ZANNA, CLAUDIA
 Distribuzione geografica
Continente #
NA - Nord America 3.787
AS - Asia 3.555
EU - Europa 3.129
AF - Africa 256
SA - Sud America 138
OC - Oceania 18
Totale 10.883
Nazione #
US - Stati Uniti d'America 3.736
CN - Cina 1.044
SG - Singapore 903
VN - Vietnam 804
IT - Italia 764
GB - Regno Unito 639
DE - Germania 356
SE - Svezia 334
HK - Hong Kong 243
FR - Francia 183
UA - Ucraina 179
IN - India 168
RU - Federazione Russa 158
KR - Corea 112
BR - Brasile 102
FI - Finlandia 100
CI - Costa d'Avorio 96
IE - Irlanda 92
JP - Giappone 76
NL - Olanda 72
ZA - Sudafrica 67
JO - Giordania 48
TG - Togo 47
EE - Estonia 41
CH - Svizzera 36
SC - Seychelles 35
CA - Canada 31
ES - Italia 26
BG - Bulgaria 23
AT - Austria 22
PL - Polonia 21
BD - Bangladesh 19
PH - Filippine 18
AU - Australia 17
BE - Belgio 17
ID - Indonesia 16
MX - Messico 14
PK - Pakistan 14
AR - Argentina 12
IQ - Iraq 12
TH - Thailandia 12
TW - Taiwan 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
LB - Libano 5
RO - Romania 5
SA - Arabia Saudita 5
CO - Colombia 4
DK - Danimarca 4
LT - Lituania 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
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
BB - Barbados 1
BO - Bolivia 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 10.883
Città #
Singapore 636
Southend 503
Ashburn 362
Chandler 312
Fairfield 298
Hefei 238
Hong Kong 234
Bologna 229
Ann Arbor 171
Santa Clara 170
Ho Chi Minh City 160
San Jose 151
Wilmington 147
Seattle 145
Woodbridge 142
Houston 132
Jacksonville 120
Dong Ket 115
Princeton 115
Hanoi 112
Beijing 103
Cambridge 100
Abidjan 96
Seoul 91
Dublin 90
Boardman 87
Helsinki 83
Los Angeles 69
Tokyo 63
Lauterbourg 54
New York 52
Padova 52
Westminster 52
Amman 48
Council Bluffs 47
Lomé 47
Dallas 46
Milan 45
Turin 42
Nanjing 40
Redmond 40
Berlin 38
Redwood City 37
Jinan 36
Bern 32
Saint Petersburg 29
Shanghai 27
Parma 26
Buffalo 24
Changsha 24
Bengaluru 23
Medford 23
Frankfurt am Main 22
Johannesburg 22
Mülheim 22
Sofia 22
Tianjin 22
Doylestown 21
Guangzhou 21
Warrington 21
Haiphong 20
Rome 19
Glasgow 18
Redondo Beach 18
São Paulo 18
Brussels 17
Shenyang 17
Florence 16
Hebei 16
Nanchang 16
Da Nang 15
Dearborn 15
London 15
San Diego 15
Amsterdam 14
Jakarta 14
Mahé 14
Munich 14
Phoenix 14
Kuban 13
Orem 13
Haikou 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
Shenzhen 10
Bangkok 9
Modena 9
Naples 9
Totale 6.862
Nome #
Eight human OPA1 isoforms, long and short: What are they for? 375
'Behr syndrome' with OPA1 compound heterozygote mutations 367
Coenzyme Q biosynthesis inhibition induces HIF-1α stabilization and metabolic switch toward glycolysis 310
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
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 270
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism 261
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy 246
A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16. 242
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
The antioxidant function of Bcl-2 preserves cytoskeletal stability of cells with defective respiratory complex I. 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
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 214
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
Genetic Basis of Mitochondrial Optic Neuropathies. 199
Mitochondrial abnormalities in fibroblasts carrying DNMT1 mutations 198
Syndromic parkinsonism and dementia associated with OPA1 missense mutations 198
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions 196
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder 194
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines. 193
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
Fine-tuning of the respiratory complexes stability and supercomplexes assembly in cells defective of complex III 190
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder 186
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
Cell death of fibroblasts derived from patients with Leber’s hereditary optic neuropathy mtDNA mutations 176
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. 176
OPA1: how much do we know to approach therapy? 176
The Pro-Oncogenic Protein IF1 Promotes Proliferation of Anoxic Cancer Cells during Re-Oxygenation 171
Effect of energetic stress and the ceramide analogue C6-ceramide on thyroid oncocytoma cell lines 171
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy 165
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). 160
Bioenergetics shapes cellular death pathways in Leber’s hereditary optic neuropathy: a model of mitochondrial neurodegeneration 157
Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation 155
Protection against oxidant-induced apoptosis by exogenous glutathione in Leber Hereditary Optic Neuropathy cybrids. 153
Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations 152
OPA3, a new regulator of mitochondrial fission? 151
DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated? 151
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
OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes 148
Why mitochondria must fuse to maintain their genome integrity 145
OPA1 Links Human Mitochondrial Genome Maintenance to mtDNA Replication and Distribution 145
OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. 140
Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy. 129
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 125
OPA1 directly interacts with respiratory complexes and AIF. 124
OPA3 IS AN INNER MITOCHONDRIAL MEMBRANE PROTEIN INVOLVED IN MITOCHONDRIAL DYNAMICS REGULATION 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
Organization of the respiratory supercomplexes in cells with defective complex III: Structural features and metabolic consequences 120
Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations. 119
Functional investigation of the mitochondrial protein OPA3 118
OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes 112
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
Totale 11.095
Categoria #
all - tutte 27.441
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 27.441


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021433 0 0 0 0 0 0 0 0 0 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
2025/20263.491 274 491 339 321 446 248 426 148 594 204 0 0
Totale 11.095