IRIS
VALLI, MAURIZIA
 Distribuzione geografica
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Continente #
NA - Nord America 2.207
AS - Asia 1.497
EU - Europa 1.308
SA - Sud America 177
Continente sconosciuto - Info sul continente non disponibili 40
AF - Africa 33
OC - Oceania 2
Totale 5.264
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Nazione #
US - Stati Uniti d'America 2.169
CN - Cina 789
SG - Singapore 325
IE - Irlanda 312
UA - Ucraina 185
FI - Finlandia 152
DE - Germania 147
HK - Hong Kong 136
RU - Federazione Russa 134
BR - Brasile 124
VN - Vietnam 111
GB - Regno Unito 82
IT - Italia 82
FR - Francia 80
SE - Svezia 44
IN - India 29
BE - Belgio 20
AR - Argentina 18
CA - Canada 17
IQ - Iraq 15
CZ - Repubblica Ceca 14
TR - Turchia 14
ZA - Sudafrica 14
JP - Giappone 13
BD - Bangladesh 12
MX - Messico 12
IR - Iran 11
NL - Olanda 11
PL - Polonia 10
EC - Ecuador 8
ES - Italia 8
CO - Colombia 7
ID - Indonesia 7
PK - Pakistan 6
CL - Cile 5
VE - Venezuela 5
MA - Marocco 4
PT - Portogallo 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
JM - Giamaica 2
LV - Lettonia 2
PA - Panama 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
BO - Bolivia 1
CH - Svizzera 1
CV - Capo Verde 1
DK - Danimarca 1
EE - Estonia 1
EU - Europa 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
JO - Giordania 1
KG - Kirghizistan 1
KR - Corea 1
KW - Kuwait 1
KZ - Kazakistan 1
MU - Mauritius 1
NP - Nepal 1
PR - Porto Rico 1
RS - Serbia 1
SR - Suriname 1
TH - Thailandia 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 5.228
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Città #
Dublin 312
Chandler 261
Jacksonville 219
Ashburn 212
San Jose 184
Dallas 172
Singapore 169
Beijing 162
Nanjing 145
Hong Kong 134
Boardman 85
Nanchang 70
Ann Arbor 67
Los Angeles 59
Shenyang 58
Council Bluffs 55
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 39
Munich 36
Hangzhou 28
Tianjin 27
Hanoi 25
Milan 24
Moscow 22
Buffalo 21
Shanghai 21
Woodbridge 21
Brussels 20
Santa Clara 19
Orem 17
Turku 17
Pavia 16
Washington 14
Johannesburg 13
Chicago 11
São Paulo 11
Tokyo 11
Verona 11
Denver 10
San Francisco 10
Auburn Hills 9
Brooklyn 9
Redondo Beach 9
Chennai 8
Montreal 8
Ardabil 7
Atlanta 7
Brno 7
Frankfurt am Main 7
Norwalk 7
Houston 6
London 6
Mexico City 6
Olomouc 6
Phoenix 6
The Dalles 6
Toronto 6
Warsaw 6
Zhengzhou 6
Baghdad 5
Belo Horizonte 5
Boston 5
Guangzhou 5
Naples 5
Ankara 4
Bogotá 4
Charlotte 4
Curitiba 4
Da Nang 4
Des Moines 4
Haiphong 4
Helena 4
Jinan 4
Padova 4
Piscataway 4
Poplar 4
Reconquista 4
Rio de Janeiro 4
Sacramento 4
Stockholm 4
Amsterdam 3
Can Tho 3
Carapicuíba 3
Chongqing 3
Columbus 3
Dearborn 3
Fairfield 3
Hải Dương 3
Manchester 3
Milwaukee 3
Mumbai 3
Totale 3.518
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Nome #
A specific nanobody prevents amyloidogenesis of D76N β2-microglobulin in vitro and modifies its tissue distribution in vivo 179
5-METHYL-PYRROLIDINONE CHITOSAN FILMS AS CARRIRERS FOR BUCCAL ADMINISTRATION OF PROTEINS 174
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. 168
An in vitro test predictive of bioadhesive properties of chitosan films for buccal application 160
Characterization of protein loaded 5-methyl-pyrrolidinone chitosan films 153
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. 153
Bioadhesive films for buccal release of proteins 150
Bioadhesive chitosan films for buccal release of proteins 144
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 139
Rescue of migratory defects of Ehlers-Danlos syndrome fibroblasts in vitro by type V collagen but not insulin-like binding protein-1. 136
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI. 132
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 131
Dipeptide loaded liposomes in photoaging: evaluation of cellular viability 129
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 128
Co-fibrillogenesis of Wild-type and D76N β2-Microglobulin: THE CRUCIAL ROLE OF FIBRILLAR SEEDS 126
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. 124
Plasminogen activation triggers transthyretin amyloidogenesis in vitro 119
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. 118
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: Clinical findings and novel COL3A1 mutations 117
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta. 111
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. 111
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. 109
Evaluation of bioadhesive performance of chitosan derivatives as films for buccal application 106
Identification of the amniotic fluid insulin-like growthfactor binding protein-1 phosphorylation sites andpropensity to proteolysis of the isoforms 105
Cutaneous metaplastic synovial cyst in Ehlers-Danlos syndrome: report of a second case. 104
"In vitro" fibril formation of type I collagen from different sources: biochemical and morphological aspects. 103
Structure and properties of the C-terminal domain of insulin-like growth factor-binding protein-1 isolated from human amniotic fluid. 95
Isolation and characterization of two proteoglycans from bovine tendon 94
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix. 93
Osteogenesis imperfecta and type I collagen mutations. A lethal variant caused by a Gly910->Ala substitution in the a1(I) chain. 91
Subependymal periventricular heterotopias in a patient with ehlers-danlos syndrome: a new case 91
Possible role of overglycosylation in the type I collagen triple helical domain in the molecular pathogenesis of osteogenesis imperfecta. 90
Osteogenesis imperfecta: clinical, biochemical and molecular findings. 86
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta. 86
Cardiac valve disease: an unreported feature in Ehlers Danlos syndrome arthrocalasia type? 85
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine a1(I) 901 substitution in a type-I collagen gene. 85
Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis. 84
Studio delle proprietà bioadesive del chitosano in funzione della veicolazione di farmaci proteici a livello buccale 83
Four new cases of lethal osteogenesis imperfecta due to glycine substitutions in COL1A1 and genes. Mutations in brief no. 152. 80
Gly85 to Val substitution in proa1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. 79
Mouse C127 cells transfection with fucosyltransferase Fuc-TIII express masked Lewis X but not Lewis X antigen 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. 78
Study of factors affecting the determination of total plasma 7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonate (SBD)-thiol derivatives by liquid chromatography. 74
Human Cells Unable to Express Decoron Produced Disorganized Extracellular Matrix Lacking “Shape Modules” (Interfibrillar Proteoglycan Bridges) 74
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor causes progressively deforming osteogenesis imperfecta with normal type I collagen. 74
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen. 65
Nuclear retention of COL1A1 messenger RNA identifies null alleles causing mild osteogenesis imperfecta. 64
Severe peripheral joint laxity is a distinctive clinical feature of spondylodysplastic-ehlers-danlos syndrome (Eds)-b4galt7 and spondylodysplastic-eds-b3galt6 58
Osteoblasts extracellular matrix induces vessel like structures through glycosylated collagen I. 48
Totale 5.264
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Categoria #
all - tutte 20.892
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 20.892
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022221 0 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
2025/20261.664 150 111 213 171 197 84 318 62 142 132 39 45
2026/202793 28 65 0 0 0 0 0 0 0 0 0 0
Totale 5.264