IRIS
VALLI, MAURIZIA
 Distribuzione geografica
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Continente #
NA - Nord America 1.778
AS - Asia 1.213
EU - Europa 1.206
SA - Sud America 118
AF - Africa 15
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 4.336
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Nazione #
US - Stati Uniti d'America 1.753
CN - Cina 756
IE - Irlanda 311
SG - Singapore 228
UA - Ucraina 184
FI - Finlandia 147
DE - Germania 145
RU - Federazione Russa 130
HK - Hong Kong 119
BR - Brasile 99
GB - Regno Unito 78
IT - Italia 66
SE - Svezia 44
FR - Francia 32
VN - Vietnam 32
BE - Belgio 19
CZ - Repubblica Ceca 13
IN - India 13
JP - Giappone 12
IR - Iran 11
CA - Canada 10
MX - Messico 9
AR - Argentina 8
BD - Bangladesh 8
ES - Italia 8
IQ - Iraq 8
TR - Turchia 8
PL - Polonia 7
ZA - Sudafrica 6
NL - Olanda 5
PY - Paraguay 4
TW - Taiwan 4
EC - Ecuador 3
ID - Indonesia 3
RO - Romania 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AT - Austria 2
AU - Australia 2
CO - Colombia 2
DO - Repubblica Dominicana 2
LT - Lituania 2
LV - Lettonia 2
MA - Marocco 2
MD - Moldavia 2
PA - Panama 2
PK - Pakistan 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
BG - Bulgaria 1
BH - Bahrain 1
CH - Svizzera 1
CV - Capo Verde 1
DZ - Algeria 1
EE - Estonia 1
EG - Egitto 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
IL - Israele 1
JM - Giamaica 1
KE - Kenya 1
KG - Kirghizistan 1
KR - Corea 1
MU - Mauritius 1
NP - Nepal 1
PE - Perù 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 4.336
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Città #
Dublin 311
Chandler 261
Jacksonville 219
Dallas 169
Beijing 159
Ashburn 158
Nanjing 145
Hong Kong 119
Singapore 108
Boardman 83
Nanchang 70
Ann Arbor 67
Shenyang 58
Changsha 50
Los Angeles 50
Lawrence 49
Medford 49
Princeton 49
Hebei 48
Wilmington 44
Jiaxing 42
Helsinki 38
Munich 36
New York 34
Hangzhou 28
Tianjin 27
Moscow 22
Shanghai 21
Woodbridge 21
Buffalo 20
Milan 20
Brussels 19
Turku 17
Ho Chi Minh City 16
Pavia 16
Washington 13
Verona 11
San Francisco 10
Tokyo 10
Auburn Hills 9
Chicago 9
Redondo Beach 9
São Paulo 9
Ardabil 7
Atlanta 7
Brno 7
Brooklyn 7
Norwalk 7
Denver 6
Frankfurt am Main 6
Hanoi 6
Houston 6
Johannesburg 6
London 6
Olomouc 6
Phoenix 6
Santa Clara 6
The Dalles 6
Zhengzhou 6
Belo Horizonte 5
Boston 5
Chennai 5
Guangzhou 5
Toronto 5
Warsaw 5
Ankara 4
Charlotte 4
Des Moines 4
Helena 4
Jinan 4
Mexico City 4
Montreal 4
Padova 4
Poplar 4
Reconquista 4
Stockholm 4
Baghdad 3
Can Tho 3
Carapicuíba 3
Chongqing 3
Columbus 3
Dearborn 3
Fairfield 3
Milwaukee 3
Orem 3
Pune 3
Rio de Janeiro 3
Sacramento 3
Seattle 3
Villaralbo 3
Andover 2
Bogotá 2
Brasília 2
Changchun 2
City of London 2
Concord 2
Curitiba 2
Falkenstein 2
Fuyang 2
Goiânia 2
Totale 2.960
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Nome #
A specific nanobody prevents amyloidogenesis of D76N β2-microglobulin in vitro and modifies its tissue distribution in vivo 153
5-METHYL-PYRROLIDINONE CHITOSAN FILMS AS CARRIRERS FOR BUCCAL ADMINISTRATION OF PROTEINS 150
An in vitro test predictive of bioadhesive properties of chitosan films for buccal application 143
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. 138
Characterization of protein loaded 5-methyl-pyrrolidinone chitosan films 134
Bioadhesive films for buccal release of proteins 126
Bioadhesive chitosan films for buccal release of proteins 124
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 120
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. 119
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1. 118
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 113
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 110
Dipeptide loaded liposomes in photoaging: evaluation of cellular viability 109
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. 108
Co-fibrillogenesis of Wild-type and D76N β2-Microglobulin: THE CRUCIAL ROLE OF FIBRILLAR SEEDS 107
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. 103
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI. 103
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: Clinical findings and novel COL3A1 mutations 99
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta. 93
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. 92
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. 92
Cutaneous metaplastic synovial cyst in Ehlers-Danlos syndrome: report of a second case. 90
Plasminogen activation triggers transthyretin amyloidogenesis in vitro 90
Evaluation of bioadhesive performance of chitosan derivatives as films for buccal application 88
"In vitro" fibril formation of type I collagen from different sources: biochemical and morphological aspects. 82
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 81
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 81
Isolation and characterization of two proteoglycans from bovine tendon 79
Subependymal periventricular heterotopias in a patient with ehlers-danlos syndrome: a new case 77
Osteogenesis imperfecta and type I collagen mutations. A lethal variant caused by a Gly910->Ala substitution in the a1(I) chain. 76
Possible role of overglycosylation in the type I collagen triple helical domain in the molecular pathogenesis of osteogenesis imperfecta. 75
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix. 74
Osteogenesis imperfecta: clinical, biochemical and molecular findings. 73
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta. 73
Four new cases of lethal osteogenesis imperfecta due to glycine substitutions in COL1A1 and genes. Mutations in brief no. 152. 71
Cardiac valve disease: an unreported feature in Ehlers Danlos syndrome arthrocalasia type? 71
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. 69
Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis. 65
Gly85 to Val substitution in proa1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. 64
Studio delle proprietà bioadesive del chitosano in funzione della veicolazione di farmaci proteici a livello buccale 64
Mouse C127 cells transfection with fucosyltransferase Fuc-TIII express masked Lewis X but not Lewis X antigen 61
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor causes progressively deforming osteogenesis imperfecta with normal type I collagen. 60
Study of factors affecting the determination of total plasma 7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonate (SBD)-thiol derivatives by liquid chromatography. 59
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine a1(I) 901 substitution in a type-I collagen gene. 59
Nuclear retention of COL1A1 messenger RNA identifies null alleles causing mild osteogenesis imperfecta. 53
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen. 53
Human Cells Unable to Express Decoron Produced Disorganized Extracellular Matrix Lacking “Shape Modules” (Interfibrillar Proteoglycan Bridges) 49
Severe peripheral joint laxity is a distinctive clinical feature of spondylodysplastic-ehlers-danlos syndrome (Eds)-b4galt7 and spondylodysplastic-eds-b3galt6 43
Osteoblasts extracellular matrix induces vessel like structures through glycosylated collagen I. 38
Totale 4.372
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Categoria #
all - tutte 17.494
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 17.494
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021191 0 0 0 0 0 39 6 46 6 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
2025/2026865 150 111 213 171 197 23 0 0 0 0 0 0
Totale 4.372