VERGANI, LODOVICA
 Distribuzione geografica
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Continente #
NA - Nord America 4.127
AS - Asia 2.317
EU - Europa 984
AF - Africa 416
SA - Sud America 374
OC - Oceania 38
Continente sconosciuto - Info sul continente non disponibili 13
AN - Antartide 1
Totale 8.270
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Nazione #
US - Stati Uniti d'America 3.909
SG - Singapore 713
CN - Cina 473
VN - Vietnam 337
BR - Brasile 242
HK - Hong Kong 207
FI - Finlandia 103
DE - Germania 102
IT - Italia 101
SE - Svezia 99
FR - Francia 95
IN - India 66
BD - Bangladesh 64
UA - Ucraina 59
GB - Regno Unito 57
IQ - Iraq 48
NL - Olanda 35
RU - Federazione Russa 34
MX - Messico 33
PL - Polonia 33
TR - Turchia 32
SA - Arabia Saudita 31
AR - Argentina 28
CA - Canada 27
PK - Pakistan 27
ZA - Sudafrica 27
BJ - Benin 26
ES - Italia 25
JP - Giappone 25
CO - Colombia 21
UZ - Uzbekistan 20
PH - Filippine 19
ID - Indonesia 18
MA - Marocco 18
ET - Etiopia 16
ML - Mali 16
PE - Perù 16
AT - Austria 15
EG - Egitto 15
KZ - Kazakistan 15
IE - Irlanda 14
PA - Panama 14
TH - Thailandia 14
VE - Venezuela 14
DK - Danimarca 13
DZ - Algeria 13
LC - Santa Lucia 13
RW - Ruanda 13
AL - Albania 12
AO - Angola 12
EC - Ecuador 12
GA - Gabon 12
JO - Giordania 12
MZ - Mozambico 12
PS - Palestinian Territory 12
SN - Senegal 12
SY - Repubblica araba siriana 12
TW - Taiwan 12
AD - Andorra 11
AE - Emirati Arabi Uniti 11
CR - Costa Rica 11
CV - Capo Verde 11
HR - Croazia 11
LB - Libano 11
PY - Paraguay 11
TN - Tunisia 11
AU - Australia 10
BY - Bielorussia 10
CU - Cuba 10
HN - Honduras 10
HU - Ungheria 10
JM - Giamaica 10
KE - Kenya 10
LA - Repubblica Popolare Democratica del Laos 10
ME - Montenegro 10
MG - Madagascar 10
MY - Malesia 10
NI - Nicaragua 10
SI - Slovenia 10
ZM - Zambia 10
AM - Armenia 9
BA - Bosnia-Erzegovina 9
BO - Bolivia 9
BS - Bahamas 9
CD - Congo 9
CH - Svizzera 9
CI - Costa d'Avorio 9
CM - Camerun 9
GH - Ghana 9
GM - Gambi 9
GN - Guinea 9
GT - Guatemala 9
HT - Haiti 9
IL - Israele 9
IS - Islanda 9
KG - Kirghizistan 9
MN - Mongolia 9
MU - Mauritius 9
NC - Nuova Caledonia 9
RS - Serbia 9
Totale 7.883
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Città #
Ashburn 458
San Jose 435
Singapore 425
Fairfield 399
Chandler 277
Woodbridge 234
Jacksonville 208
Hong Kong 189
Houston 186
Ann Arbor 140
Cambridge 137
Wilmington 137
Seattle 127
Ho Chi Minh City 90
Beijing 88
Santa Clara 84
Boardman 82
Princeton 77
Hanoi 65
Los Angeles 54
Roxbury 49
Des Moines 45
Lauterbourg 43
Dong Ket 39
Helsinki 39
New York 39
San Diego 36
Nanjing 35
The Dalles 35
Medford 33
São Paulo 29
Cotonou 26
Milan 22
Jinan 21
Munich 21
Guangzhou 19
Bytom 18
Baghdad 15
Buffalo 15
Haiphong 15
Orem 15
Tashkent 15
Addis Ababa 14
Bamako 14
Panama City 14
Turku 14
Castries 13
Jeddah 13
Kigali 13
Tokyo 13
Dakar 12
Hebei 12
Libreville 12
London 12
Amman 11
Andorra la Vella 11
Council Bluffs 11
Da Nang 11
Denver 11
Luanda 11
Nanchang 11
Shanghai 11
Tianjin 11
Brooklyn 10
Dublin 10
Frankfurt am Main 10
Havana 10
Johannesburg 10
Lahore 10
Lusaka 10
Managua 10
Montreal 10
Nairobi 10
Norwalk 10
Nuremberg 10
Padova 10
Praia 10
San José 10
Abidjan 9
Antananarivo 9
Bishkek 9
Chicago 9
Conakry 9
Dushanbe 9
Kingston 9
Lima 9
Maputo 9
Minsk 9
Nassau 9
Noumea 9
Rio de Janeiro 9
Vientiane 9
Accra 8
Atlanta 8
Changsha 8
Chennai 8
Gaborone 8
Kampala 8
Port-au-Prince 8
Riyadh 8
Totale 5.111
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Nome #
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients 342
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 283
Dominant optic atrophy caused by a novel OPA1 mutation: Disruption of the mitochondrial network with preserved bioenergetics. 259
Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNA. 245
The ALPINE–ALMA [C ii] Survey: Multiwavelength Ancillary Data and Basic Physical Measurements 243
Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants 242
Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect. 234
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 223
A pilot trial with clenbuterol in amyotrophic lateral sclerosis 213
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells. 208
Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females. 201
Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients. 196
INHIBITION OF MITOCHONDRIAL FISSION FAVOURS MUTANT OVER WILD-TYPE MITOCHONDRIAL DNA 196
Clinical and pathological findings in families with X-linked spinal and bulbar muscular atrophy (Kennedy's disease). 190
Human skeletal muscle atrophy in amyotrophic lateral sclerosis reveals a reduction in Akt and an increase in atrogin-1 182
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues 180
Antioxidant defences and reactive oxygen species homeostasis in different human mitochondrial DNA-depleted cell lines. 178
null 171
Adult acid maltase deficiency: an open trial with albuterol and branched- chain aminoacids 169
Physiological responses in McArdle's patients during maximal aerobic exercise 169
Energy matters: Mitochondrial proteomics for biomedicine 168
UV and Lyα luminosity functions of galaxies and star formation rate density at the end of HI reionization from the VIMOS UltraDeep Survey (VUDS) 157
Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient 157
Biased incorporation of ribonucleotides on the mitochondrial L-strand accounts for apparent strand-asymmetric DNA replication. 152
"Polyspecific anti-mitochondrion antibodies detect up- and down-regulated proteins in in toto muscle homogenates from MELAS patients 146
Overexpression of microRNA-206 in the skeletalmuscle from myotonic dystrophy type 1 patients 145
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathies. 142
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues 141
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubes 137
The mitochondrial fission protein hFis1 requires the endoplasmic reticulum gateway to induce apoptosis 136
Energy status and ROS production in three RHO0 cell lines with different nuclear background 134
Functional and molecular responses to stress conditions in heteroplasmic MELAS 3243 RD cybrids. 132
Hereditary protein C deficiency associated with riboflavin-responsive lipid storage myopathy 132
Polyspecific anti-Mitochondrion Antibodies for Proteomics on in toto Tissue Homogenates 132
Clinical varieties of carnitine and carnitine palmitoyltransferase deficiency 131
Carnitine deficiency induced during hemodialysis and hyperlipidemia: Effect of replacement therapy 122
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic distrophy type 1 patients. 119
Functional and molecular responses to stress conditions in heteroplasmic MELAS (3243) RD cybrids. 115
Characterisation of undifferentiated and differentiated RD-cybrids, harbouring 3243 MELAS mutation 113
ROS HOMEOSTASIS AND ENERGY STATUS IN mtDNA DEPLETION 113
Immobilized pH gradients with electrodic plateaus (and other unusual procedures for 2DE) 112
Alteration of mechanisms responsible for the homeostasis of mitochondrial flavin cofactors are correlated with adult lipid storage myopathies 109
Antioxidant capacity in cybrids harbouring the three mtDNA mutations primarly associated with Leber’s (LHON) 106
Altered mitochondrial morphology after in vitro muscle differentiation in MELAS (A3243G) RD cybrids 104
MITOCHONDRIAL PROTEINS IN RIBOFLAVIN-RESPONSIVE MYOPATIES 102
Riboflovin responsive myopathy: correlation between mitochondrial oxidative phosphorilation enzymes and mitochondrial flavocoenzyme homeostasis. 97
ANTIOXIDANT CAPACITY IN CYBRIDS HARBORING THE THREE MTDNA RELATED TO COMPLEX I MUTATIONS SUBUNITS AND PRIMARILY ASSOCIATED WITH LEBER'S (LHON) 97
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment 96
Homeostasis of reactive oxygen species in mtDNA-depleted cell lines 94
Diagnosis and therapy of myophosphorylase deficiency: experience with a group of italian patients 94
Muscle histopatology in patients with X-linked bulbar and spinal muscular atrophy (Kennedy's disease) and female carriers. 90
Decreased fatty-acid beta-oxidation in riboflavin-responsive, multiple acylcoenzyme A dehydrogenase-deficient patients is associated with an increase in uncoupling protein-3 74
MODIFICAZIONI DELLE DIFESE ANTIOSSIDANTI IN CIBRIDI MELAS CON BACKGROUND NUCLEARE MUSCOLARE INDOTTE DAL DIFFERENZIAMENTO 70
Totale 8.293
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Categoria #
all - tutte 22.268
article - articoli 16.947
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 386
Totale 39.601
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021117 0 0 0 0 0 0 0 0 0 0 55 62
2021/2022625 7 64 85 60 65 46 11 57 34 4 48 144
2022/2023561 99 68 5 57 108 89 0 38 66 5 26 0
2023/2024239 6 45 28 15 21 39 14 8 8 8 25 22
2024/20251.041 2 70 45 51 142 32 30 94 73 38 189 275
2025/20263.965 187 330 551 543 435 185 463 350 483 239 199 0
Totale 8.293