IRIS
GOFFRINI, Paola
 Distribuzione geografica
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Continente #
NA - Nord America 5.644
AS - Asia 4.531
EU - Europa 3.206
SA - Sud America 645
Continente sconosciuto - Info sul continente non disponibili 245
AF - Africa 206
OC - Oceania 8
Totale 14.485
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Nazione #
US - Stati Uniti d'America 5.480
SG - Singapore 1.719
CN - Cina 1.182
VN - Vietnam 747
IE - Irlanda 611
IT - Italia 606
BR - Brasile 473
SE - Svezia 433
HK - Hong Kong 354
FI - Finlandia 353
UA - Ucraina 324
DE - Germania 288
ZA - Sudafrica 154
FR - Francia 138
NL - Olanda 138
BD - Bangladesh 124
GB - Regno Unito 112
CA - Canada 108
TR - Turchia 108
RU - Federazione Russa 60
CL - Cile 59
IN - India 47
AR - Argentina 43
IQ - Iraq 36
BE - Belgio 32
AT - Austria 28
MX - Messico 28
KR - Corea 27
EC - Ecuador 24
JP - Giappone 24
PH - Filippine 19
ID - Indonesia 18
PK - Pakistan 17
ES - Italia 16
CO - Colombia 15
PL - Polonia 15
UZ - Uzbekistan 15
JO - Giordania 11
VE - Venezuela 11
SA - Arabia Saudita 10
EG - Egitto 9
LT - Lituania 9
TH - Thailandia 9
MA - Marocco 8
PY - Paraguay 8
TW - Taiwan 8
IL - Israele 7
KE - Kenya 7
AU - Australia 6
CI - Costa d'Avorio 6
DO - Repubblica Dominicana 6
PT - Portogallo 6
TN - Tunisia 6
UY - Uruguay 6
AE - Emirati Arabi Uniti 5
AZ - Azerbaigian 5
GE - Georgia 5
MY - Malesia 5
RO - Romania 5
BY - Bielorussia 4
EU - Europa 4
IR - Iran 4
LB - Libano 4
PE - Perù 4
CY - Cipro 3
CZ - Repubblica Ceca 3
DZ - Algeria 3
ET - Etiopia 3
GR - Grecia 3
GT - Guatemala 3
HN - Honduras 3
JM - Giamaica 3
LY - Libia 3
NP - Nepal 3
PS - Palestinian Territory 3
TT - Trinidad e Tobago 3
AL - Albania 2
BA - Bosnia-Erzegovina 2
CG - Congo 2
CH - Svizzera 2
CR - Costa Rica 2
DK - Danimarca 2
KG - Kirghizistan 2
LK - Sri Lanka 2
LV - Lettonia 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
PA - Panama 2
RS - Serbia 2
SI - Slovenia 2
SY - Repubblica araba siriana 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
BO - Bolivia 1
DM - Dominica 1
EE - Estonia 1
GA - Gabon 1
GP - Guadalupe 1
GY - Guiana 1
HR - Croazia 1
Totale 14.228
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Città #
Singapore 802
Dublin 611
Ashburn 595
San Jose 513
Chandler 482
Santa Clara 476
Jacksonville 354
Hong Kong 334
Beijing 283
Ho Chi Minh City 222
Dearborn 210
Council Bluffs 208
Boardman 190
Hanoi 161
Los Angeles 151
Ann Arbor 150
Dallas 149
Parma 147
Johannesburg 137
Nanjing 127
Princeton 111
San Mateo 98
Lauterbourg 94
New York 94
Izmir 90
Wilmington 85
Shanghai 81
Toronto 62
Munich 54
Helsinki 45
Jinan 45
Shenyang 41
Hefei 38
Moscow 38
Nanchang 37
Buffalo 36
Columbus 34
São Paulo 34
Kunming 30
Milan 30
Santiago 30
Tianjin 29
Kissimmee 27
Da Nang 26
Haiphong 26
Woodbridge 25
Changsha 24
Chicago 23
Guangzhou 23
Rome 23
Des Moines 22
Jiaxing 22
London 22
Nuremberg 22
Rio de Janeiro 22
Brooklyn 21
Brussels 21
Tokyo 20
Vienna 20
Falls Church 19
Zhengzhou 18
Bologna 17
Houston 17
The Dalles 16
Orem 15
Atlanta 14
Biên Hòa 14
Hebei 14
Baghdad 13
Phoenix 13
Tashkent 13
Brasília 12
Curitiba 12
Jakarta 12
Norwalk 12
Seattle 12
Seoul 12
Boston 11
Hải Dương 11
Modena 11
Montreal 11
Newark 11
Pittsburgh 11
Redmond 11
Warsaw 11
Amman 10
Ardea 10
Mexico City 10
Turku 10
Vitacura 10
Amsterdam 9
Belo Horizonte 9
Denver 9
Guayaquil 9
Quito 9
San Francisco 9
Berlin 8
Bogotá 8
Fremont 8
Hangzhou 8
Totale 8.406
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Nome #
Yeast-Based Functional Investigation of ELAC2 Variants in Mitochondrial Dysfunction 252
DNA polymerase [gamma] and disease: what we have learned from yeast 201
Yeast as a model for mitochondrial aminoacyl-tRNA synthetase disorders: validation of mutations in NARS2 and WARS2 195
Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy 189
Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy 189
Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration 184
Exploring Yeast as a Study Model of Pantothenate Kinase-Associated Neurodegeneration and for the Identification of Therapeutic Compounds 180
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 178
Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models 178
Functional characterization of archaic-specific variants in mitonuclear genes: insights from comparative analysis in S. cerevisiae 167
The Power of Yeast in Modelling Human Nuclear Mutations Associated with Mitochondrial Diseases 165
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy 165
S. cerevisiae carrying a MGM1/OPA1 chimeric gene: a model for the study of dominant optic atrophy and for drug discovery 164
Drug repositioning as a therapeutic strategy for neurodegenerations associated with OPA1 mutations 164
Yeast as a model of mitochondrial dysfunctions: neurodegenerative diseases and cancer. 163
Yeast as a model system for diseases associated with defective coenzyme a metabolism 163
Behaviour of Saccharomyces cerevisiae wine strains during adaptation to unfavourable conditions of fermentation on synthetic medium: Cell lipid composition, membrane integrity, viability and fermentative activity 162
The identification of beneficial molecules for mitochondrial diseases: Saccharomyces cerevisiae as powerful model 161
Autosomal dominant myopathy caused by a novel ISCU variant 159
Carbon catabolite repression in Kluyveromyces lactis: isolation and characterization of the KlDLD gene encoding the mitochondrial enzyme D-lactate ferricytochrome c oxidoreductase. 158
Saccharomyces cerevisiae as a tool for studying mutations in nuclear genes involved in diseases caused by mitochondrial DNA instability 157
A yeast model for PKAN and CoPAN neurodegeration 156
Modeling in yeast of KARS pathogenic variants associated with a progressive and multi-systemic disease: impact on cytosolic and mitochondrial isoforms 155
Cloning and characterization of the lactate-specific inducible gene KlCYB2, encoding the cytochrome b2 of Kluyveromyces lactis 152
Dominance of yeast aac2R96H and aac2R252G mutations, equivalent to pathological mutations in ant1, is due to gain of function 151
Clinical, radiological, and genetic characteristics of 16 patients with ACO2 gene defects: Delineation of an emerging neurometabolic syndrome 151
Expanded phenotype of AARS1-related white matter disease. 150
A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy. 149
Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency. 145
Bi-allelic KARS1 pathogenic variants affecting functions of cytosolic and mitochondrial isoforms are associated with a progressive and multisystem disease 144
Mitochondrial Aminoacyl-tRNA Synthetase: The Power Of Yeast In Modeling Human Pathological Mutations 143
Modeling human coasy mutations in yeast Saccharomyces cerevisiae 142
Investigation in yeast of novel variants in mitochondrial aminoacyl-tRNA synthetases WARS2, NARS2, and RARS2 genes associated with mitochondrial diseases 137
Modeling human Coenzyme A synthase mutation in yeast reveals altered mitochondrial function, lipid content and iron metabolism 137
"Miglioramento genetico di Kluyveromyces lactis per la produzione di proteine eterologhe 137
RAG1 and RAG2: nuclear genes involved in the dependence/independence on mitochondrial respiratory function for growth on sugars 136
Mitochondrial disorders caused by mutations impairing miotchondrial dynamics 136
Saccharomyces cerevisiae as a system to discover beneficial molecules for mitochondrial diseases 135
"A Kluyveromyces lactis gene homologous to AAC2 complements the Saccharomyces cerevisiae op1 mutation" 133
Case Series and DARS2 Variant Analysis in Early Severe Forms With Unexpected Presentations 133
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. 132
Extension of Chronological Lifespan by Hexokinase Mutation in Kluyveromyces lactis Involves Increased Level of the Mitochondrial Chaperonin Hsp60. 132
The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes. 132
Comparative Functional Genomics of glucose repression in laboratory and wine yeasts 131
Alterations of O-glycosylation, cell wall, and mitochondrial metabolism in Kluyveromyces lactis cells defective in KlPmr1p, the Golgi Ca2+-ATPase 131
Mitochondrial aminoacyl‐trna synthetase and disease: The yeast contribution for functional analysis of novel variants 130
Identificazione e caratterizzazione molecolare di soppressori multicopia dei mutanti fog in Kluyveromyces lactis 128
Genetic improvement of the yeast Kluyveromyces lactis for biotechnological purposes 126
The respiratory activities of four Hansenula species. 126
The power of yeast in modeling human mutations: mitochondrial aminoacyl tRNA synthetases and mitochondrial tRNA modifiers 123
A phosphoglucose isomerase gene is involved in the Rag phenotype of the yeast Kluyveromyces lactis. 122
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene 121
RAG4 Gene Encodes a Glucose Sensor in Kluyveromyces lactis 120
Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation 120
A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency 120
Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy. 119
Guidelines and recommendations on yeast cell death nomenclature. 118
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 117
The power of yeast in modeling human mutations leading to mitochondrial disease 117
Elementi regolativi implicati nel processo di repressione /derepressione da glucosio in Kluyveromyces lactis: differenze rispetto a Saccharomyces cerevisiae 115
A respiratory-deficient mutation associated with high salt sensitivity in Kluyveromyces lactis 115
Mitmed: a multicenter consortium for the identification and characterization of nuclear genes responsisble for human mitochondrial disorders 115
Oxygen is required to restore flor strain viability and lipid biosynthesis under fermentative conditions 112
Three target genes for the transcriptional activator Cat8p of Kluyveromyces lactis: acetyl coenzyme A synthetase genes KlACS1 and KlACS2 and lactate permease gene KlJEN1 112
Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 111
LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance. 111
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy. 110
Effetto del metabolismo fermentativo/ ossidativo e della repressione da glucosio nella produzione di proteine eterologhe in Kluyveromyces lactis 110
Galactose transport in Kluyveromyces lactis: a genomic approach 110
Evidence for a Conserved Function of Eukaryotic Pantothenate Kinases in the Regulation of Mitochondrial Homeostasis and Oxidative Stress 108
Genetic improvement of recombinant protein production in Kluyveromyces lactis 107
Genetic improvement of the yeast Kluyveromyces lactis for biotechnological purposes 107
ISOLATION AND CHARACTERIZATION OF CARBON CATABOLITE REPRESSION MUTANTS IN SACCHAROMYCES CEREVISIAE. 106
The Golgi Ca2+-ATPase KlPmr1p function is required for oxidative stress response by controlling the expression of the heat-shock element HSP60 in Kluyveromyces lactis 105
Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease 105
FLO11 expression and lipid biosynthesis are required for air-liquid biofilm formation in a Saccharomyces cerevisiae flor strain 105
Galactose transport in Kluyveromyces lactis: a genomic approach 105
Inactivation of the Kluyveromyces lactis KICOX14 gene leads to an alteration in the expression of KLADH3 and KLADH4 104
Isolation and molecular characterization of KlCOX14, a gene of Kluyveromyces lactis encoding a protein necessary for the assembly of the cytochrome oxidase complex 104
Respiration-dependent utilization of sugars in yeast: a determinant role of sugar transporter 103
Severe mitochondrial encephalomyopathy caused by de novo variants in OPA1 gene 102
Galactose transport in Kluyveromyces lactis 102
Genes release galactose and raffinose utilization from mitochondrial control in Kluyveromyces lactis 102
Rag4 gene encodes a glucose sensor in Kluyveromyces lactis 102
Role du facteur transcriptionel HAP2p dans l’activation du gène codant pour l’enzyme mitochondrial D-lacticodeshydrogénase chez S. cerevisiae et K. lactis 101
Galactose transport in Kluyveromyces lactis: major role of the glucose permease Hgt1 100
Regulation of primary carbon metabolism in Kluyveromyces lactis 100
The in vivo effect of acriflavine on mitochondrial functions in the petite-negative yeast Hansenula saturnus 99
Influence of mutations in hexose transporter genes on glucose repression in Kluyveromyces lactis. 98
The effects of glucose repression and fermentative/oxidative metabolism on heterologous protein production in Kluyveromyces lactis 98
MUF1 gene, a multycopy suppressor of fog mutants in Kluyveromyces lactis, encodes a transcriptional activator 96
Respiratory pathways in Hansenula saturnus 95
Improved Production of Heterologous Proteins by a Glucose Repression-Defective Mutant of Kluyveromyces lactis 95
RAG1 gene of the yeast Kluyveromyces lactis codes for a sugar transporter 94
IMP2, a gene involved in the expression of glucose-repressible gene in Saccharomyces cerevisiae 94
Saccharomyces cerevisiae genes release galactose and raffinose utilization from respiration control in Kluyveromyces lactis 94
Lipid Metabolism Related To Stuck Fermentation In Saccharomyces cerevisiae Wine Strains 93
Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase. 93
Identificazione e caratterizzazione del gene ERO1 di Kluyveromyces lactis potenzialmente coinvolto nel ripiegamento delle proteine nel reticolo endoplasmatico 92
Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation. 92
Totale 13.003
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Categoria #
all - tutte 50.079
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 50.079
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022552 0 11 5 25 22 22 84 89 30 55 40 169
2022/20231.834 216 176 117 137 156 193 21 116 622 9 52 19
2023/2024755 42 71 12 33 50 163 85 51 18 67 75 88
2024/20252.626 32 135 168 147 322 413 57 109 387 230 161 465
2025/20265.167 460 436 579 475 686 282 670 134 725 394 175 151
2026/2027391 193 198 0 0 0 0 0 0 0 0 0 0
Totale 14.485