FERRERO FORTUNATI, Iliana
 Distribuzione geografica
Continente #
NA - Nord America 4.196
AS - Asia 3.408
EU - Europa 2.879
SA - Sud America 514
AF - Africa 148
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 5
Totale 11.158
Nazione #
US - Stati Uniti d'America 4.058
SG - Singapore 1.433
CN - Cina 1.272
IE - Irlanda 732
FI - Finlandia 464
SE - Svezia 445
UA - Ucraina 423
BR - Brasile 415
DE - Germania 290
HK - Hong Kong 277
VN - Vietnam 190
IT - Italia 173
NL - Olanda 138
ZA - Sudafrica 114
CA - Canada 99
TR - Turchia 93
GB - Regno Unito 73
RU - Federazione Russa 52
AR - Argentina 45
MX - Messico 25
BD - Bangladesh 24
BE - Belgio 22
IN - India 19
FR - Francia 18
IQ - Iraq 18
EC - Ecuador 17
PL - Polonia 14
UZ - Uzbekistan 13
JP - Giappone 11
CO - Colombia 10
EG - Egitto 9
IR - Iran 9
ES - Italia 8
ID - Indonesia 8
PY - Paraguay 8
CL - Cile 7
EU - Europa 7
PK - Pakistan 6
AT - Austria 5
DO - Repubblica Dominicana 5
KE - Kenya 5
MA - Marocco 5
NP - Nepal 5
VE - Venezuela 5
JO - Giordania 4
KZ - Kazakistan 4
UY - Uruguay 4
AE - Emirati Arabi Uniti 3
CI - Costa d'Avorio 3
DK - Danimarca 3
DZ - Algeria 3
IL - Israele 3
JM - Giamaica 3
KG - Kirghizistan 3
LT - Lituania 3
NZ - Nuova Zelanda 3
PE - Perù 3
RS - Serbia 3
TN - Tunisia 3
AU - Australia 2
BH - Bahrain 2
GT - Guatemala 2
MK - Macedonia 2
MY - Malesia 2
PA - Panama 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TH - Thailandia 2
AL - Albania 1
CG - Congo 1
CR - Costa Rica 1
CY - Cipro 1
CZ - Repubblica Ceca 1
EE - Estonia 1
GA - Gabon 1
GR - Grecia 1
HN - Honduras 1
KH - Cambogia 1
LV - Lettonia 1
MC - Monaco 1
ME - Montenegro 1
NG - Nigeria 1
NO - Norvegia 1
PH - Filippine 1
PT - Portogallo 1
QA - Qatar 1
SA - Arabia Saudita 1
TZ - Tanzania 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 11.158
Città #
Dublin 732
Singapore 692
Jacksonville 498
Ashburn 472
Santa Clara 454
Chandler 418
Beijing 354
Hong Kong 274
Dearborn 187
Nanjing 162
Boardman 149
San Mateo 135
Los Angeles 124
Princeton 114
Johannesburg 112
Dallas 108
Ann Arbor 90
Toronto 80
Izmir 75
Wilmington 67
Ho Chi Minh City 64
Shanghai 63
Shenyang 62
Jinan 58
Helsinki 55
New York 50
Hanoi 49
Nanchang 47
Kunming 42
São Paulo 42
Hefei 41
Moscow 41
Parma 36
Des Moines 33
Hebei 31
Tianjin 29
Munich 27
Changsha 24
Buffalo 22
Woodbridge 22
Jiaxing 17
Guangzhou 15
Rio de Janeiro 15
Haikou 14
Norwalk 14
Warsaw 14
Brussels 13
Chicago 13
Columbus 13
Hangzhou 13
Phoenix 13
Zhengzhou 13
Belo Horizonte 12
Houston 11
Nuremberg 11
Tashkent 11
Tokyo 11
Brooklyn 10
San Francisco 10
Auburn Hills 9
Denver 9
London 9
Biên Hòa 8
Brasília 8
Fremont 8
Fuzhou 8
Lanzhou 8
The Dalles 8
Amsterdam 7
Atlanta 7
Boston 7
Cairo 7
Chengdu 7
Curitiba 7
Dhaka 7
Guayaquil 7
Montreal 7
Seattle 7
Taizhou 7
Zanjan 7
Chennai 6
Chongqing 6
Dosolo 6
Ninh Bình 6
Recife 6
Redondo Beach 6
Salvador 6
Taiyuan 6
Abbiategrasso 5
Bremen 5
Campinas 5
Charlotte 5
Da Nang 5
Milan 5
Rome 5
São Bernardo do Campo 5
Turku 5
Amman 4
Asunción 4
Baghdad 4
Totale 6.642
Nome #
A Klaac null mutant of Kluyveromyces lactis is complemented by a single copy of the Saccharomyces cerevisiae AAC1 gene 153
Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy 152
Pathogenic variants in glutamyl-tRNAGlnamidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder 150
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 147
IMP2, a nuclear gene controlling the mitochondrial dependence of galactose, maltose and raffinose utilization in Saccharomyces cerevisiae. 146
Yeast as a model of mitochondrial dysfunctions: neurodegenerative diseases and cancer. 144
Comet assay application in environmental monitoring: DNA damage in human leukocytes and plant cells in comparison with bacterial and yeast tests 140
Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive externalophthalmoplegia in humans 137
Construction and validation of a yeast model system for studying in vivo the susceptibility to stavudine of DNA polymerase gamma allelic variants 134
Allelism of IMP1 and GAL2 genes of Saccharomyces cerevisiae 131
YEAST MODEL FOR NOVEL AARS2 MUTATIONS ASSOCIATED WITH PROGRESSIVE LEUKOENCEPHALOPATHY AND CEREBELLAR ATAXIA 128
Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency. 128
Construction and validation of a yeast model system for studying in vivo the susceptibility to stavudine of Polg allelic variants 126
Carbon catabolite repression in Kluyveromyces lactis: isolation and characterization of the KlDLD gene encoding the mitochondrial enzyme D-lactate ferricytochrome c oxidoreductase. 126
Overexpression of DNA Polymerase Zeta Reduces the Mitochondrial Mutability Caused by Pathological Mutations in DNA Polymerase Gamma in Yeast 125
Costruzione di un mutante imp2 termosensibile di Saccharomyces cerevisiae 124
Catabolite repression by galactose in overexpressed GAL4 strains of Saccharomyces cerevisiae 124
Construction of a yeast model system for studying in vivo susceptibility to stavudine of Polg allelic variants 124
Cloning and characterization of the lactate-specific inducible gene KlCYB2, encoding the cytochrome b2 of Kluyveromyces lactis 122
Yeast equivalents of disease associated human POLG mutations show deleterious cooperative effects in vivo 122
Antimycin- and hydroxamate-insensitive respiration in yeast 121
Comet assay application in environmental monitoring: DNA damage in human leukocytes and plant cells in comparison with bacterial and yeast cells. 121
Klaac null mutant in K. lactis is complemented by a single copy of S. cerevisiae “silent” gene AAC1 121
Extension of Chronological Lifespan by Hexokinase Mutation in Kluyveromyces lactis Involves Increased Level of the Mitochondrial Chaperonin Hsp60. 121
Complementazione del mutante nullo in Klaac del lievito Kluyveromyces lactis con il gene AAC3 di Saaccharomyces cerevisiae 120
In vivo differentiation with trichodermin,axenomycin,emetine,anisomycin and erythromycin of cytoplasmic and mitochondrial protein synthesis in the yeasts S.cerevisiae, K.lactis and E.capsularis 120
EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia 118
Clinical and molecular features of mitochondrial DNA depletion syndromes. 117
The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes. 117
Functional study in a yeast model of a novel succinate-dehydrogenase subunit B gene germline missense mutation (C191Y) diagnosed in a patient affected by a glomus tumor. 115
LYS2 gene and its mutation in Kluyveromyces lactis 113
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency. 113
SYM1, the yeast ortholog of the MPV17 human disease gene, is required for TCA function, mtDNA stability and mitochondrial morphology in stress conditions 113
EFFECT OF CHLORAMPHENICOL, ANTIMYCIN A AND HYDROXAMATE ON THE MORPHOGENETIC DEVELOPMENT OF THE DIMORPHIC ASCOMYCETE ENDOMYCOPSIS CAPSULARIS. 112
COMMON POLG GENETIC VARIANTS INCREASE THERISK OF SODIUM VALPROATE INDUCED LIVER INJURYAND FAILURE 112
"A Kluyveromyces lactis gene homologous to AAC2 complements the Saccharomyces cerevisiae op1 mutation" 111
Genetic improvement of the yeast Kluyveromyces lactis for biotechnological purposes 110
Overexpression of DNA polymerase zeta and Rev1 reduces the mitochondrial mutability caused by pathological mutations in DNA polymerase gamma in yeast. 110
The respiratory activities of four Hansenula species. 109
SYM1, the yeast ortholog of the MPV17 human disease gene, is required for TCA function, mtDNA stability and mitochondrial morphology in stress conditions 109
Overexpression of DNA polymerase zeta reduces the mitochondrial mutability caused by pathological mutations in DNA polymerase gamma in yeast. 109
Heterologous complementation of Klaac null mutation of Kluyveromyces lactis by Saccharomyces cerevisiae AAC3 gene 109
Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation 107
Elementi regolativi implicati nel processo di repressione /derepressione da glucosio in Kluyveromyces lactis: differenze rispetto a Saccharomyces cerevisiae 105
Clinical and molecular features of mitochondrial DNA depletion syndromes. 105
RAG1 and RAG2: nuclear genes involved in the dependence/independence on mitochondrial respiratory function for growth on sugars 104
Saccharomyces cerevisiae, a model system to study the effect of mtDNA polymerase mutations associated with PEO in humans. 104
RAG4 Gene Encodes a Glucose Sensor in Kluyveromyces lactis 102
A phosphoglucose isomerase gene is involved in the Rag phenotype of the yeast Kluyveromyces lactis. 102
The role of mitochondrial particle in the regulation of the L- and D-lactate ferricytochrome c oxidoreductase in the yeast S.cerevisiae 101
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy. 100
Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome 99
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy. Neuromuscul Disorders. 98
FOG1 and FOG2 genes, required for the transcriptional activation of glucose-repressible genes of Kluyveromyces lactis are homologous to GAL83 and SNF1 of Saccharomyces cerevisiae 97
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 97
Studio del sistema ADP/ATP carrier in Kluyveromyces lactis: effetti fenotipici della distruzione del gene KlAAC e della introduzione del gene ScAAC1 nel mutante derivato. 96
Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model 96
Facing the problem of "false positives": Re-assessment and improvement of a multiplex RT-PCR procedure for the diagnosis of A. flavus mycotoxin producers 95
Multiplex RT-PCR approach to detect aflatoxigenic strains of Aspergillus Flavus 94
Mutations in AAC2, equivalent to human adPEO-associated ANT1 mutations, lead to defective oxidative phosphorylation in Saccharomyces cerevisiae and affect mitochondrial DNA stability 93
Genetic improvement of recombinant protein production in Kluyveromyces lactis 92
Effetto del metabolismo fermentativo/ ossidativo e della repressione da glucosio nella produzione di proteine eterologhe in Kluyveromyces lactis 92
Identificazione dei bersagli della proteina Imp2p in Saccharomyces cerevisiae 91
Genetic improvement of the yeast Kluyveromyces lactis for biotechnological purposes 90
Rescue by Pol zeta overexpression of mitochondrial DNA instability due to mutations in Pol gamma in S. cerevisiae 89
MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeast 89
ISOLATION AND CHARACTERIZATION OF CARBON CATABOLITE REPRESSION MUTANTS IN SACCHAROMYCES CEREVISIAE. 88
Genes release galactose and raffinose utilization from mitochondrial control in Kluyveromyces lactis 86
Isolation of DLD gene of Saccharomyces cerevisiae encoding the mitochondrial enzyme D-lactate ferricytochrome c oxidoreductase 86
Role of the mitochondriali protein synthesis in the catabolite repression of the petite-negative yeast K.lactis 85
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosis. 85
Genetic rescue by enzymes involved in mitochondrial DNA repair of Saccharomyces cerevisiae phenotypes induced by mitochondrial DNA polymerase mutations 85
Regulation of the Saccharomyces cerevisiae DLD1 gene encoding the mitochondrial protein D-lactate ferricytochrome c oxidoreductase by HAP1 and HAP2/3/4/5 85
Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy. 84
Validation of a molecular approach to detect aflatoxigenic strains of Aspergillus flavus 84
Role du facteur transcriptionel HAP2p dans l’activation du gène codant pour l’enzyme mitochondrial D-lacticodeshydrogénase chez S. cerevisiae et K. lactis 84
ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy 84
Mutation D104G in ANT1 gene: complementation study in Saccharomyces cerevisiae as a model system 83
Heterologous complementation of the Klaac null mutation of Kluyveromyces lactis by the Saccharomyces cerevisiae AAC3 gene encoding the ADP/ATP carrier. 83
Genes coding for mitochondrial proteins are more strongly biased in Kluyveromyces lactis than in Saccharomyces cerevisiae 83
Influence of mutations in hexose transporter genes on glucose repression in Kluyveromyces lactis. 82
Respiratory pathways in Hansenula saturnus 82
IMP2, a gene involved in the expression of glucose-repressible gene in Saccharomyces cerevisiae 82
Mitochondrial diseases and the role of the yeast models. 82
The in vivo effect of acriflavine on mitochondrial functions in the petite-negative yeast Hansenula saturnus 81
Yeast equivalents of disease-associated human POLG mutations show deleterious cooperative effects. 81
Regulation of primary carbon metabolism in Kluyveromyces lactis 81
Saccharomyces cerevisiae genes release galactose and raffinose utilization from respiration in Kluyveromyces lactis 80
POLG determines the risk of sodium valproate induced liver toxicity 79
Yeast equivalents of disease-associated human Polg mutations show deleterious cooperative effects in vivo 79
Identificazione e caratterizzazione del gene ERO1 di Kluyveromyces lactis potenzialmente coinvolto nel ripiegamento delle proteine nel reticolo endoplasmatico 79
Effetti fenotipici e funzionali di mutazioni del gene ANT1 responsabili della patologia umana adPEO nel lievito Saccharomyces cerevisiae 78
In vivo analysis of mtDNA replication defects in yeast 78
Role of ROS in mtDNA instability in ANT1-associated adPEO 77
IMP2, a gene involved in the expression of glucose-repressible genes in Saccharomyces cerevisiae. 74
Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase. 74
Mitochondrial functions and salt sensitivity in Kluyveromyces lactis 73
RAG1 gene of the yeast Kluyveromyces lactis codes for a sugar transporter 73
The first recessive pathological mutation in the adenine nucleotide translocator: yeast as a model system 73
Glucose transport in the yeast Kluyveromyces lactis. I. Properties of an inducible low-affinity glucose transporter gene 72
Totale 10.287
Categoria #
all - tutte 39.934
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 39.934


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021461 0 0 0 0 0 13 102 12 183 15 124 12
2021/2022543 6 4 3 10 12 6 89 105 30 64 40 174
2022/20231.791 214 153 109 111 146 187 18 117 684 4 40 8
2023/2024812 30 63 13 26 73 170 103 67 15 104 67 81
2024/20252.303 15 132 138 107 298 384 46 65 334 212 147 425
2025/20262.385 399 366 406 385 621 208 0 0 0 0 0 0
Totale 11.230