IRIS
PETRUZZELLA, Vittoria
 Distribuzione geografica
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Continente #
NA - Nord America 6.658
AS - Asia 2.567
EU - Europa 1.896
SA - Sud America 629
AF - Africa 94
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.855
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Nazione #
US - Stati Uniti d'America 6.565
SG - Singapore 1.136
CN - Cina 577
BR - Brasile 492
IT - Italia 370
HK - Hong Kong 316
SE - Svezia 303
RU - Federazione Russa 241
DE - Germania 237
UA - Ucraina 165
FI - Finlandia 159
FR - Francia 137
VN - Vietnam 133
GB - Regno Unito 122
IN - India 82
BD - Bangladesh 48
AR - Argentina 47
CA - Canada 38
IQ - Iraq 36
TR - Turchia 35
ID - Indonesia 33
MX - Messico 33
NL - Olanda 31
BE - Belgio 28
JP - Giappone 25
PK - Pakistan 23
CI - Costa d'Avorio 20
CO - Colombia 20
ZA - Sudafrica 20
VE - Venezuela 19
IE - Irlanda 18
EC - Ecuador 17
PL - Polonia 17
CL - Cile 16
ES - Italia 16
AT - Austria 14
AE - Emirati Arabi Uniti 13
SA - Arabia Saudita 13
MA - Marocco 11
UZ - Uzbekistan 11
EG - Egitto 9
JO - Giordania 9
KE - Kenya 9
MY - Malesia 9
LT - Lituania 8
PH - Filippine 8
KR - Corea 7
TN - Tunisia 7
GR - Grecia 6
KZ - Kazakistan 6
NP - Nepal 6
PY - Paraguay 6
AU - Australia 5
BO - Bolivia 5
IL - Israele 5
OM - Oman 5
AZ - Azerbaigian 4
ET - Etiopia 4
JM - Giamaica 4
MD - Moldavia 4
SN - Senegal 4
AO - Angola 3
BG - Bulgaria 3
CR - Costa Rica 3
DZ - Algeria 3
EU - Europa 3
IR - Iran 3
NI - Nicaragua 3
PA - Panama 3
PE - Perù 3
PS - Palestinian Territory 3
QA - Qatar 3
SY - Repubblica araba siriana 3
TT - Trinidad e Tobago 3
BH - Bahrain 2
BY - Bielorussia 2
CZ - Repubblica Ceca 2
GY - Guiana 2
HN - Honduras 2
HU - Ungheria 2
KG - Kirghizistan 2
KW - Kuwait 2
LU - Lussemburgo 2
NZ - Nuova Zelanda 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
AL - Albania 1
AM - Armenia 1
BN - Brunei Darussalam 1
CY - Cipro 1
DK - Danimarca 1
GA - Gabon 1
GF - Guiana Francese 1
GT - Guatemala 1
HR - Croazia 1
HT - Haiti 1
KH - Cambogia 1
LB - Libano 1
MN - Mongolia 1
MT - Malta 1
Totale 11.844
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Città #
Fairfield 676
Ashburn 626
Singapore 593
Woodbridge 519
Chandler 518
Houston 390
Jacksonville 377
San Jose 365
Hong Kong 313
Cambridge 303
Seattle 278
Ann Arbor 268
Nyköping 222
Wilmington 206
Beijing 169
Bari 116
Lauterbourg 107
Nanjing 105
Lawrence 104
Roxbury 102
New York 101
Los Angeles 89
Dallas 84
Des Moines 71
Boardman 60
Princeton 53
Helsinki 52
Munich 46
Brooklyn 43
Ho Chi Minh City 43
San Diego 41
Santa Clara 40
Foggia 39
Nanchang 39
São Paulo 39
Buffalo 36
Dearborn 36
Inglewood 35
Council Bluffs 34
London 30
Chicago 26
Brussels 24
Frankfurt am Main 22
Hanoi 22
Hebei 22
Rio de Janeiro 22
Shenyang 22
Abidjan 20
Denver 20
Jiaxing 20
Tokyo 19
Jakarta 18
Stockholm 18
Dublin 17
Montreal 17
Nuremberg 17
Belo Horizonte 16
Dong Ket 16
Phoenix 16
Baghdad 15
Orem 15
Changsha 14
Falkenstein 14
Mexico City 14
Brasília 13
Salt Lake City 13
Warsaw 13
Conversano 12
Moscow 12
Tianjin 12
Turku 12
Boston 11
Chennai 11
Grafing 11
Nijmegen 11
San Francisco 11
Washington 11
Amsterdam 10
Johannesburg 10
Tashkent 10
The Dalles 10
Amman 9
Milan 9
Monopoli 9
Norwalk 9
Quito 9
Rome 9
Atlanta 8
Da Nang 8
Elk Grove Village 8
Mottola 8
Pescara 8
Poplar 8
Santiago 8
Sorocaba 8
Toronto 8
Cairo 7
Erbil 7
Guangzhou 7
Nairobi 7
Totale 8.161
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Nome #
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers 206
High Mitochondrial DNA Copy Number is a Protective Factor From Vision Loss in Heteroplasmic Leber’s Hereditary Optic Neuropathy (LHON) 197
ACTN3/ACE GENOTYPES AND MITOCHONDRIAL GENOME IN PROFESSIONAL SOCCER PLAYERS’ PERFORMANCE 191
HmtDB, a genomic resource for mitochondrion-based human variability studies 188
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation 187
Author Response: Increased mtDNA Copy Number Protects Against LHON 180
Interaction of COMT Val108/158Met genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 162
Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers 160
Leber's hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G>A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene - case report 159
A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndrome 154
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H 154
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesis 152
Age-dependent structural variations in rat brain mitochondrial DNA 150
Author response: Do high mtDNA copy numbers truly prevent LHON manifestations? 149
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10 148
NEW MORPHOLOGICAL APPROACHES TO THE STUDY OF MITOCHONDRIAL ENCEPHALOMYOPATHIES 148
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit 147
The oxidative phosphorylation system in mammalian mitochondria 146
Deep sequencing unearths NumtS under LHON-associated false heteroplasmic mitochondrial DNA variants 145
Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System 145
Dysfunction of mitochondrial respiratory chain complex I in neurological disorders: genetics and pathogenetic mechanisms 142
MOLECULAR ANALYSIS OF THE MUSCLE PATHOLOGY ASSOCIATED WITH MITOCHONDRIAL-DNA DELETIONS 141
ACETYL-L-CARNITINE INCREASES CYTOCHROME-OXIDASE SUBUNIT-I MESSENGER-RNA CONTENT IN HYPOTHYROID RAT-LIVER 136
Bilateral progressive visual loss in an epileptic, mentally retarded boy 134
Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio). 133
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 132
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene 130
TRIM8 blunts the pro-proliferative action of ΔNp63α in a p53 wild-type background 130
The regulation of PTC containing transcripts of the human NDUFS4 gene of complex I of respiratory chain and the impact of pathological mutations 128
Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases. 128
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy 127
The cAMP cascade and mitochondrial oxidative phosphorylation. Physiopathological implications 124
IS A POINT MUTATION IN THE MITOCHONDRIAL ND2 GENE ASSOCIATED WITH ALZHEIMERS-DISEASE 124
ALTERAZIONI STRUTTURALI DEL DNA MITOCONDRIALE IN TESSUTI DI RATTO VECCHIO 120
Decrease of D-loop frequency in heart and cerebral hemispheres mitochondrial DNA of aged rat 115
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I RID D-6064-2011 114
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 113
A novel insertion mutation (A(169i)) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient 113
Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects 113
In vivo effect of acetyl-L-carnitine on succinate oxidation, adenine nucleotide pool and lipid composition of synaptic and non-synaptic mitochondria from cerebral hemispheres of senescent rats 113
Cerebellar ataxia as atypical manifestation of the 3243A > G MELAS mutation 112
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia 111
Reduced synthesis of mtRNA in isolated mitochondria of senescent rat brain 111
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. 109
Differential expression of ATPAF1 and ATPAF2 genes encoding F-1-ATPase assembly proteins in mouse tissues 108
Late-onset Leber hereditary optic neuropathy mimicking Susac's syndrome 105
cAMP-dependent phosphorylation and dephosphorylation of mitochondrial proteins. Molecular aspects and physiopathological implications 105
Survey of genes involved in mitochondrial biogenesis in early development of zebrafish as candidates for mitochondrial pathologies 103
Respiratory complex I in brian development and genetic disease 101
null 101
A Gel-Based Proteomic Analysis Reveals Synovial α-Enolase and Fibrinogen β-Chain Dysregulation in Knee Osteoarthritis: A Controlled Trial 100
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I 100
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 98
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 97
The nuclear NDUFS4 gene of complex I (NADH-ubiquinone oxidoreductase): expression products and function 96
CMT2A harboring mitofusin 2 mutation with optic nerve atrophy and normal visual acuity 96
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts 96
The NADH: Ubiquinone oxidoreductase (complex 1) of the mammalian respiratory chain and the cAMP cascade 93
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGING 92
LIPID-COMPOSITION IN SYNAPTIC AND NONSYNAPTIC MITOCHONDRIA FROM RAT BRAINS AND EFFECT OF AGING 92
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 91
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 91
A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P 90
Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutation 90
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases 89
Faithful and highly efficient RNA synthesis in isolated mitochondria from rat liver 89
Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain 88
EXTREMELY HIGH-LEVELS OF MUTANT MTDNAS CO-LOCALIZE WITH CYTOCHROME-C OXIDASE-NEGATIVE RAGGED-RED FIBERS IN PATIENTS HARBORING A POINT MUTATION AT NT-3243 88
Mitochondrial dysfunction as a mechanism of CNS injury. 88
CLINICAL AND MOLECULAR IMPLICATION IN A FAMILY WITH 3460 LEBER HEREDITARY OPTIC NEUROPATHY 87
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 86
Structure, Redox-Coupled Protonmotive activity, and Pathological Disorders of Respiratory Chain Complexes 83
Complementation tests and sequence analysis of seven genes controlling the formation of cytochrome c oxidase in Leigh disease 83
Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3 82
Clinical and molecular characterization of a novel INCL mutation in an Italian patient 82
Deep sequencing unearths Nuclear mitochondrial sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants 79
The NDUFS4 nuclear gene of complex I encodes a subunit essential for the assembly and cAMP-dependent regulation of the activity of the complex 79
Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain 79
Complex I and the cAMP cascade in human physiopathology 78
MITOCHONDRIAL DNA TRANSCRIPTION IN AGING RAT 75
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 75
Disorders of nuclear-mitochondrial intergenomic signalling 74
The cAMP cascade regulates mitochondrial respiration in mammalian cells. The role of complex I 74
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 74
Tackling dysfunction of mitochondrial bioenergetics in the brain 74
null 72
Top level professional soccer players: association between gene polymorphisms and myDNA copy number as potential factors in modulating exercise-related phenotypes 72
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 70
Deficit complesso V mitocondriale e fenotipo epilettico. Descrizione di un caso clinico 70
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGED RAT TISSUES 70
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts 68
NMD of mutated and alternatively spliced transcripts in human complex I deficiency 67
MITOCHONDRIAL DISEASE MIMIKING POLYMYOSITIS: A CASE REPORT 67
MECCANISMO D'AZIONE DELL'ACETIL-L-CARNITINA SULL'ESPRESSIONE DEL DNA MITOCONDRIALE IN CERVELLO DI RATTO INVECCHIATO 67
DNA MITOCONDRIALE E INVECCHIAMENTO 66
Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutation 65
GRM3 genotype and olanzapine treatment: Differential effects on prefrontal cortical function during working memory in patients with schizophrenia 65
The effect of GRM3 genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 64
null 64
REDUCED SYNTHESIS OF MESSENGER TRANSFER-RNA IN ISOLATED-MITOCHONDRIA OF SENESCENT RAT-BRAIN 64
Totale 10.883
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Categoria #
all - tutte 49.339
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 49.339
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021320 0 0 0 0 0 0 0 0 0 178 61 81
2021/2022773 36 132 4 22 43 46 49 39 56 37 130 179
2022/20231.284 184 99 87 159 151 176 9 137 222 10 25 25
2023/2024459 42 94 31 31 50 106 16 18 4 22 13 32
2024/20251.851 35 19 148 60 38 135 132 171 80 86 323 624
2025/20263.465 633 162 241 389 443 258 432 120 430 357 0 0
Totale 12.078