MONTOSI, Giuliana
 Distribuzione geografica
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Continente #
NA - Nord America 5.787
EU - Europa 2.461
AS - Asia 2.371
SA - Sud America 397
AF - Africa 29
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 4
Totale 11.059
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Nazione #
US - Stati Uniti d'America 5.727
GB - Regno Unito 1.019
CN - Cina 912
SG - Singapore 680
SE - Svezia 357
BR - Brasile 336
HK - Hong Kong 272
IT - Italia 249
DE - Germania 201
VN - Vietnam 151
UA - Ucraina 136
KR - Corea 135
RU - Federazione Russa 129
FI - Finlandia 115
TR - Turchia 71
FR - Francia 61
BG - Bulgaria 52
CA - Canada 39
BE - Belgio 30
IN - India 27
NL - Olanda 25
ID - Indonesia 24
AR - Argentina 23
JP - Giappone 20
PL - Polonia 19
BD - Bangladesh 17
MY - Malesia 16
IE - Irlanda 15
AT - Austria 13
EC - Ecuador 10
ES - Italia 10
IQ - Iraq 10
MX - Messico 9
IR - Iran 8
LT - Lituania 8
ZA - Sudafrica 8
AU - Australia 7
CL - Cile 7
CO - Colombia 6
MA - Marocco 6
PE - Perù 5
RO - Romania 5
CZ - Repubblica Ceca 4
OM - Oman 4
PY - Paraguay 4
CH - Svizzera 3
EU - Europa 3
HU - Ungheria 3
KE - Kenya 3
NZ - Nuova Zelanda 3
PK - Pakistan 3
TH - Thailandia 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
BO - Bolivia 2
BZ - Belize 2
DK - Danimarca 2
DZ - Algeria 2
EG - Egitto 2
HN - Honduras 2
LV - Lettonia 2
PS - Palestinian Territory 2
RS - Serbia 2
SA - Arabia Saudita 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BY - Bielorussia 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GT - Guatemala 1
JM - Giamaica 1
JO - Giordania 1
KZ - Kazakistan 1
LB - Libano 1
NP - Nepal 1
PA - Panama 1
PH - Filippine 1
QA - Qatar 1
SC - Seychelles 1
SN - Senegal 1
SR - Suriname 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
UG - Uganda 1
ZW - Zimbabwe 1
Totale 11.059
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Città #
Southend 768
Santa Clara 590
Fairfield 537
Woodbridge 478
Ashburn 464
Singapore 428
Chandler 398
Hefei 376
Houston 323
Jacksonville 304
Ann Arbor 279
Hong Kong 272
Wilmington 208
Seattle 197
Dearborn 189
Nyköping 188
Cambridge 187
Beijing 135
London 123
Seoul 122
Modena 106
Los Angeles 90
Chicago 86
Helsinki 61
New York 60
Des Moines 52
Sofia 51
Princeton 49
Buffalo 48
Ho Chi Minh City 48
San Diego 48
Eugene 46
Shanghai 46
Moscow 41
São Paulo 38
The Dalles 36
Hanoi 35
Council Bluffs 30
Brussels 29
Munich 27
Columbus 23
Izmir 23
Falls Church 20
Philadelphia 20
Bremen 19
Redwood City 19
San Mateo 19
Bologna 18
Frankfurt am Main 18
Jakarta 18
Brooklyn 17
Milan 17
Yalova 17
Ottawa 16
Dublin 15
Auburn Hills 14
Dallas 14
Norwalk 13
Salt Lake City 13
Elk Grove Village 11
San Francisco 10
Tampa 10
Toronto 10
Warsaw 10
Boardman 9
Montreal 9
Phoenix 9
Seongnam 9
Tokyo 9
Turku 9
Kent 8
Lakewood 8
Baghdad 7
Boston 7
Denver 7
Haiphong 7
Kunming 7
Orem 7
Belo Horizonte 6
Biên Hòa 6
Brasília 6
Dong Ket 6
Fuzhou 6
Nanjing 6
Nuremberg 6
Rio de Janeiro 6
Stockholm 6
Xi'an 6
Atlanta 5
Campinas 5
Guangzhou 5
Jinan 5
Johannesburg 5
Kilburn 5
Lancaster 5
North Bergen 5
Quito 5
Ravarino 5
Recife 5
Reggio Emilia 5
Totale 8.209
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Nome #
Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene 348
Gluconeogenic Signals Regulate Iron Homeostasis via Hepcidin in Mice. 319
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene 318
Human macrophage ferroportin biology and the basis for the ferroportin disease 299
Hepcidin expression does not rescue the iron-poor phenotype of Kupffer cells in Hfe-null mice after liver transplantation. 287
VITAMIN-E SUPPLEMENTATION PREVENTS HEPATIC CIRRHOSIS DUE TO IRON OVERLOAD IN RODENTS 281
ER stress controls iron metabolism through induction of hepcidin. 281
Bone Morphogenetic Protein Signaling Is Impaired in an Hfe Knockout Mouse Model of Hemochromatosis. 281
Hepatic stellate cells are not subjected to oxidant stress during iron-induced fibrogenesis in rodents 277
Kupffer cells and macrophages are not required for hepatic hepcidin activation during iron overload 277
The role of the iron responsive element in the control of ferroportin1/IREG1/MTP1 gene expression 273
Duodenal ferritin synthesis in genetic hemochromatosis 273
Heterogeneity of hemochromatosis in Italy 269
Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy 269
BMP6 treatment compensates for the molecular defect and ameliorates hemochromatosis in Hfe knockout mice. 264
MOLECULAR AND CELLULAR ASPECTS OF IRON-INDUCED HEPATIC CIRRHOSIS IN RODENTS 263
The SMAD pathway is required for hepcidin response during endoplasmic reticulum stress 254
WISP-2 expression induced by Teriparatide treatment affects in vitro osteoblast differentiation and improves in vivo osteogenesis 250
Enhanced hepatic collagen type I mRNA expression into fat-storing cells in a rodent model of hemochromatosis. 249
Excess iron into hepatocytes is required for activation of collagen type I gene during experimental siderosis 245
Expression of the duodenal iron transporters divalent-metal transporter 1 and ferroportin 1 in iron deficiency and iron overload 242
THE MOLECULAR BASIS FOR THE HEPATIC REGULATION OF HEPCIDIN, THE IRON HORMONE, BY BONE MORPHOGENETIC PROTEINS. 237
Diacerhein blocks iron regulatory protein activation in inflamed human monocytes 236
Antioxidant activity of silybin in vivo during long-term iron overload in rats 236
Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene 236
Huh-7: a human hemochromatotic cell line. 224
Lack of enterocyte iron accumulation in the ferroportin disease 222
GLUCONEOGENIC SIGNALS DIRECTLY CONTROL IRON HOMEOSTASIS THROUGH HEPCIDIN 216
Wild-type HFE protein normalizes transferrin iron accumulation in macrophages from subjects with hereditary hemochromatosis 211
Defective control or iron metabolism in pre-neoplastic liver nodules during experimental carcinogenesis 210
IRON IS A MITOGENIC AND PROFIBROGENIC FACTOR IN EXPERIMENTAL LIVER FIBROSIS DUE TO IRON OVERLOAD 210
Inappropriately high iron regulatory protein activity in monocytes of patients with genetic hemochromatosis 203
Osteocytes signaling events induced by intermittent vs continuous Teriparatide treatment affect in vitro osteoblast differentiation and mineralization 203
Wisp2 overexpression induced by short Teriparatide treatment affects IDG-SW3 osteogenic differentiation. 195
Effect of anti-osteoarthritic drugs on interleukin 1-dependent activation of NF-kappa B in human chondrocytes 194
C/EBP-beta/LAP controls down-regulation of albumin gene transcription during liver regeneration 194
Iron-induced oxidant stress in nonparenchymal liver cells: Mitochondrial derangement and fibrosis in acutely iron-dosed gerbils and its prevention by silybin 192
Ursodeoxycholic acid complexation with 2-hydroxypropyl-beta-cyclodextrin increases ursodeoxycholic acid biliary excretion after single oral administration in rats 191
SEX HORMONES DIFFERENTLY REGULATE HEPCIDIN EXPRESSION AND IRON HOMEOSTASIS IN VIVO. 190
Iron overload in rodents leads to hepatic cirrhosis through enhancement of collagen gene expression into non-parenchymal cells. 188
No HFE, no HLA, no 6p-linked adult hemochromatosis: A new genetic iron overload condition 184
Spatial and temporal dynamics of hepatic stellate cell activation during oxidant-stress-induced fibrogenesis 180
MOLECULAR AND CELLULAR ASPECTS OF LIVER-DISEASE IN GENETIC HEMOCHROMATOSIS 172
Iron-induced oxidant stress leads to irreversible mitochondrial dysfunctions and fibrosis in the liver of chronic iron-dosed gerbils. The effect of silybin 164
HLA-H mutations in Italian patients with genetic hemochromatosis: Evidence of genetic heterogeneity 159
CREB-H is a stress-regulator of hepcidin gene expression during early postnatal development 138
Oxidant stress: cell signalling and gene response in the liver: the iron-oxygen connection. 136
Erratum: Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene (Blood Cells, Molecules, and Diseases (2003) 31 (299-304) DOI: 10.1016/S1079-9796(03)00164-5) 101
SEX HORMONES DIFFERENTLY REGULATE HEPATIC HEPCIDIN EXPRESSION AND SYSTEMIC IRON HOMEOSTASIS IN VIVO 61
Totale 11.102
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Categoria #
all - tutte 41.441
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 41.441
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021715 0 0 0 0 0 114 142 155 35 125 83 61
2021/2022940 40 128 76 83 35 44 58 39 92 74 162 109
2022/20231.077 113 138 58 128 121 178 13 130 111 11 38 38
2023/2024507 20 38 68 47 78 48 55 54 14 21 17 47
2024/20252.381 128 16 45 153 459 387 176 109 182 88 340 298
2025/20261.976 353 235 425 388 501 74 0 0 0 0 0 0
Totale 11.102