Search Results - "SCAVUZZO, CATALDO"

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  1. 1

    LDOC1 expression in fibroblasts of patients with Down syndrome by Salemi, Michele, Barone, Concetta, Romano, Carmelo, Caniglia, Salvatore, Ragalmuto, Alda, Scillato, Francesco, Salluzzo, Maria Grazia, Scavuzzo, Cataldo, Vinci, Mirella, Salluzzo, Roberto, Romano, Corrado, Bosco, Paolo

    Published in Open life sciences (11-03-2015)
    “…Down syndrome (DS) is characterised by intellectual disability and is caused by trisomy 21. Apoptosis is a programmed cell death process and is involved in…”
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    Journal Article
  2. 2

    Poly (ADP-ribose) polymerase 1 expression in fibroblasts of Down syndrome subjects by Salemi, Michele, Barone, Concetta, Romano, Corrado, Romano, Carmelo, Scavuzzo, Cataldo, Salluzzo, Maria Grazia, Tirolo, Cataldo, Cantarella, Rita Anna, Ragalmuto, Alda, Paola, Sandro Santa, Bosco, Paolo

    Published in Central European journal of medicine (01-12-2013)
    “…Down syndrome (DS) is the most common chromosomal disorder. It is featured by intellectual disability and is caused by trisomy 21. People with DS can develop…”
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    Journal Article
  3. 3

    KIF21A mRNA expression in patients with Down syndrome by Salemi, Michele, Barone, Concetta, Romano, Carmelo, Ridolfo, Federico, Scavuzzo, Cataldo, Cantarella, Rita Anna, Salluzzo, Maria Grazia, Calogero, Aldo E., Romano, Corrado, Bosco, Paolo

    Published in Neurological sciences (01-04-2013)
    “…Down syndrome (DS) is a chromosomal disorder caused by chromosome 21 trisomy and is the most frequent genetic cause of intellectual disability. The gene for…”
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    Journal Article
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    Differential expression of PARP1 mRNA in leucocytes of patients with Down’s syndrome by SALEMI, MICHELE, BARONE, CONCETTA, ROMANO, CARMELO, RIDOLFO, FEDERICO, GULOTTA, ELEONORA, SCAVUZZO, CATALDO, SALLUZZO, MARIA GRAZIA, GIAMBIRTONE, MARIACONCETTA, CARACI, FILIPPO, ROMANO, CORRADO, BOSCO, PAOLO

    Published in Journal of genetics (01-12-2011)
    “…Downs syndrome (DS) is one of the most common numerical chromosomal aberrations, usually caused by trisomy of chromosome 21, and is the most frequent genetic…”
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    Journal Article
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