IRIS
CETTA, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 2.174
EU - Europa 1.669
AS - Asia 1.062
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
AF - Africa 1
SA - Sud America 1
Totale 4.913
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Nazione #
US - Stati Uniti d'America 2.162
CN - Cina 1.015
IE - Irlanda 550
UA - Ucraina 321
FI - Finlandia 226
DE - Germania 155
IT - Italia 111
GB - Regno Unito 97
SE - Svezia 91
FR - Francia 40
BE - Belgio 32
SG - Singapore 22
IR - Iran 17
RU - Federazione Russa 17
CA - Canada 9
CZ - Repubblica Ceca 9
NL - Olanda 9
RO - Romania 6
IN - India 4
A2 - ???statistics.table.value.countryCode.A2??? 3
JP - Giappone 3
MX - Messico 3
AU - Australia 2
BO - Bolivia 1
CH - Svizzera 1
EU - Europa 1
HU - Ungheria 1
LV - Lettonia 1
MD - Moldavia 1
MU - Mauritius 1
PL - Polonia 1
TR - Turchia 1
Totale 4.913
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Città #
Dublin 550
Chandler 505
Jacksonville 375
Nanjing 254
Ann Arbor 171
Beijing 163
Ashburn 146
Nanchang 110
Lawrence 82
Princeton 82
Wilmington 81
Medford 80
Shenyang 77
Changsha 72
Hebei 65
Helsinki 64
Jiaxing 63
Boardman 59
Shanghai 58
Hangzhou 57
Woodbridge 54
Tianjin 50
Milan 47
Brussels 32
Verona 26
Auburn Hills 22
Washington 20
Los Angeles 18
Houston 16
New York 16
Singapore 15
Norwalk 13
Dearborn 10
Kunming 10
Chicago 9
Seattle 9
Ardabil 8
Brno 8
Fairfield 7
Munich 7
Pavia 7
Des Moines 6
Falkenstein 6
Ningbo 6
Jinan 5
Monmouth Junction 5
Tappahannock 5
Zhengzhou 5
Ottawa 4
Sacramento 4
Detroit 3
Duncan 3
Falls Church 3
Lanzhou 3
Leawood 3
Rome 3
San Miguel de Allende 3
Toronto 3
Andover 2
Fuzhou 2
Monza 2
Orange 2
St Petersburg 2
Teano 2
Winnipeg 2
Augusta 1
Austin 1
Berlin 1
Brdo 1
Budapest 1
Changchun 1
Chisinau 1
Cupertino 1
Groningen 1
Gunzenhausen 1
Henderson 1
Kish 1
London 1
Melbourne 1
Montereale Valcellina 1
Moscow 1
Ornavasso 1
Piscataway 1
Pitesti 1
Polska 1
Pune 1
Qingdao 1
Redwood City 1
Rockville 1
Shiraz 1
Simi Valley 1
Taganrog 1
Taiyuan 1
Tokyo 1
Tomsk 1
Voronezh 1
Zanjan 1
Zurich 1
Totale 3.635
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Nome #
Micellar electrokinetic chromatography for analyzing active site specificity of Pseudomonas aeruginosa elastase. 93
In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation. 90
Separation of closely related peptide substrates of human proteinases by micellar electrokinetic chromatography with anionic and nonionic surfactants. 88
Cartilage histogenesis in a murine model of chondrodysplasia 87
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. 86
Adesion proteins in CHO cells. 86
Effects of lactitol compared to polyethylene glicol-3350 on fecal short chain fatty acids and microflora in old patients with idiopathic chronic constipation. 86
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. 84
Biodegradable microspheres for prolidase delivery to human cultured fibroblasts 81
Sequencing prolidase from pig kidney using multiple enzymatic digestion and LC-ESI-QTOF 81
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts 79
Investigation on transcellular delivery of active enzyme relased from PLGA microspheres 78
Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies. 78
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 78
Effect of enamel matrix derivative on human periodontal fibroblasts: proliferation, morphology and root surface colonization. An in vitro study 78
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 78
A quantitative and qualitative method for direct 2-DE analysis of murine cartilage 75
Use of capillary zone electrophoresis for analysis of imidodipeptides in urine of prolidase-deficient patients. 73
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. 71
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 71
Capillary electrophoresis with laser-induced fluorescence detection as a novel sensitive approach for the analysis of desmosines in real samples. 71
Enzyme replacement as a new therapy for prolidase deficiency 70
Micellar electrokinetic chromatography for the determination of urinary desmosine and isodesmosine in patients affected by chronic obstructive pulmonary disease 70
Intracellular delivery of liposome-encapsulated prolidase in cultured fibroblasts from prolidase-deficient patients 70
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship. 69
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI. 69
Rapid detection of ornithine transcarbamylase activity by micellar electrokinetic chromatography. 68
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. 67
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 67
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency. 66
Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta. 66
Alpha1-antitrypsin in serum determined by capillary isoelectric focusing 65
Beta2-microglobulin isoforms display an heterogeneous affinity for type I collagen. 64
Optimization of a capillary electrophoretic method to detect and quantify the Gly-Pro dipeptide in complex matrices from long term cultured prolidase deficiency fibroblasts 63
Micellar electrokinetic chromatography: a convenient alternative to colorimetric and high performance liquid chromatographic detection for monitoring protease activity. 63
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. 63
Intracellular release of a liposome-incapsulated biologically active protein 62
Stability of type I collagen peptide trimers. 62
The role of emerging techniques in the investigation of prolidase deficiency: from diagnosis to the development of a possible therapeutical approach 62
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations 62
Effect of the triterpenoid fraction of Centella asiatica on macromolecules of the connective matrix in human skin fibroblast cultures. 62
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. 61
High levels of desmosines in urine and plasma of patients with pseudoxanthoma elasticum. 60
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. 60
Insights from a transgenic mouse model on the role of SLC26A2 in health and disease. 60
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta. 59
N-benzyloxycarbonyl-L-proline: an in vitro inhibitor of prolidase. 58
Inhibition of human neutrophil elastase by erythromycin andflurythromycin, two macrolide antibiotics. 55
Type I collagen CNBr peptides: species and behavior in solution 55
Micellar electrokinetic chromatographic and capillary zone electrophoretic methods for screening urinary biomarkers of human disorders: a critical review of the state-of-the-art. 55
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. 55
Micellar electrokinetic chromatography as a complementary method to sodium dodecyl sulfate-polyacrylamide gel electrophoresis for studying limited proteolysis of proteins. 55
Activity of different proteases in a complex mixture and 'in vitro' study of their reciprocal interferences by micellar electrokinetic chromatography. 53
Osteogenesis imperfecta and type I collagen mutations. A lethal variant caused by a Gly910->Ala substitution in the a1(I) chain. 52
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 52
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. 51
Possible role of overglycosylation in the type I collagen triple helical domain in the molecular pathogenesis of osteogenesis imperfecta. 50
Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects. 50
Capillary electrophoresis as a modern tool for determining proteolytic activities in purified specimens and in real samples 50
Diastrophic dysplasia sulfate transporter (DTDST) gene is not involved in pseudodiastrophic dysplasia 49
Evaluation of the TiMo12Zr6Fe2 alloy for orthopaedic implants: in vitro biocompatibility study by using primary human fibroblasts and osteoblasts 49
Defective proteoglycan sulfation of the growth plate zones causes reduced chondrocyte proliferation via an altered Indian hedgehog signalling 49
Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for a Leu483Pro substitution in the diastrophic dysplasia sulfate transporter 48
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix. 48
Gly85 to Val substitution in proa1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. 47
Effect of different surfactants on the separation by micellar electrokinetic chromatography of a complex mixture of dipeptides in urine of prolidase-deficient patients. 47
Complete resolution of imidodipeptide mixtures in urine of prolidase-deficient patients using micellar electrokinetic chromatography. 47
Mild, late-onset prolidase deficiency: another Italian case. 46
Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta. 45
Therapeutic apheresis exchange in two patients with prolidase deficiency 44
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 43
Simultaneous determination of Pseudomonas aeruginosa elastase, human leukocyte elastase and cathepsin G activities by micellar electrokinetic chromatography 43
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype 43
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine a1(I) 901 substitution in a type-I collagen gene. 39
Proteoglycan modifications in cultured Osteogenesis Imperfecta skin fibroblasts. 38
In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias 38
Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2 38
Serum type I and type III procollagen peptide levels in sarcoidosis. 37
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen. 34
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta. 33
Relationship between changes in alveolar surfactant levels and lung defence mechanisms. 32
Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients. 27
Totale 4.957
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Categoria #
all - tutte 16.833
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 16.833
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.202 329 424 3 59 6 59 14 72 7 117 111 1
2020/2021560 75 54 14 60 4 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
2024/202536 36 0 0 0 0 0 0 0 0 0 0 0
Totale 4.957