IRIS
CETTA, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 3.685
AS - Asia 2.639
EU - Europa 2.364
SA - Sud America 302
AF - Africa 78
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 4
Totale 9.077
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Nazione #
US - Stati Uniti d'America 3.592
CN - Cina 1.396
IE - Irlanda 550
SG - Singapore 539
UA - Ucraina 326
RU - Federazione Russa 277
FI - Finlandia 270
DE - Germania 263
HK - Hong Kong 244
BR - Brasile 220
VN - Vietnam 195
GB - Regno Unito 149
FR - Francia 133
IT - Italia 120
SE - Svezia 105
IN - India 63
ZA - Sudafrica 46
CA - Canada 45
BE - Belgio 37
MX - Messico 36
AR - Argentina 32
TR - Turchia 30
BD - Bangladesh 29
IQ - Iraq 24
PL - Polonia 22
ES - Italia 20
NL - Olanda 19
IR - Iran 18
JP - Giappone 18
CZ - Repubblica Ceca 17
EC - Ecuador 14
CO - Colombia 13
ID - Indonesia 13
PK - Pakistan 13
LT - Lituania 11
AT - Austria 9
MA - Marocco 9
PH - Filippine 8
UZ - Uzbekistan 8
RO - Romania 7
SA - Arabia Saudita 7
AL - Albania 6
MY - Malesia 6
VE - Venezuela 6
CL - Cile 5
DZ - Algeria 5
TW - Taiwan 5
AU - Australia 4
BO - Bolivia 4
ET - Etiopia 4
JM - Giamaica 4
PY - Paraguay 4
A2 - ???statistics.table.value.countryCode.A2??? 3
DO - Repubblica Dominicana 3
EG - Egitto 3
JO - Giordania 3
KE - Kenya 3
LV - Lettonia 3
NP - Nepal 3
PA - Panama 3
PT - Portogallo 3
TN - Tunisia 3
BG - Bulgaria 2
GR - Grecia 2
HU - Ungheria 2
KG - Kirghizistan 2
LB - Libano 2
MD - Moldavia 2
PE - Perù 2
RS - Serbia 2
SN - Senegal 2
TH - Thailandia 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
AZ - Azerbaigian 1
BH - Bahrain 1
BY - Bielorussia 1
CG - Congo 1
CH - Svizzera 1
CR - Costa Rica 1
EE - Estonia 1
EU - Europa 1
GA - Gabon 1
HR - Croazia 1
IL - Israele 1
KR - Corea 1
LK - Sri Lanka 1
MK - Macedonia 1
MM - Myanmar 1
MU - Mauritius 1
OM - Oman 1
QA - Qatar 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SR - Suriname 1
TM - Turkmenistan 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 9.077
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Città #
Dublin 550
Chandler 505
Jacksonville 376
Beijing 323
Ashburn 312
Singapore 290
Dallas 268
San Jose 263
Nanjing 255
Hong Kong 238
Ann Arbor 171
Boardman 143
Nanchang 110
Los Angeles 100
Lawrence 82
Princeton 82
Wilmington 81
Medford 80
Shenyang 80
Changsha 79
Helsinki 75
Munich 71
Hebei 65
Lauterbourg 65
Jiaxing 63
Shanghai 61
Hangzhou 60
Ho Chi Minh City 59
Moscow 55
Woodbridge 55
Tianjin 54
Milan 49
Hanoi 46
New York 46
Johannesburg 40
Buffalo 39
Orem 39
Brussels 36
Turku 33
São Paulo 30
Frankfurt am Main 27
Verona 26
Houston 23
Santa Clara 23
Auburn Hills 22
Washington 22
Chicago 20
Brooklyn 19
Chennai 19
Warsaw 16
Denver 14
Mexico City 14
Montreal 14
Stockholm 14
The Dalles 14
Tokyo 14
Haiphong 13
London 13
Norwalk 13
Redondo Beach 13
Toronto 13
Atlanta 12
Ankara 11
Seattle 11
Dearborn 10
Falkenstein 10
Kunming 10
Da Nang 9
Pavia 9
Ardabil 8
Boston 8
Brno 8
Des Moines 8
Ningbo 8
Poplar 8
Belo Horizonte 7
Fairfield 7
New Delhi 7
Olomouc 7
Ottawa 7
Rio de Janeiro 7
San Francisco 7
Tashkent 7
Amsterdam 6
Baghdad 6
Biên Hòa 6
Casablanca 6
City of London 6
Dhaka 6
Istanbul 6
Jinan 6
Ninh Bình 6
Phoenix 6
Quito 6
Bogotá 5
Buenos Aires 5
Columbus 5
Curitiba 5
Jakarta 5
Manchester 5
Totale 6.077
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Nome #
A quantitative and qualitative method for direct 2-DE analysis of murine cartilage 175
Adesion proteins in CHO cells. 167
Biodegradable microspheres for prolidase delivery to human cultured fibroblasts 162
Alpha1-antitrypsin in serum determined by capillary isoelectric focusing 161
Micellar electrokinetic chromatography for analyzing active site specificity of Pseudomonas aeruginosa elastase. 159
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
Cartilage histogenesis in a murine model of chondrodysplasia 156
Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family. 149
Effects of lactitol compared to polyethylene glicol-3350 on fecal short chain fatty acids and microflora in old patients with idiopathic chronic constipation. 146
Insights from a transgenic mouse model on the role of SLC26A2 in health and disease. 143
Sequencing prolidase from pig kidney using multiple enzymatic digestion and LC-ESI-QTOF 142
Separation of closely related peptide substrates of human proteinases by micellar electrokinetic chromatography with anionic and nonionic surfactants. 141
Capillary electrophoresis with laser-induced fluorescence detection as a novel sensitive approach for the analysis of desmosines in real samples. 141
In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation. 137
Investigation on transcellular delivery of active enzyme relased from PLGA microspheres 136
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 135
Differential expression of both extracellular and intracellular proteins is involved in the lethal or nonlethal phenotypic variation of BrtlIV, a murine model for osteogenesis imperfecta 133
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts 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
Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies. 128
Beta2-microglobulin isoforms display an heterogeneous affinity for type I collagen. 128
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 127
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 125
Intracellular delivery of liposome-encapsulated prolidase in cultured fibroblasts from prolidase-deficient patients 122
Activity of different proteases in a complex mixture and 'in vitro' study of their reciprocal interferences by micellar electrokinetic chromatography. 122
Effect of enamel matrix derivative on human periodontal fibroblasts: proliferation, morphology and root surface colonization. An in vitro study 122
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship. 121
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
Complete resolution of imidodipeptide mixtures in urine of prolidase-deficient patients using micellar electrokinetic chromatography. 120
Diagnosis of late-infantile neuronal ceroid lipofuscinosis: a new sensitive method to assay lysosomal pepstatin-insensitive proteinase activity in human and animal specimens by capillary electrophoresis. 119
Capillary electrophoresis as a modern tool for determining proteolytic activities in purified specimens and in real samples 118
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype 118
Intracellular release of a liposome-incapsulated biologically active protein 117
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
Use of capillary zone electrophoresis for analysis of imidodipeptides in urine of prolidase-deficient patients. 116
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency. 115
Rapid detection of ornithine transcarbamylase activity by micellar electrokinetic chromatography. 115
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations 115
Optimization of a capillary electrophoretic method to detect and quantify the Gly-Pro dipeptide in complex matrices from long term cultured prolidase deficiency fibroblasts 114
N-benzyloxycarbonyl-L-proline: an in vitro inhibitor of prolidase. 114
Enzyme replacement as a new therapy for prolidase deficiency 113
Inhibition of human neutrophil elastase by erythromycin andflurythromycin, two macrolide antibiotics. 112
Micellar electrokinetic chromatography for the determination of urinary desmosine and isodesmosine in patients affected by chronic obstructive pulmonary disease 110
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta. 109
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knock-in murine model for classical, dominant osteogenesis imperfecta 109
The role of emerging techniques in the investigation of prolidase deficiency: from diagnosis to the development of a possible therapeutical approach 108
Micellar electrokinetic chromatographic and capillary zone electrophoretic methods for screening urinary biomarkers of human disorders: a critical review of the state-of-the-art. 108
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. 107
Effect of the triterpenoid fraction of Centella asiatica on macromolecules of the connective matrix in human skin fibroblast cultures. 107
Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta. 107
Micellar electrokinetic chromatography as a complementary method to sodium dodecyl sulfate-polyacrylamide gel electrophoresis for studying limited proteolysis of proteins. 107
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. 106
Stability of type I collagen peptide trimers. 105
Micellar electrokinetic chromatography: a convenient alternative to colorimetric and high performance liquid chromatographic detection for monitoring protease activity. 104
Defective proteoglycan sulfation of the growth plate zones causes reduced chondrocyte proliferation via an altered Indian hedgehog signalling 103
High levels of desmosines in urine and plasma of patients with pseudoxanthoma elasticum. 100
Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects. 97
Type I procollagen in the severe non-lethal form of osteogenesis imperfecta. Defective pro-alpha 1(I) chains in a patient with abnormal proteoglycan metabolism and mineral deposits in the dermis. 95
Mild, late-onset prolidase deficiency: another Italian case. 93
Therapeutic apheresis exchange in two patients with prolidase deficiency 93
Effect of different surfactants on the separation by micellar electrokinetic chromatography of a complex mixture of dipeptides in urine of prolidase-deficient patients. 91
Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta. 90
Type I collagen CNBr peptides: species and behavior in solution 89
Evaluation of the TiMo12Zr6Fe2 alloy for orthopaedic implants: in vitro biocompatibility study by using primary human fibroblasts and osteoblasts 89
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
Possible role of overglycosylation in the type I collagen triple helical domain in the molecular pathogenesis of osteogenesis imperfecta. 85
Diastrophic dysplasia sulfate transporter (DTDST) gene is not involved in pseudodiastrophic dysplasia 83
Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for a Leu483Pro substitution in the diastrophic dysplasia sulfate transporter 83
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta. 83
Simultaneous determination of Pseudomonas aeruginosa elastase, human leukocyte elastase and cathepsin G activities by micellar electrokinetic chromatography 83
In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias 80
Proteoglycan modifications in cultured Osteogenesis Imperfecta skin fibroblasts. 76
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. 74
Gly85 to Val substitution in proa1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. 73
Serum type I and type III procollagen peptide levels in sarcoidosis. 73
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
Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2 68
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production 66
Relationship between changes in alveolar surfactant levels and lung defence mechanisms. 64
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen. 61
Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients. 57
Totale 9.121
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Categoria #
all - tutte 33.427
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 33.427
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021172 0 0 0 0 0 0 0 0 0 84 73 15
2021/2022417 7 12 18 8 10 7 11 29 17 12 67 219
2022/20231.445 129 142 13 113 161 123 5 61 622 20 42 14
2023/2024504 72 90 31 48 51 104 26 29 9 18 17 9
2024/20251.331 40 97 46 34 37 63 69 33 360 39 197 316
2025/20262.869 242 190 372 383 384 176 557 122 286 157 0 0
Totale 9.121