VALLI, MAURIZIA
 Distribuzione geografica
Continente #
NA - Nord America 2.036
AS - Asia 1.486
EU - Europa 1.293
SA - Sud America 171
AF - Africa 33
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 5.025
Nazione #
US - Stati Uniti d'America 2.005
CN - Cina 788
SG - Singapore 318
IE - Irlanda 312
UA - Ucraina 185
FI - Finlandia 152
DE - Germania 147
HK - Hong Kong 134
RU - Federazione Russa 134
BR - Brasile 124
VN - Vietnam 111
GB - Regno Unito 82
FR - Francia 80
IT - Italia 74
SE - Svezia 44
IN - India 29
BE - Belgio 19
AR - Argentina 16
CA - Canada 15
IQ - Iraq 15
CZ - Repubblica Ceca 14
TR - Turchia 14
ZA - Sudafrica 14
JP - Giappone 13
BD - Bangladesh 12
IR - Iran 11
MX - Messico 10
PL - Polonia 10
EC - Ecuador 8
ES - Italia 8
NL - Olanda 8
ID - Indonesia 6
PK - Pakistan 6
CL - Cile 5
VE - Venezuela 5
CO - Colombia 4
MA - Marocco 4
PY - Paraguay 4
TW - Taiwan 4
KE - Kenya 3
LT - Lituania 3
MD - Moldavia 3
MY - Malesia 3
PE - Perù 3
PH - Filippine 3
RO - Romania 3
TN - Tunisia 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AL - Albania 2
AT - Austria 2
AU - Australia 2
AZ - Azerbaigian 2
BH - Bahrain 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EG - Egitto 2
ET - Etiopia 2
IL - Israele 2
LV - Lettonia 2
PA - Panama 2
PT - Portogallo 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
BO - Bolivia 1
CH - Svizzera 1
CV - Capo Verde 1
EE - Estonia 1
EU - Europa 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
JM - Giamaica 1
JO - Giordania 1
KG - Kirghizistan 1
KR - Corea 1
KW - Kuwait 1
KZ - Kazakistan 1
MU - Mauritius 1
NP - Nepal 1
RS - Serbia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 5.025
Città #
Dublin 312
Chandler 261
Jacksonville 219
Ashburn 199
Dallas 169
Singapore 167
Beijing 162
Nanjing 145
San Jose 145
Hong Kong 132
Boardman 83
Nanchang 70
Ann Arbor 67
Los Angeles 58
Shenyang 58
Changsha 50
Lawrence 49
Medford 49
Princeton 49
Hebei 48
Wilmington 44
Helsinki 43
Lauterbourg 43
Jiaxing 42
Ho Chi Minh City 39
New York 37
Munich 36
Hangzhou 28
Tianjin 27
Hanoi 25
Milan 24
Moscow 22
Buffalo 21
Shanghai 21
Woodbridge 21
Brussels 19
Turku 17
Orem 16
Pavia 16
Johannesburg 13
Washington 13
Santa Clara 11
São Paulo 11
Tokyo 11
Verona 11
Chicago 10
Denver 10
San Francisco 10
Auburn Hills 9
Redondo Beach 9
Chennai 8
Ardabil 7
Atlanta 7
Brno 7
Brooklyn 7
Frankfurt am Main 7
Montreal 7
Norwalk 7
Houston 6
London 6
Olomouc 6
Phoenix 6
The Dalles 6
Warsaw 6
Zhengzhou 6
Baghdad 5
Belo Horizonte 5
Boston 5
Guangzhou 5
Toronto 5
Ankara 4
Charlotte 4
Curitiba 4
Da Nang 4
Des Moines 4
Haiphong 4
Helena 4
Jinan 4
Mexico City 4
Padova 4
Piscataway 4
Poplar 4
Reconquista 4
Rio de Janeiro 4
Stockholm 4
Amsterdam 3
Bogotá 3
Can Tho 3
Carapicuíba 3
Chongqing 3
Columbus 3
Dearborn 3
Fairfield 3
Hải Dương 3
Manchester 3
Milwaukee 3
Mumbai 3
Nairobi 3
Paris 3
Pune 3
Totale 3.380
Nome #
A specific nanobody prevents amyloidogenesis of D76N β2-microglobulin in vitro and modifies its tissue distribution in vivo 177
5-METHYL-PYRROLIDINONE CHITOSAN FILMS AS CARRIRERS FOR BUCCAL ADMINISTRATION OF PROTEINS 168
A de novo G to T transversion in a pro-a1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain. 159
An in vitro test predictive of bioadhesive properties of chitosan films for buccal application 156
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. 151
Characterization of protein loaded 5-methyl-pyrrolidinone chitosan films 150
Bioadhesive films for buccal release of proteins 143
Bioadhesive chitosan films for buccal release of proteins 143
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 135
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1. 132
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI. 130
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 127
Dipeptide loaded liposomes in photoaging: evaluation of cellular viability 126
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 125
Co-fibrillogenesis of Wild-type and D76N β2-Microglobulin: THE CRUCIAL ROLE OF FIBRILLAR SEEDS 123
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta. 121
Anomalous cysteine in type I collagen. Localisation by chemical cleavage of the protein using 2-nitro-5-thiocyanobenzoic acid and by mismatch analysis of cDNA heteroduplexes. 116
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: Clinical findings and novel COL3A1 mutations 114
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta. 109
Plasminogen activation triggers transthyretin amyloidogenesis in vitro 108
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. 107
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. 106
Cutaneous metaplastic synovial cyst in Ehlers-Danlos syndrome: report of a second case. 102
Evaluation of bioadhesive performance of chitosan derivatives as films for buccal application 101
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 99
"In vitro" fibril formation of type I collagen from different sources: biochemical and morphological aspects. 98
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 92
Isolation and characterization of two proteoglycans from bovine tendon 91
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix. 87
Osteogenesis imperfecta and type I collagen mutations. A lethal variant caused by a Gly910->Ala substitution in the a1(I) chain. 86
Subependymal periventricular heterotopias in a patient with ehlers-danlos syndrome: a new case 85
Osteogenesis imperfecta: clinical, biochemical and molecular findings. 85
Possible role of overglycosylation in the type I collagen triple helical domain in the molecular pathogenesis of osteogenesis imperfecta. 85
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta. 84
Cardiac valve disease: an unreported feature in Ehlers Danlos syndrome arthrocalasia type? 82
Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis. 79
Four new cases of lethal osteogenesis imperfecta due to glycine substitutions in COL1A1 and genes. Mutations in brief no. 152. 78
Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutation. 75
Studio delle proprietà bioadesive del chitosano in funzione della veicolazione di farmaci proteici a livello buccale 75
Gly85 to Val substitution in proa1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. 74
Study of factors affecting the determination of total plasma 7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonate (SBD)-thiol derivatives by liquid chromatography. 72
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor causes progressively deforming osteogenesis imperfecta with normal type I collagen. 72
Mouse C127 cells transfection with fucosyltransferase Fuc-TIII express masked Lewis X but not Lewis X antigen 70
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine a1(I) 901 substitution in a type-I collagen gene. 70
Human Cells Unable to Express Decoron Produced Disorganized Extracellular Matrix Lacking “Shape Modules” (Interfibrillar Proteoglycan Bridges) 69
Nuclear retention of COL1A1 messenger RNA identifies null alleles causing mild osteogenesis imperfecta. 63
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen. 61
Severe peripheral joint laxity is a distinctive clinical feature of spondylodysplastic-ehlers-danlos syndrome (Eds)-b4galt7 and spondylodysplastic-eds-b3galt6 54
Osteoblasts extracellular matrix induces vessel like structures through glycosylated collagen I. 46
Totale 5.061
Categoria #
all - tutte 18.803
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 18.803


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202194 0 0 0 0 0 0 0 0 0 48 40 6
2021/2022226 5 5 11 5 3 2 7 9 13 3 34 129
2022/2023798 77 60 2 70 88 74 1 37 353 10 18 8
2023/2024304 25 55 22 37 26 81 4 26 1 7 13 7
2024/2025724 30 55 28 24 17 31 26 29 178 30 112 164
2025/20261.554 150 111 213 171 197 84 318 62 142 106 0 0
Totale 5.061