BOSCO, PAOLO
BOSCO, PAOLO
Università degli Studi di CATANIA
Allele ε4 of apolipoprotein E gene is less frequent in Down syndrome patient of the Sicilian population and has no influence on the grade of mental retardation
2001-01-01 Anello, G.; Gueant, J. -L.; Romano, C.; Barone, C.; Pettinato, R.; Pillot, T.; Rodriguez, R. -M.; Romano, A.; Bosco, P.
DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome
2013-01-01 Coppede, F.; Bosco, P.; Tannorella, P.; Romano, C.; Antonucci, I.; Stuppia, L.; Romano, C.; Migliore, L.
Environmental influence on the worldwide prevalence of a 776C→G variant in the transcobalamin gene (TCN2)
file da validare2007-01-01 Gueant, J. -L.; Chabi, N. W.; Gueant-Rodriguez, R. -M.; Mutchinick, O. M.; Debard, R.; Payet, C.; Lu, X.; Villaume, C.; Bronowicki, J. -P.; Quadros, E. V.; Sanni, A.; Amouzou, E.; Xia, B.; Chen, M.; Anello, G.; Bosco, P.; Romano, C.; Arrieta, H. R.; Sanchez, B. E.; Romano, A.; Herbeth, B.; Anwar, W.; Namour, F.
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability
2015-01-01 Gandin, I.; Faletra, F.; Faletra, F.; Carella, M.; Pecile, V.; Ferrero, G. B.; Biamino, E.; Palumbo, P.; Palumbo, O.; Bosco, P.; Romano, C.; Belcaro, C.; Vozzi, D.; D'Adamo, A. P.
Genetic determinants of folate and vitamin B12 metabolism: A common pathway in neural tube defect and Down syndrome?
2003-01-01 Gueant, J. -L.; Gueant-Rodriguez, R. -M.; Anello, G.; Bosco, P.; Brunaud, L.; Romano, C.; Ferri, R.; Romano, A.; Candito, M.; Namour, B.
Homocysteine and related genetic polymorphisms in Down's syndrome IQ
2005-01-01 Gueant, J. -L.; Anello, G.; Bosco, P.; Gueant-Rodriguez, R. -M.; Romano, A.; Barone, C.; Gerard, P.; Romano, C.
Killer-specific secretory (Ksp37) gene expression in subjects with Down’s syndrome
file da validare2016-01-01 Salemi, M.; Barone, C.; Morale, M. C.; Caniglia, S.; Romano, C.; Salluzzo, M. G.; Rando, R. G. G.; Ragalmuto, A.; Bosco, P.; Romano, C.
LDOC1 expression in fibroblasts of patients with Down syndrome
2015-01-01 Salemi, M.; Barone, C.; Romano, C.; Caniglia, S.; Ragalmuto, A.; Scillato, F.; Salluzzo, M. G.; Scavuzzo, C.; Vinci, M.; Salluzzo, R.; Romano, C.; Bosco, P.
NF-kB1 gene expression in Down syndrome patients
2015-01-01 Salemi, M.; Barone, C.; Romano, C.; Scillato, F.; Ragalmuto, A.; Caniglia, S.; Salluzzo, M. G.; Sciuto, G.; Ridolfo, F.; Romano, C.; Bosco, P.
Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: A comparative study in Mexican, West African, and European populations
2006-01-01 Gueant-Rodriguez, R. -M.; Gueant, J. -L.; Debard, R.; Thirion, S.; Lu, X. H.; Bronowicki, J. -P.; Namour, F.; Chabi, N. W.; Sanni, A.; Anello, G.; Bosco, P.; Romano, C.; Amouzou, E.; Arrieta, H. R.; Sanchez, B. E.; Romano, A.; Herbeth, B.; Guilland, J. -C.; Mutchinick, O. M.
Searching for disease-modifying drugs in AD: can we combine neuropsychological tools with biological markers?
file da validare2014-01-01 Caraci, Filippo; Castellano, Sabrina; Salomone, Salvatore; Drago, Filippo; Bosco, Paolo; Di Nuovo, Santo
Simultaneous determination of ochratoxin A and aflatoxins by LCMS/MS in fetus-maternal biological fluids
2010-01-01 Ritieni, A; Santini, A; Mussap, M; Ferracane, R; Gazzolo, D; Galvano, F; Bosco, Paolo
Spectral phasor analysis using 4 detectors of a commercial microscope for fast spectral imaging
file da validare2024-01-01 Lanzano', Luca; Bosco, Paolo; Di Franco, Elisabetta; Longo, Elisa; Privitera, Anna P.; Scalisi, Silvia
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability
2015-01-01 Morgan, A.; Gandin, I.; Belcaro, C.; Palumbo, P.; Palumbo, O.; Biamino, E.; Dal Col, V.; Laurini, E.; Pricl, S.; Bosco, P.; Carella, M.; Ferrero, G. B.; Romano, C.; D'Adamo, A. P.; Faletra, F.; Vozzi, D.
The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: A case-control study and a meta-analysis
2014-01-01 Coppede, F.; Bosco, P.; Lorenzoni, V.; Denaro, M.; Anello, G.; Antonucci, I.; Barone, C.; Stuppia, L.; Romano, C.; Migliore, L.
The role of antioxidant supplement in immune system, neoplastic, and neurodegenerative disorders: A point of view for an assessment of the risk/benefit profile
file da validare2008-01-01 Brambilla, D.; Mancuso, C.; Scuderi, M. R.; Bosco, P.; Cantarella, G.; Lempereur, L.; Di Benedetto, G.; Pezzino, S.; Bernardini, R.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Allele ε4 of apolipoprotein E gene is less frequent in Down syndrome patient of the Sicilian population and has no influence on the grade of mental retardation | 1-gen-2001 | Anello, G.; Gueant, J. -L.; Romano, C.; Barone, C.; Pettinato, R.; Pillot, T.; Rodriguez, R. -M.; Romano, A.; Bosco, P. | |
DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome | 1-gen-2013 | Coppede, F.; Bosco, P.; Tannorella, P.; Romano, C.; Antonucci, I.; Stuppia, L.; Romano, C.; Migliore, L. | |
Environmental influence on the worldwide prevalence of a 776C→G variant in the transcobalamin gene (TCN2) | 1-gen-2007 | Gueant, J. -L.; Chabi, N. W.; Gueant-Rodriguez, R. -M.; Mutchinick, O. M.; Debard, R.; Payet, C.; Lu, X.; Villaume, C.; Bronowicki, J. -P.; Quadros, E. V.; Sanni, A.; Amouzou, E.; Xia, B.; Chen, M.; Anello, G.; Bosco, P.; Romano, C.; Arrieta, H. R.; Sanchez, B. E.; Romano, A.; Herbeth, B.; Anwar, W.; Namour, F. | file da validare |
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability | 1-gen-2015 | Gandin, I.; Faletra, F.; Faletra, F.; Carella, M.; Pecile, V.; Ferrero, G. B.; Biamino, E.; Palumbo, P.; Palumbo, O.; Bosco, P.; Romano, C.; Belcaro, C.; Vozzi, D.; D'Adamo, A. P. | |
Genetic determinants of folate and vitamin B12 metabolism: A common pathway in neural tube defect and Down syndrome? | 1-gen-2003 | Gueant, J. -L.; Gueant-Rodriguez, R. -M.; Anello, G.; Bosco, P.; Brunaud, L.; Romano, C.; Ferri, R.; Romano, A.; Candito, M.; Namour, B. | |
Homocysteine and related genetic polymorphisms in Down's syndrome IQ | 1-gen-2005 | Gueant, J. -L.; Anello, G.; Bosco, P.; Gueant-Rodriguez, R. -M.; Romano, A.; Barone, C.; Gerard, P.; Romano, C. | |
Killer-specific secretory (Ksp37) gene expression in subjects with Down’s syndrome | 1-gen-2016 | Salemi, M.; Barone, C.; Morale, M. C.; Caniglia, S.; Romano, C.; Salluzzo, M. G.; Rando, R. G. G.; Ragalmuto, A.; Bosco, P.; Romano, C. | file da validare |
LDOC1 expression in fibroblasts of patients with Down syndrome | 1-gen-2015 | Salemi, M.; Barone, C.; Romano, C.; Caniglia, S.; Ragalmuto, A.; Scillato, F.; Salluzzo, M. G.; Scavuzzo, C.; Vinci, M.; Salluzzo, R.; Romano, C.; Bosco, P. | |
NF-kB1 gene expression in Down syndrome patients | 1-gen-2015 | Salemi, M.; Barone, C.; Romano, C.; Scillato, F.; Ragalmuto, A.; Caniglia, S.; Salluzzo, M. G.; Sciuto, G.; Ridolfo, F.; Romano, C.; Bosco, P. | |
Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: A comparative study in Mexican, West African, and European populations | 1-gen-2006 | Gueant-Rodriguez, R. -M.; Gueant, J. -L.; Debard, R.; Thirion, S.; Lu, X. H.; Bronowicki, J. -P.; Namour, F.; Chabi, N. W.; Sanni, A.; Anello, G.; Bosco, P.; Romano, C.; Amouzou, E.; Arrieta, H. R.; Sanchez, B. E.; Romano, A.; Herbeth, B.; Guilland, J. -C.; Mutchinick, O. M. | |
Searching for disease-modifying drugs in AD: can we combine neuropsychological tools with biological markers? | 1-gen-2014 | Caraci, Filippo; Castellano, Sabrina; Salomone, Salvatore; Drago, Filippo; Bosco, Paolo; Di Nuovo, Santo | file da validare |
Simultaneous determination of ochratoxin A and aflatoxins by LCMS/MS in fetus-maternal biological fluids | 1-gen-2010 | Ritieni, A; Santini, A; Mussap, M; Ferracane, R; Gazzolo, D; Galvano, F; Bosco, Paolo | |
Spectral phasor analysis using 4 detectors of a commercial microscope for fast spectral imaging | 1-gen-2024 | Lanzano', Luca; Bosco, Paolo; Di Franco, Elisabetta; Longo, Elisa; Privitera, Anna P.; Scalisi, Silvia | file da validare |
Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability | 1-gen-2015 | Morgan, A.; Gandin, I.; Belcaro, C.; Palumbo, P.; Palumbo, O.; Biamino, E.; Dal Col, V.; Laurini, E.; Pricl, S.; Bosco, P.; Carella, M.; Ferrero, G. B.; Romano, C.; D'Adamo, A. P.; Faletra, F.; Vozzi, D. | |
The MTRR 66A>G polymorphism and maternal risk of birth of a child with Down syndrome in Caucasian women: A case-control study and a meta-analysis | 1-gen-2014 | Coppede, F.; Bosco, P.; Lorenzoni, V.; Denaro, M.; Anello, G.; Antonucci, I.; Barone, C.; Stuppia, L.; Romano, C.; Migliore, L. | |
The role of antioxidant supplement in immune system, neoplastic, and neurodegenerative disorders: A point of view for an assessment of the risk/benefit profile | 1-gen-2008 | Brambilla, D.; Mancuso, C.; Scuderi, M. R.; Bosco, P.; Cantarella, G.; Lempereur, L.; Di Benedetto, G.; Pezzino, S.; Bernardini, R. | file da validare |