn 15
London 15
Jakarta 14
Mahé 14
Munich 14
Orem 14
Kuban 13
Haikou 12
Naples 12
Ningbo 12
Vienna 12
Zhengzhou 12
Dongjak-gu 11
Hangzhou 11
Taiyuan 11
Taizhou 11
Warsaw 11
Brooklyn 10
Can Tho 10
Chennai 10
Des Moines 10
Minsk 10
Olalla 10
San Francisco 10
Shenzhen 10
Bangkok 9
Totale 7.011
Nome #
Eight human OPA1 isoforms, long and short: What are they for? 386
'Behr syndrome' with OPA1 compound heterozygote mutations 377
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy 320
Coenzyme Q biosynthesis inhibition induces HIF-1α stabilization and metabolic switch toward glycolysis 318
Respiratory complex I deficiency triggers OMA1-mediated integrated stress response and affects lipid homeostasis during glucose restriction 306
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 286
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 267
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 250
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 243
The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity. 234
Apoptosis induced by staurosporine in ECV304 cells requires cell shrinkage and upregulation of Cl- conductance 229
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. 223
Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder 221
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 214
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 211
Metabolomics hallmarks OPA1 variants correlating with their in-vitro phenotype and predicting clinical severity 208
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein mutant 207
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions. 202
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 202
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations 201
Genetic Basis of Mitochondrial Optic Neuropathies. 200
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 200
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 198
The cytochrome B p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes 195
Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G. 195
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 193
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III 192
The Pro-Oncogenic Protein IF1 Promotes Proliferation of Anoxic Cancer Cells during Re-Oxygenation 188
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 186
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 184
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 182
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations 180
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 179
OPA1: how much do we know to approach therapy? 179
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 176
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 166
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). 164
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation 159
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. 158
Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration 158
OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes 154
OPA3, a new regulator of mitochondrial fission? 153
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? 152
Dominant optic neuropathy: analysis of the energetic efficiency and mitochondrial dynamics 149
AIF and endonuclease G are involved in the caspase-indepenent death of cybrids with LHON mutations 149
OPA1 Links Human Mitochondrial Genome Maintenance to mtDNA Replication and Distribution 149
Why mitochondria must fuse to maintain their genome integrity 147
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. 141
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. 136
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 128
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 128
OPA1 directly interacts with respiratory complexes and AIF. 127
Functional investigation of the mitochondrial protein OPA3 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 123
Organization of the respiratory supercomplexes in cells with defective complex III: Structural features and metabolic consequences 122
OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes 116
Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies. 111
Respiratory Chain Function and Mitochondrial Dynamics in Leber's Hereditary Optic Neuropathy (LHON) and OPA1-Related Dominant Optic Atrophy (DOA) Fibroblasts. 96
Totale 11.397
Categoria #
all - tutte 29.062
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 29.062


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021322 0 0 0 0 0 0 0 0 0 0 0 322
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
2025/20263.793 274 491 339 321 446 248 426 148 594 250 142 114
Totale 11.397