Search Results - "Ceratto, N."
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Antioxidant role of metallothioneins: a comparative overview
Published in Cellular and molecular biology (Noisy-le-Grand, France) (01-03-2000)“…Metallothioneins (MTs) are sulfhydryl-rich proteins binding essential and non-essential heavy metals. MTs display in vitro oxyradical scavenging capacity,…”
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Effect of hydrogen peroxide on antioxidant enzymes and metallothionein level in the digestive gland of Mytilus galloprovincialis
Published in Comparative biochemistry and physiology. Toxicology & pharmacology (2002)“…The pro-oxidant effect of H 2O 2 at a concentration of 20 μM was examined in the digestive gland of Mytilus galloprovincialis, a bivalve mollusc frequently…”
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Cloning and sequencing of a novel metallothionein gene in Mytilus galloprovincialis Lam
Published in Comparative biochemistry and physiology. Toxicology & pharmacology (01-03-2002)“…Metallothionein (MT) is a ubiquitous, metal-inducible protein with an important role in the homeostasis and in the detoxification of heavy metals. This work…”
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PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population
Published in Journal of inherited metabolic disease (01-01-1996)“…Summary The results of the neonatal screening for phenylalanine hydroxylase (PAH) deficiency in Sicily show that its incidence is higher than previously…”
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Human type I cytokeratin genes are a compact cluster
Published in Cytogenetics and cell genetics (01-01-1997)“…A YAC clone (211F11) containing approximately 0.5 Mb of human DNA was isolated from a human genomic library by PCR-based screening with cytokeratin (KRT)…”
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Identification of two new phenylalanine hydroxylase alleles in Sicilian phenylketonuric families
Published in Journal of inherited metabolic disease (01-05-1993)Get full text
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Association between haplotypes, hind III-VNTR alleles and mutations at the PAH locus in Sicily
Published in Acta pædiatrica (Oslo, Norway : 1992). Supplement (01-12-1994)“…In this study we report previously undescribed associations between mutations, haplotypes and a minisatellite polymorphism (Hind III VNTR) of the PAH gene in…”
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Chromosomal mapping of human cytokeratin 13 gene (KRT13)
Published in Genomics (San Diego, Calif.) (01-10-1992)“…In the present study the human cytokeratin 13 gene (KRT13), encoding a polypeptide characteristic of internal stratified epithelia, has been mapped with the…”
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Assignment of the human cytokeratin 3 gene (KRT3) to 12q12-->q13 by FISH
Published in Cytogenetics and cell genetics (01-01-1994)“…We used fluorescence in situ hybridization to localize the human gene for cytokeratin 3 (KRT3), a member of the type II subfamily of cytokeratins, within the…”
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Effect of hydrogen peroxide on antioxidant enzymes and metallothionein level in the digestive gland of Mytilus galloprovincialis. cavalett@unipmn.it
Published in Comparative biochemistry and physiology. Toxicology & pharmacology (01-04-2002)“…The pro-oxidant effect of H2O2 at a concentration of 20 microM was examined in the digestive gland of Mytilus galloprovincialis, a bivalve mollusc frequently…”
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Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304
Published in American journal of medical genetics (01-02-1991)“…A new RFLP marker U6.2 defining the locus DXS304 was recently mapped to the distal long arm of the X chromosome. In the present study we report the results of…”
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Preliminary studies on the molecular basis of hyperphenylalaninemia in Egypt
Published in Human genetics (01-07-1996)“…Mutation analysis at the phenylalanine hydroxylase (PAH) locus was undertaken in 56 Egyptian hyperphenylalaninemic patients. Selected screening for 11 known…”
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Two novel PAH gene mutations detected in Italian phenylketonuric patients
Published in Human genetics (01-02-1997)“…We report the identification by denaturing gradient gel electrophoresis and sequence analysis of two new phenylalanine hydroxylase (PAH) gene mutations…”
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Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuria
Published in Prenatal diagnosis (01-10-1994)“…A polymorphic short tandem repeat (STR) in intron 3 (Goltsov et al., 1993) and a variable number of tandem repeats (Hind III-VNTR) flanked by two constant Hind…”
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Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe
Published in Human molecular genetics (01-10-1993)“…Hyperphenylalaninemia due to a deficiency of hepatic phenylalanine hydroxylase (PAH) is the most common inborn error of amino acid metabolism. Clinically, the…”
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