IRIS
PETRUZZELLA, Vittoria
 Distribuzione geografica
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Continente #
NA - Nord America 6.905
AS - Asia 2.603
EU - Europa 2.319
SA - Sud America 635
AF - Africa 94
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 4
Totale 12.567
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Nazione #
US - Stati Uniti d'America 6.798
SG - Singapore 1.149
IT - Italia 784
CN - Cina 580
BR - Brasile 494
HK - Hong Kong 321
SE - Svezia 303
RU - Federazione Russa 241
DE - Germania 237
UA - Ucraina 167
FI - Finlandia 159
FR - Francia 138
VN - Vietnam 133
GB - Regno Unito 123
IN - India 83
BD - Bangladesh 61
AR - Argentina 47
CA - Canada 47
IQ - Iraq 36
TR - Turchia 35
ID - Indonesia 33
MX - Messico 33
NL - Olanda 33
BE - Belgio 28
JP - Giappone 26
PK - Pakistan 23
CO - Colombia 22
CI - Costa d'Avorio 20
ZA - Sudafrica 20
VE - Venezuela 19
EC - Ecuador 18
IE - Irlanda 18
PL - Polonia 18
CL - Cile 17
ES - Italia 17
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
JM - Giamaica 5
OM - Oman 5
TT - Trinidad e Tobago 5
AZ - Azerbaigian 4
CR - Costa Rica 4
ET - Etiopia 4
MD - Moldavia 4
SN - Senegal 4
AO - Angola 3
BG - Bulgaria 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
AL - Albania 2
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
PR - Porto Rico 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
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
Totale 12.556
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Città #
Fairfield 676
Ashburn 647
Singapore 599
Woodbridge 519
Chandler 518
San Jose 428
Houston 391
Jacksonville 378
Hong Kong 318
Cambridge 303
Seattle 280
Ann Arbor 268
Milan 236
Nyköping 222
Wilmington 207
Beijing 169
Bari 119
Lauterbourg 107
New York 107
Nanjing 105
Lawrence 104
Roxbury 102
Dallas 92
Los Angeles 91
Des Moines 71
Rome 65
Boardman 64
Princeton 54
Helsinki 52
Santa Clara 49
Brooklyn 46
Munich 46
Ho Chi Minh City 43
San Diego 41
Foggia 39
Nanchang 39
São Paulo 39
Buffalo 38
Dearborn 36
Inglewood 35
Council Bluffs 34
Figino 31
Columbus 30
London 30
Chicago 27
Brussels 24
Frankfurt am Main 22
Hanoi 22
Hebei 22
Rio de Janeiro 22
Shenyang 22
Denver 21
Abidjan 20
Jiaxing 20
Tokyo 20
Montreal 19
Jakarta 18
Stockholm 18
Dublin 17
Nuremberg 17
Phoenix 17
Belo Horizonte 16
Dong Ket 16
Orem 16
Baghdad 15
Changsha 14
Falkenstein 14
Mexico City 14
Brasília 13
Salt Lake City 13
Warsaw 13
Conversano 12
Moscow 12
San Francisco 12
Tianjin 12
Turku 12
Washington 12
Boston 11
Chennai 11
Grafing 11
Nijmegen 11
The Dalles 11
Turin 11
Amsterdam 10
Johannesburg 10
Tashkent 10
Amman 9
Florence 9
Monopoli 9
Norwalk 9
Quito 9
Santiago 9
Toronto 9
Atlanta 8
Da Nang 8
Elk Grove Village 8
Mottola 8
Pescara 8
Poplar 8
Sorocaba 8
Totale 8.647
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Nome #
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers 219
High Mitochondrial DNA Copy Number is a Protective Factor From Vision Loss in Heteroplasmic Leber’s Hereditary Optic Neuropathy (LHON) 211
HmtDB, a genomic resource for mitochondrion-based human variability studies 195
ACTN3/ACE GENOTYPES AND MITOCHONDRIAL GENOME IN PROFESSIONAL SOCCER PLAYERS’ PERFORMANCE 194
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation 192
Author Response: Increased mtDNA Copy Number Protects Against LHON 186
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 170
Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers 166
Interaction of COMT Val108/158Met genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 165
Author response: Do high mtDNA copy numbers truly prevent LHON manifestations? 164
NEW MORPHOLOGICAL APPROACHES TO THE STUDY OF MITOCHONDRIAL ENCEPHALOMYOPATHIES 161
Age-dependent structural variations in rat brain mitochondrial DNA 161
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H 161
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesis 160
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 160
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10 155
Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System 155
The oxidative phosphorylation system in mammalian mitochondria 153
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit 153
Deep sequencing unearths NumtS under LHON-associated false heteroplasmic mitochondrial DNA variants 151
MOLECULAR ANALYSIS OF THE MUSCLE PATHOLOGY ASSOCIATED WITH MITOCHONDRIAL-DNA DELETIONS 147
Dysfunction of mitochondrial respiratory chain complex I in neurological disorders: genetics and pathogenetic mechanisms 144
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 142
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene 139
ACETYL-L-CARNITINE INCREASES CYTOCHROME-OXIDASE SUBUNIT-I MESSENGER-RNA CONTENT IN HYPOTHYROID RAT-LIVER 139
Bilateral progressive visual loss in an epileptic, mentally retarded boy 139
Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases. 135
Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio). 135
TRIM8 blunts the pro-proliferative action of ΔNp63α in a p53 wild-type background 133
The cAMP cascade and mitochondrial oxidative phosphorylation. Physiopathological implications 132
The regulation of PTC containing transcripts of the human NDUFS4 gene of complex I of respiratory chain and the impact of pathological mutations 131
IS A POINT MUTATION IN THE MITOCHONDRIAL ND2 GENE ASSOCIATED WITH ALZHEIMERS-DISEASE 130
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy 128
ALTERAZIONI STRUTTURALI DEL DNA MITOCONDRIALE IN TESSUTI DI RATTO VECCHIO 125
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 124
Decrease of D-loop frequency in heart and cerebral hemispheres mitochondrial DNA of aged rat 124
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia 122
A novel insertion mutation (A(169i)) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient 122
Differential expression of ATPAF1 and ATPAF2 genes encoding F-1-ATPase assembly proteins in mouse tissues 120
Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects 120
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. 119
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I RID D-6064-2011 117
Survey of genes involved in mitochondrial biogenesis in early development of zebrafish as candidates for mitochondrial pathologies 114
Reduced synthesis of mtRNA in isolated mitochondria of senescent rat brain 114
Cerebellar ataxia as atypical manifestation of the 3243A > G MELAS mutation 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
Late-onset Leber hereditary optic neuropathy mimicking Susac's syndrome 112
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 108
cAMP-dependent phosphorylation and dephosphorylation of mitochondrial proteins. Molecular aspects and physiopathological implications 107
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts 107
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 104
A Gel-Based Proteomic Analysis Reveals Synovial α-Enolase and Fibrinogen β-Chain Dysregulation in Knee Osteoarthritis: A Controlled Trial 104
Respiratory complex I in brian development and genetic disease 103
A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P 102
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I 102
CMT2A harboring mitofusin 2 mutation with optic nerve atrophy and normal visual acuity 102
Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutation 101
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 101
null 101
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 101
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGING 99
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 97
The nuclear NDUFS4 gene of complex I (NADH-ubiquinone oxidoreductase): expression products and function 96
The NADH: Ubiquinone oxidoreductase (complex 1) of the mammalian respiratory chain and the cAMP cascade 96
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases 96
Structure, Redox-Coupled Protonmotive activity, and Pathological Disorders of Respiratory Chain Complexes 94
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 94
LIPID-COMPOSITION IN SYNAPTIC AND NONSYNAPTIC MITOCHONDRIA FROM RAT BRAINS AND EFFECT OF AGING 93
Complementation tests and sequence analysis of seven genes controlling the formation of cytochrome c oxidase in Leigh disease 92
CLINICAL AND MOLECULAR IMPLICATION IN A FAMILY WITH 3460 LEBER HEREDITARY OPTIC NEUROPATHY 91
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 91
Faithful and highly efficient RNA synthesis in isolated mitochondria from rat liver 90
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 89
Mitochondrial dysfunction as a mechanism of CNS injury. 89
Complex I and the cAMP cascade in human physiopathology 85
Clinical and molecular characterization of a novel INCL mutation in an Italian patient 84
Tackling dysfunction of mitochondrial bioenergetics in the brain 83
The NDUFS4 nuclear gene of complex I encodes a subunit essential for the assembly and cAMP-dependent regulation of the activity of the complex 82
Deep sequencing unearths Nuclear mitochondrial sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants 81
Disorders of nuclear-mitochondrial intergenomic signalling 81
MITOCHONDRIAL DNA TRANSCRIPTION IN AGING RAT 81
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 80
Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain 80
Deficit complesso V mitocondriale e fenotipo epilettico. Descrizione di un caso clinico 78
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 77
The cAMP cascade regulates mitochondrial respiration in mammalian cells. The role of complex I 77
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 76
DNA MITOCONDRIALE E INVECCHIAMENTO 75
OPA1 mutation affects autophagy and triggers senescence in autosomal dominant optic atrophy plus fibroblasts 73
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGED RAT TISSUES 73
Top level professional soccer players: association between gene polymorphisms and myDNA copy number as potential factors in modulating exercise-related phenotypes 73
MECCANISMO D'AZIONE DELL'ACETIL-L-CARNITINA SULL'ESPRESSIONE DEL DNA MITOCONDRIALE IN CERVELLO DI RATTO INVECCHIATO 72
null 72
NMD of mutated and alternatively spliced transcripts in human complex I deficiency 71
MITOCHONDRIAL DISEASE MIMIKING POLYMYOSITIS: A CASE REPORT 71
Mitochondrial DNA transcription and translation in aged rat: effect of acetyl-L-carnitine 70
The effect of GRM3 genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 68
GRM3 genotype and olanzapine treatment: Differential effects on prefrontal cortical function during working memory in patients with schizophrenia 68
REDUCED SYNTHESIS OF MESSENGER TRANSFER-RNA IN ISOLATED-MITOCHONDRIA OF SENESCENT RAT-BRAIN 68
Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA 67
Totale 11.481
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Categoria #
all - tutte 53.297
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 53.297
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20264.088 633 162 241 389 443 258 432 120 430 424 119 437
2026/202790 90 0 0 0 0 0 0 0 0 0 0 0
Totale 12.791