Sfoglia per Autore
GSTA1 gene variation associated with gestational hypertension and its involvement in pregnancy-related pathogenic conditions
2015-01-01 Iorio, A; Spinelli, M; Polimanti, R; Lorenzi, F; Valensise, H; Manfellotto, D; Fuciarelli, M
From adaptive licensing to adaptive pathways: Delivering a flexible life-span approach to bring new drugs to patients
2015-01-01 Eichler, H-; Baird, Lg; Barker, R; Bloechl-Daum, B; Borlum-Kristensen, F; Brown, J; Chua, R; Del Signore, S; Dugan, U; Ferguson, J; Garner, S; Goettsch, W; Haigh, J; Honig, P; Hoos, A; Huckle, P; Kondo, T; Le Cam, Y; Leufkens, H; Lim, R; Longson, C; Lumpkin, M; Maraganore, J; O'Rourke, B; Oye, K; Pezalla, E; Pignatti, F; Raine, J; Rasi, G; Salmonson, T; Samaha, D; Schneeweiss, S; Siviero, Pd; Skinner, M; Teagarden, Jr; Tominaga, T; Trusheim, Mr; Tunis, S; Unger, Tf; Vamvakas, S; Hirsch, G
Deletion polymorphism of GSTT1 gene as protective marker for allergic rhinitis
2015-01-01 Iorio, A; Polimanti, R; Piacentini, S; Liumbruno, Gm; Manfellotto, D; Fuciarelli, M
Most recent common ancestor of TTR Val30Met mutation in Italian population and its potential role in genotype-phenotype correlation
2015-01-01 Iorio, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Pradotto, L; Mauro, A; Manfellotto, D; Fuciarelli, M; Polimanti, R
Haplotype differences for copy number variants in the 22q11.23 region among human populations: A pigmentation-based model for selective pressure
2015-01-01 Polimanti, R; Piacentini, S; Iorio, A; De Angelis, F; Kozlov, A; Novelletto, A; Fuciarelli, M
GPX1*Pro198Leu AND GPX3 rs2070593 as genetic risk markers for Italian asthmatic patients
2016-01-01 Iorio, A; Velocci, M; Graziano, Me; Piacentini, S; Polimanti, R; Manfellotto, D; Fuciarelli, M
Explorative genetic association study of GSTT2B copy number variant in complex disease risks
2016-05-01 Iorio, A; Polimanti, R; Calandro, M; Graziano, Me; Piacentini, S; Bucossi, S; Squitti, R; Lazzarin, N; Scano, G; Limbruno, Gm; Manfellotto, D; Fuciarelli, M
Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis
2017-01-01 Iorio, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Pradotto, Lg; Mazzeo, A; Frusconi, S; My, F; Manfellotto, D; Fuciarelli, M; Polimanti, R
Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis
2017-01-01 Iorio, A; De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Pradotto, L; Mauro, A; Mazzeo, A; Stancanelli, C; Perfetto, F; Frusconi, S; My, F; Manfellotto, D; Fuciarelli, M; Polimanti, R
Effect of the GSTM1 gene deletion on glycemic variability, sympatho-vagal balance and arterial stiffness in patients with metabolic syndrome, but without diabetes
2018-04-01 Iorio, A; Ylli, D; Polimanti, R; Picconi, F; Maggio, P; Francomano, D; Aversa, A; Manfellotto, D; Fuciarelli, M; Frontoni, S
Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses
2019-10-29 De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R
Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis
2020-01-01 De Lillo, A; Pathak, Ga; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Perfetto, F; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R
Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank.
2021-01-01 De Lillo, A; D'Antona, S; Pathak, G; Wendt, F; De Angelis, F; Fuciarelli, M; Polimanti, R
Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms
2021-01-01 Pathak, G; Wendt, F; De Lillo, A; Nunez, Y; Goswami, A; De Angelis, F; Fuciarelli, M; Kranzler, H; Gelernter, J; Polimanti, R
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2015 | GSTA1 gene variation associated with gestational hypertension and its involvement in pregnancy-related pathogenic conditions | Iorio, A; Spinelli, M; Polimanti, R; Lorenzi, F; Valensise, H; Manfellotto, D; Fuciarelli, M | Articolo su rivista | |
| 1-gen-2015 | From adaptive licensing to adaptive pathways: Delivering a flexible life-span approach to bring new drugs to patients | Eichler, H-; Baird, Lg; Barker, R; Bloechl-Daum, B; Borlum-Kristensen, F; Brown, J; Chua, R; Del Signore, S; Dugan, U; Ferguson, J; Garner, S; Goettsch, W; Haigh, J; Honig, P; Hoos, A; Huckle, P; Kondo, T; Le Cam, Y; Leufkens, H; Lim, R; Longson, C; Lumpkin, M; Maraganore, J; O'Rourke, B; Oye, K; Pezalla, E; Pignatti, F; Raine, J; Rasi, G; Salmonson, T; Samaha, D; Schneeweiss, S; Siviero, Pd; Skinner, M; Teagarden, Jr; Tominaga, T; Trusheim, Mr; Tunis, S; Unger, Tf; Vamvakas, S; Hirsch, G | Articolo su rivista | |
| 1-gen-2015 | Deletion polymorphism of GSTT1 gene as protective marker for allergic rhinitis | Iorio, A; Polimanti, R; Piacentini, S; Liumbruno, Gm; Manfellotto, D; Fuciarelli, M | Articolo su rivista | |
| 1-gen-2015 | Most recent common ancestor of TTR Val30Met mutation in Italian population and its potential role in genotype-phenotype correlation | Iorio, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Pradotto, L; Mauro, A; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-gen-2015 | Haplotype differences for copy number variants in the 22q11.23 region among human populations: A pigmentation-based model for selective pressure | Polimanti, R; Piacentini, S; Iorio, A; De Angelis, F; Kozlov, A; Novelletto, A; Fuciarelli, M | Articolo su rivista | |
| 1-gen-2016 | GPX1*Pro198Leu AND GPX3 rs2070593 as genetic risk markers for Italian asthmatic patients | Iorio, A; Velocci, M; Graziano, Me; Piacentini, S; Polimanti, R; Manfellotto, D; Fuciarelli, M | Articolo su rivista | |
| 1-mag-2016 | Explorative genetic association study of GSTT2B copy number variant in complex disease risks | Iorio, A; Polimanti, R; Calandro, M; Graziano, Me; Piacentini, S; Bucossi, S; Squitti, R; Lazzarin, N; Scano, G; Limbruno, Gm; Manfellotto, D; Fuciarelli, M | Articolo su rivista | |
| 1-gen-2017 | Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis | Iorio, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Pradotto, Lg; Mazzeo, A; Frusconi, S; My, F; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-gen-2017 | Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis | Iorio, A; De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Pradotto, L; Mauro, A; Mazzeo, A; Stancanelli, C; Perfetto, F; Frusconi, S; My, F; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-apr-2018 | Effect of the GSTM1 gene deletion on glycemic variability, sympatho-vagal balance and arterial stiffness in patients with metabolic syndrome, but without diabetes | Iorio, A; Ylli, D; Polimanti, R; Picconi, F; Maggio, P; Francomano, D; Aversa, A; Manfellotto, D; Fuciarelli, M; Frontoni, S | Articolo su rivista | |
| 29-ott-2019 | Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses | De Lillo, A; De Angelis, F; Di Girolamo, M; Luigetti, M; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-gen-2020 | Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosis | De Lillo, A; Pathak, Ga; De Angelis, F; Di Girolamo, M; Luigetti, M; Sabatelli, M; Perfetto, F; Frusconi, S; Manfellotto, D; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-gen-2021 | Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank. | De Lillo, A; D'Antona, S; Pathak, G; Wendt, F; De Angelis, F; Fuciarelli, M; Polimanti, R | Articolo su rivista | |
| 1-gen-2021 | Epigenomic Profiles of African-American Transthyretin Val122Ile Carriers Reveals Putatively Dysregulated Amyloid Mechanisms | Pathak, G; Wendt, F; De Lillo, A; Nunez, Y; Goswami, A; De Angelis, F; Fuciarelli, M; Kranzler, H; Gelernter, J; Polimanti, R | Articolo su rivista |
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