Search Results - "Ceratto, N."

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  1. 1

    Antioxidant role of metallothioneins: a comparative overview by Viarengo, A, Burlando, B, Ceratto, N, Panfoli, I

    “…Metallothioneins (MTs) are sulfhydryl-rich proteins binding essential and non-essential heavy metals. MTs display in vitro oxyradical scavenging capacity,…”
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  2. 2

    Effect of hydrogen peroxide on antioxidant enzymes and metallothionein level in the digestive gland of Mytilus galloprovincialis by Cavaletto, M., Ghezzi, A., Burlando, B., Evangelisti, V., Ceratto, N., Viarengo, A.

    “…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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  3. 3

    Cloning and sequencing of a novel metallothionein gene in Mytilus galloprovincialis Lam by Ceratto, Nadia, Dondero, Francesco, van de Loo, Jan-Willem, Burlando, Bruno, Viarengo, Aldo

    “…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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  4. 4

    PAH deficiency in Italy: correlation of genotype with phenotype in the Sicilian population by Romano, V., Guldberg, P., Güttler, F., Meli, C., Mollica, F., Pavone, L., Giovannini, M., Riva, E., Biasucci, G., Luotti, D., Palillo, L., Calí, F., Ceratto, N., Anello, G., Bosco, P.

    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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  5. 5

    Human type I cytokeratin genes are a compact cluster by Ceratto, N, Dobkin, C, Carter, M, Jenkins, E, Yao, X L, Cassiman, J J, Aly, M S, Bosco, P, Leube, R, Langbein, L, Feo, S, Romano, V

    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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    Association between haplotypes, hind III-VNTR alleles and mutations at the PAH locus in Sicily by Romano, V, Calì, F, Guldberg, P, Güttler, F, Indelicato, A, Bosco, P, Ceratto, N

    “…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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  8. 8

    Chromosomal mapping of human cytokeratin 13 gene (KRT13) by Romano, V, Raimondi, E, Bosco, P, Feo, S, Di Pietro, C, Leube, R E, Troyanovsky, S M, Ceratto, N

    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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  9. 9

    Assignment of the human cytokeratin 3 gene (KRT3) to 12q12-->q13 by FISH by Raimondi, E, Moralli, D, De Carli, L, Ceratto, N, Balzaretti, M, Leube, R, Collin, C, Romano, V

    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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  10. 10

    Effect of hydrogen peroxide on antioxidant enzymes and metallothionein level in the digestive gland of Mytilus galloprovincialis. cavalett@unipmn.it by Cavaletto, M, Ghezzi, A, Burlando, B, Evangelisti, V, Ceratto, N, Viarengo, A

    “…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 by Goonewardena, P, Brown, W T, Gross, A C, Ferrando, C, Dobkin, C, Romano, V, Bosco, P, Ceratto, N, Pettersson, U, Dahl, N

    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 by HASHEM, N, BOSCO, P, CHIAVETTA, V, CALI, F, CERATTO, N, ROMANO, V

    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 by ARGIOLAS, A, BOSCO, P, CALI, F, CERATTO, N, ANELLO, G, RIVA, E, BIASUCCI, G, CARDUCCI, C, ROMANO, V

    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 by Romano, V, Dianzani, I, Ponzone, A, Zammarchi, E, Eisensmith, R, Ceratto, N, Bosco, P, Indelicato, A

    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 by Guldberg, P, Romano, V, Ceratto, N, Bosco, P, Ciuna, M, Indelicato, A, Mollica, F, Meli, C, Giovannini, M, Riva, E

    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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