IRIS
CETTA, GIUSEPPE
 Distribuzione geografica
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Continente #
NA - Nord America 4.434
AS - Asia 2.683
EU - Europa 2.454
SA - Sud America 309
AF - Africa 85
Continente sconosciuto - Info sul continente non disponibili 55
OC - Oceania 4
Totale 10.024
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Nazione #
US - Stati Uniti d'America 4.272
CN - Cina 1.410
SG - Singapore 552
IE - Irlanda 551
UA - Ucraina 326
RU - Federazione Russa 291
FI - Finlandia 270
DE - Germania 265
HK - Hong Kong 248
BR - Brasile 225
VN - Vietnam 195
IT - Italia 170
GB - Regno Unito 159
FR - Francia 137
SE - Svezia 105
CA - Canada 63
IN - India 63
ZA - Sudafrica 46
BE - Belgio 38
MX - Messico 38
AR - Argentina 33
BD - Bangladesh 32
TR - Turchia 30
IQ - Iraq 24
ES - Italia 22
NL - Olanda 22
PL - Polonia 22
IR - Iran 18
JP - Giappone 18
CZ - Repubblica Ceca 17
CO - Colombia 14
EC - Ecuador 14
ID - Indonesia 14
PK - Pakistan 13
HN - Honduras 11
LT - Lituania 11
CR - Costa Rica 10
AT - Austria 9
MA - Marocco 9
NI - Nicaragua 8
PH - Filippine 8
UZ - Uzbekistan 8
IL - Israele 7
RO - Romania 7
SA - Arabia Saudita 7
AL - Albania 6
CW - ???statistics.table.value.countryCode.CW??? 6
MY - Malesia 6
VE - Venezuela 6
CL - Cile 5
DZ - Algeria 5
JM - Giamaica 5
SV - El Salvador 5
TN - Tunisia 5
TW - Taiwan 5
AU - Australia 4
BO - Bolivia 4
ET - Etiopia 4
GP - Guadalupe 4
GT - Guatemala 4
KE - Kenya 4
NP - Nepal 4
PR - Porto Rico 4
PT - Portogallo 4
PY - Paraguay 4
SC - Seychelles 4
A2 - ???statistics.table.value.countryCode.A2??? 3
DO - Repubblica Dominicana 3
EG - Egitto 3
JO - Giordania 3
LV - Lettonia 3
PA - Panama 3
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
EE - Estonia 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
TT - Trinidad e Tobago 2
AM - Armenia 1
AZ - Azerbaigian 1
BH - Bahrain 1
BY - Bielorussia 1
CG - Congo 1
CH - Svizzera 1
DK - Danimarca 1
EU - Europa 1
GA - Gabon 1
GL - Groenlandia 1
HR - Croazia 1
KR - Corea 1
KZ - Kazakistan 1
LK - Sri Lanka 1
MK - Macedonia 1
Totale 9.969
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Città #
Dublin 551
Chandler 505
Jacksonville 376
San Jose 355
Ashburn 351
Beijing 328
Singapore 292
Dallas 275
Nanjing 255
Hong Kong 242
Council Bluffs 188
Ann Arbor 171
Boardman 144
Los Angeles 115
Nanchang 110
Princeton 84
Wilmington 83
Lawrence 82
Medford 80
Shenyang 80
Changsha 79
Helsinki 75
Munich 71
Hebei 65
Lauterbourg 65
Shanghai 64
Jiaxing 63
Hangzhou 60
Ho Chi Minh City 59
Moscow 55
Woodbridge 55
Milan 54
Tianjin 54
New York 53
Hanoi 46
Buffalo 40
Johannesburg 40
Santa Clara 40
Orem 39
Brussels 37
Turku 33
São Paulo 30
Frankfurt am Main 27
Houston 26
Verona 26
Chicago 25
Washington 25
Auburn Hills 22
Brooklyn 20
Chennai 19
Mexico City 16
Montreal 16
Warsaw 16
Atlanta 15
Denver 15
Norwalk 14
Stockholm 14
The Dalles 14
Tokyo 14
Haiphong 13
London 13
Redondo Beach 13
Toronto 13
Seattle 12
Ankara 11
Dearborn 10
Falkenstein 10
Kunming 10
Rome 10
San José 10
Da Nang 9
Pavia 9
Amsterdam 8
Ardabil 8
Boston 8
Brno 8
Des Moines 8
Ningbo 8
Phoenix 8
Poplar 8
San Francisco 8
Belo Horizonte 7
Dhaka 7
Fairfield 7
Managua 7
New Delhi 7
Olomouc 7
Ottawa 7
Rio de Janeiro 7
Tashkent 7
Baghdad 6
Biên Hòa 6
Bogotá 6
Casablanca 6
City of London 6
Columbus 6
Istanbul 6
Jinan 6
Manchester 6
Ninh Bình 6
Totale 6.506
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Nome #
A quantitative and qualitative method for direct 2-DE analysis of murine cartilage 195
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. 181
Adesion proteins in CHO cells. 177
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. 174
Alpha1-antitrypsin in serum determined by capillary isoelectric focusing 173
Biodegradable microspheres for prolidase delivery to human cultured fibroblasts 170
Micellar electrokinetic chromatography for analyzing active site specificity of Pseudomonas aeruginosa elastase. 168
Sequencing prolidase from pig kidney using multiple enzymatic digestion and LC-ESI-QTOF 163
Cartilage histogenesis in a murine model of chondrodysplasia 163
Capillary electrophoresis with laser-induced fluorescence detection as a novel sensitive approach for the analysis of desmosines in real samples. 158
Effects of lactitol compared to polyethylene glicol-3350 on fecal short chain fatty acids and microflora in old patients with idiopathic chronic constipation. 154
Separation of closely related peptide substrates of human proteinases by micellar electrokinetic chromatography with anionic and nonionic surfactants. 150
Insights from a transgenic mouse model on the role of SLC26A2 in health and disease. 149
In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation. 147
Mutation analysis of five new patients affected by prolidase deficiency: the lack of enzyme activity causes necrosis-like cell death in cultured fibroblasts 146
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 146
Investigation on transcellular delivery of active enzyme relased from PLGA microspheres 144
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 143
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 143
Intracellular delivery of liposome-encapsulated prolidase in cultured fibroblasts from prolidase-deficient patients 142
Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies. 140
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship. 139
Beta2-microglobulin isoforms display an heterogeneous affinity for type I collagen. 139
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI. 138
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 136
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype 136
Inhibition of human neutrophil elastase by erythromycin andflurythromycin, two macrolide antibiotics. 133
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. 130
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. 129
Activity of different proteases in a complex mixture and 'in vitro' study of their reciprocal interferences by micellar electrokinetic chromatography. 129
Effect of enamel matrix derivative on human periodontal fibroblasts: proliferation, morphology and root surface colonization. An in vitro study 129
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations 128
Complete resolution of imidodipeptide mixtures in urine of prolidase-deficient patients using micellar electrokinetic chromatography. 127
Capillary electrophoresis as a modern tool for determining proteolytic activities in purified specimens and in real samples 125
N-benzyloxycarbonyl-L-proline: an in vitro inhibitor of prolidase. 125
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency. 124
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. 124
Optimization of a capillary electrophoretic method to detect and quantify the Gly-Pro dipeptide in complex matrices from long term cultured prolidase deficiency fibroblasts 123
Intracellular release of a liposome-incapsulated biologically active protein 123
Effect of the triterpenoid fraction of Centella asiatica on macromolecules of the connective matrix in human skin fibroblast cultures. 123
Use of capillary zone electrophoresis for analysis of imidodipeptides in urine of prolidase-deficient patients. 122
The role of emerging techniques in the investigation of prolidase deficiency: from diagnosis to the development of a possible therapeutical approach 121
Rapid detection of ornithine transcarbamylase activity by micellar electrokinetic chromatography. 121
Stability of type I collagen peptide trimers. 119
Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta. 119
Micellar electrokinetic chromatographic and capillary zone electrophoretic methods for screening urinary biomarkers of human disorders: a critical review of the state-of-the-art. 119
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. 119
Enzyme replacement as a new therapy for prolidase deficiency 118
Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta. 118
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 117
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. 116
Micellar electrokinetic chromatography for the determination of urinary desmosine and isodesmosine in patients affected by chronic obstructive pulmonary disease 115
High levels of desmosines in urine and plasma of patients with pseudoxanthoma elasticum. 114
Micellar electrokinetic chromatography as a complementary method to sodium dodecyl sulfate-polyacrylamide gel electrophoresis for studying limited proteolysis of proteins. 114
Defective proteoglycan sulfation of the growth plate zones causes reduced chondrocyte proliferation via an altered Indian hedgehog signalling 113
Micellar electrokinetic chromatography: a convenient alternative to colorimetric and high performance liquid chromatographic detection for monitoring protease activity. 112
Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects. 108
Mild, late-onset prolidase deficiency: another Italian case. 107
Type I collagen CNBr peptides: species and behavior in solution 105
Therapeutic apheresis exchange in two patients with prolidase deficiency 103
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. 102
Evaluation of the TiMo12Zr6Fe2 alloy for orthopaedic implants: in vitro biocompatibility study by using primary human fibroblasts and osteoblasts 98
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix. 98
Osteogenesis imperfecta and type I collagen mutations. A lethal variant caused by a Gly910->Ala substitution in the a1(I) chain. 97
Effect of different surfactants on the separation by micellar electrokinetic chromatography of a complex mixture of dipeptides in urine of prolidase-deficient patients. 97
Simultaneous determination of Pseudomonas aeruginosa elastase, human leukocyte elastase and cathepsin G activities by micellar electrokinetic chromatography 97
Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta. 97
Possible role of overglycosylation in the type I collagen triple helical domain in the molecular pathogenesis of osteogenesis imperfecta. 96
Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for a Leu483Pro substitution in the diastrophic dysplasia sulfate transporter 95
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta. 95
Diastrophic dysplasia sulfate transporter (DTDST) gene is not involved in pseudodiastrophic dysplasia 93
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine a1(I) 901 substitution in a type-I collagen gene. 89
Gly85 to Val substitution in proa1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion. 87
In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias 86
Proteoglycan modifications in cultured Osteogenesis Imperfecta skin fibroblasts. 84
Serum type I and type III procollagen peptide levels in sarcoidosis. 82
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. 81
Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2 80
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 76
Relationship between changes in alveolar surfactant levels and lung defence mechanisms. 73
Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen. 69
Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients. 66
Totale 10.024
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Categoria #
all - tutte 40.036
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 40.036
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022372 0 0 0 0 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
2025/20263.034 242 190 372 383 384 176 557 122 286 208 57 57
2026/2027738 51 156 179 294 58 0 0 0 0 0 0 0
Totale 10.024