LANTIERI, FRANCESCA
LANTIERI, FRANCESCA
100011 - Dipartimento di Scienze della salute
A COMMON HAPLOTYPE AT THE 5' END OF THE RET PROTO-ONCOGENE, OVERREPRESENTED IN HIRSCHSPRUNG PATIENTS, IS ASSOCIATED WITH REDUCED GENE EXPRESSION
2005-01-01 Griseri, P; Bachetti, T; Puppo, F; Lantieri, Francesca; Ravazzolo, Roberto; Devoto, M; Ceccherini, I.
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung disease
2007-01-01 Griseri, P; Lantieri, Francesca; Puppo, F; Bachetti, T; DI DUCA, M; Ravazzolo, Roberto; Ceccherini, I.
A metagenomics study on Hirschsprung's disease associated enterocolitis: Biodiversity and gut microbial homeostasis depend on resection length and patient's clinical history
2019-01-01 Prato, A. P.; Bartow-McKenney, C.; Hudspeth, K.; Mosconi, M.; Rossi, V.; Avanzini, S.; Faticato, M. G.; Ceccherini, I.; Lantieri, F.; Mattioli, G.; Larson, D.; Pavan, W.; De Filippo, C.; Di Paola, M.; Mavilio, D.; Cavalieri, D.
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities
2010-01-01 Bachetti, T; DI ZANNI, E; Lantieri, Francesca; Caroli, F; Regis, S; Filocamo, M; Rainero, I; Gallone, S; Cilia, R; Romano, S; Savoiardo, M; Pareyson, D; Biancheri, R; Ravazzolo, Roberto; Ceccherini, I.
A pilot study on school of medicine students’ perception of ethical issues related to human specimens in anatomical museums
2024-01-01 Ciliberti, R.; Lantieri, F.; Bagnara, D.; Fais, F.
A prospective observational study of associated anomalies in Hirschsprung's disease.
2013-01-01 Pini Prato, A; Rossi, V; Mosconi, M; Holm, C; Lantieri, Francesca; Griseri, P; Ceccherini, I; Mavilio, D; Jasonni, Vincenzo; Tuo, G; Derchi, M; Marasini, M; Magnano, G; Granata, C; Ghiggeri, G; Priolo, E; Sposetti, L; Porcu, A; Buffa, P; Mattioli, Girolamo
A Survey on Undergraduate Medical Students’ Perception of COVID-19 Vaccination
2022-01-01 Ciliberti, Rosagemma; Lantieri, Francesca; Barranco, Rosario; Tettamanti, Camilla; Bonsignore, Alessandro; Ventura, Francesco
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum
2010-01-01 Lantieri, Francesca; J. T., Glessner; H., Hakonarson; J., Elia; M., Devoto
Behavior of non-classical soluble HLA class G antigens in human immunodeficiency virus 1-infected patients before and after HAART: comparison with classical soluble HLA-A, -B, -C antigens and potential role in immune-reconstitution.
2009-01-01 Murdaca, Giuseppe; Contini, Paola; Setti, M.; Cagnati, P.; Lantieri, Francesca; Indiveri, Francesco; Puppo, Francesco
Behavior of serum human major histocompatibility complex class I antigen levels in human immunodeficiency virus-infected patients during antiretroviral therapy: correlation with clinical outcome
2007-01-01 Murdaca, Giuseppe; Contini, P.; Setti, M.; Cagnati, P.; Villa, R.; Lantieri, Francesca; Indiveri, Francesco; Puppo, Francesco
Behavior of soluble HLA-A, -B, -C and HLA-G molecules in patients with chronic hepatitis C virus infection undergoing pegylated interferon-α and ribavirin treatment: potential role as markers of response to antiviral therapy
2017-01-01 Murdaca, Giuseppe; Contini, Paola; Cagnati, Paola; Marenco, Simona; Pieri, Giulia; Lantieri, Francesca; Picciotto, Antonino; Puppo, Francesco
Beneficial effects of long-term treatment with bosentan on the development of pulmonary arterial hypertension in patients with systemic sclerosis
2016-01-01 Murdaca, Giuseppe; Lantieri, Francesca; Puppo, Francesco; Bezante, Gian Paolo; Balbi, Manrico
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A
2009-01-01 J., Elia; M., Capasso; Z., Zaheer; Lantieri, Francesca; P., Ambrosini; W., Berrettini; M., Devoto; H., Hakonarson
CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation
2001-01-01 Della Torre, G; Pasini, B; Frigerio, S; Donghi, R; Rovini, D; Delia, D; Peters, G; Huot, Tj; Bianchi, Giovanna; Lantieri, Francesca; Rodolfo, M; Parmiani, G; Pierotti, Ma
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study
2009-01-01 Lantieri, Francesca; M. A., Jhun; J., Park; T., Park; M., Devoto
Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease
2019-01-01 Lantieri, F.; Gimelli, S.; Viaggi, C.; Stathaki, E.; Malacarne, M.; Santamaria, G.; Grossi, A.; Mosconi, M.; Sloan-Bena, F.; Prato, A. P.; Coviello, D.; Ceccherini, I.
Correction: Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from hirschsprung patients (PLoS ONE)
2013-01-01 Rusmini, M.; Griseri, P.; Lantieri, F.; Matera, I.; Hudspeth, K. L.; Roberto, A.; Mikulak, J.; Avanzini, S.; Rossi, V.; Mattioli, G.; Jasonni, V.; Ravazzolo, R.; Pavan, W. J.; Pini-Prato, A.; Ceccherini, I.; Mavilio, D.
Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant Validation.
2017-01-01 Lantieri, Francesca; Malacarne, M; Gimelli, S; Santamaria, G; Coviello, D; Ceccherini, I.
Deprescribing Strategies: A Prospective Study on Proton Pump Inhibitors
2023-01-01 Calvini, G.; Baiardi, G.; Mattioli, F.; Milano, G.; Calautti, F.; Zunino, A.; Fraguglia, C. E.; Caccavale, F.; Lantieri, F.; Antonucci, G.
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability
2010-01-01 E. S., Emison; M., GARCIA BARCELO; E. A., Grice; Lantieri, Francesca; J., Amiel; G., Burzynski; R. M., Fernandez; L., Hao; C., Kashuk; K., West; X., Miao; P. K., Tam; P., Griseri; I., Ceccherini; A., Pelet; A. S., Jannot; L., DE PONTUAL; A., HENRION CAUDE; S., Lyonnet; J. B., Verheij; R. M., Hofstra; G., Antiñolo; S., Borrego; A. S., Mccallion; A., Chakravarti
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A COMMON HAPLOTYPE AT THE 5' END OF THE RET PROTO-ONCOGENE, OVERREPRESENTED IN HIRSCHSPRUNG PATIENTS, IS ASSOCIATED WITH REDUCED GENE EXPRESSION | 1-gen-2005 | Griseri, P; Bachetti, T; Puppo, F; Lantieri, Francesca; Ravazzolo, Roberto; Devoto, M; Ceccherini, I. | |
| A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung disease | 1-gen-2007 | Griseri, P; Lantieri, Francesca; Puppo, F; Bachetti, T; DI DUCA, M; Ravazzolo, Roberto; Ceccherini, I. | |
| A metagenomics study on Hirschsprung's disease associated enterocolitis: Biodiversity and gut microbial homeostasis depend on resection length and patient's clinical history | 1-gen-2019 | Prato, A. P.; Bartow-McKenney, C.; Hudspeth, K.; Mosconi, M.; Rossi, V.; Avanzini, S.; Faticato, M. G.; Ceccherini, I.; Lantieri, F.; Mattioli, G.; Larson, D.; Pavan, W.; De Filippo, C.; Di Paola, M.; Mavilio, D.; Cavalieri, D. | |
| A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities | 1-gen-2010 | Bachetti, T; DI ZANNI, E; Lantieri, Francesca; Caroli, F; Regis, S; Filocamo, M; Rainero, I; Gallone, S; Cilia, R; Romano, S; Savoiardo, M; Pareyson, D; Biancheri, R; Ravazzolo, Roberto; Ceccherini, I. | |
| A pilot study on school of medicine students’ perception of ethical issues related to human specimens in anatomical museums | 1-gen-2024 | Ciliberti, R.; Lantieri, F.; Bagnara, D.; Fais, F. | |
| A prospective observational study of associated anomalies in Hirschsprung's disease. | 1-gen-2013 | Pini Prato, A; Rossi, V; Mosconi, M; Holm, C; Lantieri, Francesca; Griseri, P; Ceccherini, I; Mavilio, D; Jasonni, Vincenzo; Tuo, G; Derchi, M; Marasini, M; Magnano, G; Granata, C; Ghiggeri, G; Priolo, E; Sposetti, L; Porcu, A; Buffa, P; Mattioli, Girolamo | |
| A Survey on Undergraduate Medical Students’ Perception of COVID-19 Vaccination | 1-gen-2022 | Ciliberti, Rosagemma; Lantieri, Francesca; Barranco, Rosario; Tettamanti, Camilla; Bonsignore, Alessandro; Ventura, Francesco | |
| Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum | 1-gen-2010 | Lantieri, Francesca; J. T., Glessner; H., Hakonarson; J., Elia; M., Devoto | |
| Behavior of non-classical soluble HLA class G antigens in human immunodeficiency virus 1-infected patients before and after HAART: comparison with classical soluble HLA-A, -B, -C antigens and potential role in immune-reconstitution. | 1-gen-2009 | Murdaca, Giuseppe; Contini, Paola; Setti, M.; Cagnati, P.; Lantieri, Francesca; Indiveri, Francesco; Puppo, Francesco | |
| Behavior of serum human major histocompatibility complex class I antigen levels in human immunodeficiency virus-infected patients during antiretroviral therapy: correlation with clinical outcome | 1-gen-2007 | Murdaca, Giuseppe; Contini, P.; Setti, M.; Cagnati, P.; Villa, R.; Lantieri, Francesca; Indiveri, Francesco; Puppo, Francesco | |
| Behavior of soluble HLA-A, -B, -C and HLA-G molecules in patients with chronic hepatitis C virus infection undergoing pegylated interferon-α and ribavirin treatment: potential role as markers of response to antiviral therapy | 1-gen-2017 | Murdaca, Giuseppe; Contini, Paola; Cagnati, Paola; Marenco, Simona; Pieri, Giulia; Lantieri, Francesca; Picciotto, Antonino; Puppo, Francesco | |
| Beneficial effects of long-term treatment with bosentan on the development of pulmonary arterial hypertension in patients with systemic sclerosis | 1-gen-2016 | Murdaca, Giuseppe; Lantieri, Francesca; Puppo, Francesco; Bezante, Gian Paolo; Balbi, Manrico | |
| Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A | 1-gen-2009 | J., Elia; M., Capasso; Z., Zaheer; Lantieri, Francesca; P., Ambrosini; W., Berrettini; M., Devoto; H., Hakonarson | |
| CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation | 1-gen-2001 | Della Torre, G; Pasini, B; Frigerio, S; Donghi, R; Rovini, D; Delia, D; Peters, G; Huot, Tj; Bianchi, Giovanna; Lantieri, Francesca; Rodolfo, M; Parmiani, G; Pierotti, Ma | |
| Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study | 1-gen-2009 | Lantieri, Francesca; M. A., Jhun; J., Park; T., Park; M., Devoto | |
| Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease | 1-gen-2019 | Lantieri, F.; Gimelli, S.; Viaggi, C.; Stathaki, E.; Malacarne, M.; Santamaria, G.; Grossi, A.; Mosconi, M.; Sloan-Bena, F.; Prato, A. P.; Coviello, D.; Ceccherini, I. | |
| Correction: Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from hirschsprung patients (PLoS ONE) | 1-gen-2013 | Rusmini, M.; Griseri, P.; Lantieri, F.; Matera, I.; Hudspeth, K. L.; Roberto, A.; Mikulak, J.; Avanzini, S.; Rossi, V.; Mattioli, G.; Jasonni, V.; Ravazzolo, R.; Pavan, W. J.; Pini-Prato, A.; Ceccherini, I.; Mavilio, D. | |
| Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant Validation. | 1-gen-2017 | Lantieri, Francesca; Malacarne, M; Gimelli, S; Santamaria, G; Coviello, D; Ceccherini, I. | |
| Deprescribing Strategies: A Prospective Study on Proton Pump Inhibitors | 1-gen-2023 | Calvini, G.; Baiardi, G.; Mattioli, F.; Milano, G.; Calautti, F.; Zunino, A.; Fraguglia, C. E.; Caccavale, F.; Lantieri, F.; Antonucci, G. | |
| Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability | 1-gen-2010 | E. S., Emison; M., GARCIA BARCELO; E. A., Grice; Lantieri, Francesca; J., Amiel; G., Burzynski; R. M., Fernandez; L., Hao; C., Kashuk; K., West; X., Miao; P. K., Tam; P., Griseri; I., Ceccherini; A., Pelet; A. S., Jannot; L., DE PONTUAL; A., HENRION CAUDE; S., Lyonnet; J. B., Verheij; R. M., Hofstra; G., Antiñolo; S., Borrego; A. S., Mccallion; A., Chakravarti |