CNR Institutional Research Information System

MARRA, ERSILIA
 Distribuzione geografica
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Continente #
AS - Asia 2.187
NA - Nord America 1.376
EU - Europa 362
SA - Sud America 354
AF - Africa 36
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 1
Totale 4.321
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Nazione #
US - Stati Uniti d'America 1.305
SG - Singapore 972
CN - Cina 550
BR - Brasile 287
HK - Hong Kong 219
VN - Vietnam 170
FR - Francia 120
KR - Corea 82
IT - Italia 48
NL - Olanda 44
BD - Bangladesh 43
JP - Giappone 35
IN - India 31
CA - Canada 30
AR - Argentina 28
GB - Regno Unito 26
ID - Indonesia 18
FI - Finlandia 16
DE - Germania 15
MX - Messico 14
IL - Israele 13
EC - Ecuador 11
ES - Italia 11
PL - Polonia 10
ZA - Sudafrica 10
CL - Cile 8
SA - Arabia Saudita 8
TR - Turchia 8
RU - Federazione Russa 7
IQ - Iraq 6
MA - Marocco 6
PY - Paraguay 6
SE - Svezia 6
UA - Ucraina 6
CO - Colombia 5
CZ - Repubblica Ceca 5
DO - Repubblica Dominicana 5
IE - Irlanda 5
PE - Perù 5
AU - Australia 4
CR - Costa Rica 4
HU - Ungheria 4
KE - Kenya 4
PK - Pakistan 4
RO - Romania 4
UZ - Uzbekistan 4
AO - Angola 3
AT - Austria 3
AZ - Azerbaigian 3
BG - Bulgaria 3
DZ - Algeria 3
EE - Estonia 3
GR - Grecia 3
GT - Guatemala 3
JM - Giamaica 3
LV - Lettonia 3
NO - Norvegia 3
PH - Filippine 3
PT - Portogallo 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
BY - Bielorussia 2
CY - Cipro 2
EG - Egitto 2
HR - Croazia 2
JO - Giordania 2
KZ - Kazakistan 2
NI - Nicaragua 2
PR - Porto Rico 2
PS - Palestinian Territory 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
VE - Venezuela 2
AG - Antigua e Barbuda 1
AL - Albania 1
BO - Bolivia 1
BS - Bahamas 1
BW - Botswana 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CW - ???statistics.table.value.countryCode.CW??? 1
DK - Danimarca 1
ET - Etiopia 1
GD - Grenada 1
GP - Guadalupe 1
HN - Honduras 1
IM - Isola di Man 1
IR - Iran 1
LT - Lituania 1
LU - Lussemburgo 1
MN - Mongolia 1
MY - Malesia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
OM - Oman 1
RS - Serbia 1
SI - Slovenia 1
SV - El Salvador 1
TC - Turks e Caicos 1
TT - Trinidad e Tobago 1
Totale 4.317
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Città #
Santa Clara 553
Singapore 549
Hong Kong 216
Hefei 200
San Jose 147
Beijing 123
Ashburn 114
Lauterbourg 99
Seoul 82
Ho Chi Minh City 64
Hanoi 40
Los Angeles 39
São Paulo 36
Dallas 32
New York 25
Tokyo 20
Guangzhou 15
Helsinki 15
Rio de Janeiro 15
Haiphong 14
Orem 14
Milan 11
Minamishinagawa 11
Atlanta 9
Bengaluru 9
Montreal 9
Warsaw 9
Chennai 8
Boston 7
Buenos Aires 7
Buffalo 7
Curitiba 7
Denver 7
Wuhan 7
Biên Hòa 6
Brasília 6
Can Tho 6
Dhaka 6
Stockholm 6
Campinas 5
Dublin 5
Guayaquil 5
Houston 5
London 5
Madrid 5
Mumbai 5
Porto Alegre 5
Prague 5
Rome 5
Shanghai 5
Toronto 5
Baltimore 4
Belo Horizonte 4
Betim 4
Brooklyn 4
Caxias do Sul 4
Charlotte 4
Chicago 4
Da Nang 4
Jakarta 4
Johannesburg 4
Miami 4
Milwaukee 4
Nairobi 4
Phoenix 4
Poplar 4
Riyadh 4
Santiago 4
Tashkent 4
The Bronx 4
Tucson 4
Amsterdam 3
Ankara 3
Asunción 3
Baghdad 3
Baku 3
Boardman 3
Elk Grove Village 3
Falkenstein 3
Frankfurt am Main 3
Guarulhos 3
Hòa Bình 3
Hải Dương 3
Istanbul 3
Jeddah 3
Juiz de Fora 3
Lima 3
Lisbon 3
Luanda 3
Manchester 3
Mogi das Cruzes 3
Palermo 3
Paris 3
Queens 3
Querétaro 3
Rabat 3
Recife 3
Riga 3
San Bernardino 3
San José 3
Totale 2.777
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Nome #
Upregulation of Skp2 after prostate cancer cell adhesion to basement membranes results in BRCA2 degradation and cell proliferation 81
Beta1 integrins modulate cell adhesion by regulating insulin-like growth factor-II levels in the microenvironment. 75
Cytochrome c, released from cerebellar granule cells undergoing apoptosis or excytotoxic death, can generate protonmotive force and drive ATP synthesis in isolated mitochondria. 75
A transient proteasome activation is needed for acetic acid-induce programmed cell death to occur in Saccharomyces cerevisiae 73
Genetic heterogeneity in five Italian regions: Analysis of PAH mutations and minihaplotypes 72
YCA1 participates in the acetic acid induced yeast programmed cell death also in a manner unrelated to its caspase-like activity. 67
Cytochrome c is released from coupled mitochondria of yeast en route to acetic acid-induced programmed cell death and can work as an electron donor and a ROS scavenger. 66
Achievements and perspectives in yeast acetic acid-induced programmed cell death pathways 64
Mitochondrial DNA depletion sensitizes cancer cells to PARP inhibitors by translational and post-translational repression of BRCA2 62
Loss of BRCA2 promotes prostate cancer cell invasion through up-regulation of matrix metalloproteinase-9. 61
Glutamate neurotoxicity in rat cerebellar granule cells involves cytochrome c release from mitochondria and mitochondrial shuttle impairment. 58
Silencing of BRCA2 decreases anoikis and its heterologous expression sensitizes yeast cells to acetic acid-induced programmed cell death. 57
Regulation of beta1C and beta1A integrin expression in prostate carcinoma cells 54
An increase in the ATP levels occurs in cerebellar granule cells en route to apoptosis in which ATP derives from both oxidative phosphorylation and ... 54
Yeast growth in raffinose results in resistance to acetic-acid induced programmed cell death mostly due to the activation of the mitochondrial retrograde pathway. 52
Mitochondrial retrograde signaling contributes to acetic acid-induced programmed cell death resistance in yeast 52
Hepatocyte 'priming' and increase in transforming growth factor-beta1 mRNA expression are delayed in hypothyroid versus euthyroid rats during liver regeneration. 51
The in vitro-synthesized precursor and mature mitochondrial aspartate aminotransferase share the same import pathway in isolated mitochondria. 50
Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria model 50
Use of protease sensitivity to probe the conformations of newly synthesised mutant forms of mitochondrial aspartate aminotransferase. 49
Production of reactive oxygen species, alteration of cytosolic ascorbate peroxidase, and impairment of mitochondrial metabolism are early events in heat shock-induced programmed cell death in tobacco Bright-Yellow 2 cells. 48
Skp2 overexpression is associated with loss of BRCA2 protein in human prostate cancer 48
A DOUBLE ALTERATION OF THE ADP/ATP TRANSLOCATOR, WHICH DEPENDS ON BOTH ROS PRODUCTION AND CASPASES, TRIGGERS THE MITOCHONDRIAL PERMEABILITY TRANSITION, DISPENSABLE DURING CEREBELLAR GRANULE CELL APOPTOSIS 45
Transcriptional regulation of beta(1) integrin expression in the physio/pathological states of human endometrial tissues 45
Photomodulation of cellular and subcellular activities by He-Ne laser 44
Alzheimer's proteins, oxidative stress, and mitochondrial dysfunction interplay in a neuronal model of Alzheimer's disease 44
Molecular mechanisms of programmed cell death induced by acetic acid in Saccharomyces cerevisiae 44
Thyroid hormone treatment of hypothyroid rats restores the regenerative capacity and the mitochondrial membrane permeability properties of the liver after partial hepatectomy. 44
Yeast programmed cell death pathway: a new experimental platform for biomedical and agri-food sciences 43
The yeast Saccharomyces cerevisiae is a model to elucidate the mechanism of programmed cell death in eukaryotes. 43
Multifactorial Impairment of mitochondrial oxidative phosphorylation in human skin fibroblasts with chromosome 21 trisomy 43
Molecular mechanisms of Saccharomyces cerevisiae stress adaptation and programmed cell death in response to acetic acid. 43
ATP at a Crossroads: Cell Life or Death? 43
Mitochondrial retrograde signaling involvement in acetic acid-induced programmed cell death in yeast Saccharomyces cerevisiae 42
Proteasome function is required for activation of programmed cell death in heat shocked tobacco Bright-Yellow 2 cells 42
Different sources of reactive oxygen species contribute to low-potassium induced apoptosis in cerebellar granule cells 41
Mitochondrial DNA depletion in prostate epithelial cells promotes anoikisis resistance and invasion through activation of PI3K/Akt2 41
Thyroid hormone administration to hypothyroid rats restores the mitochondrial membrane permeability properties 41
Mitochondrial impairment induces excitotoxic death in cerebellar granule cells 41
Yeast programmed cell death: integration of cell adaptation and death pathways through mitochondrial stress response pathways 40
The temporal correlation of molecular events occurring in neuronal apoptosis 40
Genotypic hetereogeneity of the molecular basis of cystic fibrosis: the paradigm of lithuanian population genetic testing 40
On the role of mitochondria in cell life and death decisions in a yeast model 40
Mitochondrial stress response and cell adaptation in Saccharomyces cerevisiae 40
NITRIC OXIDE SYNTHASE UPREGULATION IN THE EARLY PHASE OF CEREBELLAR GRANULE CELLS APOPTOSIS 40
Pro-death and pro-life cellular strategies in yeast: the role of mitochondria 39
Nitric oxide production, NOS activity and nNOS protein expression in the early phase of cerebellar granule cells apoptosis 39
Impairment of ATPase, adenine nucleotide translocator and adenylate kinase causes mitochondrial energy deficit in human skin fibroblasts with chromosome 21 trisomy 39
Impairment of F1F0-ATPase, adenine nucleotide translocator and adenylate kinase causes mitochondrial energy deficit in human skin fibroblasts with chromosome 21 trisomy 39
Silencing of the tumor suppressor BRCA2 decreases anoikis and its heterologous expression exacerbates acetic acid-induced programmed cell death in yeast cells 39
Characterization of phenylketonuria alleles in the Italian population. 39
Molecular basis of cystic fibrosis in Lithuania. Incomplete CFTR mutation detection by PCR-based screening protocols 39
Alternatively Spliced Variants of Beta1 Integrin Are Involved in the Modulation of Human Endometrial Transformation in Different Physiological/Pathological Conditions 39
Upregulation of Skp2 after Prostate Cancer Cell Adhesion to Extracellular Matrix Proteins 38
Proteasome inhibitors prevent cytochrome c release during apoptosis but not in excitotoxic death of cerebellar granule neurons 38
ROLE OF MITOCHONDRIAL DYSFUNCTIONS IN DOWN SYNDROME PATHOGENESIS: NEW MOLECULAR TARGETS AND THERAPEUTIC STRATEGIES 38
Kinetic properties and thermal stabilities of mutant forms of mitochondrial aspartate aminotransferase. 37
Deficit of complex I activity in human skin fibroblasts with chromosome 21 trisomy and overproduction of reactive oxygen species by mitochondria: involvement of the cAMP/PKA signalling pathway 37
Yeast as a tool to study signalling pathways in mitochondrial stress response and cytoprotection 37
Ultrastructural zonal heterogeneity of hepatocytes and mitochondria within the hepatic acinus during liver regeneration after partial hepatectomy. 37
The role of mitochondria in yeast programmed cell death 36
Cytochrome c Is Released in a Reactive Oxygen Species-Dependent Manner and Is Degraded via Caspase-Like Proteases in Tobacco Bright-Yellow 2 Cells en Route to Heat Shock-Induced Cell Death. 36
Inhibition of the uptake of mitochondrial aspartate aminotransferase by cytoplasmically synthesized protein 35
Cytochrome c Trp65Ser substitution results in inhibition of acetic acid-induced programmed cell death in Saccharomyces cerevisiae 35
Constitutive activation of MAPK/ERK inhibits prostate cancer cell proliferation through upregulation of BRCA2. 34
Knock-out of metacaspase and/or cytochrome c results in the activation of a ROS-independent acetic acid-induced programmed cell death pathway in yeast 34
Phenylketonuria mutations and linked haplotypes in the Lithuanian population: origin of the most common R408W mutation. 34
Identification of mitochondrial DNA lesions in hereditary cardiomyoapthies. 34
L-lactate metabolism can occur in normal and cancer prostate cells via the novel mitochondrial L-lactate dehydrogenase 34
Photomodulation of cellular and subcellular activities by He-Ne laser. 33
Changes in mitochondrial function and ultrastructure during rat liver regeneration 33
Yeast acetic acid-induced programmed cell death can occur without cytochrome c release which requires metacaspase YCA1 33
Rapid uncoupling of oxidative phosphorylation accompanies glutamate toxicity in rat cerebellar granule cells 32
A transient proteasome activation is needed for acetic acid-induced programmed cell death to occur in Saccharomyces cerevisiae. 32
The apoptosis/necrosis transition in cerebellar granule cells depends on the mutual relationship of the antioxidant and the proteolytic systems which regulate ROS production and cytochrome c release en route to death. 32
The mitochondria in cerebellar granule cells 31
Acid stress adaptation protects Saccharomyces cerevisiae from acetic acid-induced programmed cell death. 31
Mitochondrial DNA depletion reduces PARP-1 levels and promotes progression of the neoplastic phenotype in prostate carcinoma 31
The N-acetylcysteine-insensitive acetic acid-induced yeast programmed cell death occurs without macroautophagy 31
Cumulative effects of mutations in newly synthesised mitochondrial aspartate aminotransferase on uptake into mitochondria. 30
Mitochondrial Bioenergetics in Human skin fibroblasts with chromosome 21 trisomy: deficiency in complex I and production of mitochondrial ATP and increase in mitochondrial mass, reactive oxygen species and production of lactate 29
In the early phase of programmed cell death in Tobacco Bright Yellow 2 cells the mitochondrial adenine nucleotide translocator, adenylate kinase and nucleoside diphosphate kinase are impaired in a reactive oxygen species-dependent manner. 29
Caspase-dependent alteration of the ADP/ATP translocator triggers the mitochondrial permeability transition which is not required for the low-potassium-dependent apoptosis of cerebellar granule cells 29
Programmed cell death in Saccharomyces cerevisiae. 28
Certain N-terminal peptides inhibit uptake of mature aspartate aminotransferase by isolated mitochondria. 28
Apoptosis and cytochrome c release in cerebellar granule cells. 28
Import of mutant forms of mitochondrial aspartate aminotransferase into isolated mitochondria 28
The molecular evolution of B6 enzymes: ribonuclease A as a model pyridoxal-5 -phosphate-dependent protoenzyme. 28
Down-regulation of BRCA2 expression by collagen type I promotes prostate cancer cell proliferation. 28
Hydrogen peroxide and superoxide anion production during acetic acid-induced yeast programmed cell death. 28
Glutamate Neurotoxicity in Rat Cerebellar Granule Cells: a major role for xanthine oxidase in oxygen radical formation 28
Unbalance of the ascorbate and glutathione redox state and downregulation of the cytosolic ascorbate peroxidase are early events in the programmed cell death induced by heat shock in tobacco BY-2 cells 27
Abnormal transport of inorganic phosphate in left ventricular mitochondria from spontaneously hypertensive rats. 26
Mitochondria from the left heart ventricles of both normotensive and spontaneously hypertensive rats oxidize externally added NADH mostly via a novel malate/oxaloacetate shuttle as reconstructed in vitro. 26
The rate of ATP export in the extramitochondrial phase via the adenine nucleotide translocator changes in aging in mitochondria isolated from heart left ventricle of either normotensive or spontaneously hypertensive rats 26
Non-radioactive detection of five common microsatellite markers for ATP7B gene in Wilson Disease patients. 26
The N-terminal region of mature mitochondrial aspartate aminotransferase can direct cytosolic dihydrofolate reductase into mitochondria in vitro. 25
Yeast programmed cell death triggered by aceti acid: ROS involvement and cytochrome c release. 24
Transport and metabolism of L-lactate occur in mitochondria from cerebellar granule cells and are modified in cells undergoing low potassium dependent apoptosis 24
Molecular evolution of B6 enzymes: binding of pyridoxal-5'-phosphate and Lys41Arg substitution turn ribonuclease A into a model B6 protoenzyme. 24
Totale 4.062
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Categoria #
all - tutte 15.338
article - articoli 11.664
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 947
Totale 27.949
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202441 0 0 0 0 0 0 0 0 1 0 36 4
2024/20251.724 6 1 153 69 436 111 44 101 51 43 356 353
2025/20262.450 119 250 202 417 512 86 305 116 136 154 96 57
2026/2027106 106 0 0 0 0 0 0 0 0 0 0 0
Totale 4.321