DONATO, Rosario Francesco
 Distribuzione geografica
Continente #
NA - Nord America 10.898
EU - Europa 8.541
AS - Asia 6.660
SA - Sud America 1.401
AF - Africa 105
Continente sconosciuto - Info sul continente non disponibili 27
OC - Oceania 14
Totale 27.646
Nazione #
US - Stati Uniti d'America 10.721
SG - Singapore 2.852
UA - Ucraina 2.064
IE - Irlanda 1.357
BR - Brasile 1.188
SE - Svezia 1.180
HK - Hong Kong 1.164
IT - Italia 1.044
CN - Cina 1.013
RU - Federazione Russa 832
VN - Vietnam 627
DE - Germania 560
KR - Corea 453
FI - Finlandia 437
GB - Regno Unito 315
FR - Francia 153
TR - Turchia 140
RO - Romania 125
AR - Argentina 88
PL - Polonia 85
CA - Canada 83
CH - Svizzera 72
IN - India 67
AT - Austria 66
MX - Messico 59
BE - Belgio 53
UZ - Uzbekistan 49
BD - Bangladesh 45
NL - Olanda 45
EC - Ecuador 42
IQ - Iraq 41
ZA - Sudafrica 39
JP - Giappone 37
ES - Italia 28
LB - Libano 26
CO - Colombia 25
CZ - Repubblica Ceca 23
EU - Europa 23
ID - Indonesia 21
PK - Pakistan 21
GR - Grecia 20
MA - Marocco 18
SK - Slovacchia (Repubblica Slovacca) 17
CL - Cile 16
LT - Lituania 15
PH - Filippine 15
PY - Paraguay 14
JM - Giamaica 13
AZ - Azerbaigian 11
KE - Kenya 11
PE - Perù 11
AU - Australia 10
BG - Bulgaria 10
EG - Egitto 10
VE - Venezuela 10
AE - Emirati Arabi Uniti 9
AL - Albania 9
IL - Israele 7
SA - Arabia Saudita 7
TN - Tunisia 7
JO - Giordania 6
KZ - Kazakistan 6
DK - Danimarca 5
DO - Repubblica Dominicana 5
MY - Malesia 5
NP - Nepal 5
TH - Thailandia 5
LV - Lettonia 4
MD - Moldavia 4
PT - Portogallo 4
UY - Uruguay 4
XK - ???statistics.table.value.countryCode.XK??? 4
CR - Costa Rica 3
GE - Georgia 3
GT - Guatemala 3
HR - Croazia 3
IR - Iran 3
KW - Kuwait 3
NZ - Nuova Zelanda 3
PA - Panama 3
RS - Serbia 3
SN - Senegal 3
TW - Taiwan 3
ZM - Zambia 3
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
BO - Bolivia 2
DZ - Algeria 2
HN - Honduras 2
KH - Cambogia 2
MK - Macedonia 2
MN - Mongolia 2
NG - Nigeria 2
NO - Norvegia 2
TT - Trinidad e Tobago 2
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AO - Angola 1
BT - Bhutan 1
BY - Bielorussia 1
Totale 27.623
Città #
Singapore 1.906
Chandler 1.724
Dublin 1.356
Hong Kong 1.157
Jacksonville 1.139
San Mateo 796
Boardman 563
Ashburn 550
Seoul 434
Wilmington 426
Santa Clara 422
Medford 355
Princeton 353
Perugia 335
Ann Arbor 293
Moscow 276
Dong Ket 245
Altamura 229
Andover 201
Beijing 197
Piscataway 183
Lawrence 172
Ho Chi Minh City 135
Los Angeles 127
Munich 121
Saint Petersburg 115
Bucharest 110
São Paulo 107
Des Moines 102
New York 102
Izmir 99
Helsinki 87
Dearborn 85
Norwalk 82
Shanghai 82
Hanoi 78
Redmond 70
Woodbridge 67
Falls Church 65
The Dalles 60
Council Bluffs 54
Brussels 52
Philadelphia 45
Dallas 40
Rio de Janeiro 40
Houston 39
Montreal 37
Vienna 35
Boston 34
Brooklyn 33
Rome 33
Shenzhen 33
Chicago 32
Warsaw 32
Frankfurt am Main 31
Tokyo 29
Auburn Hills 28
Chennai 28
Stockholm 27
Johannesburg 26
Belo Horizonte 25
Phoenix 25
Turku 25
Milan 24
Orem 23
Brasília 21
Denver 21
Guangzhou 21
London 21
San Jose 21
Atlanta 19
Campinas 19
Da Nang 19
Guayaquil 19
Tashkent 19
Den Haag 18
Falkenstein 18
Haiphong 18
Poplar 18
San Francisco 17
Ankara 16
Bratislava 16
Columbus 16
Lausanne 16
Redwood City 16
Manchester 15
Mexico City 15
Nanning 15
Kraków 14
Osasco 14
Porto Alegre 14
Baghdad 13
Dhaka 13
Bologna 12
Nuremberg 12
Toronto 12
Zhengzhou 12
Baku 11
Caxias do Sul 11
Charlotte 11
Totale 16.399
Nome #
Le proteine S100 230
Artesunate induces ROS- and p38 MAPK-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells 180
Intraperitoneal injection of microencapsulated Sertoli cells restores muscle morphology and performance in dystrophic mice 155
Annexins V and VI in rat tissues during post-natal development: immunochemical measurements 147
Annexins V and VI in skeletal muscle cells: relationships with the calcium-modulated proteins, S100A1 and S100B 146
Artesunate induces ROS-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells. 141
Analysis of S100A1, S100B and annexins V and VI in developing and adult avian skeletal muscles 140
An HMGB1/RAGE/p38 MAPK/Myogenin Axis Modulates Pax7 Expression in Myoblasts by Both Transcriptional and Post-Transcriptional Mechanisms 139
Forced expression of S100B in a neuronal cell line (PC12) results in increased proliferation and reduced sensitivity to NGF 137
Immunocytochemical detection of the calcium-regulated proteins, S100B and S100A1, in bovine retina: their calcium-dependent stimulation of a membrane-bound guanylate cyclase activity as investigated by ultracytochemistry 135
Biological effects of astrocyte-derived S100-beta protein on BV-2 microglial cell line 129
Extracellular S100B causes nuclear translocation of NF-?B in rat L6 myoblasts likely by binding to RAGE 129
RAGE in the pathophysiology of skeletal muscle. 128
Calcium- and protein kinase C-dependent association of S100A11 with S100B and vimentin intermediate filaments in LLC-PK1 renal cells 127
Glucocorticoid-Induced Leucine Zipper (GILZ) and Long GILZ Inhibit Myogenic Differentiation and Mediate Anti-myogenic Effects of Glucocorticoids 127
Annexin V as a probe of the contribution of anionic phospholipids to the procoagulant activity of tumour cell surfaces 124
Generation of an mdx/Ager–/– double mutant mouse. Preliminary data on skeletal muscle architecture. 124
Activation of RAGE in myoblasts and rhabdomyosarcoma cells results in downregulation of Pax7 expression 123
Differential expression of S100B protein and RAGE in young and aged human satellite cells. 123
Targeting RAGE prevents muscle wasting and prolongs survival in cancer cachexia 123
Sertoli cells protect C2C12 myotubes against atrophy and induce utrophin expression in canine and human dystrophic myotubes. 122
The Pathophysiological Role of Microglia in Dynamic Surveillance, Phagocytosis and Structural Remodeling of the Developing CNS 121
Amphoterin-induced myogenic differentiation of RAGE-transfected rhabdomyosarcoma TE671 cells 120
Oxidative stress-induced S100B accumulation converts myoblasts into brown adipocytes via an NF-κB/YY1/miR-133 axis and NF-κB/YY1/BMP-7 axis 120
S100B protein regulates myoblast and macrophage functions in skeletal muscle regeneration 120
A braking circuit between pathogen- and danger-sensing signaling pathways restrains lung inflammation: role of S100B protein, RAGE and Toll-like receptors. 119
Microglia and Aging: The Role of the TREM2-DAP12 and CX3CL1-CX3CR1 Axes 117
RAGE signalling in myoblasts and embryonal rhabdomyosarcoma cells represses Pax7 expression via p38 MAPK-dependent induction of myogenin. 116
Aged vs young human satellite cells: altered expression of S100B and RAGE, and defective ability in conditioning the medium contribute to impaired myogenic potential. 116
Annexin VI binds S100A1 and S100B and blocks the ability of S100A1 and S100B to inhibit desmin and GFAP assemblies into intermediate filaments 115
Cellular and molecular mechanisms of sarcopenia: the S100B perspective 115
Microglia-glioma cross-talk: a two way approach to new strategies against glioma 114
PP242 counteracts glioblastoma cell proliferation, migration, invasiveness and stemness properties by inhibiting mTORC2/AKT 114
Probing Internalization Effects and Biocompatibility of Ultrasmall Zirconium Metal-Organic Frameworks UiO-66 NP in U251 Glioblastoma Cancer Cells 114
Toward the identification of receptor for advanced glycation end-products (RAGE) as a muscle biomarker of cancer cachexia. 114
RAGE expression in rhabdomyosarcoma cells results in reduced proliferation, migration, and invasiveness in vitro and tumor growth in vivo 113
Annexin II2-p112 (calpactin I) stimulates the assembly of GFAP in a calcium- and pH-dependent manner. 112
Amphoterin stimulates myogenesis and counteracts the anti-myogenic factors, bFGF and S100B, via RAGE binding 110
RAGE and its ligands, S100B and HMGB1, are molecular determinants of cancer-induced muscle wasting. 110
The calcium-modulated proteins, S100A1 and S100B, as potential regulators of the dynamics of the type III intermediate filaments 108
S-100 proteins and microtubules: analysis of the effects of rat brain S-100 (S-100b) and ox brain S-l00ao, S-l00a and S-l00b on microtubule assembly-disassembly 107
S-100 protein in cerebral cortex synaptosomes 107
Targeting RAGE as a potential therapeutic approach to Duchenne muscular dystrophy 107
Targeting mTOR in Glioblastoma: Rationale and Preclinical/Clinical Evidence 107
Immunolocalization of secretory phospholipases A2 (sPLA2) in neural cells 105
Absence of RAGE in an animal experimental model of Duchenne muscular dystrophy results in reduced muscle necrosis and inflammation 103
Interaction of annexins with S100 proteins. 102
Implication of RAGE and Amphoterin in Myogenesis 102
S100B protein in myoblasts modulates myogenic differentiation via NF-?B-dependent inhibition of MyoD expression. 102
Glial S100B protein in neuroprotection and neurodegeneration 101
Role of the C-terminal extension in the interaction of S100A1 with GFAP, tubulin, the S100A1- and S100B-inhibitory peptide, TRTK-12, and a peptide derived from p53, and the S100A1 inhibitory effect on GFAP polymerization 101
S-100 protein binds to annexin II and p11, the heavy and light chains of calpactin I 100
Riflessioni in merito al problema: Identikit dell’Anatomico, in “Tavola rotonda sull’Identità dell’Anatomia” 99
S100B-mediated inhibition of the phosphorylation of GFAP is prevented by TRTK-12 99
Group II phospholipase A2 (GIIA) is involved in neuritogenesis in NGF-treated PC12 cells. 99
S100B neuroprotective effect against ßamyloid-driven neurotoxicity 98
Codistribution of S100A1 with synapsin I in discrete brain areas: S100A1 inhibits the F-actin bundling activity of synapsin I 98
Immunohistochemical localization of annexin V (CaBP33) in rat organs 98
Annexin V, annexin VI, S100A1 and S100B in developing and adult avian skeletal muscles 98
S100B in myoblasts regulates the transition from activation to quiescence and from quiescence to activation, and reduces apoptosis 98
S100B retards the biochemical differentiation of myoblasts and their fusion into myotubes 97
Immunocytochemical localization of S100A11 (S100C) in developing and adult avian skeletal muscles 97
Different intrinsic properties of young and aged human satellite cells. 97
EFFECT OF NGF ON PHOSPHOLIPASES A2 LOCALIZATION IN PC12 CELLS 97
Hypoxia Promotes Danger-mediated Inflammation via Receptor for Advanced Glycation End Products in Cystic Fibrosis 97
S100B inhibits myotube formation 96
Human S100B protein localizes to the nucleus in Nicotiana Tabacum 96
The Glucocorticoid-Induced Leucine Zipper (GILZ) inhibits skeletal myogenesis by counteracting MyoD activity 96
Calpactin I binds to the glial fibrillary acidic protein (GFAP) and to glial filaments in a Ca2+-dependent manner. Implications for concerted regulatory effects of calpactin I and S100 protein on glial filaments 95
"Neuron-specific" protein gene product 9.5 (PGP 9.5) is also expressed in glioma cell lines and its expression depends on cellular growth 95
Immunocytochemical localization of S-100b protein in olfactory and supporting cells of lamb olfactory epithelium 95
Bovine annexin V isoforms: a molecular weight difference of 4 kDa by SDS-PAGE, 9 D by mass spectrometry 95
Effects of S100B and S100A1 on cytoplasmic microtubules in triton-cytoskeletons from cell lines 94
Intracellular functions of S100B: S100B inhibits myoblast differentiation via stimulation of NF-kappaB transcriptional activity 94
S100B protein interacts with and activates Src kinase in astrocytes thereby regulating cell shape and migration: implications for astrocyte development, activation and tumor growth. 94
Association of S100B with intermediate filaments and microtubules in glial cells 94
Immunocytochemical localization of S-100b protein in degenerating and regenerating rat sciatic nerves 94
NGF Induces the Expression of Group IIA Secretory Phospholipase A2 in PC12 Cells: The Newly Synthesized Enzyme Is Addressed to Growing Neurites 94
Membrane-bound guanylate cyclase as the receptor of natriuretic peptides. A Minireview 93
Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice 93
Effects of extracellular S100B, a calcium-binding protein of the EF-hand type, on a skeletal muscle cell line 92
Anti-myogenic activity of S100B in myoblasts 92
Immunocytochemical detection of S100A1 and S100B in fused myotubes and related immunochemical analyses 92
Effect of NGF on the Subcellular Localization of Group IIA Secretory Phospholipase A2 (GIIA) in PC12 Cells: Role in Neuritogenesis. 92
Appropriate levels of extracellular S100B protein in injured muscle are required for correct muscle regeneration. 92
Synergistic regulation of neurite outgrowth and cell survival by amphoterin and S100 proteins through RAGE activation 91
RAGE engagement in myoblasts modulates proliferation, apoptosis, adhesiveness, migration and invasiveness 91
Cellular and subcellular distribution of secretory PLA2 in neural cells 91
Is the binding of S100A1 (and S100B) to synapsin I physiologically relevant? 91
Time-resolved fluorescence of S-100a protein in absence and presence of calcium and phospholipids 90
Transplantation of microencapsulated Sertoli cells: a new potential antiinflammatory approach to Duchenne muscular dystrophy (DMD). 90
S100B in myoblasts inhibits myotube formation by interfering with MyoD 89
Relationships of annexins V and VI with the calcium-modulated proteins, S100A1 and S100B, in skeletal muscles 89
Opposing regulatory roles of S100B and amphoterin in myogenic differentiation: RAGE-dependence of amphoterin stimulatory effects vs. RAGE-independence of S100B inhibitory effects 88
S100B in myoblasts interferes with MyoD expression 88
S100B protein, a damage-associated molecular pattern protein in the brain and heart, and beyond 88
Levels of S100B protein drive the reparative process in acute muscle injury and muscular dystrophy 88
Characterization of mammalian heart annexins with special reference to CaBP33 (annexin V) 88
S100B-stimulated NO production by BV-2 microglia is independent of RAGE transducing activity but dependent on RAGE extracellular domain 87
Distribution of secretory phospholipase A2 (PLA2) in neural cells 87
Totale 10.847
Categoria #
all - tutte 119.438
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 119.438


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.902 0 0 0 0 0 235 367 12 463 122 357 346
2021/20223.247 74 573 117 221 143 42 52 917 28 124 390 566
2022/20235.142 425 800 80 437 444 559 13 285 1.848 16 177 58
2023/20242.069 107 221 111 68 44 25 494 78 350 43 262 266
2024/20254.672 52 530 358 148 668 121 298 395 875 198 737 292
2025/20265.560 702 764 523 1.584 1.238 749 0 0 0 0 0 0
Totale 28.294