IRIS
CETTA, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 3.257
EU - Europa 2.225
AS - Asia 2.176
SA - Sud America 220
AF - Africa 29
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 3
Totale 7.915
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Nazione #
US - Stati Uniti d'America 3.178
CN - Cina 1.328
IE - Irlanda 550
SG - Singapore 418
UA - Ucraina 325
RU - Federazione Russa 274
FI - Finlandia 269
DE - Germania 249
HK - Hong Kong 214
BR - Brasile 182
GB - Regno Unito 138
IT - Italia 115
SE - Svezia 105
VN - Vietnam 66
FR - Francia 61
CA - Canada 41
BE - Belgio 36
IN - India 34
MX - Messico 28
TR - Turchia 21
AR - Argentina 19
IR - Iran 18
CZ - Repubblica Ceca 17
PL - Polonia 17
JP - Giappone 16
NL - Olanda 15
ES - Italia 14
ZA - Sudafrica 13
BD - Bangladesh 12
LT - Lituania 10
IQ - Iraq 8
AT - Austria 7
CO - Colombia 6
ID - Indonesia 6
RO - Romania 6
MA - Marocco 5
PK - Pakistan 5
SA - Arabia Saudita 5
TW - Taiwan 5
UZ - Uzbekistan 5
JM - Giamaica 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AU - Australia 3
CL - Cile 3
EC - Ecuador 3
KE - Kenya 3
LV - Lettonia 3
NP - Nepal 3
PA - Panama 3
AL - Albania 2
BG - Bulgaria 2
BO - Bolivia 2
DZ - Algeria 2
EG - Egitto 2
JO - Giordania 2
VE - Venezuela 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BH - Bahrain 1
BY - Bielorussia 1
CH - Svizzera 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
EU - Europa 1
GR - Grecia 1
HR - Croazia 1
HU - Ungheria 1
IL - Israele 1
KG - Kirghizistan 1
LK - Sri Lanka 1
MD - Moldavia 1
MK - Macedonia 1
MU - Mauritius 1
MY - Malesia 1
OM - Oman 1
PT - Portogallo 1
PY - Paraguay 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SR - Suriname 1
TM - Turkmenistan 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 7.915
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Città #
Dublin 550
Chandler 505
Jacksonville 376
Beijing 317
Dallas 267
Nanjing 255
Ashburn 249
Hong Kong 214
Singapore 210
Ann Arbor 171
Boardman 143
Nanchang 110
Los Angeles 96
Lawrence 82
Princeton 82
Wilmington 81
Medford 80
Shenyang 80
Changsha 79
Helsinki 74
Munich 71
Hebei 65
Jiaxing 63
Hangzhou 60
Shanghai 59
Moscow 55
Woodbridge 55
Tianjin 54
Milan 47
New York 46
Buffalo 37
Brussels 35
Turku 33
Verona 26
São Paulo 25
Houston 23
Auburn Hills 22
Washington 22
Ho Chi Minh City 21
Chicago 20
Brooklyn 19
Orem 19
Frankfurt am Main 17
Santa Clara 17
Stockholm 14
The Dalles 14
Chennai 13
Denver 13
Hanoi 13
Norwalk 13
Redondo Beach 13
Tokyo 13
Toronto 13
Warsaw 13
London 12
Mexico City 12
Ankara 11
Atlanta 11
Johannesburg 11
Montreal 11
Seattle 11
Dearborn 10
Falkenstein 10
Kunming 10
Pavia 9
Ardabil 8
Boston 8
Brno 8
Ningbo 8
Poplar 8
Fairfield 7
Olomouc 7
San Francisco 7
Belo Horizonte 6
Des Moines 6
Jinan 6
Ottawa 6
Columbus 5
Manchester 5
Monmouth Junction 5
Phoenix 5
Rio de Janeiro 5
Tappahannock 5
Zhengzhou 5
Bogotá 4
Casablanca 4
Dhaka 4
Elk Grove Village 4
Haiphong 4
Jackson 4
Jakarta 4
Kingston 4
Lanzhou 4
Ninh Bình 4
Quận Bảy 4
Riyadh 4
Rome 4
Sacramento 4
Tashkent 4
Amsterdam 3
Totale 5.365
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Nome #
A quantitative and qualitative method for direct 2-DE analysis of murine cartilage 152
Adesion proteins in CHO cells. 146
Alpha1-antitrypsin in serum determined by capillary isoelectric focusing 141
Biodegradable microspheres for prolidase delivery to human cultured fibroblasts 141
Cartilage histogenesis in a murine model of chondrodysplasia 139
Micellar electrokinetic chromatography for analyzing active site specificity of Pseudomonas aeruginosa elastase. 138
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. 138
Separation of closely related peptide substrates of human proteinases by micellar electrokinetic chromatography with anionic and nonionic surfactants. 130
Capillary electrophoresis with laser-induced fluorescence detection as a novel sensitive approach for the analysis of desmosines in real samples. 130
In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation. 127
Effects of lactitol compared to polyethylene glicol-3350 on fecal short chain fatty acids and microflora in old patients with idiopathic chronic constipation. 125
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. 122
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 122
Sequencing prolidase from pig kidney using multiple enzymatic digestion and LC-ESI-QTOF 122
Investigation on transcellular delivery of active enzyme relased from PLGA microspheres 121
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 121
Insights from a transgenic mouse model on the role of SLC26A2 in health and disease. 117
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 114
Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies. 113
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts 113
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 110
Effect of enamel matrix derivative on human periodontal fibroblasts: proliferation, morphology and root surface colonization. An in vitro study 110
Beta2-microglobulin isoforms display an heterogeneous affinity for type I collagen. 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. 109
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship. 108
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. 107
Intracellular delivery of liposome-encapsulated prolidase in cultured fibroblasts from prolidase-deficient patients 107
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency. 105
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations 105
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. 104
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI. 104
Capillary electrophoresis as a modern tool for determining proteolytic activities in purified specimens and in real samples 103
Complete resolution of imidodipeptide mixtures in urine of prolidase-deficient patients using micellar electrokinetic chromatography. 103
Optimization of a capillary electrophoretic method to detect and quantify the Gly-Pro dipeptide in complex matrices from long term cultured prolidase deficiency fibroblasts 102
Rapid detection of ornithine transcarbamylase activity by micellar electrokinetic chromatography. 102
Intracellular release of a liposome-incapsulated biologically active protein 101
Activity of different proteases in a complex mixture and 'in vitro' study of their reciprocal interferences by micellar electrokinetic chromatography. 101
Use of capillary zone electrophoresis for analysis of imidodipeptides in urine of prolidase-deficient patients. 99
N-benzyloxycarbonyl-L-proline: an in vitro inhibitor of prolidase. 99
Enzyme replacement as a new therapy for prolidase deficiency 97
Micellar electrokinetic chromatography for the determination of urinary desmosine and isodesmosine in patients affected by chronic obstructive pulmonary disease 97
Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta. 97
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta. 96
Micellar electrokinetic chromatographic and capillary zone electrophoretic methods for screening urinary biomarkers of human disorders: a critical review of the state-of-the-art. 96
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 96
The role of emerging techniques in the investigation of prolidase deficiency: from diagnosis to the development of a possible therapeutical approach 95
Effect of the triterpenoid fraction of Centella asiatica on macromolecules of the connective matrix in human skin fibroblast cultures. 95
Inhibition of human neutrophil elastase by erythromycin andflurythromycin, two macrolide antibiotics. 93
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. 92
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. 92
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype 92
Stability of type I collagen peptide trimers. 91
Micellar electrokinetic chromatography: a convenient alternative to colorimetric and high performance liquid chromatographic detection for monitoring protease activity. 90
High levels of desmosines in urine and plasma of patients with pseudoxanthoma elasticum. 88
Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects. 88
Micellar electrokinetic chromatography as a complementary method to sodium dodecyl sulfate-polyacrylamide gel electrophoresis for studying limited proteolysis of proteins. 88
Defective proteoglycan sulfation of the growth plate zones causes reduced chondrocyte proliferation via an altered Indian hedgehog signalling 86
Mild, late-onset prolidase deficiency: another Italian case. 82
Therapeutic apheresis exchange in two patients with prolidase deficiency 82
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. 80
Evaluation of the TiMo12Zr6Fe2 alloy for orthopaedic implants: in vitro biocompatibility study by using primary human fibroblasts and osteoblasts 79
Type I collagen CNBr peptides: species and behavior in solution 78
Effect of different surfactants on the separation by micellar electrokinetic chromatography of a complex mixture of dipeptides in urine of prolidase-deficient patients. 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. 76
Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta. 75
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix. 74
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta. 73
Simultaneous determination of Pseudomonas aeruginosa elastase, human leukocyte elastase and cathepsin G activities by micellar electrokinetic chromatography 73
Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for a Leu483Pro substitution in the diastrophic dysplasia sulfate transporter 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. 70
Proteoglycan modifications in cultured Osteogenesis Imperfecta skin fibroblasts. 68
Diastrophic dysplasia sulfate transporter (DTDST) gene is not involved in pseudodiastrophic dysplasia 67
Gly85 to Val substitution in proa1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. 65
Serum type I and type III procollagen peptide levels in sarcoidosis. 65
In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias 62
Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2 61
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 60
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
Relationship between changes in alveolar surfactant levels and lung defence mechanisms. 57
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen. 53
Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients. 47
Totale 7.959
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Categoria #
all - tutte 31.437
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 31.437
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021353 0 0 0 0 0 66 9 93 13 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
2025/20261.707 242 190 372 383 384 136 0 0 0 0 0 0
Totale 7.959