CARRI', MARIA TERESA
 Distribuzione geografica
Continente #
NA - Nord America 42.852
EU - Europa 3.749
AS - Asia 3.298
SA - Sud America 539
AF - Africa 40
Continente sconosciuto - Info sul continente non disponibili 12
OC - Oceania 12
Totale 50.502
Nazione #
US - Stati Uniti d'America 42.736
SG - Singapore 1.539
DE - Germania 700
CN - Cina 660
UA - Ucraina 603
BR - Brasile 451
RU - Federazione Russa 413
PL - Polonia 404
FR - Francia 381
HK - Hong Kong 347
IE - Irlanda 322
VN - Vietnam 310
IT - Italia 226
GB - Regno Unito 201
FI - Finlandia 173
SE - Svezia 166
KR - Corea 123
JP - Giappone 95
CA - Canada 80
IN - India 55
NL - Olanda 39
BD - Bangladesh 29
ID - Indonesia 27
AR - Argentina 26
MX - Messico 24
GR - Grecia 22
BE - Belgio 17
ES - Italia 17
IQ - Iraq 16
ZA - Sudafrica 16
AT - Austria 15
TR - Turchia 15
EC - Ecuador 13
VE - Venezuela 13
CL - Cile 11
CZ - Repubblica Ceca 11
EU - Europa 11
IL - Israele 11
PK - Pakistan 11
UZ - Uzbekistan 11
AU - Australia 10
CO - Colombia 10
PH - Filippine 8
MA - Marocco 7
PY - Paraguay 7
RO - Romania 7
CH - Svizzera 6
DK - Danimarca 6
MY - Malesia 6
SA - Arabia Saudita 6
KG - Kirghizistan 4
LT - Lituania 4
UY - Uruguay 4
DZ - Algeria 3
EG - Egitto 3
IR - Iran 3
SV - El Salvador 3
TN - Tunisia 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
AZ - Azerbaigian 2
BG - Bulgaria 2
BY - Bielorussia 2
HU - Ungheria 2
JM - Giamaica 2
JO - Giordania 2
KE - Kenya 2
LB - Libano 2
LV - Lettonia 2
NP - Nepal 2
OM - Oman 2
PE - Perù 2
TW - Taiwan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CR - Costa Rica 1
CY - Cipro 1
DM - Dominica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GE - Georgia 1
GH - Ghana 1
GY - Guiana 1
HN - Honduras 1
KI - Kiribati 1
KW - Kuwait 1
KZ - Kazakistan 1
MK - Macedonia 1
MT - Malta 1
MU - Mauritius 1
MZ - Mozambico 1
NI - Nicaragua 1
PA - Panama 1
PS - Palestinian Territory 1
PT - Portogallo 1
RW - Ruanda 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 50.497
Città #
Woodbridge 12.914
Wilmington 10.781
Houston 10.287
Fairfield 1.315
Ann Arbor 1.004
Singapore 879
Ashburn 760
Jacksonville 545
Seattle 501
Chandler 484
Cambridge 440
Kraków 389
Hong Kong 339
San Jose 334
Dublin 314
Dearborn 290
Medford 258
Beijing 254
The Dalles 162
Santa Clara 126
Lawrence 122
New York 109
Council Bluffs 105
Los Angeles 101
Ho Chi Minh City 96
Mülheim 94
Tokyo 80
Buffalo 76
Hanoi 74
Rome 66
San Diego 66
Menlo Park 55
Helsinki 53
Moscow 46
Dallas 45
Norwalk 45
Falls Church 38
Detroit 37
Mountain View 37
Munich 37
Toronto 36
Zhengzhou 36
Lauterbourg 35
London 32
Milan 32
University Park 31
Boardman 29
Phoenix 27
São Paulo 27
Chicago 26
Guangzhou 26
Redwood City 23
Saint Petersburg 22
Jakarta 21
Amsterdam 19
Montreal 18
Thessaloniki 18
Verona 18
Brussels 17
Frankfurt am Main 16
Nanjing 16
Nürnberg 16
Haiphong 15
Orem 15
Hefei 14
Kunming 14
Rio de Janeiro 14
Atlanta 13
Da Nang 13
Denver 13
Nuremberg 13
Shanghai 13
Warsaw 13
Brooklyn 12
San Francisco 12
Chennai 11
Columbus 11
Jinan 11
San Mateo 11
Kaiserslautern 10
Stockholm 10
Brasília 9
Brno 9
Johannesburg 9
Kyiv 9
Ankara 8
Campinas 8
Hounslow 8
Poplar 8
Baghdad 7
Dong Ket 7
Hangzhou 7
Redondo Beach 7
Belo Horizonte 6
Indiana 6
Manchester 6
Mumbai 6
New Delhi 6
Palo Alto 6
Porto Alegre 6
Totale 44.675
Nome #
S -Nitrosoglutathione Reductase Plays Opposite Roles in SH-SY5Y Models of Parkinson's Disease and Amyotrophic Lateral Sclerosis 539
Mutation of Lys-120 and Lys-134 drastically reduces the catalytic rate of Cu,Zn superoxide dismutase 519
Bcl2a1 serves as a switch in death of motor neurons in amyotrophic lateral sclerosis 507
Differential role of superoxide and glutathione in S-nitrosoglutathione-mediated apoptosis: a rationale for mild forms of familial amyotrophic lateral sclerosis associated with less active Cu,Zn superoxide dismutase mutants 500
Amyotrophic lateral sclerosis: from current developments in the laboratory to clinical implications 492
Three-dimensional structure of Xenopus laevis Cu,Zn superoxide dismutase b determined by X-ray crystallography at 1.5 A resolution 489
Activation and induction by copper of Cu/Zn superoxide dismutase in Saccharomyces cerevisiae. Presence of an inactive proenzyme in anaerobic yeast 489
Inactivation of cytochrome c oxidase by mutant SOD1s in mouse motoneuronal NSC-34 cells is independent from copper availability but is because of nitric oxide 487
2-DE and MALDI-TOF-MS for a comparative analysis of proteins expressed in different cellular models of amyotrophic lateral sclerosis 487
Copper depletion increases the mitochondrial-associated SOD1 in neuronal cells 486
Regulation of CU, ZNSOD by metals in S-Cereivisiae and Zea-Mays 484
Structural insights into the multi-determinant aggregation of TDP-43 in motor neuron-like cells 482
Neurodegeneration in amyotrophic lateral sclerosis: the role of oxidative stress and altered homeostasis of metals 479
Developmental expression of Cu,Zn superoxide dismutase in Xenopus. Constant level of the enzyme in oogenesis and embryogenesis 479
Apoptotic mechanisms in mutant LRRK2-mediated cell death 475
A study of the dual role of copper in superoxide dismutase as antioxidant and pro-oxidant in cellular models of amyotrophic lateral sclerosis 471
Dynamic NAD(P)H post-synaptic autofluorescence signals for the assessment of mitochondrial function in a neurodegenerative disease: monitoring the primary motor cortex of G93A mice, an amyotrophic lateral sclerosis model 469
Effect of Lys->Arg mutation on the thermal stability of Cu,Zn superoxide dismutase: Influence on the monomer-dimer equilibrium 468
Resistance to striatal dopamine depletion induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice expressing human mutant Cu,Zn superoxide dismutase 463
Xenopus laevis U1 snRNA genes: characterisation of transcriptionally active genes reveals major and minor repeated gene families 463
The NADPH oxidase pathway is dysregulated by the P2X7 receptor in the SOD1-G93A microglia model of amyotrophic lateral sclerosis. 463
Abnormal sensitivity of cannabinoid CB1 receptors in the striatum of mice with experimental amyotrophic lateral sclerosis 462
Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS 462
Beta-amyloid causes downregulation of calcineurin in neurons through induction of oxidative stress 461
An electron microscope study of chromosomal DNA replication in different eukaryotic systems 459
Xenopus laevis Cu,Zn superoxide dismutase B cDNA sequence 459
Apoptosome inactivation rescues proneural and neural cells from neurodegeneration 458
Purification and characterization of Ag,Zn-superoxide dismutase from Saccharomyces cerevisiae exposed to silver 458
Amyotrophic Lateral Sclerosis: New Insights into Underlying Molecular Mechanisms and Opportunities for Therapeutic Intervention 458
ALS: focus on purinergic signalling 457
Role of zinc-coordination and of the glutathione redox couple in the redox susceptibility of human transcription factor Sp1 457
The unfolded protein response in models of human mutant G93A amyotrophic lateral sclerosis 456
Treatment with lithium carbonate does not improve disease progression in two different strains of SOD1 mutant mice 455
Impairment of glutamate transport and increased vulnerability to oxidative stress in neuroblastoma SH-SY5Y cells expressing a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis 453
Copper-dependent oxidative stress and neurodegeneration 451
Superoxide dismutase 1 modulates expression of transferrin receptor 451
Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials 451
Interaction of cisplatin with human superoxide dismutase 451
Metal uptake of recombinant cambialistic superoxide dismutase from Propionitbacterium shermanii is affected by growth conditions of host Escherichia coli cells 449
Tissue-specific deregulation of selected HDACs characterizes ALS progression in mouse models: pharmacological characterization of SIRT1 and SIRT2 pathways 449
Voltage-activated sodium currents in a cell line expressing a Cu,Zn superoxide dismutase typical of familial ALS 447
Minocycline for patients with ALS. 446
Cu,Zn-superoxide dismutase-dependent apoptosis induced by nitric oxide in neuronal cells 446
Temperature-dependent protein folding in vivo--lower growth temperature increases yield of two genetic variants of Xenopus laevis Cu,Zn superoxide dismutase in Escherichia coli 445
The relationship between chromosomal origins of replication and the nuclear matrix during the cell cycle 444
Oligomerization of mutant SOD1 in mitochondria of motoneuronal cells drives mitochondrial damage and cell toxicity 443
Impaired copper binding by the H46R mutant of human Cu,Zn superoxide dismutase, involved in amyotrophic lateral sclerosis 442
Amyotrophic lateral sclerosis: mechanisms and countermeasures 439
Evidence for co-regulation of Cu,Zn superoxide dismutase and metallothionein gene expression in yeast through transcriptional control by copper via the ACE 1 factor 439
LRRK2 affects vesicle trafficking, neurotransmitter extracellular level and membrane receptor localization 438
Mitochondrial damage modulates alternative splicing in neuronal cells: implications for neurodegeneration 436
Differential role of superoxide and glutathione in S-nitrosoglutathione-mediated apoptosis: A rationale for mild forms of familial amyotrophic lateral sclerosis associated with less active Cu,Zn superoxide dismutase mutants 435
Lessons from models of SOD1-linked familial ALS 435
Glutaredoxin 1 is a major player in copper metabolism in neuroblastoma cells 435
Oxidative stress and mitochondrial damage: Importance in non-SOD1 ALS 435
Activity of protein phosphatase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosispatients 433
Continuous monitoring of ascorbate transport through neuroblastoma cells with a ruthenium oxide hexacyanoferrate modified microelectrode 433
Expression of a Cu, Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of neuroblastoma cells to infectious injury 432
Impairment of mitochondrial calcium handling in a mtSOD1 cell culture model of motoneuron disease 432
Chromosome length and DNA loop size during early embryonic development of Xenopus laevis 431
Pur-alpha functionally interacts with FUS carrying ALS-associated mutations 431
Neuronal RNA-binding proteins in health and disease 430
Which TDP-43 aggregates are toxic in ALS? 430
Bcl2-A1 interacts with pro-caspase-3: Implications for amyotrophic lateral sclerosis. 429
Altered gene expression, mitochondrial damage and oxidative stress: converging routes in motor neuron degeneration 429
Cystatin B and SOD1: protein–protein interaction and possible relation to neurodegeneration 429
Glutaredoxin 2 prevents aggregation of mutant SOD1 in mitochondria and abolishes its toxicity 426
Primary structure from amino acid and cDNA sequences of two Cu,Zn superoxide dismutase variants from Xenopus laevis 426
SIRT3 and mitochondrial metabolism in neurodegenerative diseases 426
Apoptosome-deficient cells lose cytochrome c through proteasomal degradation but survive by autophagy-dependent glycolysis 425
Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis 425
The proinflammatory action of microglial P2 receptors is enhanced in SOD1 models for amyotrophic lateral sclerosis 423
Cell death in amyotrophic lateral sclerosis: interplay between neuronal and glial cells 423
The intriguing case of motor neuron disease: ALS and SMA come closer 422
Mitochondria and ALS: Implications from novel genes and pathways 421
Pathways to mitochondrial dysfunction in ALS pathogenesis 421
Mitochondrial dynamism and the pathogenesis of Amyotrophic Lateral Sclerosis 420
The role of metals and their effect on oxidative stress in amyotrophic lateral sclerosis 418
Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase 416
SOD1 and mitochondria in ALS: a dangerous liaison. 414
Apaf1 mediates apoptosis and mitochondrial damage induced by mutant human SOD1s typical of familial amyotrophic lateral sclerosis 413
Cysteine modifications in the pathogenesis of ALS 410
A relationship between replicon size and supercoiled loop domains in the eukaryotic genome 405
Copper-dependent oxidative stress, alteration of signal transduction and neurodegeneration in amyotrophic lateral sclerosis 403
Increase of Cu,Zn-superoxide dismutase activity during differentiation of human K562 cells involves activation by copper of a constantly expressed copper-deficient protein 402
Inflammatory cytokines increase mitochondrial damage in motoneuronal cells expressing mutant SOD1 400
The Cu,Zn superoxide dismutase isoenzymes of Xenopus laevis: purification, identification of a heterodimer and differential heat sensitivity 400
Oxidative stress and mitochondrial damage in the pathogenesis of ALS: New perspectives 395
Oxidative modulation of nuclear factor-kappaB in human cells expressing mutant fALS-typical superoxide dismutases 394
Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca2+ concentration in transfected neuroblastoma SH-SY5Y cells 394
Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis 392
Mutant SOD1 and mitochondrial damage alter expression and splicing of genes controlling neuritogenesis in models of neurodegeneration 391
Mitochondrial dysfunction in ALS 391
Mislocalised FUS mutants stall spliceosomal snRNPs in the cytoplasm. 388
Crystal structure of the cyanide-inhibited Xenopus laevis Cu,Zn superoxide dismutase at 98 K 385
Increased SOD1 association with chromatin, DNA damage, p53 activation, and apoptosis in a cellular model of SOD1-linked ALS 384
Mitochondrial redox signalling by p66Shc mediates ALS-like disease through Rac1 inactivation 384
The sinister side of Italian soccer 383
Philanthropy: ice-bucket challenge should jolt funding 382
Aberrant copper chemistry as a major mediator of oxidative stress in a human cellular model of amyotrophic lateral sclerosis 379
Totale 43.973
Categoria #
all - tutte 101.654
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 101.654


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021312 0 0 0 0 0 0 0 0 0 0 253 59
2021/20221.265 55 143 71 58 34 115 70 51 100 105 78 385
2022/20231.376 150 104 25 212 101 315 115 61 130 6 128 29
2023/2024347 61 6 17 8 36 111 10 20 4 2 1 71
2024/20252.314 92 533 250 128 52 227 157 165 201 172 192 145
2025/20263.795 299 237 508 327 325 123 448 538 439 532 19 0
Totale 50.889