Sfoglia per Autore
MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1
2009-01-01 Menghini, R; Casagrande, V; Cardellini, M; Martelli, E; Terrinoni, A; Amati, F; Vasa Nicotera, M; Ippoliti, A; Novelli, G; Melino, G; Lauro, R; Federici, M
Gene expression analysis during development by high-throughput methods
2009-01-01 Amati, F; Chillemi, G; Novelli, G
Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist
2010-01-01 Amati, F; Diano, L; Campagnolo, L; Vecchione, L; Cipollone, D; Bueno, S; Prosperini, G; Desideri, A; Siracusa, G; Chillemi, G; Marino, B; Novelli, G
Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events.
2010-01-01 Predazzi, I; MARTINEZ-LABARGA, Mc; Vecchione, L; Mango, R; Ciccacci, C; Amati, F; Ottoni, C; Crawford, M; Rickards, O; Romeo, F; Novelli, G
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism.
2011-01-01 Minella, D; Wannenes, F; Biancolella, M; Amati, F; Testa, B; Nardone, A; Bueno, S; Fabbri, A; Lauro, D; Novelli, G; Moretti, C
Practical guidelines for managing patients with 22q11.2 deletion syndrome.
2011-01-01 Bassett, A; McDonald McGinn, D; Devriendt, K; Digilio, M; Goldenberg, P; Habel, A; Marino, B; Oskarsdottir, S; Philip, N; Sullivan, K; Swillen, A; Vorstman, J; Abadie, V; Allgrove, J; Amati, F; Baker, K; Baylis, A; Beaujard, M; Beemer, F; Boers, M; Bolton, P; Boot, E; Brigstocke, S; Burtey, S; Campbell, L; Chabloz, M; Chow, E; Clayton Smith, J; Cubells, J; Debbané, M; Delrue, M; De Smedt, B; Duijff, S; Eicher, P; Emanuel, B; Evers, L; Flahault, A; Forsythe, A; Frebourg, T; Gennery, A; Goldmuntz, E; Gosling, A; Handler, S; Heine Suñer, D; Hilmarsson, A; Hogan, A; Hordijk, R; Howley, S; Illingworth, E; Jackson, O; Joyce, H; Kawame, H; Kelly, R; Kemp, A; Kempf, L; Kimpen, J; Kirschner, R; Klaassen, P; Kumararatne, D; Lambert, M; Lima, K; Lindsay, E; Macerola, S; Malki, M; Marlin, S; Mascarenhas, M; Monks, S; Moran, V; Morrow, B; Moss, E; Murphy, C; Naqvi, N; Nielsen, B; Niklasson, L; Nordgarden, H; Oenema Mostert, C; Ottet, M; Pasca, C; Pasquariello, P; Persson, C; Portnoi, M; Prasad, S; Rockers, K; Saitta, S; Scambler, P; Schaer, M; Schneider, M; Sell, D; Solot, C; Sommerlad, B; Unanue, N; Sundram, F; Van Aken, K; van Amelsvoort, T; van der Molen, A; Widdershoven, J; Zackai, E
Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population.
2012-01-01 Predazzi, I; Norata, G; Vecchione, L; Garlaschelli, K; Amati, F; Grigore, L; Cutuli, L; Pirillo, A; Tramontana, S; Romeo, F; Novelli, G; Catapano, Al
Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis.
2012-01-01 Vecchione, L; Diano, L; Campagnolo, L; Rocchi, L; Ferrè, F; Mehta, J; Novelli, G; Amati, F
LOX-1 Inhibition in ApoE KO Mice Using a Schizophyllan-based Antisense Oligonucleotide Therapy.
2012-01-01 Amati, F; Diano, L; Vecchione, L; Norata, G; Koyama, Y; Cutuli, L; Catapano, A; Romeo, F; Ando, H; Novelli, G
Application of Next Generation Sequencing for personalized medicine for sudden cardiac death
2015-01-01 Morini, E; Sangiuolo, Fc; Caporossi, D; Novelli, G; Amati, F
Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways.
2015-02-09 Massimiani, M; Vecchione, L; Piccirilli, D; Spitalieri, P; Amati, F; Salvi, S; Ferrazzani, S; Stuhlmann, H; Campagnolo, L
Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways
2015-05-01 Massimiani, M; Vecchione, L; Piccirilli, D; Spitalieri, P; Amati, F; Salvi, S; Ferrazzani, S; Stuhlmann, H; Campagnolo, L
Mutational Analysis of Mitochondrial DNA in Brugada Syndrome
2016-01-01 Stocchi, L; Polidori, E; Potenza, L; Rocchi, M; Calcabrini, C; Busacca, P; Capalbo, M; Potenza, D; Amati, F; Mango, R; Romeo, F; Novelli, G; Stocchi, V
The human rs1050286 polymorphism alters LOX-1 expression through modifying miR-24 binding
2016-01-01 Morini, E; Rizzacasa, B; Pucci, S; Polidoro, C; Ferrè, F; Caporossi, D; HELMER CITTERICH, M; Novelli, G; Amati, F
Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies
2017-01-01 Rizzacasa, B; Morini, E; Pucci, S; Murdocca, M; Novelli, G; Amati, F
OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study
2017-06-01 Bruno, V; Rizzacasa, B; Pietropolli, A; Capogna, M; Massoud, R; Ticconi, C; Piccione, E; Cortese, C; Novelli, G; Amati, F
MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study
2019-01-01 Rizzacasa, B; Morini, E; Mango, R; Vancheri, C; Budassi, S; Massaro, G; Maletta, S; Macrini, M; D'Annibale, S; Romeo, F; Novelli, G; Amati, F
Epigenetic Modification in Coronary Atherosclerosis
2019-01-01 Rizzacasa, B; Amati, F; Romeo, F; Novelli, G; Mehta, Jl
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes
2019-01-18 Pucci, S; Polidoro, C; Greggi, C; Amati, F; Morini, E; Murdocca, M; Biancolella, M; Orlandi, A; Sangiuolo, F; Novelli, G
Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome
2020-01-01 D'Apice, Mr; De Dominicis, A; Murdocca, M; Amati, F; Botta, A; Sangiuolo, F; Lattanzi, G; Federici, M; Novelli, G
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-2009 | MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 | Menghini, R; Casagrande, V; Cardellini, M; Martelli, E; Terrinoni, A; Amati, F; Vasa Nicotera, M; Ippoliti, A; Novelli, G; Melino, G; Lauro, R; Federici, M | Articolo su rivista | |
1-gen-2009 | Gene expression analysis during development by high-throughput methods | Amati, F; Chillemi, G; Novelli, G | Contributo in libro | |
1-gen-2010 | Hif1α down-regulation is associated with transposition of great arteries in mice treated with a retinoic acid antagonist | Amati, F; Diano, L; Campagnolo, L; Vecchione, L; Cipollone, D; Bueno, S; Prosperini, G; Desideri, A; Siracusa, G; Chillemi, G; Marino, B; Novelli, G | Articolo su rivista | |
1-gen-2010 | Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events. | Predazzi, I; MARTINEZ-LABARGA, Mc; Vecchione, L; Mango, R; Ciccacci, C; Amati, F; Ottoni, C; Crawford, M; Rickards, O; Romeo, F; Novelli, G | Articolo su rivista | |
1-gen-2011 | SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. | Minella, D; Wannenes, F; Biancolella, M; Amati, F; Testa, B; Nardone, A; Bueno, S; Fabbri, A; Lauro, D; Novelli, G; Moretti, C | Articolo su rivista | |
1-gen-2011 | Practical guidelines for managing patients with 22q11.2 deletion syndrome. | Bassett, A; McDonald McGinn, D; Devriendt, K; Digilio, M; Goldenberg, P; Habel, A; Marino, B; Oskarsdottir, S; Philip, N; Sullivan, K; Swillen, A; Vorstman, J; Abadie, V; Allgrove, J; Amati, F; Baker, K; Baylis, A; Beaujard, M; Beemer, F; Boers, M; Bolton, P; Boot, E; Brigstocke, S; Burtey, S; Campbell, L; Chabloz, M; Chow, E; Clayton Smith, J; Cubells, J; Debbané, M; Delrue, M; De Smedt, B; Duijff, S; Eicher, P; Emanuel, B; Evers, L; Flahault, A; Forsythe, A; Frebourg, T; Gennery, A; Goldmuntz, E; Gosling, A; Handler, S; Heine Suñer, D; Hilmarsson, A; Hogan, A; Hordijk, R; Howley, S; Illingworth, E; Jackson, O; Joyce, H; Kawame, H; Kelly, R; Kemp, A; Kempf, L; Kimpen, J; Kirschner, R; Klaassen, P; Kumararatne, D; Lambert, M; Lima, K; Lindsay, E; Macerola, S; Malki, M; Marlin, S; Mascarenhas, M; Monks, S; Moran, V; Morrow, B; Moss, E; Murphy, C; Naqvi, N; Nielsen, B; Niklasson, L; Nordgarden, H; Oenema Mostert, C; Ottet, M; Pasca, C; Pasquariello, P; Persson, C; Portnoi, M; Prasad, S; Rockers, K; Saitta, S; Scambler, P; Schaer, M; Schneider, M; Sell, D; Solot, C; Sommerlad, B; Unanue, N; Sundram, F; Van Aken, K; van Amelsvoort, T; van der Molen, A; Widdershoven, J; Zackai, E | Articolo su rivista | |
1-gen-2012 | Association between OLR1 K167N SNP and Intima Media Thickness of the Common Carotid Artery in the General Population. | Predazzi, I; Norata, G; Vecchione, L; Garlaschelli, K; Amati, F; Grigore, L; Cutuli, L; Pirillo, A; Tramontana, S; Romeo, F; Novelli, G; Catapano, Al | Articolo su rivista | |
1-gen-2012 | Functional characterization and expression analysis of novel alternative splicing isoforms of Olr1 gene during mouse embryogenesis. | Vecchione, L; Diano, L; Campagnolo, L; Rocchi, L; Ferrè, F; Mehta, J; Novelli, G; Amati, F | Articolo su rivista | |
1-gen-2012 | LOX-1 Inhibition in ApoE KO Mice Using a Schizophyllan-based Antisense Oligonucleotide Therapy. | Amati, F; Diano, L; Vecchione, L; Norata, G; Koyama, Y; Cutuli, L; Catapano, A; Romeo, F; Ando, H; Novelli, G | Articolo su rivista | |
1-gen-2015 | Application of Next Generation Sequencing for personalized medicine for sudden cardiac death | Morini, E; Sangiuolo, Fc; Caporossi, D; Novelli, G; Amati, F | Articolo su rivista | |
9-feb-2015 | Epidermal growth factor-like domain 7 (EGFL7) promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways. | Massimiani, M; Vecchione, L; Piccirilli, D; Spitalieri, P; Amati, F; Salvi, S; Ferrazzani, S; Stuhlmann, H; Campagnolo, L | Articolo su rivista | |
1-mag-2015 | Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways | Massimiani, M; Vecchione, L; Piccirilli, D; Spitalieri, P; Amati, F; Salvi, S; Ferrazzani, S; Stuhlmann, H; Campagnolo, L | Articolo su rivista | |
1-gen-2016 | Mutational Analysis of Mitochondrial DNA in Brugada Syndrome | Stocchi, L; Polidori, E; Potenza, L; Rocchi, M; Calcabrini, C; Busacca, P; Capalbo, M; Potenza, D; Amati, F; Mango, R; Romeo, F; Novelli, G; Stocchi, V | Articolo su rivista | |
1-gen-2016 | The human rs1050286 polymorphism alters LOX-1 expression through modifying miR-24 binding | Morini, E; Rizzacasa, B; Pucci, S; Polidoro, C; Ferrè, F; Caporossi, D; HELMER CITTERICH, M; Novelli, G; Amati, F | Articolo su rivista | |
1-gen-2017 | Lox-1 and its splice variants: a new challenge for atherosclerosis and cancer-targeted therapies | Rizzacasa, B; Morini, E; Pucci, S; Murdocca, M; Novelli, G; Amati, F | Articolo su rivista | |
1-giu-2017 | OLR1 and Loxin Expression in PBMCs of Women with a History of Unexplained Recurrent Miscarriage: A Pilot Study | Bruno, V; Rizzacasa, B; Pietropolli, A; Capogna, M; Massoud, R; Ticconi, C; Piccione, E; Cortese, C; Novelli, G; Amati, F | Articolo su rivista | |
1-gen-2019 | MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study | Rizzacasa, B; Morini, E; Mango, R; Vancheri, C; Budassi, S; Massaro, G; Maletta, S; Macrini, M; D'Annibale, S; Romeo, F; Novelli, G; Amati, F | Articolo su rivista | |
1-gen-2019 | Epigenetic Modification in Coronary Atherosclerosis | Rizzacasa, B; Amati, F; Romeo, F; Novelli, G; Mehta, Jl | Articolo su rivista | |
18-gen-2019 | Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes | Pucci, S; Polidoro, C; Greggi, C; Amati, F; Morini, E; Murdocca, M; Biancolella, M; Orlandi, A; Sangiuolo, F; Novelli, G | Articolo su rivista | |
1-gen-2020 | Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome | D'Apice, Mr; De Dominicis, A; Murdocca, M; Amati, F; Botta, A; Sangiuolo, F; Lattanzi, G; Federici, M; Novelli, G | Articolo su rivista |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile