IRIS - Res&Arch Institutional Research Information System - Research & Archive

SORCI, Guglielmo
 Distribuzione geografica
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Continente #
NA - Nord America 6.830
EU - Europa 5.375
AS - Asia 5.257
SA - Sud America 971
AF - Africa 134
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 14
Totale 18.596
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Nazione #
US - Stati Uniti d'America 6.664
SG - Singapore 2.342
IT - Italia 968
UA - Ucraina 898
BR - Brasile 780
HK - Hong Kong 763
IE - Irlanda 732
CN - Cina 730
RU - Federazione Russa 636
SE - Svezia 575
VN - Vietnam 429
DE - Germania 346
FR - Francia 285
KR - Corea 272
FI - Finlandia 235
GB - Regno Unito 204
TR - Turchia 128
IN - India 127
NL - Olanda 84
RO - Romania 80
AT - Austria 76
CA - Canada 75
IQ - Iraq 67
BD - Bangladesh 64
PL - Polonia 58
AR - Argentina 57
MX - Messico 54
JP - Giappone 48
CH - Svizzera 45
ZA - Sudafrica 43
PK - Pakistan 38
PH - Filippine 37
CO - Colombia 36
ES - Italia 31
UZ - Uzbekistan 31
EC - Ecuador 30
BE - Belgio 28
ID - Indonesia 28
VE - Venezuela 25
MA - Marocco 21
CZ - Repubblica Ceca 18
SA - Arabia Saudita 18
LB - Libano 16
MY - Malesia 15
CL - Cile 12
JO - Giordania 12
PY - Paraguay 12
TN - Tunisia 12
EG - Egitto 11
EU - Europa 11
JM - Giamaica 11
LT - Lituania 11
AU - Australia 10
AZ - Azerbaigian 10
KE - Kenya 10
IR - Iran 9
AE - Emirati Arabi Uniti 8
GR - Grecia 8
MD - Moldavia 8
PE - Perù 8
SK - Slovacchia (Repubblica Slovacca) 8
BG - Bulgaria 7
DZ - Algeria 7
IL - Israele 7
CR - Costa Rica 6
ET - Etiopia 6
OM - Oman 6
TH - Thailandia 6
TW - Taiwan 6
BO - Bolivia 5
DO - Repubblica Dominicana 5
KG - Kirghizistan 5
KH - Cambogia 5
NP - Nepal 5
UY - Uruguay 5
AL - Albania 4
BA - Bosnia-Erzegovina 4
HU - Ungheria 4
KZ - Kazakistan 4
LV - Lettonia 4
NZ - Nuova Zelanda 4
PA - Panama 4
BY - Bielorussia 3
DK - Danimarca 3
GE - Georgia 3
GT - Guatemala 3
KW - Kuwait 3
NI - Nicaragua 3
PS - Palestinian Territory 3
RS - Serbia 3
SN - Senegal 3
XK - ???statistics.table.value.countryCode.XK??? 3
AM - Armenia 2
BH - Bahrain 2
CY - Cipro 2
GA - Gabon 2
HR - Croazia 2
ME - Montenegro 2
MG - Madagascar 2
MN - Mongolia 2
Totale 18.563
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Città #
Singapore 1.770
Chandler 869
Hong Kong 749
Dublin 728
San Jose 540
Jacksonville 490
Ashburn 470
San Mateo 418
Perugia 297
Boardman 296
Santa Clara 265
Moscow 238
Seoul 202
Wilmington 188
Medford 186
Princeton 185
Lauterbourg 178
Beijing 149
Dong Ket 140
Ann Arbor 129
The Dalles 120
Andover 114
Ho Chi Minh City 107
Los Angeles 104
Altamura 100
Munich 87
New York 79
Piscataway 79
Izmir 68
Lawrence 68
São Paulo 68
Bucharest 64
Des Moines 61
Vienna 59
Hanoi 55
Saint Petersburg 55
Dearborn 53
Norwalk 53
Redmond 52
Shanghai 50
Helsinki 47
Orem 44
Falls Church 41
Council Bluffs 37
Tokyo 37
Montreal 33
Rome 32
Warsaw 31
Bologna 30
Philadelphia 30
Rio de Janeiro 30
Shenzhen 29
Woodbridge 28
Brussels 27
Johannesburg 27
Amsterdam 23
Phoenix 23
Baghdad 22
Boston 22
Houston 22
Stockholm 22
Chennai 21
Dallas 21
Falkenstein 21
Frankfurt am Main 21
London 21
Turku 21
Atlanta 20
Brooklyn 20
Chicago 19
Denver 19
Milan 19
Nuremberg 19
Seongnam-si 19
Brasília 17
Da Nang 17
Guangzhou 17
Belo Horizonte 16
Manchester 16
Tashkent 16
Lahore 15
Redwood City 15
Ankara 13
Cebu City 13
Dhaka 13
San Francisco 13
Tijuana 13
Toronto 13
Mumbai 12
Olomouc 12
Parma 12
Quito 12
Auburn Hills 11
Haiphong 11
Istanbul 11
Porto Alegre 11
Amman 10
Baku 10
Guayaquil 10
Poplar 10
Totale 11.220
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Nome #
Le proteine S100 253
Artesunate induces ROS- and p38 MAPK-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells 202
An HMGB1/RAGE/p38 MAPK/Myogenin Axis Modulates Pax7 Expression in Myoblasts by Both Transcriptional and Post-Transcriptional Mechanisms 177
Histological muscle characterization in hypertrophied Marchigiana cattle breed 171
Intraperitoneal injection of microencapsulated Sertoli cells restores muscle morphology and performance in dystrophic mice 169
Artesunate induces ROS-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells. 163
IDO1 suppresses inhibitor development in hemophilia A treated with factor VIII 161
Targeting RAGE prevents muscle wasting and prolongs survival in cancer cachexia 146
Identification of natural products able to counteract the formation of advanced glycation end-products (AGEs) sustaining muscle atrophy 145
RAGE in the pathophysiology of skeletal muscle. 144
Extracellular S100B causes nuclear translocation of NF-?B in rat L6 myoblasts likely by binding to RAGE 144
Biological effects of astrocyte-derived S100-beta protein on BV-2 microglial cell line 141
Differential expression of S100B protein and RAGE in young and aged human satellite cells. 141
Generation of an mdx/Ager–/– double mutant mouse. Preliminary data on skeletal muscle architecture. 138
S100B protein regulates myoblast and macrophage functions in skeletal muscle regeneration 138
Pharmacological targeting of the receptor for advanced glycation end-products (RAGE) to counteract cancer cachexia 136
A braking circuit between pathogen- and danger-sensing signaling pathways restrains lung inflammation: role of S100B protein, RAGE and Toll-like receptors. 136
Absence of RAGE in an animal experimental model of Duchenne muscular dystrophy results in reduced muscle necrosis and inflammation 135
Sertoli cells protect C2C12 myotubes against atrophy and induce utrophin expression in canine and human dystrophic myotubes. 134
Amphoterin-induced myogenic differentiation of RAGE-transfected rhabdomyosarcoma TE671 cells 133
Activation of RAGE in myoblasts and rhabdomyosarcoma cells results in downregulation of Pax7 expression 133
Effect of recombinant murine tumor necrosis factor on the generation of natural killer cells in bone marrow cultures 133
Cellular and molecular mechanisms of sarcopenia: the S100B perspective 133
Toward the identification of receptor for advanced glycation end-products (RAGE) as a muscle biomarker of cancer cachexia. 133
Equisetum arvense standardized extract hinders age-related sarcopenia 132
Beneficial effects of horsetail (Equisetum arvense) in experimental models of sarcopenia and osteoporosis 131
Natural products to counteract muscle atrophy 131
RAGE signalling in myoblasts and embryonal rhabdomyosarcoma cells represses Pax7 expression via p38 MAPK-dependent induction of myogenin. 128
Aged vs young human satellite cells: altered expression of S100B and RAGE, and defective ability in conditioning the medium contribute to impaired myogenic potential. 128
An ultrastructural study of Sertoli cells inside alginate microcapsules. 127
Screening of 100 plant extracts for the development of a herbal product effective against muscle atrophy 127
Sertoli cell-secreted factors have promyogenic and antifibrotic properties on human DMD myoblasts with different mutations. 126
The calcium-modulated proteins, S100A1 and S100B, as potential regulators of the dynamics of the type III intermediate filaments 125
RAGE and its ligands, S100B and HMGB1, are molecular determinants of cancer-induced muscle wasting. 125
Targeting RAGE as a potential therapeutic approach to Duchenne muscular dystrophy 122
Amphoterin stimulates myogenesis and counteracts the anti-myogenic factors, bFGF and S100B, via RAGE binding 121
S100B protein, a damage-associated molecular pattern protein in the brain and heart, and beyond 120
Hypoxia Promotes Danger-mediated Inflammation via Receptor for Advanced Glycation End Products in Cystic Fibrosis 120
Histological Muscle Characterization in Hypertrophied Marchigiana Beef Cattle Breed 119
Implication of RAGE and Amphoterin in Myogenesis 118
RAGE expression in rhabdomyosarcoma cells results in reduced proliferation, migration, and invasiveness in vitro and tumor growth in vivo 118
"Neuron-specific" protein gene product 9.5 (PGP 9.5) is also expressed in glioma cell lines and its expression depends on cellular growth 118
Glial S100B protein in neuroprotection and neurodegeneration 115
Different intrinsic properties of young and aged human satellite cells. 115
Appropriate levels of extracellular S100B protein in injured muscle are required for correct muscle regeneration. 111
Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice 109
Mdx/Ager–/– mice show reduced muscle necrosis and inflammation compared with mdx mice 109
S100B retards the biochemical differentiation of myoblasts and their fusion into myotubes 107
Association of S100B with intermediate filaments and microtubules in glial cells 107
Synergistic regulation of neurite outgrowth and cell survival by amphoterin and S100 proteins through RAGE activation 106
Involvement of a RAGE/p38MAPK/myogenin axis in cancer cachexia. 106
S100B inhibits myotube formation 105
Role of calcium-binding proteins (S100B, annexin II2-p112, annexin VI) in the regulation of GFAP intermediate filament dynamics 105
Receptor for advanced glycation end-products (RAGE) as a biomarker of muscle wasting in cancer conditions 105
Microencapsulated Sertoli cells sustain myoblast proliferation without affecting the myogenic potential. In vitro data 105
KYMASIN UP Natural Product Inhibits Osteoclastogenesis and Improves Osteoblast Activity by Modulating Src and p38 MAPK 104
S100B neuroprotective effect against ßamyloid-driven neurotoxicity 104
RAGE engagement in myoblasts modulates proliferation, apoptosis, adhesiveness, migration and invasiveness 104
Young and Aged Human Muscle Satellite Cells Show Differential Expression of S100B Protein and RAGE. 104
Transplantation of microencapsulated Sertoli cells: a new potential antiinflammatory approach to Duchenne muscular dystrophy (DMD). 104
Employment of Microencapsulated Sertoli Cells as a New Tool to Treat Duchenne Muscular Dystrophy 104
S100B causes apoptosis in a myoblast cell line in a RAGE-independent manner 103
Effects of S100B and S100A1 on cytoplasmic microtubules in triton-cytoskeletons from cell lines 102
Immunocytochemical detection of S100A1 and S100B in fused myotubes and related immunochemical analyses 102
Causes of elevated serum levels of S100B protein in athletes 102
RAGE signaling in myoblasts and rhabdomyosarcoma cells causes downregulation of Pax7 expression via p38 MAPK activation and upregulation of myogenin expression 101
Genetically-determined hyperfunction of the S100B/RAGE axis is a risk factor for aspergillosis in stem cell transplant recipients 101
Immunocytochemistry of S100B, annexin V and annexin VI in glial and microglial cells. 101
Hyperactivated rage in comorbidities as a risk factor for severe covid-19—the role of rage-ras crosstalk 101
Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? 100
The calcium-modulated proteins, S100A1 and S100B, as potential regulators of the dynamics of type III intermediate filaments 99
The danger signal S100B integrates pathogen- and danger-sensing pathways to restrain inflammation 99
S100B protein in tissue development, repair and regeneration 99
Levels of S100B protein drive the reparative process in acute muscle injury and muscular dystrophy 99
Use of Sertoli cells to treat DMD patients is supported by their immunomodulatory rather than immunosuppressive effect 99
Identification of Withania somnifera-Silybum marianum-Trigonella foenum-graecum Formulation as a Nutritional Supplement to Contrast Muscle Atrophy and Sarcopenia 99
Ablation of RAGE (receptor for advanced glycation end-products) translates into reduced tumorigenic and cachectic potential in LLC-tumor bearing mice 98
Effects of extracellular S100B, a calcium-binding protein of the EF-hand type, on a skeletal muscle cell line 98
Colocalization of S100B with intermediate filaments and microtubules in L6 myoblasts and U251 glial cells. 98
Cellular growth state-dependent expression of annexin V in glioma cell lines. 98
Caveolins and cavins in muscle-derived tumours. 98
Is the binding of S100A1 (and S100B) to synapsin I physiologically relevant? 98
Equisetum arvense standardized dried extract hinders age-related osteosarcopenia. 97
The role of a mindful movement-based program (Movimento Biologico) in health promotion: results of a pre-post intervention study 97
The calcium-modulated proteins, S100B and S100A1, disassemble cytoplasmic microtubules in situ. An in vitro study using triton-cytoskeletons from cell lines 97
The effects of microgravity on human skeletal muscle regeneration. 97
Defective RAGE activity in embryonal rhabdomyosarcoma cells results in high PAX7 levels that sustain migration and invasiveness 96
Effects of deletion of RAGE in muscle regeneration: preliminary observations. 95
S100B protein differentially regulates myoblast differentiation via direct binding to RAGE and bFGF-mediated activation of FGFR1 in low-density and high-density cultures, respectively 94
Human muscle satellite cells show age-related differential expression of S100B protein and RAGE. 94
Functions of S100 proteins 94
Opposing regulatory roles of S100B and amphoterin in myogenic differentiation: RAGE-dependence of amphoterin stimulatory effects vs. RAGE-independence of S100B inhibitory effects 93
Detection of membrane-bound guanylate cyclase activity in rat C6 glioma cells at different growth states following activation by natriuretic peptides 93
S100B and S100A1 disassemble cytoplasmic microtubules in triton-cytoskeletons from glioma and myoblast cells 92
S100B modulates beta-amyloid-induced neurotoxicity 92
Complex regulatory effects of extracellular S100B on myoblast differentiation: S100B activates quiescent myoblats and satellite cells 92
S100B engages RAGE or bFGF/FGFR1 in myoblasts depending on its own concentration and myoblast density. Implications for muscle regeneration 92
The receptor RAGE: a potential molecular target in cancer cachexia 92
Reductive stress in striated muscle cells 92
Colocalization of S100B with type III intermediate filaments and taxol-stabilized microtubules suggests that S100B might crosslink intermediate filaments to microtubules 91
Totale 11.689
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Categoria #
all - tutte 74.172
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 74.172
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021391 0 0 0 0 0 0 0 0 0 60 155 176
2021/20221.692 32 305 42 123 61 24 31 496 22 56 202 298
2022/20232.622 218 375 43 219 228 288 7 137 970 10 91 36
2023/20241.242 62 98 53 51 53 32 319 41 149 40 153 191
2024/20253.476 69 323 236 152 480 139 275 307 556 173 561 205
2025/20266.178 438 383 291 927 850 631 1.139 348 711 460 0 0
Totale 18.990