IRIS
PETRUZZELLA, Vittoria
 Distribuzione geografica
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Continente #
NA - Nord America 5.137
EU - Europa 1.196
AS - Asia 561
SA - Sud America 6
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 2
Totale 6.908
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Nazione #
US - Stati Uniti d'America 5.128
CN - Cina 360
IT - Italia 307
SE - Svezia 285
SG - Singapore 165
UA - Ucraina 158
DE - Germania 150
FI - Finlandia 124
GB - Regno Unito 74
BE - Belgio 27
IE - Irlanda 17
NL - Olanda 16
VN - Vietnam 16
FR - Francia 15
CA - Canada 9
IN - India 8
RU - Federazione Russa 6
BR - Brasile 4
ES - Italia 4
BG - Bulgaria 3
EU - Europa 3
GR - Grecia 3
HK - Hong Kong 3
AT - Austria 2
IR - Iran 2
JP - Giappone 2
KR - Corea 2
MA - Marocco 2
AR - Argentina 1
AU - Australia 1
CL - Cile 1
CZ - Repubblica Ceca 1
EG - Egitto 1
ID - Indonesia 1
KH - Cambogia 1
LU - Lussemburgo 1
MD - Moldavia 1
MT - Malta 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
Totale 6.908
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Città #
Fairfield 675
Chandler 527
Woodbridge 519
Houston 378
Jacksonville 377
Ashburn 328
Cambridge 303
Seattle 275
Ann Arbor 268
Nyköping 223
Wilmington 205
Singapore 125
Bari 111
Lawrence 105
Nanjing 104
Roxbury 102
Des Moines 70
New York 70
Beijing 62
Boardman 60
Princeton 53
San Diego 41
Foggia 39
Nanchang 39
Dearborn 35
Inglewood 35
Helsinki 30
Brooklyn 27
Santa Clara 24
Brussels 23
Hebei 22
Shenyang 22
Jiaxing 20
London 19
Dong Ket 16
Dublin 16
Los Angeles 16
Changsha 13
Munich 13
Conversano 12
Tianjin 12
Grafing 11
Nijmegen 11
Washington 11
Monopoli 9
Norwalk 9
Mottola 8
Venezia 7
Giovinazzo 6
Paris 6
Rome 6
Shanghai 6
Leawood 5
Pescara 5
Pune 5
Wuhan 5
Augusta 4
Frankfurt am Main 4
Indiana 4
Kunming 4
Milan 4
Ningbo 4
San Mateo 4
Toronto 4
Zhengzhou 4
Bologna 3
Falls Church 3
Guangzhou 3
Jinan 3
Jinhua 3
Palermo 3
Sofia 3
Suffolk 3
Triggiano 3
Turin 3
Ardabil 2
Athens 2
Auburn Hills 2
Barletta 2
Bisceglie 2
Bova Marina 2
Brescia 2
Chiswick 2
Florence 2
Gravina In Puglia 2
Hefei 2
Hounslow 2
Islington 2
Johnson City 2
Madrid 2
Metairie 2
New Orleans 2
Ohain 2
Ottawa 2
Padova 2
Rabat 2
Redwood City 2
Stockholm 2
São Paulo 2
Tappahannock 2
Totale 5.640
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Nome #
HmtDB, a genomic resource for mitochondrion-based human variability studies 137
Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers 127
NEW MORPHOLOGICAL APPROACHES TO THE STUDY OF MITOCHONDRIAL ENCEPHALOMYOPATHIES 126
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation 125
High Mitochondrial DNA Copy Number is a Protective Factor From Vision Loss in Heteroplasmic Leber’s Hereditary Optic Neuropathy (LHON) 123
ACTN3/ACE GENOTYPES AND MITOCHONDRIAL GENOME IN PROFESSIONAL SOCCER PLAYERS’ PERFORMANCE 113
Author Response: Increased mtDNA Copy Number Protects Against LHON 112
MOLECULAR ANALYSIS OF THE MUSCLE PATHOLOGY ASSOCIATED WITH MITOCHONDRIAL-DNA DELETIONS 110
Interaction of COMT Val108/158Met genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 107
Dysfunction of mitochondrial respiratory chain complex I in neurological disorders: genetics and pathogenetic mechanisms 102
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 102
Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene 101
null 101
The oxidative phosphorylation system in mammalian mitochondria 100
Respiratory chain complex I, a main regulatory target of the cAMP/PKA pathway is defective in different human diseases. 100
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy 98
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesis 97
IS A POINT MUTATION IN THE MITOCHONDRIAL ND2 GENE ASSOCIATED WITH ALZHEIMERS-DISEASE 96
Age-dependent structural variations in rat brain mitochondrial DNA 96
Mitochondrial DNA copy number differentiates the Leber's hereditary optic neuropathy affected individuals from the unaffected mutation carriers 96
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 91
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit 91
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H 91
Cerebellar ataxia as atypical manifestation of the 3243A > G MELAS mutation 90
Mitochondrial DNA metabolism in early development of zebrafish (Danio rerio). 89
The regulation of PTC containing transcripts of the human NDUFS4 gene of complex I of respiratory chain and the impact of pathological mutations 88
Fishing in the Cell Powerhouse: Zebrafish as A Tool for Exploration of Mitochondrial Defects Affecting the Nervous System 87
Decrease of D-loop frequency in heart and cerebral hemispheres mitochondrial DNA of aged rat 86
Deep sequencing unearths NumtS under LHON-associated false heteroplasmic mitochondrial DNA variants 86
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 85
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I RID D-6064-2011 83
The cAMP cascade and mitochondrial oxidative phosphorylation. Physiopathological implications 82
Differential expression of ATPAF1 and ATPAF2 genes encoding F-1-ATPase assembly proteins in mouse tissues 81
Bilateral progressive visual loss in an epileptic, mentally retarded boy 81
Author response: Do high mtDNA copy numbers truly prevent LHON manifestations? 81
Respiratory complex I in brian development and genetic disease 80
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. 77
ACETYL-L-CARNITINE INCREASES CYTOCHROME-OXIDASE SUBUNIT-I MESSENGER-RNA CONTENT IN HYPOTHYROID RAT-LIVER 76
Reduced synthesis of mtRNA in isolated mitochondria of senescent rat brain 76
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 75
Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I 72
null 72
LIPID-COMPOSITION IN SYNAPTIC AND NONSYNAPTIC MITOCHONDRIA FROM RAT BRAINS AND EFFECT OF AGING 72
Late-onset Leber hereditary optic neuropathy mimicking Susac's syndrome 70
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 69
Survey of genes involved in mitochondrial biogenesis in early development of zebrafish as candidates for mitochondrial pathologies 65
cAMP-dependent phosphorylation and dephosphorylation of mitochondrial proteins. Molecular aspects and physiopathological implications 65
Faithful and highly efficient RNA synthesis in isolated mitochondria from rat liver 65
null 64
TRIM8 blunts the pro-proliferative action of ΔNp63α in a p53 wild-type background 63
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia 62
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 60
null 60
Mitochondrial dysfunction as a mechanism of CNS injury. 60
Structure, Redox-Coupled Protonmotive activity, and Pathological Disorders of Respiratory Chain Complexes 59
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 59
Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases 59
Dysfunctional prefrontal activation during working memory in schizophrenia controlling for performance and COMT Val(108/158)Met genotype 58
CLINICAL AND MOLECULAR IMPLICATION IN A FAMILY WITH 3460 LEBER HEREDITARY OPTIC NEUROPATHY 58
ALTERAZIONI STRUTTURALI DEL DNA MITOCONDRIALE IN TESSUTI DI RATTO VECCHIO 58
The nuclear NDUFS4 gene of complex I (NADH-ubiquinone oxidoreductase): expression products and function 57
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 56
Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects 56
Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants 54
Clinical and molecular characterization of a novel INCL mutation in an Italian patient 54
The NADH: Ubiquinone oxidoreductase (complex 1) of the mammalian respiratory chain and the cAMP cascade 54
Top level professional soccer players: association between gene polymorphisms and myDNA copy number as potential factors in modulating exercise-related phenotypes 54
Complex I and the cAMP cascade in human physiopathology 53
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGING 53
Complementation tests and sequence analysis of seven genes controlling the formation of cytochrome c oxidase in Leigh disease 52
A novel insertion mutation (A(169i)) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient 51
Disorders of nuclear-mitochondrial intergenomic signalling 47
The NDUFS4 nuclear gene of complex I encodes a subunit essential for the assembly and cAMP-dependent regulation of the activity of the complex 47
STRUCTURAL ALTERATIONS OF MITOCHONDRIAL DNA IN AGED RAT TISSUES 45
Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complex 45
MITOCHONDRIAL DNA TRANSCRIPTION IN AGING RAT 45
The cAMP cascade regulates mitochondrial respiration in mammalian cells. The role of complex I 43
Mitochondrial ND5 geme nucleotide variants in a patient with ptical atrophy and renal involvement 41
GRM3 genotype and olanzapine treatment: Differential effects on prefrontal cortical function during working memory in patients with schizophrenia 41
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 40
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 39
Mitochondrial DNA transcription and translation in aged rat: effect of acetyl-L-carnitine 38
The effect of GRM3 genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia 37
NMD of mutated and alternatively spliced transcripts in human complex I deficiency 36
REDUCED TRANSCRIPTION OF MITOCHONDRIAL DNA IN THE SENESCENT RAT. TISSUE DEPENDENCE AND EFFECT OF ACETYL-L-CARNITINE 36
MITOCHONDRIAL DISEASE MIMIKING POLYMYOSITIS: A CASE REPORT 36
Expression of ATPAF1 and ATPAF2 genes encoding F1-ATPase assembly proteins in mammalian tissues 35
null 35
Mutations in the NDUFS4 gene of complex I are associated with fatal neurological Leigh-like syndrome 34
REDUCED SYNTHESIS OF MESSENGER TRANSFER-RNA IN ISOLATED-MITOCHONDRIA OF SENESCENT RAT-BRAIN 34
DNA MITOCONDRIALE E INVECCHIAMENTO 33
Deficit complesso V mitocondriale e fenotipo epilettico. Descrizione di un caso clinico 33
null 32
MECCANISMO D'AZIONE DELL'ACETIL-L-CARNITINA SULL'ESPRESSIONE DEL DNA MITOCONDRIALE IN CERVELLO DI RATTO INVECCHIATO 32
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 32
Deep sequencing unearths Nuclear mitochondrial sequences under Leber's hereditary optic neuropathy-associated false heteroplasmic mitochondrial DNA variants 31
CMT2A harboring mitofusin 2 mutation with optic nerve atrophy and normal visual acuity 31
Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA 30
THE NDUFS4 NUCLEAR GENE OF COMPLEX I ENCODED A SUBUNIT ESSENTIAL FOR THE ASSEMBLY AND CAMP-DEPENDENT REGULATION OF THE ACTIVITY OF THE COMPLEX 28
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts 24
Totale 6.769
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Categoria #
all - tutte 31.853
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 31.853
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.243 0 0 0 0 216 123 202 168 233 89 159 53
2020/20211.062 90 90 99 77 116 45 59 61 105 178 61 81
2021/2022773 36 132 4 22 43 46 49 39 56 37 130 179
2022/20231.302 185 101 87 160 153 177 10 143 225 10 26 25
2023/2024465 42 95 32 32 51 108 16 18 4 22 13 32
2024/2025302 35 19 149 66 33 0 0 0 0 0 0 0
Totale 7.088