CARRI', MARIA TERESA
 Distribuzione geografica
Continente #
NA - Nord America 43.580
EU - Europa 3.832
AS - Asia 3.401
SA - Sud America 551
Continente sconosciuto - Info sul continente non disponibili 399
AF - Africa 42
OC - Oceania 12
Totale 51.817
Nazione #
US - Stati Uniti d'America 43.432
SG - Singapore 1.547
DE - Germania 700
CN - Cina 680
UA - Ucraina 604
BR - Brasile 455
RU - Federazione Russa 413
PL - Polonia 405
FR - Francia 382
HK - Hong Kong 353
IE - Irlanda 323
VN - Vietnam 315
IT - Italia 293
GB - Regno Unito 205
FI - Finlandia 173
SE - Svezia 169
KR - Corea 123
CA - Canada 100
JP - Giappone 95
BD - Bangladesh 84
IN - India 55
NL - Olanda 42
ID - Indonesia 28
AR - Argentina 26
MX - Messico 24
GR - Grecia 22
ES - Italia 19
EC - Ecuador 18
BE - Belgio 17
IQ - Iraq 16
ZA - Sudafrica 16
AT - Austria 15
TR - Turchia 15
VE - Venezuela 14
CL - Cile 12
IL - Israele 12
CO - Colombia 11
CZ - Repubblica Ceca 11
EU - Europa 11
PK - Pakistan 11
UZ - Uzbekistan 11
AU - Australia 10
PH - Filippine 10
MY - Malesia 9
MA - Marocco 7
PY - Paraguay 7
RO - Romania 7
SA - Arabia Saudita 7
CH - Svizzera 6
CR - Costa Rica 6
DK - Danimarca 6
JM - Giamaica 5
EG - Egitto 4
KG - Kirghizistan 4
LT - Lituania 4
SV - El Salvador 4
UY - Uruguay 4
AE - Emirati Arabi Uniti 3
DZ - Algeria 3
IR - Iran 3
TN - Tunisia 3
AL - Albania 2
AZ - Azerbaigian 2
BG - Bulgaria 2
BY - Bielorussia 2
HN - Honduras 2
HU - Ungheria 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
BF - Burkina Faso 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CY - Cipro 1
DM - Dominica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GE - Georgia 1
GH - Ghana 1
GY - Guiana 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
PR - Porto Rico 1
PS - Palestinian Territory 1
PT - Portogallo 1
RW - Ruanda 1
Totale 51.422
Città #
Woodbridge 12.914
Wilmington 10.782
Houston 10.287
Fairfield 1.315
Ann Arbor 1.004
Singapore 885
Ashburn 851
Jacksonville 546
Seattle 504
Chandler 484
Cambridge 446
Kraków 389
San Jose 349
Hong Kong 345
Dublin 314
Dearborn 290
Medford 258
Beijing 257
The Dalles 205
Council Bluffs 176
New York 162
Santa Clara 161
Lawrence 122
Los Angeles 116
Ho Chi Minh City 98
Mülheim 94
Buffalo 83
Tokyo 80
Hanoi 77
Rome 76
San Diego 66
Menlo Park 55
Helsinki 53
Dallas 49
Moscow 46
Norwalk 46
Detroit 39
Milan 39
Falls Church 38
Toronto 38
Mountain View 37
Munich 37
Zhengzhou 36
Lauterbourg 35
Phoenix 35
London 32
University Park 31
Boardman 30
Reading 29
Chicago 27
São Paulo 27
Guangzhou 26
North Bergen 26
Montreal 23
Redwood City 23
Saint Petersburg 22
Jakarta 21
Verona 20
Amsterdam 19
Thessaloniki 18
Brussels 17
Denver 17
Brooklyn 16
Frankfurt am Main 16
Nanjing 16
Nürnberg 16
Haiphong 15
Hefei 15
Orem 15
Atlanta 14
Kunming 14
Rio de Janeiro 14
San Francisco 14
Shanghai 14
Columbus 13
Da Nang 13
Nuremberg 13
Warsaw 13
Chennai 11
Jinan 11
San Mateo 11
Kaiserslautern 10
Kyiv 10
Manchester 10
Stockholm 10
Brasília 9
Brno 9
Johannesburg 9
Ankara 8
Campinas 8
Hounslow 8
North Charleston 8
Poplar 8
Baghdad 7
Dong Ket 7
Hangzhou 7
Naples 7
Redondo Beach 7
Belo Horizonte 6
Indiana 6
Totale 45.145
Nome #
S -Nitrosoglutathione Reductase Plays Opposite Roles in SH-SY5Y Models of Parkinson's Disease and Amyotrophic Lateral Sclerosis 546
Mutation of Lys-120 and Lys-134 drastically reduces the catalytic rate of Cu,Zn superoxide dismutase 523
Bcl2a1 serves as a switch in death of motor neurons in amyotrophic lateral sclerosis 512
Three-dimensional structure of Xenopus laevis Cu,Zn superoxide dismutase b determined by X-ray crystallography at 1.5 A resolution 509
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 507
Superoxide dismutase 1 modulates expression of transferrin receptor 501
Amyotrophic lateral sclerosis: from current developments in the laboratory to clinical implications 500
2-DE and MALDI-TOF-MS for a comparative analysis of proteins expressed in different cellular models of amyotrophic lateral sclerosis 499
Copper depletion increases the mitochondrial-associated SOD1 in neuronal cells 497
Activation and induction by copper of Cu/Zn superoxide dismutase in Saccharomyces cerevisiae. Presence of an inactive proenzyme in anaerobic yeast 491
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 490
A study of the dual role of copper in superoxide dismutase as antioxidant and pro-oxidant in cellular models of amyotrophic lateral sclerosis 489
Regulation of CU, ZNSOD by metals in S-Cereivisiae and Zea-Mays 486
Apoptotic mechanisms in mutant LRRK2-mediated cell death 485
Neurodegeneration in amyotrophic lateral sclerosis: the role of oxidative stress and altered homeostasis of metals 485
Structural insights into the multi-determinant aggregation of TDP-43 in motor neuron-like cells 485
Developmental expression of Cu,Zn superoxide dismutase in Xenopus. Constant level of the enzyme in oogenesis and embryogenesis 481
Effect of Lys->Arg mutation on the thermal stability of Cu,Zn superoxide dismutase: Influence on the monomer-dimer equilibrium 480
Treatment with lithium carbonate does not improve disease progression in two different strains of SOD1 mutant mice 478
The NADPH oxidase pathway is dysregulated by the P2X7 receptor in the SOD1-G93A microglia model of amyotrophic lateral sclerosis. 478
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 475
Beta-amyloid causes downregulation of calcineurin in neurons through induction of oxidative stress 475
Familial ALS-superoxide dismutases associate with mitochondria and shift their redox potentials 472
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 470
Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS 470
Xenopus laevis Cu,Zn superoxide dismutase B cDNA sequence 469
Apoptosome inactivation rescues proneural and neural cells from neurodegeneration 466
Abnormal sensitivity of cannabinoid CB1 receptors in the striatum of mice with experimental amyotrophic lateral sclerosis 465
Xenopus laevis U1 snRNA genes: characterisation of transcriptionally active genes reveals major and minor repeated gene families 465
Role of zinc-coordination and of the glutathione redox couple in the redox susceptibility of human transcription factor Sp1 465
Interaction of cisplatin with human superoxide dismutase 465
Copper-dependent oxidative stress and neurodegeneration 464
An electron microscope study of chromosomal DNA replication in different eukaryotic systems 464
Purification and characterization of Ag,Zn-superoxide dismutase from Saccharomyces cerevisiae exposed to silver 463
Amyotrophic Lateral Sclerosis: New Insights into Underlying Molecular Mechanisms and Opportunities for Therapeutic Intervention 462
ALS: focus on purinergic signalling 461
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 460
Impaired copper binding by the H46R mutant of human Cu,Zn superoxide dismutase, involved in amyotrophic lateral sclerosis 459
Voltage-activated sodium currents in a cell line expressing a Cu,Zn superoxide dismutase typical of familial ALS 458
The unfolded protein response in models of human mutant G93A amyotrophic lateral sclerosis 458
Metal uptake of recombinant cambialistic superoxide dismutase from Propionitbacterium shermanii is affected by growth conditions of host Escherichia coli cells 457
Oligomerization of mutant SOD1 in mitochondria of motoneuronal cells drives mitochondrial damage and cell toxicity 455
Cu,Zn-superoxide dismutase-dependent apoptosis induced by nitric oxide in neuronal cells 453
Tissue-specific deregulation of selected HDACs characterizes ALS progression in mouse models: pharmacological characterization of SIRT1 and SIRT2 pathways 453
The proinflammatory action of microglial P2 receptors is enhanced in SOD1 models for amyotrophic lateral sclerosis 451
The relationship between chromosomal origins of replication and the nuclear matrix during the cell cycle 451
Minocycline for patients with ALS. 450
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 449
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 445
Amyotrophic lateral sclerosis: mechanisms and countermeasures 444
LRRK2 affects vesicle trafficking, neurotransmitter extracellular level and membrane receptor localization 443
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 441
Bcl2-A1 interacts with pro-caspase-3: Implications for amyotrophic lateral sclerosis. 441
Continuous monitoring of ascorbate transport through neuroblastoma cells with a ruthenium oxide hexacyanoferrate modified microelectrode 440
Oxidative stress and mitochondrial damage: Importance in non-SOD1 ALS 440
Expression of a Cu, Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of neuroblastoma cells to infectious injury 439
Mitochondrial damage modulates alternative splicing in neuronal cells: implications for neurodegeneration 439
Lessons from models of SOD1-linked familial ALS 438
Glutaredoxin 1 is a major player in copper metabolism in neuroblastoma cells 438
Chromosome length and DNA loop size during early embryonic development of Xenopus laevis 437
Neuronal RNA-binding proteins in health and disease 437
Pathways to mitochondrial dysfunction in ALS pathogenesis 436
The intriguing case of motor neuron disease: ALS and SMA come closer 435
Pur-alpha functionally interacts with FUS carrying ALS-associated mutations 435
Activity of protein phosphatase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosispatients 434
Impairment of mitochondrial calcium handling in a mtSOD1 cell culture model of motoneuron disease 433
Cell death in amyotrophic lateral sclerosis: interplay between neuronal and glial cells 433
Which TDP-43 aggregates are toxic in ALS? 433
Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis 431
Altered gene expression, mitochondrial damage and oxidative stress: converging routes in motor neuron degeneration 431
Cystatin B and SOD1: protein–protein interaction and possible relation to neurodegeneration 431
Primary structure from amino acid and cDNA sequences of two Cu,Zn superoxide dismutase variants from Xenopus laevis 430
SIRT3 and mitochondrial metabolism in neurodegenerative diseases 429
Glutaredoxin 2 prevents aggregation of mutant SOD1 in mitochondria and abolishes its toxicity 428
Mitochondria and ALS: Implications from novel genes and pathways 428
Apoptosome-deficient cells lose cytochrome c through proteasomal degradation but survive by autophagy-dependent glycolysis 427
Mitochondrial dynamism and the pathogenesis of Amyotrophic Lateral Sclerosis 423
The role of metals and their effect on oxidative stress in amyotrophic lateral sclerosis 420
A relationship between replicon size and supercoiled loop domains in the eukaryotic genome 418
Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase 418
SOD1 and mitochondria in ALS: a dangerous liaison. 417
Cysteine modifications in the pathogenesis of ALS 417
Apaf1 mediates apoptosis and mitochondrial damage induced by mutant human SOD1s typical of familial amyotrophic lateral sclerosis 416
Increase of Cu,Zn-superoxide dismutase activity during differentiation of human K562 cells involves activation by copper of a constantly expressed copper-deficient protein 412
Copper-dependent oxidative stress, alteration of signal transduction and neurodegeneration in amyotrophic lateral sclerosis 407
Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis 402
The Cu,Zn superoxide dismutase isoenzymes of Xenopus laevis: purification, identification of a heterodimer and differential heat sensitivity 402
Inflammatory cytokines increase mitochondrial damage in motoneuronal cells expressing mutant SOD1 401
Oxidative stress and mitochondrial damage in the pathogenesis of ALS: New perspectives 401
Mitochondrial dysfunction in ALS 399
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 399
Oxidative modulation of nuclear factor-kappaB in human cells expressing mutant fALS-typical superoxide dismutases 398
Increased SOD1 association with chromatin, DNA damage, p53 activation, and apoptosis in a cellular model of SOD1-linked ALS 396
Mutant SOD1 and mitochondrial damage alter expression and splicing of genes controlling neuritogenesis in models of neurodegeneration 393
Crystal structure of the cyanide-inhibited Xenopus laevis Cu,Zn superoxide dismutase at 98 K 393
Mitochondrial redox signalling by p66Shc mediates ALS-like disease through Rac1 inactivation 392
Mislocalised FUS mutants stall spliceosomal snRNPs in the cytoplasm. 389
Philanthropy: ice-bucket challenge should jolt funding 389
Aberrant copper chemistry as a major mediator of oxidative stress in a human cellular model of amyotrophic lateral sclerosis 386
The sinister side of Italian soccer 384
Totale 44.715
Categoria #
all - tutte 107.724
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 107.724


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.067 0 0 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
2025/20264.193 299 237 508 327 325 123 448 538 439 532 221 196
2026/2027530 268 236 26 0 0 0 0 0 0 0 0 0
Totale 51.817