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

DONATO, Rosario Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 9.221
EU - Europa 7.385
AS - Asia 2.608
SA - Sud America 40
Continente sconosciuto - Info sul continente non disponibili 24
AF - Africa 7
OC - Oceania 6
Totale 19.291
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Nazione #
US - Stati Uniti d'America 9.195
UA - Ucraina 2.043
IE - Irlanda 1.355
SE - Svezia 1.154
SG - Singapore 999
IT - Italia 949
HK - Hong Kong 739
DE - Germania 402
FI - Finlandia 390
CN - Cina 386
RU - Federazione Russa 311
VN - Vietnam 246
GB - Regno Unito 233
RO - Romania 121
FR - Francia 101
TR - Turchia 101
CH - Svizzera 70
AT - Austria 55
BE - Belgio 50
PL - Polonia 46
KR - Corea 41
BR - Brasile 34
UZ - Uzbekistan 30
LB - Libano 25
EU - Europa 23
NL - Olanda 23
GR - Grecia 20
CZ - Repubblica Ceca 19
MX - Messico 15
SK - Slovacchia (Repubblica Slovacca) 15
PH - Filippine 12
CA - Canada 11
BG - Bulgaria 7
AU - Australia 5
TH - Thailandia 5
DK - Danimarca 4
ES - Italia 4
JP - Giappone 4
IL - Israele 3
MD - Moldavia 3
PT - Portogallo 3
TW - Taiwan 3
ZM - Zambia 3
CO - Colombia 2
IN - India 2
IQ - Iraq 2
LT - Lituania 2
NO - Norvegia 2
PK - Pakistan 2
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
AZ - Azerbaigian 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
MA - Marocco 1
ME - Montenegro 1
MY - Malesia 1
NG - Nigeria 1
NZ - Nuova Zelanda 1
PE - Perù 1
PY - Paraguay 1
RS - Serbia 1
TN - Tunisia 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 19.291
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Città #
Chandler 1.724
Dublin 1.354
Jacksonville 1.138
San Mateo 796
Singapore 789
Hong Kong 734
Boardman 563
Wilmington 426
Santa Clara 404
Medford 355
Princeton 353
Perugia 310
Ann Arbor 293
Ashburn 263
Dong Ket 245
Altamura 229
Andover 201
Lawrence 172
Saint Petersburg 115
Bucharest 110
Beijing 105
Des Moines 102
Izmir 97
Dearborn 85
Norwalk 81
Redmond 70
Shanghai 70
Helsinki 67
Woodbridge 67
Falls Church 65
Brussels 50
Philadelphia 45
Seoul 38
Los Angeles 36
Shenzhen 30
Auburn Hills 28
New York 27
Vienna 27
Munich 25
Rome 22
Dallas 19
Houston 19
Den Haag 18
Lausanne 16
Redwood City 16
Bratislava 14
Kraków 14
Moscow 13
Nanning 13
Edinburgh 11
Milan 11
Terni 11
San Paolo di Civitate 10
Guangzhou 9
Olomouc 9
San Diego 9
Cebu City 8
Tijuana 8
Chicago 7
Glasgow 7
London 7
Phoenix 7
Belém 6
Frankfurt Am Main 6
Frankfurt am Main 6
Nanjing 6
Tappahannock 6
Zhengzhou 6
Kunming 5
Padova 5
Simi Valley 5
Bragadiru 4
Copenhagen 4
Empoli 4
Fremont 4
Jinan 4
Ludwigshafen 4
Montreal 4
Ottawa 4
Paris 4
Quanzhou 4
Renton 4
Sofia 4
Timisoara 4
Xiamen 4
Albuquerque 3
Bologna 3
Chisinau 3
Città Di Castello 3
Cosenza 3
Florence 3
Kiev 3
Lappeenranta 3
Lisbon 3
Madrid 3
Nanchang 3
Napoli 3
Perth 3
Pollenza 3
Prague 3
Totale 12.119
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Nome #
Le proteine S100 165
Artesunate induces ROS- and p38 MAPK-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells 130
Intraperitoneal injection of microencapsulated Sertoli cells restores muscle morphology and performance in dystrophic mice 119
Annexins V and VI in rat tissues during post-natal development: immunochemical measurements 115
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 105
Artesunate induces ROS-mediated apoptosis and counteracts tumor growth in vivo in embryonal rhabdomyosarcoma cells. 105
Forced expression of S100B in a neuronal cell line (PC12) results in increased proliferation and reduced sensitivity to NGF 104
Annexins V and VI in skeletal muscle cells: relationships with the calcium-modulated proteins, S100A1 and S100B 101
RAGE in the pathophysiology of skeletal muscle. 101
RAGE signalling in myoblasts and embryonal rhabdomyosarcoma cells represses Pax7 expression via p38 MAPK-dependent induction of myogenin. 99
Analysis of S100A1, S100B and annexins V and VI in developing and adult avian skeletal muscles 99
Glucocorticoid-Induced Leucine Zipper (GILZ) and Long GILZ Inhibit Myogenic Differentiation and Mediate Anti-myogenic Effects of Glucocorticoids 97
An HMGB1/RAGE/p38 MAPK/Myogenin Axis Modulates Pax7 Expression in Myoblasts by Both Transcriptional and Post-Transcriptional Mechanisms 95
The Pathophysiological Role of Microglia in Dynamic Surveillance, Phagocytosis and Structural Remodeling of the Developing CNS 95
RAGE expression in rhabdomyosarcoma cells results in reduced proliferation, migration, and invasiveness in vitro and tumor growth in vivo 94
Extracellular S100B causes nuclear translocation of NF-?B in rat L6 myoblasts likely by binding to RAGE 94
Generation of an mdx/Ager–/– double mutant mouse. Preliminary data on skeletal muscle architecture. 91
Annexin V as a probe of the contribution of anionic phospholipids to the procoagulant activity of tumour cell surfaces 90
Calcium- and protein kinase C-dependent association of S100A11 with S100B and vimentin intermediate filaments in LLC-PK1 renal cells 89
Sertoli cells protect C2C12 myotubes against atrophy and induce utrophin expression in canine and human dystrophic myotubes. 89
S100B protein regulates myoblast and macrophage functions in skeletal muscle regeneration 88
Activation of RAGE in myoblasts and rhabdomyosarcoma cells results in downregulation of Pax7 expression 87
Probing Internalization Effects and Biocompatibility of Ultrasmall Zirconium Metal-Organic Frameworks UiO-66 NP in U251 Glioblastoma Cancer Cells 86
Glial S100B protein in neuroprotection and neurodegeneration 85
S100B neuroprotective effect against ßamyloid-driven neurotoxicity 84
Biological effects of astrocyte-derived S100-beta protein on BV-2 microglial cell line 84
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 84
Interaction of annexins with S100 proteins. 83
Immunolocalization of secretory phospholipases A2 (sPLA2) in neural cells 83
Riflessioni in merito al problema: Identikit dell’Anatomico, in “Tavola rotonda sull’Identità dell’Anatomia” 82
S-100 protein in cerebral cortex synaptosomes 82
Microglia and Aging: The Role of the TREM2-DAP12 and CX3CL1-CX3CR1 Axes 82
The calcium-modulated proteins, S100A1 and S100B, as potential regulators of the dynamics of the type III intermediate filaments 81
S100B retards the biochemical differentiation of myoblasts and their fusion into myotubes 80
Implication of RAGE and Amphoterin in Myogenesis 80
Microglia-glioma cross-talk: a two way approach to new strategies against glioma 80
S100B-mediated inhibition of the phosphorylation of GFAP is prevented by TRTK-12 79
Amphoterin-induced myogenic differentiation of RAGE-transfected rhabdomyosarcoma TE671 cells 79
Differential expression of S100B protein and RAGE in young and aged human satellite cells. 79
S100B inhibits myotube formation 78
PP242 counteracts glioblastoma cell proliferation, migration, invasiveness and stemness properties by inhibiting mTORC2/AKT 78
Targeting RAGE as a potential therapeutic approach to Duchenne muscular dystrophy 78
Effects of extracellular S100B, a calcium-binding protein of the EF-hand type, on a skeletal muscle cell line 77
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 77
Cellular and molecular mechanisms of sarcopenia: the S100B perspective 77
Is the binding of S100A1 (and S100B) to synapsin I physiologically relevant? 77
Toward the identification of receptor for advanced glycation end-products (RAGE) as a muscle biomarker of cancer cachexia. 77
S100B protein in myoblasts modulates myogenic differentiation via NF-?B-dependent inhibition of MyoD expression. 76
Membrane-bound guanylate cyclase as the receptor of natriuretic peptides. A Minireview 76
Aged vs young human satellite cells: altered expression of S100B and RAGE, and defective ability in conditioning the medium contribute to impaired myogenic potential. 76
Targeting mTOR in Glioblastoma: Rationale and Preclinical/Clinical Evidence 76
Opposing regulatory roles of S100B and amphoterin in myogenic differentiation: RAGE-dependence of amphoterin stimulatory effects vs. RAGE-independence of S100B inhibitory effects 75
Synergistic regulation of neurite outgrowth and cell survival by amphoterin and S100 proteins through RAGE activation 75
Immunocytochemical localization of S100A11 (S100C) in developing and adult avian skeletal muscles 75
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 75
Effects of S100B and S100A1 on cytoplasmic microtubules in triton-cytoskeletons from cell lines 74
Potential role of S100B in the pathophysiology of neurodegenerative disorders 74
Heterogeneity of the S-100 protein specific binding sites in synaptosomal particulate fractions 74
Time-resolved fluorescence of S-100a protein in absence and presence of calcium and phospholipids 74
Annexin II2-p112 (calpactin I) stimulates the assembly of GFAP in a calcium- and pH-dependent manner. 74
Relationships of annexins V and VI with the calcium-modulated proteins, S100A1 and S100B, in skeletal muscles 74
Targeting RAGE prevents muscle wasting and prolongs survival in cancer cachexia 74
Intracellular functions of S100B: S100B inhibits myoblast differentiation via stimulation of NF-kappaB transcriptional activity 73
S-100 protein binds to annexin II and p11, the heavy and light chains of calpactin I 73
S100B and S100A1 disassemble cytoplasmic microtubules in triton-cytoskeletons from glioma and myoblast cells 72
Le vie e i centri del dolore cefalico: anatomia topografica e funzionale 72
S100B protein interacts with and activates Src kinase in astrocytes thereby regulating cell shape and migration: implications for astrocyte development, activation and tumor growth. 72
Amphoterin stimulates myogenesis and counteracts the anti-myogenic factors, bFGF and S100B, via RAGE binding 72
RAGE and its ligands, S100B and HMGB1, are molecular determinants of cancer-induced muscle wasting. 72
RAGE signaling in myoblasts and rhabdomyosarcoma cells causes downregulation of Pax7 expression via p38 MAPK activation and upregulation of myogenin expression 71
Annexin VI binds S100A1 and S100B and blocks the ability of S100A1 and S100B to inhibit desmin and GFAP assemblies into intermediate filaments 71
RAGE-independence of S100B inhibition of myogenic differentiation and myotube formation 71
The calcium-modulated proteins, S100B and S100A1, disassemble cytoplasmic microtubules in situ. An in vitro study using triton-cytoskeletons from cell lines 70
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 70
Le vie ed i centri del dolore cefalico: anatomia topografica e funzionale 70
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 70
Annexin V, annexin VI, S100A1 and S100B in developing and adult avian skeletal muscles 70
Transplantation of microencapsulated Sertoli cells: a new potential antiinflammatory approach to Duchenne muscular dystrophy (DMD). 70
Intracellular and extracellular roles of S100 proteins 69
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 69
EFFECT OF NGF ON PHOSPHOLIPASES A2 LOCALIZATION IN PC12 CELLS 69
NGF Induces the Expression of Group IIA Secretory Phospholipase A2 in PC12 Cells: The Newly Synthesized Enzyme Is Addressed to Growing Neurites 69
Transplantation of microencapsulated Sertoli cells in mdx mice reduces muscle inflammation and promotes muscle regeneration 69
Role of Intracellular S100B in the Transition of Myoblasts from Quiescence to Proliferation and from Proliferation to Quiescence, and in Apoptosis. 68
Chlorpromazine inhibits the calcium-mediated effects of S-100 protein(s) on assembled brain microtubule proteins, but not those on microtubule protein assembly 68
Further studies on the specific interaction of S-100 protein with synaptosomal particulates 68
Soluble and membrane-bound S-100 protein in cerebral cortex synaptosomes. Properties of the S-100 receptor 68
S100a6 68
S100B in myoblasts regulates the transition from activation to quiescence and from quiescence to activation, and reduces apoptosis 68
In planta expression of the vertebrate S100B protein as a tool for its funcional study. CNB 7. 7th National Biotechnology Congress 68
S100B in myoblasts interferes with MyoD expression 67
Effects of deletion of RAGE in muscle regeneration: preliminary observations. 67
Muscular dystrophies share pathogenetic mechanisms with muscle sarcomas 67
Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice 67
Differential relocation of calcium-binding proteins in a renal cell line exposed to calcium ionophores or PMA 66
RAGE engagement in myoblasts modulates proliferation, apoptosis, adhesiveness, migration and invasiveness 66
A braking circuit between pathogen- and danger-sensing signaling pathways restrains lung inflammation: role of S100B protein, RAGE and Toll-like receptors. 66
Genetically-determined hyperfunction of the S100B/RAGE axis is a risk factor for aspergillosis in stem cell transplant recipients 66
The danger signal S100B integrates pathogen- and danger-sensing pathways to restrain inflammation 66
Effects of astrocyte-secreted S100B Ca2+-binding protein on microglial cells 65
Totale 8.009
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Categoria #
all - tutte 79.023
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 79.023
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.259 0 0 0 0 0 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
2023/20242.069 107 221 111 68 44 25 494 78 350 43 262 266
2024/20251.871 52 530 358 148 668 115 0 0 0 0 0 0
Totale 19.933