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

DONATO, Rosario Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 8.110
EU - Europa 7.257
AS - Asia 1.482
Continente sconosciuto - Info sul continente non disponibili 23
SA - Sud America 10
AF - Africa 5
OC - Oceania 5
Totale 16.892
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Nazione #
US - Stati Uniti d'America 8.096
UA - Ucraina 2.043
IE - Irlanda 1.354
SE - Svezia 1.154
IT - Italia 902
HK - Hong Kong 738
FI - Finlandia 377
DE - Germania 374
RU - Federazione Russa 311
CN - Cina 289
VN - Vietnam 245
GB - Regno Unito 225
RO - Romania 120
TR - Turchia 99
FR - Francia 94
CH - Svizzera 70
AT - Austria 55
BE - Belgio 48
PL - Polonia 46
UZ - Uzbekistan 29
LB - Libano 24
EU - Europa 23
GR - Grecia 20
NL - Olanda 20
SG - Singapore 13
SK - Slovacchia (Repubblica Slovacca) 13
PH - Filippine 12
KR - Corea 10
CZ - Repubblica Ceca 9
MX - Messico 9
BR - Brasile 8
BG - Bulgaria 6
AU - Australia 5
CA - Canada 5
TH - Thailandia 5
DK - Danimarca 4
JP - Giappone 4
ES - Italia 3
TW - Taiwan 3
ZM - Zambia 3
IL - Israele 2
IN - India 2
IQ - Iraq 2
MD - Moldavia 2
PT - Portogallo 2
AF - Afghanistan, Repubblica islamica di 1
BD - Bangladesh 1
BT - Bhutan 1
CI - Costa d'Avorio 1
CL - Cile 1
CY - Cipro 1
EC - Ecuador 1
HR - Croazia 1
IR - Iran 1
LT - Lituania 1
ME - Montenegro 1
NG - Nigeria 1
NO - Norvegia 1
RS - Serbia 1
Totale 16.892
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Città #
Chandler 1.724
Dublin 1.353
Jacksonville 1.138
San Mateo 796
Hong Kong 733
Wilmington 426
Medford 355
Princeton 353
Perugia 303
Ann Arbor 293
Ashburn 246
Dong Ket 245
Altamura 229
Andover 201
Lawrence 172
Saint Petersburg 115
Bucharest 110
Beijing 104
Des Moines 102
Izmir 97
Dearborn 85
Norwalk 81
Redmond 70
Woodbridge 67
Falls Church 65
Shanghai 64
Boardman 62
Helsinki 55
Brussels 48
Philadelphia 45
Los Angeles 31
Shenzhen 29
Auburn Hills 28
Vienna 27
New York 26
Houston 19
Den Haag 18
Rome 17
Lausanne 16
Redwood City 16
Kraków 14
Moscow 13
Nanning 13
Bratislava 12
Edinburgh 11
Terni 11
San Paolo di Civitate 10
Milan 9
San Diego 9
Cebu City 8
Tijuana 8
Chicago 7
Glasgow 7
Seoul 7
Belém 6
Frankfurt Am Main 6
Nanjing 6
Tappahannock 6
Frankfurt am Main 5
Guangzhou 5
Kunming 5
Padova 5
Simi Valley 5
Bragadiru 4
Copenhagen 4
Empoli 4
Fremont 4
Jinan 4
Ludwigshafen 4
Montreal 4
Phoenix 4
Quanzhou 4
Renton 4
Timisoara 4
Xiamen 4
Zhengzhou 4
Albuquerque 3
Bologna 3
Città Di Castello 3
Cosenza 3
Kiev 3
Nanchang 3
Napoli 3
Paris 3
Perth 3
Siena 3
Sofia 3
Ancona 2
Aquila 2
Athens 2
Aurora 2
Bangkok 2
Cagliari 2
Central 2
Cerro Maggiore 2
Changsha 2
Chisinau 2
Chur 2
Collazzone 2
Dumaguete 2
Totale 10.263
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Nome #
Le proteine S100 131
Artesunate induces ROS- and p38 MAPK-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells 120
Intraperitoneal injection of microencapsulated Sertoli cells restores muscle morphology and performance in dystrophic mice 111
Annexins V and VI in rat tissues during post-natal development: immunochemical measurements 106
Forced expression of S100B in a neuronal cell line (PC12) results in increased proliferation and reduced sensitivity to NGF 97
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 95
Artesunate induces ROS-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells. 95
Annexins V and VI in skeletal muscle cells: relationships with the calcium-modulated proteins, S100A1 and S100B 92
The Pathophysiological Role of Microglia in Dynamic Surveillance, Phagocytosis and Structural Remodeling of the Developing CNS 92
Analysis of S100A1, S100B and annexins V and VI in developing and adult avian skeletal muscles 89
RAGE signalling in myoblasts and embryonal rhabdomyosarcoma cells represses Pax7 expression via p38 MAPK-dependent induction of myogenin. 88
Glucocorticoid-Induced Leucine Zipper (GILZ) and Long GILZ Inhibit Myogenic Differentiation and Mediate Anti-myogenic Effects of Glucocorticoids 88
RAGE in the pathophysiology of skeletal muscle. 88
Extracellular S100B causes nuclear translocation of NF-?B in rat L6 myoblasts likely by binding to RAGE 87
Generation of an mdx/Ager–/– double mutant mouse. Preliminary data on skeletal muscle architecture. 85
RAGE expression in rhabdomyosarcoma cells results in reduced proliferation, migration, and invasiveness in vitro and tumor growth in vivo 81
Annexin V as a probe of the contribution of anionic phospholipids to the procoagulant activity of tumour cell surfaces 81
S100B neuroprotective effect against ßamyloid-driven neurotoxicity 79
Glial S100B protein in neuroprotection and neurodegeneration 79
Calcium- and protein kinase C-dependent association of S100A11 with S100B and vimentin intermediate filaments in LLC-PK1 renal cells 78
Activation of RAGE in myoblasts and rhabdomyosarcoma cells results in downregulation of Pax7 expression 78
An HMGB1/RAGE/p38 MAPK/Myogenin Axis Modulates Pax7 Expression in Myoblasts by Both Transcriptional and Post-Transcriptional Mechanisms 78
Interaction of annexins with S100 proteins. 77
Immunolocalization of secretory phospholipases A2 (sPLA2) in neural cells 77
Riflessioni in merito al problema: Identikit dell’Anatomico, in “Tavola rotonda sull’Identità dell’Anatomia” 76
Biological effects of astrocyte-derived S100-beta protein on BV-2 microglial cell line 76
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 76
Microglia and Aging: The Role of the TREM2-DAP12 and CX3CL1-CX3CR1 Axes 76
S100B retards the biochemical differentiation of myoblasts and their fusion into myotubes 74
Sertoli cells protect C2C12 myotubes against atrophy and induce utrophin expression in canine and human dystrophic myotubes. 74
Targeting RAGE as a potential therapeutic approach to Duchenne muscular dystrophy 74
Is the binding of S100A1 (and S100B) to synapsin I physiologically relevant? 74
S100B inhibits myotube formation 73
Implication of RAGE and Amphoterin in Myogenesis 73
S100B-mediated inhibition of the phosphorylation of GFAP is prevented by TRTK-12 73
Microglia-glioma cross-talk: a two way approach to new strategies against glioma 72
Probing Internalization Effects and Biocompatibility of Ultrasmall Zirconium Metal-Organic Frameworks UiO-66 NP in U251 Glioblastoma Cancer Cells 72
Immunocytochemical localization of S100A11 (S100C) in developing and adult avian skeletal muscles 71
Amphoterin-induced myogenic differentiation of RAGE-transfected rhabdomyosarcoma TE671 cells 71
S100B protein-dependent activation of microglia: RAGE ligation by S100B results in stimulation of IL-1beta and TNF-alpha secretion via MEK-ERK- and p38 MAPK-dependent activation of NF-kB 71
Opposing regulatory roles of S100B and amphoterin in myogenic differentiation: RAGE-dependence of amphoterin stimulatory effects vs. RAGE-independence of S100B inhibitory effects 70
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 70
Membrane-bound guanylate cyclase as the receptor of natriuretic peptides. A Minireview 70
Targeting mTOR in Glioblastoma: Rationale and Preclinical/Clinical Evidence 70
Potential role of S100B in the pathophysiology of neurodegenerative disorders 69
S100B protein in myoblasts modulates myogenic differentiation via NF-?B-dependent inhibition of MyoD expression. 69
S-100 protein in cerebral cortex synaptosomes 69
Time-resolved fluorescence of S-100a protein in absence and presence of calcium and phospholipids 69
PP242 counteracts glioblastoma cell proliferation, migration, invasiveness and stemness properties by inhibiting mTORC2/AKT 69
Relationships of annexins V and VI with the calcium-modulated proteins, S100A1 and S100B, in skeletal muscles 69
Effects of extracellular S100B, a calcium-binding protein of the EF-hand type, on a skeletal muscle cell line 68
The calcium-modulated proteins, S100A1 and S100B, as potential regulators of the dynamics of the type III intermediate filaments 68
Synergistic regulation of neurite outgrowth and cell survival by amphoterin and S100 proteins through RAGE activation 68
RAGE-independence of S100B inhibition of myogenic differentiation and myotube formation 68
Heterogeneity of the S-100 protein specific binding sites in synaptosomal particulate fractions 67
Effects of S100B and S100A1 on cytoplasmic microtubules in triton-cytoskeletons from cell lines 66
The calcium-modulated proteins, S100B and S100A1, disassemble cytoplasmic microtubules in situ. An in vitro study using triton-cytoskeletons from cell lines 66
Le vie e i centri del dolore cefalico: anatomia topografica e funzionale 66
Intracellular functions of S100B: S100B inhibits myoblast differentiation via stimulation of NF-kappaB transcriptional activity 66
Individual halves of annexin VI bind to distinct sites on S100B and S100A1 and differentially affect the inhibitory effects of S100B and S100A1 on GFAP assembly 65
Le vie ed i centri del dolore cefalico: anatomia topografica e funzionale 65
S100B protein interacts with and activates Src kinase in astrocytes thereby regulating cell shape and migration: implications for astrocyte development, activation and tumor growth. 65
Differential expression of S100B protein and RAGE in young and aged human satellite cells. 65
Intracellular and extracellular roles of S100 proteins 65
S100a6 65
Annexin II2-p112 (calpactin I) stimulates the assembly of GFAP in a calcium- and pH-dependent manner. 65
Amphoterin stimulates myogenesis and counteracts the anti-myogenic factors, bFGF and S100B, via RAGE binding 65
Toward the identification of receptor for advanced glycation end-products (RAGE) as a muscle biomarker of cancer cachexia. 65
S100B and S100A1 disassemble cytoplasmic microtubules in triton-cytoskeletons from glioma and myoblast cells 64
Cellular and molecular mechanisms of sarcopenia: the S100B perspective 64
Chlorpromazine inhibits the calcium-mediated effects of S-100 protein(s) on assembled brain microtubule proteins, but not those on microtubule protein assembly 63
Further studies on the specific interaction of S-100 protein with synaptosomal particulates 63
Annexin VI binds S100A1 and S100B and blocks the ability of S100A1 and S100B to inhibit desmin and GFAP assemblies into intermediate filaments 63
S-100 protein binds to annexin II and p11, the heavy and light chains of calpactin I 63
Aged vs young human satellite cells: altered expression of S100B and RAGE, and defective ability in conditioning the medium contribute to impaired myogenic potential. 63
Transplantation of microencapsulated Sertoli cells: a new potential antiinflammatory approach to Duchenne muscular dystrophy (DMD). 63
In planta expression of the vertebrate S100B protein as a tool for its funcional study. CNB 7. 7th National Biotechnology Congress 63
Role of Intracellular S100B in the Transition of Myoblasts from Quiescence to Proliferation and from Proliferation to Quiescence, and in Apoptosis. 62
The danger signal S100B integrates pathogen- and danger-sensing pathways to restrain inflammation 62
Muscular dystrophies share pathogenetic mechanisms with muscle sarcomas 62
Transplantation of microencapsulated Sertoli cells in mdx mice reduces muscle inflammation and promotes muscle regeneration 62
RAGE engagement in myoblasts modulates proliferation, apoptosis, adhesiveness, migration and invasiveness 61
S100B in myoblasts interferes with MyoD expression 61
RAGE signaling in myoblasts and rhabdomyosarcoma cells causes downregulation of Pax7 expression via p38 MAPK activation and upregulation of myogenin expression 61
EFFECT OF NGF ON PHOSPHOLIPASES A2 LOCALIZATION IN PC12 CELLS 61
Molecular mechanism of S100B-dependent inhibition of myoblast differentiation 61
Differential relocation of calcium-binding proteins in a renal cell line exposed to calcium ionophores or PMA 60
S100B/IFNgamma-stimulated NO secretion is mediated by p38 and SAPK/JNK kinases and is independent of RAGE signaling 60
S100B in myoblasts regulates the transition from activation to quiescence and from quiescence to activation, and reduces apoptosis 60
Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice 60
RAGE and its ligands, S100B and HMGB1, are molecular determinants of cancer-induced muscle wasting. 60
Effects of astrocyte-secreted S100B Ca2+-binding protein on microglial cells 59
Probing the mechanisms for interferon-? induction of inducible nitric oxide synthase in microglia (BV-2) cells 59
Effects of deletion of RAGE in muscle regeneration: preliminary observations. 59
Soluble and membrane-bound S-100 protein in cerebral cortex synaptosomes. Properties of the S-100 receptor 59
Genetically-determined hyperfunction of the S100B/RAGE axis is a risk factor for aspergillosis in stem cell transplant recipients 59
NGF Induces the Expression of Group IIA Secretory Phospholipase A2 in PC12 Cells: The Newly Synthesized Enzyme Is Addressed to Growing Neurites 59
Annexin V, annexin VI, S100A1 and S100B in developing and adult avian skeletal muscles 58
S100A11 (S100C) in developing and adult avian skeletal muscles 57
Role of S100B in neurosphere formation in the MIO-M1 Müller cell line 57
Totale 7.178
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Categoria #
all - tutte 57.492
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 57.492
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019155 0 0 0 0 0 0 0 0 0 0 143 12
2019/20201.899 13 17 296 13 301 78 336 25 457 82 25 256
2020/20213.685 7 297 149 293 1.037 235 367 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
2023/20241.541 107 221 111 68 44 25 494 78 350 43 0 0
Totale 17.534