SQUARZONI, STEFANO
 Distribuzione geografica
Continente #
AS - Asia 2.178
NA - Nord America 1.667
EU - Europa 499
SA - Sud America 423
Continente sconosciuto - Info sul continente non disponibili 67
AF - Africa 38
OC - Oceania 4
Totale 4.876
Nazione #
US - Stati Uniti d'America 1.569
SG - Singapore 896
CN - Cina 526
BR - Brasile 321
HK - Hong Kong 220
VN - Vietnam 206
IT - Italia 166
FR - Francia 141
KR - Corea 109
IN - India 44
BD - Bangladesh 40
FI - Finlandia 40
CA - Canada 38
NL - Olanda 36
JP - Giappone 35
AR - Argentina 34
GB - Regno Unito 28
CO - Colombia 24
MX - Messico 23
DE - Germania 22
EC - Ecuador 18
IQ - Iraq 14
IL - Israele 13
ZA - Sudafrica 13
ID - Indonesia 12
PL - Polonia 10
VE - Venezuela 10
JM - Giamaica 9
MY - Malesia 8
SE - Svezia 8
PH - Filippine 7
PK - Pakistan 7
CL - Cile 6
CR - Costa Rica 6
ES - Italia 6
MA - Marocco 6
PT - Portogallo 6
RU - Federazione Russa 6
BO - Bolivia 5
EG - Egitto 5
TR - Turchia 5
TT - Trinidad e Tobago 5
AL - Albania 4
DO - Repubblica Dominicana 4
DZ - Algeria 4
KZ - Kazakistan 4
NP - Nepal 4
AE - Emirati Arabi Uniti 3
GR - Grecia 3
HN - Honduras 3
JO - Giordania 3
LV - Lettonia 3
OM - Oman 3
PY - Paraguay 3
RO - Romania 3
SA - Arabia Saudita 3
TW - Taiwan 3
UA - Ucraina 3
AT - Austria 2
AU - Australia 2
BE - Belgio 2
CZ - Repubblica Ceca 2
EE - Estonia 2
GT - Guatemala 2
IE - Irlanda 2
KE - Kenya 2
KG - Kirghizistan 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
PA - Panama 2
SC - Seychelles 2
TN - Tunisia 2
UY - Uruguay 2
UZ - Uzbekistan 2
AG - Antigua e Barbuda 1
AZ - Azerbaigian 1
BJ - Benin 1
BW - Botswana 1
CM - Camerun 1
CU - Cuba 1
CY - Cipro 1
DK - Danimarca 1
GD - Grenada 1
HR - Croazia 1
KW - Kuwait 1
LT - Lituania 1
MN - Mongolia 1
NG - Nigeria 1
PS - Palestinian Territory 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TC - Turks e Caicos 1
TH - Thailandia 1
TJ - Tagikistan 1
Totale 4.809
Città #
Santa Clara 610
Singapore 509
Hefei 272
Hong Kong 215
San Jose 193
Ashburn 123
Seoul 109
Lauterbourg 97
Beijing 77
Ho Chi Minh City 70
Hanoi 47
Los Angeles 45
Helsinki 32
Pavia 27
São Paulo 26
Tokyo 20
Buffalo 18
New York 18
Dallas 17
Orem 17
Da Nang 16
Milan 16
Bologna 15
Minamishinagawa 15
Chicago 13
Rio de Janeiro 12
Council Bluffs 11
Phoenix 11
Bengaluru 10
Frankfurt am Main 10
Montreal 10
Chennai 9
Belo Horizonte 8
Denver 8
London 8
Baghdad 7
Brasília 7
Düsseldorf 7
Guayaquil 7
Haiphong 7
Johannesburg 7
Kingston 7
Quito 7
Rome 7
San Francisco 7
Sorocaba 7
Amsterdam 6
Brooklyn 6
Catania 6
Houston 6
San José 6
Atlanta 5
Biên Hòa 5
Bogotá 5
Cleveland 5
Dayton 5
Hải Dương 5
Lappeenranta 5
Naples 5
Philadelphia 5
Saint-Martin-d'Hères 5
San Antonio 5
Tampa 5
Toronto 5
Boardman 4
Boston 4
Cincinnati 4
Curitiba 4
Guarulhos 4
La Paz 4
Lisbon 4
Medellín 4
Memphis 4
Pittsburgh 4
Recife 4
Stockholm 4
São Bernardo do Campo 4
The Bronx 4
Thái Bình 4
Tirana 4
Verona 4
Warsaw 4
Washington 4
Wroclaw 4
Albignasego 3
Albuquerque 3
Amman 3
Anápolis 3
Belleville 3
Cairo 3
City of London 3
Dhaka 3
Elk Grove Village 3
Goiânia 3
Guangzhou 3
Indianapolis 3
Joinville 3
Kansas City 3
Las Vegas 3
Lexington 3
Totale 3.014
Nome #
Collagen VI Deficiency Impairs Tendon Fibroblasts Mechanoresponse in Ullrich Congenital Muscular Dystrophy 125
Long term breeding of the Lmna G609G progeric mouse: Characterization of homozygous and heterozygous models 108
Characterization of new genetic defects in mad 103
A new Ag-nanostructured hydroxyapatite porous scaffold: Antibacterial effect and cytotoxicity study. 93
Dual-functional nano-functionalized titanium scaffolds to inhibit bacterial growth and enhance osteointegration 92
Barrier-to-Autointegration Factor (BAF) evaluation during DNA-damage response. 89
Emerin increase in regenerating muscle fibers, 86
Lamin A Involvement in Ageing Processes 86
Interleukin-6 neutralization ameliorates symptoms in prematurely aged mice 82
Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition. 79
Lamin A-dependent heterochromatin dynamics in control and progeria syndrome fibroblasts, 74
The Italian Network for Laminopathies. 73
Drugs affecting prelamin A processing: Effects on heterochromatin organization. 73
The empowerment of translational research: lessons from laminopathies. 72
Lamin A/C sustains PcG proteins architecture maintaining transcriptional repression at target genes 67
Emerin Phosphorylation during the Early Phase of the Oxidative Stress Response Influences Emerin-BAF Interaction and BAF Nuclear Localization 65
New roles for lamins, nuclear envelope proteins and actin in the nucleus, 64
Aging research from bench to bedside and beyond: What we learned from Sammy Basso 59
Early diagnosis of ceramic liner fracture. Guidelines based on a twelve-year clinical experience, 58
Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes. 58
Ceramic Debris in Hip Prosthesis: Correlation Between Synovial Fluid and Joint Capsule 57
Synovial fluid microanalysis allows early diagnosis of ceramic hip prosthesis damage. 57
Effect on collagen VI extra-cellular assembly of COL6A1 and COL6A2 C-terminal mutationsi in Ullrich congenital muscular dystrophy. 56
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy, 54
3D ECM-rich environment sustains the identity of naive human iPSCs 53
Collagen VI-NG2 axis in human tendon fibroblasts under conditions mimicking injury response 51
Autosomal recessive Bethlem myopathy. 51
A new method for isolation of polyethylene wear debris from tissue and synovial fluid, 50
Prelamin A processing and functional effects in restrictive dermopathy. 50
Emerin-prelamin A interplay in human fibroblasts. 50
Prelamin A processing and heterochromatin dynamics in laminopathies. 49
Pre-Lamin A processing is linked to heterochromatin organization 48
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy, 48
Muscular laminopathies: Role of prelamin A in early steps of muscle differentiation. 48
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment. 47
Muscular laminopathies: role of prelamin a in early steps of muscle differentiation 46
Immunoelectron Microscopy Methods 46
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning 46
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment, 44
A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome 44
Barrier-to-Autointegration Factor (BAF) involvement in prelamin A-related chromatin organization changes. 44
Characterization of prelamin A forms accumulated in Mandibuloacral Dysplasia and prospects for therapy 42
New drug treatments in progeria cells: modulating mutated lamins to improve cell quality 41
Report of a novel ATP7A mutation causing distal motor neuropathy 41
Diverse lamin-dependent mechanisms interact to control chromatin dynamics: Focus on laminopathies 41
A recently developed bifacial platelet-rich fibrin matrix. 41
Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases, 40
Lamin A precursor induces barrier-to-autointegration factor nuclear localization. 40
Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains, 39
Effect of mechanical strain on the collagen VI pericellular matrix in anterior cruciate ligament fibroblasts 39
Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics 39
Nuclear Defects In Syndromic Laminopathies With Muscle Involvement 39
Prelamin A is involved in early steps of muscle differentiation. 39
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. 38
Antimicrobial Effect and Cytotoxic Evaluation of Mg-Doped Hydroxyapatite Functionalized with Au-Nano Rods 38
Laminopathies: a chromatin affair, 38
Prelamin A degradation pathways and progeria 38
A new method for isolation of polyethylene wear debris from tissue and synovial fluid, 37
Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy, 37
Pre-lamin A is modulated during muscle cell differentiation,. Implications for Emery-Dreifuss muscular dystrofy. 37
Innovative Composite HA Scaffold Rapid Prototyping for Bone Reconstruction: an In-Vitro Pilot Study 36
All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype. 36
Prelamin A-emerin interplay in human fibroblasts. 36
Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation 36
Nuclear envelope proteins and chromatin arrangem ent: a pathogenic mechanism for laminopathies, 36
Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by Collagen VI myopathies. 35
A case report of fracture of ceramic head in total hip arthroplasty: histological and biochemical features of perimplant tissues, 34
Honey flavonoids inhibit Candida albicans morphogenesis by affecting DNA behavior and mitochondrial function 34
Modulation of TGFbeta 2 levels by lamin A in U2-OS osteoblast-like cells: understanding the osteolytic process triggered by altered lamins 34
Effects on Collagen VI mrna Stability and Microfibrillar Assembly of Three COL6A2 Mutations in Two Families with Ullrich Congenital Muscular Dystrophy 34
Barrier-to-autointegration factors nuclear localization and LAP2alpha mislocalization are a common features in laminopathies with defective prelamin A processing. 33
Detection of mitochondrial defects in collagen VI deficient muscle cultures from UCMD patients and Col6a1 knockout mice: an ultrastructural study, 33
Effects of prelamin A processing inhibitors on the differentiation and activity of human osteoclasts. 33
Expression of the Collagen VI alpha5 and alpha6 Chains in Normal Human Skin and in Skin of Patients with Collagen VI-Related Myopathies 33
Differential and restricted expression of novel collagen VI chains in mouse. 33
Defective collagen VI alpha 6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies 33
Isolation and characterization of wear debris generated in patients wearing polyethylene Hylamer inserts, gamma irradiated in air, 32
Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology 32
Expression of collagen VI alpha5 and alpha6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis. 32
Effect on collagen VI extra-cellular assembly of COL6A1 and COL6A2 C-terminal mutationsi in Ullrich congenital muscular dystrophy 32
Barrier-to-autointegration factor nuclear localization is a common feature in prelamin A accumulating cells under pathological or physiological conditions. 32
Pre-Lamin A processing is linked to heterochromatin organization. 32
Lamin A precursor induces barrier-to-autointegration factor nuclear localization. 32
Mineralization behaviour with mesenchymal stromal cells in a biomimetic hyaluronic acid-based scaffold 32
Ultrastructural changes in muscle cells of patients with collagen VI-related myopathies. 32
The effect of gentamicin sulphate on the fracture properties of a manually mixed bone cement. 32
Prelamin A is involved in early steps of muscle differentiation 30
Barrier-to-autointegration factor involvement in prelamin A-related chromatin remodeling 30
Prelamin A in diverse tissues. What happens in health and disease? 30
Collagen type VI deficiency disrupts basal lamina-extracellular matrix binding in Ullrich congenital muscular dysystrophy and COL6A1 null mutant skeletal muscle 30
Heterochromatin dynamics in hutchinson-gilford progeria sindrome fibroblasts, 30
Autosomal recessive myosclerosis myopathy is a collagen VI disorder. 30
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription. 30
Implications for nuclear organization and gene transcription of lamin A/C specific mutations, 29
Barrier-to-autointegration factor involvement in prelamin A-related chromatin remodeling 29
At the nucleus of the problem: nuclear proteins and disease 29
Involvement of cytoskeletal and extracellular matrix structural components in LGND21 muscle: report of one case, 28
Drugs affecting prelamin A processing: Effects on heterochromatin organization 27
Altered pre-lamin A processing in laminopathies featuring lipodystrophy 26
Immunofluorescence and morphological alterations of capillary wall in skeletal muscle of two Myosclerosis myopathy patients 26
Totale 4.662
Categoria #
all - tutte 16.538
article - articoli 12.403
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 166
Totale 29.107


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/20248 0 0 0 0 0 0 0 0 3 0 3 2
2024/20251.896 2 7 120 64 554 112 53 88 66 65 413 352
2025/20262.474 141 353 224 423 396 108 363 97 115 124 90 40
2026/2027498 152 103 243 0 0 0 0 0 0 0 0 0
Totale 4.876