Search Results - "Sercia, L"

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  1. 1

    Allele-specific CRISPR-Cas9 editing of dominant epidermolysis bullosa simplex in human epidermal stem cells by Cattaneo, C, Enzo, E, De Rosa, L, Sercia, L, Consiglio, F, Forcato, M, Bicciato, S, Paiardini, A, Basso, G, Tagliafico, E, Paganelli, A, Fiorentini, C, Magnoni, C, Latella, M C, De Luca, M

    Published in Molecular therapy (07-02-2024)
    “…Epidermolysis bullosa simplex (EBS) is a rare skin disease inherited mostly in an autosomal dominant manner. Patients display a skin fragility that leads to…”
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    Journal Article
  2. 2

    Multi-centre evaluation of mass spectrometric identification of anaerobic bacteria using the VITEK® MS system by Garner, O., Mochon, A., Branda, J., Burnham, C.-A., Bythrow, M., Ferraro, M., Ginocchio, C., Jennemann, R., Manji, R., Procop, G.W., Richter, S., Rychert, J., Sercia, L., Westblade, L., Lewinski, M.

    Published in Clinical microbiology and infection (01-04-2014)
    “…Accurate and timely identification of anaerobic bacteria is critical to successful treatment. Classic phenotypic methods for identification require long…”
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    Multi-centre evaluation of mass spectrometric identification of anaerobic bacteria using the VITEK super( registered ) MS system by Garner, O, Mochon, A, Branda, J, Burnham, C-A, Bythrow, M, Ferraro, M, Ginocchio, C, Jennemann, R, Manji, R, Procop, G W, Richter, S, Rychert, J, Sercia, L, Westblade, L, Lewinski, M

    Published in Clinical microbiology and infection (01-04-2014)
    “…Accurate and timely identification of anaerobic bacteria is critical to successful treatment. Classic phenotypic methods for identification require long…”
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    Journal Article
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    Expression of caveolin-1 in renal neoplasms by Zhou, M., Tamaskar, I., Sercia, L., Rini, B. I., Bukowski, R. M.

    Published in Journal of clinical oncology (20-06-2006)
    “…Abstract only 14509 Background: Caveolin-1 is the major structural and functional component of caveolae, which are specialized lipid raft microdomains on cell…”
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  9. 9

    Detection of a novel point mutation of the prothrombin gene at position 20209 by Warshawsky, Ilka, Hren, Carol, Sercia, Linda, Shadrach, Bonnie, Deitcher, Steven R, Newton, Erin, Kottke-Marchant, Kandice

    Published in Diagnostic molecular pathology (01-09-2002)
    “…Detection of the prothrombin G20210A mutation was performed on the LightCycler Instrument (Roche Molecular Biochemicals, Mannheim, Germany) using commercially…”
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    Journal Article