LANTIERI, FRANCESCA

LANTIERI, FRANCESCA  

100011 - Dipartimento di Scienze della salute  

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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 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
Absence of melanocortin 1 receptor variants in Ligurian G101W families 1-gen-2001 Lantieri, Francesca; Pastorino, P.; Barile, M.; Santi, P. L.; Bianchi, Giovanna
Absence of melanocortin 1 receptor variants in Ligurian Gly101trp families 1-gen-2001 Lantieri, Francesca; Pastorino, Lorenza; Barile, M.; Santi, Pierluigi; Bianchi, Giovanna; Ciotti, Paola
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
Attention-deficit hyperactivity disorder 1-gen-2012 Elia, J; Lantieri, Francesca; Takeda, T; Gai, X; White, Ps; Devoto, M; Hakonarson, H.
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.
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.
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
DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients 1-gen-2008 Vitale, C.; Gulli, R.; Ciotti, P.; Scaglione, C.; Bellone, Emilia; Avanzino, Laura; Lantieri, Francesca; Abbruzzese, Giovanni; Martinelli, P.; Barone, P.; Mandich, Paola