15 results match your criteria: "Universita' degli Studi di Cagliari[Affiliation]"

Microfibres are one of the most ubiquitous particulate pollutants, occurring in all environmental compartments. They are often assumed to be microplastics, but include natural as well as synthetic textile fibres and are perhaps best treated as a separate class of pollutants given the challenges they pose in terms of identification and contamination. Microfibres have been largely ignored by traditional methods used to sample floating microplastics at sea, which use 300-500 μm mesh nets that are too coarse to sample most textile fibres.

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We describe a case of Wilson's disease (WD) diagnosed at 5 years after routine biochemical test showed increased aminotransferases. Mutation analysis of the ATP7B gene revealed a 3039-bp deletion in the homozygous state spanning from the terminal part of intron 1 to nt position 368 of exon 2. This deletion results in the activation of 3 cryptic splice sites: an AG acceptor splice site in nt positions 578-579 producing a different breakpoint and removing the first 577 nts of exon 2, an acceptor and a donor splice site in nt positions 20363-4 and 20456-7, respectively, in intron 1, resulting in the activation of a 94-bp cryptic Alu exon being incorporated into the mature transcript.

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Refractive error (RE) is a complex, multifactorial disorder characterized by a mismatch between the optical power of the eye and its axial length that causes object images to be focused off the retina. The two major subtypes of RE are myopia (nearsightedness) and hyperopia (farsightedness), which represent opposite ends of the distribution of the quantitative measure of spherical refraction. We performed a fixed effects meta-analysis of genome-wide association results of myopia and hyperopia from 9 studies of European-derived populations: AREDS, KORA, FES, OGP-Talana, MESA, RSI, RSII, RSIII and ERF.

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A dental unit water line (DUWL) equipped with a device designed to automatically and continually flush a bacteriostatic solution of hydrogen peroxide (WHE) and a discontinuous disinfecting system (BIOSTER) was evaluated. In the first instance a preliminary sensitivity test on a large number of microorganisms (bacteria and fungi) was tried with a H(2)O(2) range from 100 to 800 ppm. The bacteria frequently reported in DUWL (including Pseudomonas spp, Streptococcus spp.

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Metal-induced pre-organisation for anion recognition in a neutral platinum-containing receptor.

Chem Commun (Camb)

November 2009

Universita' degli Studi di Cagliari, Dipartimento di Chimica Inorganica ed Analitica, S.S. 554 Bivio per Sestu, Monserrato (CA), Italy.

The presence of Pt(II) allows pre-organisation of 4,4'-dicarboxamidoindole-2,2'-bipyridine, enhancing anion affinity with the resulting complex displaying selectivity for dihydrogen phosphate in DMSO-d6-0.5% water. Moreover the Pt(II) complex behaves as a colorimetic sensor for fluoride.

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In Vitro evaluation of Enterococcus faecalis adhesion on various endodontic medicaments.

Open Dent J

June 2009

Oral Biotechnology Laboratory (OBL), Dipartimento di Chirurgia e Scienze Odontostomatologiche, Universita' Degli Studi di Cagliari, Cagliari, Italy.

E. faecalis in endodontic infection represents a biofilm type of disease, which explains the bacteria's resistance to various antimicrobial compounds and the subsequent failure after endodontic treatment. The purpose of this study was to compare antimicrobial activities and bacteria kinetic adhesion in vitro for three endodontic medicaments with a clinical isolate of E.

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Risk assessment does not explain high prevalence of gestational diabetes mellitus in a large group of Sardinian women.

Reprod Biol Endocrinol

July 2008

Dipartimento Chirurgico Materno Infantile e di Scienza delle Immagini, Sezione di Clinica Ginecologica, Ostetrica e Fisiopatologia della Riproduzione Umana, Universita' degli Studi di Cagliari, Italy.

Background: A very high prevalence (22.3%) of gestational diabetes mellitus (GDM) was recently reported following our study on a large group of Sardinian women. In order to explain such a high prevalence we sought to characterise our obstetric population through the analysis of risk factors and their association with the development of GDM.

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Autoimmunity in gestational diabetes mellitus in Sardinia: a preliminary case-control report.

Reprod Biol Endocrinol

June 2008

Dipartimento Chirurgico Materno Infantile e di Scienza delle Immagini, Sezione di Clinica Ginecologica, Ostetrica e Fisiopatologia della Riproduzione Umana, Universita' degli Studi di Cagliari, Italy.

Background: We previously reported a high prevalence (22.3%) of gestational diabetes mellitus (GDM) in a large group of Sardinian women, in contrast with the prevalence of Type 2 diabetes. Sardinia has an unusual distribution of haplotypes and genotypes, with the highest population frequency of HLA DR3 in the world, and after Finland, the highest prevalence of Type 1 diabetes and Autoimmune-related Diseases.

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Alpha1-Antitrypsin deficiency is an autosomal codominant inherited disorder, with increased risk of developing lung and liver disease. The large majority of subjects affected by alpha1-antitrypsin deficiency carry the PIZZ or PISZ genotypes, which can be easily detected using several molecular methods. Another pathologic allele, the M-Malton variant (also known as Mnichinan and Mcagliari), can mimic the Pi Z clinical phenotype, but this alpha1-antitrypsin deficiency variant is not easily recognizable and, therefore, seems to be more under-recognized than the Z or S alleles.

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Hepatitis E Virus (HEV) is the causative agent of an acute and self-limited form of hepatitis. The virus is transmitted by the faecal-oral route and is a major cause of viral hepatitis in much of the developing world where it causes sporadic infections and large-scale epidemics. A simple and rapid protocol for the measurement of HEV faecal shedding by a real-time polymerase chain reaction (PCR) with the SYBR Green method on a LightCycler instrument, is described.

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Computerized quantitative color analysis for histological study of pulmonary fibrosis.

Anticancer Res

March 2003

Universita' degli Studi di Cagliari, Dipartimento di Sanita' Pubblica, Sezione di Medicina Legale, Via Porcell, 4, 09124, Cagliari, Italy.

Background: Color segmentation is a process through which particular structures can be identified and isolated by the same image according to their color. This may prove particularly useful for the quantification of human pulmonary fibrosis through computerized color segmentation methods applied to trichromic stainings. The aim of this study was to develop and verify a reliable method in order to obtain reproducible parameters of fibrosis using trichromic stainings.

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A poly(ethylene glycol)-supported quaternary ammonium salt: An efficient, recoverable, and recyclable phase-transfer catalyst.

Org Lett

June 2000

Centro CNR and Dipartimento di Chimica Organica e Industriale, Universita' degli Studi di Milano, via Golgi 19, I-20133 - Milano, Italy, and Dipartimento Farmaco Chimico Tecnologico, Universita' degli Studi di Cagliari, via Ospedale 72, I-09.

A quaternary ammonium salt readily immobilized on a soluble poly(ethylene glycol) polymer support efficiently catalyzes different reactions carried out under phase-transfer catalysis conditions; the catalyst, easily recovered by precipitation and filtration, shows no appreciable loss of activity when recycled three times.

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Anti-HIV-1 integrase drugs: how far from the shelf?

Curr Pharm Des

March 2000

Dipartimento di Biologia Sperimentale, Sezione di Microbiologia, Universita' degli Studi di Cagliari, Italy.

Chemotherapy of HIV-1 infection/AIDS currently employs inhibitors of two products of the viral pol gene, the reverse transcriptase and protease enzymes. However, a third product of the pol gene is essential for retroviral multiplication, the integrase. As no cellular homologue of HIV integrase has been described, potential inhibitors could be relatively nontoxic.

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In this study, we analyzed the phenotypic manifestations resulting from the interaction of heterozygous beta zero-thalassemia(beta zero-39 nonsense mutation) with the functional loss of three alpha-globin structural genes in six subjects, of whom four had the [-alpha/--]alpha-globin genotype and two the [--/alpha Th alpha] alpha-globin genotype. The beta-thalassemia defect was in all cases the nonsense mutation at codon 39. The nondeletion alpha-thalassemia alpha th was the initiation codon mutation (AUG----GUG) of the alpha-2 gene.

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Diagnosis of beta-thalassemia intermedia at presentation.

Birth Defects Orig Artic Ser

August 1988

Istituto di Clinica e Biologia dell'Eta' Evolutiva, Universita' degli Studi di Cagliari, Sardinia, Italy.

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