Search Results - "SCILLATO, FRANCESCO"
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LDOC1 expression in fibroblasts of patients with Down syndrome
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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A polymorphism (rs1042522) in TP53 gene is a risk factor for Down Syndrome in Sicilian mothers
Published in The journal of maternal-fetal & neonatal medicine (01-11-2017)“…Trisomy 21 is the most frequent genetic cause of intellectual disability. Tumor Protein 53 (TP53) gene down-regulation triggers chromosomal instability. A TP53…”
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Poly (ADP-ribose) polymerase-1 (PARP-1) − 410C/T polymorphism in Sicilian patients with Parkinson's disease
Published in Journal of the neurological sciences (15-04-2016)Get full text
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NF-kB1 gene expression in Down syndrome patients
Published in Neurological sciences (01-06-2015)Get full text
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Gene expression profiling and qRT-PCR expression of RRP1B, PCNT, KIF21A and ADRB2 in leucocytes of Down’s syndrome subjects
Published in Journal of genetics (01-12-2014)“…Down's syndrome (DS) is one of the most common numerical chromosomal aberrations in humans, usually caused by trisomy of chromosome 21, and is the most…”
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Gene expression profiling and qRT-PCR expression of RRP1B, PCNT, KIF21A and ADRB2 in leucocytes of Down's syndrome subjects
Published in Journal of genetics (13-03-2012)Get full text
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Expression of LDOC1 mRNA in leucocytes of patients with Down’s syndrome
Published in Journal of genetics (01-04-2012)Get full text
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SPANX-B and SPANX-C (Xq27 region) gene dosage analysis in Down’s syndrome subjects with undescended testes
Published in Journal of genetics (01-04-2009)“…The function of SPANX gene-encoded proteins is currently unknown, and it is also not known if all the members or some of them are normally expressed in the…”
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A polymorphism (rs1042522) in TP53 gene is a risk factor for Down Syndrome in Sicilian mothers
Published in The Journal of Maternal-Fetal & Neonatal Medicine (17-11-2017)“…Objective: Trisomy 21 is the most frequent genetic cause of intellectual disability. Tumor Protein 53 (TP53) gene down-regulation triggers chromosomal…”
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