Search Results - "RIDOLFO, FEDERICO"

Evidence for long noncoding RNA GAS5 up-regulationin patients with Klinefelter syndrome by Salemi, Michele, Cannarella, Rossella, Condorelli, Rosita A, Cimino, Laura, Ridolfo, Federico, Giurato, Giorgio, Romano, Corrado, La Vignera, Sandro, Calogero, Aldo E

“…Klinefelter syndrome (KS) is characterized by the presence of at least one supernumerary X chromosome. KS typical symptoms include tall stature, gynecomastia,…”
Get full text

Expression of miR-132 in Down syndrome subjects by Salemi, Michele, Barone, Concetta, Salluzzo, Maria Grazia, Giambirtone, Mariaconcetta, Ridolfo, Federico, Romano, Corrado

Get full text

Mitochondrial mRNA expression in fibroblasts of Down syndrome subjects by Salemi, Michele, Giambirtone, Mariaconcetta, Barone, Concetta, Salluzzo, Maria Grazia, Russo, Roberto, Giudice, Mariangela Lo, Cutuli, Salvatore, Ridolfo, Federico, Romano, Corrado

Get full text

PARP-1 and CASP3 genes are up-regulated in LNCaP and PC-3 prostate cancer cell lines by Salemi, Michele, Condorelli, Rosita A., La Vignera, Sandro, Barone, Nunziata, Ridolfo, Federico, Giuffrida, Maria C., Vicari, Enzo, Calogero, Aldo E.

Get full text

Humanin gene expression in subjects with Parkinson’s disease by Salemi, Michele, Ridolfo, Federico, Salluzzo, Maria Grazia, Schillaci, Francesca A., Caniglia, Salvatore, Lanuzza, Bartolo, Cantone, Mariagiovanna, Ferri, Raffaele

“…Background Bradykinesia, tremor, rigidity and postural instability are the hallmark of Parkinson’s disease (PD). Non-motor symptoms including cognitive,…”
Get full text

A polymorphism (rs1042522) in TP53 gene is a risk factor for Down Syndrome in Sicilian mothers by Salemi, Michele, Barone, Concetta, Salluzzo, Maria Grazia, Giambirtone, Mariaconcetta, Scillato, Francesco, Galati Rando, Rosanna, Romano, Carmelo, Morale, Maria Concetta, Ridolfo, Federico, Romano, Corrado

“…Trisomy 21 is the most frequent genetic cause of intellectual disability. Tumor Protein 53 (TP53) gene down-regulation triggers chromosomal instability. A TP53…”
Get full text

Cerebellar degeneration-related protein 1 expression in fibroblasts of patients affected by down syndrome by Salemi, Michele, Rappazzo, Giancarlo, Ridolfo, Federico, Salluzzo, Maria Grazia, Cannarella, Rossella, Castiglione, Roberto, Caniglia, Salvatore, Tirolo, Cataldo, Calogero, Aldo E., Romano, Corrado

Get full text

NF-kB1 gene expression in Down syndrome patients by Salemi, Michele, Barone, Concetta, Romano, Carmelo, Scillato, Francesco, Ragalmuto, Alda, Caniglia, Salvatore, Salluzzo, Maria Grazia, Sciuto, Graziella, Ridolfo, Federico, Romano, Corrado, Bosco, Paolo

Get full text

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

“…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…”
Get full text

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

“…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…”
Get full text

Expression of LDOC1 mRNA in leucocytes of patients with Down’s syndrome by SALEMI, MICHELE, BARONE, CONCETTA, ROMANO, CARMELO, RIDOLFO, FEDERICO, SALLUZZO, ROBERTO, SCILLATO, FRANCESCO, SCAVUZZO, CATALDO, CARACI, FILIPPO, CALOGERO, ALDO E., ROMANO, CORRADO, BOSCO, PAOLO

Get full text

Humanin gene expression in fibroblast of Down syndrome subjects by Salemi, Michele, Ridolfo, Federico, Salluzzo, Maria Grazia, Cannarrella, Rossella, Giambirtone, Mariaconcetta, Caniglia, Salvatore, Tirolo, Cataldo, Ferri, Raffaele, Romano, Corrado

“…Down syndrome (DS) is characterized by trisomy of chromosome 21 and peculiar phenotype. Humanin (HN) is a mitochondrial short 24-residue polypeptide whit…”
Get full text

A polymorphism (rs1042522) in TP53 gene is a risk factor for Down Syndrome in Sicilian mothers by Salemi, Michele, Barone, Concetta, Salluzzo, Maria Grazia, Giambirtone, Mariaconcetta, Scillato, Francesco, Galati Rando, Rosanna, Romano, Carmelo, Morale, Maria Concetta, Ridolfo, Federico, Romano, Corrado

“…Objective: Trisomy 21 is the most frequent genetic cause of intellectual disability. Tumor Protein 53 (TP53) gene down-regulation triggers chromosomal…”
Get full text

Multicast Voice Transmission over Vehicular Ad Hoc Networks: Issues and Challenges by Bucciol, P., Ridolfo, F., De Martin, J.C.

“…In this paper we analyze the challenges and issues of transmitting multicast voice streams in a vehicular ad hoc network (VANET). The considered scenario…”
Get full text

Hybrid bitrate/PSNR control for H.264 video streaming to roaming users by De Vito, F., Ridolfo, F., De Martin, J.C.

“…In wireless communications, the available throughput depends on several parameters, like physical layer, base station distance, fading and interference. Users…”
Get full text