CASCINO, ISABELLA
CASCINO, ISABELLA
Istituto di Biologia Cellulare e Neurobiologia - IBCN - Sede Monterotondo Scalo (attivo dal 18/11/1923 al 31/12/2021)
Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity.
2017 Teveroni, Emanuela; Pellegrino, Marsha; Sacconi, Sabrina; Calandra, Patrizia; Cascino, Isabella; Fariolivecchioli, Stefano; Puma, Angela; Garibaldi, Matteo; Morosetti, Roberta; Tasca, Giorgio; Ricci, Enzo; Trevisan Carlo, Pietro; Galluzzi, Giuliana; Pontecorvi, Alfredo; Crescenzi, Marco; Deidda, Giancarlo; Moretti, Fabiola
Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2
2016 Calandra, P; Cascino, I; Lemmers, Rj; Galluzzi, G; Teveroni, E; Monforte, M; Tasca, G; Ricci, E; Moretti, F; van der Maarel, Sm; Deidda, G
Estrogens improve differentiation of facioscapulohumeral muscular dystrophy myoblasts by antagonizing DUX4 activity.
2016 Emanuela Teveroni; Marsha Pellegrino; Sabrina Sacconi; Patrizia Calandra; Isabella Cascino; Stefano FarioliVecchioli; Roberta Morosetti; Giorgio Tasca; Enzo Ricci; Giuliana Galluzzi; Alfredo Pontecorvi; Marco Crescenzi; Giancarlo Deidda; Fabiola Moretti;
Advances in the development of a methylation assay for FSHD
2015 Calandra P.; Cascino I.; Lemmers R.J.; Teveroni E.; Ricci E.; Galluzzi G.; Monforte M.; Tasca G.; Moretti F.; van der Maarel S.M.; Deidda G.
Development of a new methylation assay for FSHD diagnosis
2014 Calandra P.; Cascino I.; Lemmers R.J.; Teveroni E.; Ricci E.; Galluzzi G.; Monforte M.; Tasca G.; Moretti F.; van der Maarel S.M.; Deidda G.
Age-dependent association of idiopathic achalasia with vasoactive intestinal peptide receptor 1 gene.
2009 Paladini F.; Cocco E.; Cascino I.; Belfiore F.; Badiali D.; Piretta L.; Alghisi F.; Anzini F.; Fiorillo M.T.; Corazziari E.;Sorrentino R.
HLA-E gene polymorphism associates with ankylosing spondylitis in Sardinia
2009 Paladini F.; Belfiore F.; Cocco E.; Carcassi C.; Cauli A.; Vacca A.; Fiorillo M.T.; Mathieu A.; Cascino I.; Sorrentino R.
A functional polymorphism of the vA functional polymorphism of the vasoactive intestinal peptide receptor 1 gene correlates with the presence of HLA-B*2705 in Sardinia
2008 Paladini F; Cocco E; Cauli A; Cascino I; Vacca A; Belfiore F; Fiorillo MT; Mathieu A; Sorrentino R.
Co-ordinator report, JDRF-Telethon Project IDDM locus analysis in T1DM- Identification and characterization of functional polymorphisms , 2006-07
2007 Cascino, I; Ruberti, G
High risk of congenital hypothyroidism in multiple pregnancies.
2007 Olivieri, A; Medda, E; De Angelis, S; Valensise, H; De Felice, M; Fazzini, C; Cascino, I; Cordeddu, V; Sorcini, M; Stazi, Ma; the Study Group for Congenital, Hypothyroidism
IDDM12 Locus analysis in T1DM: identification and characterization of functional polymorphisms
2007 Ruberti G.; Belfiore F.; Malquori L.; Carsetti L.;Cascino I
Identification of Previously Unrecognized Predisposing Factors for Ankylosing Spondylitis From Analysis of HLA-B27 Extended Haplotypes in Sardinia.
2007 Cascino, I; Paladini, F; Belfiore, F; Cauli, A; Angelini, C; Fiorillo, Mt; Mathieu, A; Sorrentino, R
Multiple Sclerosis in Twins from Continental Italy and Sardinia: A Nationwide Study
2006 Ristori, G; Cannoni, S; Stazi, Ma; Vanacore, N; Cotichini, R; Alfo, M; Pugliatti, M; Sotgiu, S; Solaro, C; Bomprezzi, R; Di Giovanni, S; Figa Talamanca, L; Nistico, L; Fagnani, C; Neale, Mc; Cascino, I; Giorgi, G; Battaglia, Ma; Buttinelli, C; Tosi, R; Salvetti, M
CT60 single nucleotide polymorphisms of the cytotoxic T-lymphocyte-associated antigen-4 gene region is associated with Graves' disease in an Italian population.
2005 Petrone, A; Giorgi, G; Galgani, A; Alemanno, I; Corsello, Sm; Signore, A; Di Mario, U; Nistico, L; Cascino, I; Buzzetti, R
Co-ordinator report, ISS Grant Fattori genetici ed ambientali nelle malattie multifattoriali: istituzione di un registro nazionale di gemelli Sclerosi Multipla: modificazioni postzigotiche o epigenetiche in gemelli monozigoti discordanti
2003 Cascino I.
CTLA-4 in Type 1 Diabetes Mellitus
2003 Nisticò, L; Cascino, I; Buzzatti, R; Pozzilli, P
Type 1 diabetes and IDDM12 locus in different genetic backgrounds: analysis in affected families of mixed ancestry
2003 Tosi, R; Giorgi, G; Nisticò, L; Pozzilli, P; Cascino, I
IL12B polymorphism and type 1 diabetes in the Italian population: a case-control study
2002 Nisticò, L; Giorgi, G; Giordano, M; Galgani, A; Petrone, A; D'Alfonso, S; Federici, M; Di Mario, U; Pozzilli, P; Buzzetti, R; Cascino, I
. IL12B polymorphism and type 1 diabetes in the Italian population - A case-control study.
2001 Nisticò L; Giordano M; Mellai M; Giorgi G; Galgani a; Buzzetti R;Cascino I
Association of DRB1*04-0301 haplotype and lack of association of two polymorphic sites at CTLA-4 gene with Hashimoto?s thyroiditis in a Italian population.
2001 Petrone, A; Giorgi, G; Mesturino, Ca; Capizzi, M; Cascino, I; Nisticò, L; Osborn, J; Di Mario, U; Buzzetti, R
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity. | 1-gen-2017 | Teveroni, Emanuela; Pellegrino, Marsha; Sacconi, Sabrina; Calandra, Patrizia; Cascino, Isabella; Fariolivecchioli, Stefano; Puma, Angela; Garibaldi, Matteo; Morosetti, Roberta; Tasca, Giorgio; Ricci, Enzo; Trevisan Carlo, Pietro; Galluzzi, Giuliana; Pontecorvi, Alfredo; Crescenzi, Marco; Deidda, Giancarlo; Moretti, Fabiola | |
| Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2 | 1-gen-2016 | Calandra, P; Cascino, I; Lemmers, Rj; Galluzzi, G; Teveroni, E; Monforte, M; Tasca, G; Ricci, E; Moretti, F; van der Maarel, Sm; Deidda, G | |
| Estrogens improve differentiation of facioscapulohumeral muscular dystrophy myoblasts by antagonizing DUX4 activity. | 1-gen-2016 | Emanuela Teveroni; Marsha Pellegrino; Sabrina Sacconi; Patrizia Calandra; Isabella Cascino; Stefano FarioliVecchioli; Roberta Morosetti; Giorgio Tasca; Enzo Ricci; Giuliana Galluzzi; Alfredo Pontecorvi; Marco Crescenzi; Giancarlo Deidda; Fabiola Moretti; | |
| Advances in the development of a methylation assay for FSHD | 1-gen-2015 | Calandra P.; Cascino I.; Lemmers R.J.; Teveroni E.; Ricci E.; Galluzzi G.; Monforte M.; Tasca G.; Moretti F.; van der Maarel S.M.; Deidda G. | |
| Development of a new methylation assay for FSHD diagnosis | 1-gen-2014 | Calandra P.; Cascino I.; Lemmers R.J.; Teveroni E.; Ricci E.; Galluzzi G.; Monforte M.; Tasca G.; Moretti F.; van der Maarel S.M.; Deidda G. | |
| Age-dependent association of idiopathic achalasia with vasoactive intestinal peptide receptor 1 gene. | 1-gen-2009 | Paladini F.; Cocco E.; Cascino I.; Belfiore F.; Badiali D.; Piretta L.; Alghisi F.; Anzini F.; Fiorillo M.T.; Corazziari E.;Sorrentino R. | |
| HLA-E gene polymorphism associates with ankylosing spondylitis in Sardinia | 1-gen-2009 | Paladini F.; Belfiore F.; Cocco E.; Carcassi C.; Cauli A.; Vacca A.; Fiorillo M.T.; Mathieu A.; Cascino I.; Sorrentino R. | |
| A functional polymorphism of the vA functional polymorphism of the vasoactive intestinal peptide receptor 1 gene correlates with the presence of HLA-B*2705 in Sardinia | 1-gen-2008 | Paladini F; Cocco E; Cauli A; Cascino I; Vacca A; Belfiore F; Fiorillo MT; Mathieu A; Sorrentino R. | |
| Co-ordinator report, JDRF-Telethon Project IDDM locus analysis in T1DM- Identification and characterization of functional polymorphisms , 2006-07 | 1-gen-2007 | Cascino, I; Ruberti, G | |
| High risk of congenital hypothyroidism in multiple pregnancies. | 1-gen-2007 | Olivieri, A; Medda, E; De Angelis, S; Valensise, H; De Felice, M; Fazzini, C; Cascino, I; Cordeddu, V; Sorcini, M; Stazi, Ma; the Study Group for Congenital, Hypothyroidism | |
| IDDM12 Locus analysis in T1DM: identification and characterization of functional polymorphisms | 1-gen-2007 | Ruberti G.; Belfiore F.; Malquori L.; Carsetti L.;Cascino I | |
| Identification of Previously Unrecognized Predisposing Factors for Ankylosing Spondylitis From Analysis of HLA-B27 Extended Haplotypes in Sardinia. | 1-gen-2007 | Cascino, I; Paladini, F; Belfiore, F; Cauli, A; Angelini, C; Fiorillo, Mt; Mathieu, A; Sorrentino, R | |
| Multiple Sclerosis in Twins from Continental Italy and Sardinia: A Nationwide Study | 1-gen-2006 | Ristori, G; Cannoni, S; Stazi, Ma; Vanacore, N; Cotichini, R; Alfo, M; Pugliatti, M; Sotgiu, S; Solaro, C; Bomprezzi, R; Di Giovanni, S; Figa Talamanca, L; Nistico, L; Fagnani, C; Neale, Mc; Cascino, I; Giorgi, G; Battaglia, Ma; Buttinelli, C; Tosi, R; Salvetti, M | |
| CT60 single nucleotide polymorphisms of the cytotoxic T-lymphocyte-associated antigen-4 gene region is associated with Graves' disease in an Italian population. | 1-gen-2005 | Petrone, A; Giorgi, G; Galgani, A; Alemanno, I; Corsello, Sm; Signore, A; Di Mario, U; Nistico, L; Cascino, I; Buzzetti, R | |
| Co-ordinator report, ISS Grant Fattori genetici ed ambientali nelle malattie multifattoriali: istituzione di un registro nazionale di gemelli Sclerosi Multipla: modificazioni postzigotiche o epigenetiche in gemelli monozigoti discordanti | 1-gen-2003 | Cascino I. | |
| CTLA-4 in Type 1 Diabetes Mellitus | 1-gen-2003 | Nisticò, L; Cascino, I; Buzzatti, R; Pozzilli, P | |
| Type 1 diabetes and IDDM12 locus in different genetic backgrounds: analysis in affected families of mixed ancestry | 1-gen-2003 | Tosi, R; Giorgi, G; Nisticò, L; Pozzilli, P; Cascino, I | |
| IL12B polymorphism and type 1 diabetes in the Italian population: a case-control study | 1-gen-2002 | Nisticò, L; Giorgi, G; Giordano, M; Galgani, A; Petrone, A; D'Alfonso, S; Federici, M; Di Mario, U; Pozzilli, P; Buzzetti, R; Cascino, I | |
| . IL12B polymorphism and type 1 diabetes in the Italian population - A case-control study. | 1-gen-2001 | Nisticò L; Giordano M; Mellai M; Giorgi G; Galgani a; Buzzetti R;Cascino I | |
| Association of DRB1*04-0301 haplotype and lack of association of two polymorphic sites at CTLA-4 gene with Hashimoto?s thyroiditis in a Italian population. | 1-gen-2001 | Petrone, A; Giorgi, G; Mesturino, Ca; Capizzi, M; Cascino, I; Nisticò, L; Osborn, J; Di Mario, U; Buzzetti, R |