PROVERBIO, MARIA CARLA
PROVERBIO, MARIA CARLA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Genetic variants of PARP4 gene and PARP4P2 pseudogene in patients with multiple primary tumors including thyroid cancer.
2019 V. Cirello, C. Colombo, G. Pogliaghi, M. Proverbio, S. Rossi, E. Mussani, D. Tosi, G. Bulfamante, E. Bonoldi, G. Gherardi, L. Persani, L. Fugazzola
Impact of Mutation Density and Heterogeneity on Papillary Thyroid Cancer Clinical Features and Remission Probability
2019 C. Colombo, M. Muzza, M.C. Proverbio, D. Tosi, D. Soranna, C. Pesenti, S. Rossi, V. Cirello, S. De Leo, N. Fusco, M. Miozzo, G. Bulfamante, L. Vicentini, S. Ferrero, A. Zambon, S. Tabano, L. Fugazzola
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma : the PTC-MA assay
2018 C. Pesenti, M. Muzza, C. Colombo, M.C. Proverbio, C. Faré, S. Ferrero, M. Miozzo, L. Fugazzola, S. Tabano
Transcriptional profiling of human bronchial epithelial cell BEAS-2B exposed to diesel and biomass ultrafine particles
2018 A. Grilli, R. Bengalli, E. Longhin, L. Capasso, M.C. Proverbio, M. Forcato, S. Bicciato, M. Gualtieri, C. Battaglia, M. Camatini
Letter regarding the article: "Multiple HABP2 variants in familial papillary thyroid carcinoma: Contribution of a group of "thyroid-checked" controls" by Kern et al
2018 C. Colombo, L. Fugazzola, M. Muzza, M. Proverbio, V. Cirello
Segregation and expression analyses of hyaluronan-binding protein 2 (HABP2) : insights from a large series of familial non-medullary thyroid cancers and literature review
2017 C. Colombo, M. Muzza, M. Proverbio, G. Ercoli, M. Perrino, V. Cirello, L. Vicentini, S. Ferrero, L. Fugazzola
The role of IL-6 released from pulmonary epithelial cells in diesel UFP-induced endothelial activation
2017 R. Bengalli, E. Longhin, S. Marchetti, M.C. Proverbio, C. Battaglia, M. Camatini
Expression of S561F CDKAL1 variant modifies the constitutive trafficking and affects insulin release in INS1E cells
2017 E.S. Di Cairano, C. Cosentino, A. Galli, M.C. Proverbio, C. Battaglia, C. Perego
S561f cdkal1 variant, identified by whole exome sequencing of congenital hyperinsulinism patients, affects insulin content and release in ins1-e cells
2015 C. Cosentino, E. Di Cairano, M.C. Proverbio, E. Mangano, S. Moretti, C. Perego, C. Battaglia
Gene expression profiling of human bronchial epithelial cells exposed to seasonal Milan particulate matter
2014 E. Longhin, L. Capasso, C. Battaglia, C. Cosentino, M.C. Proverbio, I. Cifola, E. Mangano, M. Camatini, M. Gualtieri
Congenital Hyperinsulinism of Infancy (CHI) : hunt for new genes
2014 C. Battaglia, C. Cosentino, M. Proverbio, A. Pietrelli, E. Mangano, R. Bordoni, C. Perego, E. Di Cairano, A. Maggi, L. Tattini, G. De Bellis
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism
2013 M.C. Proverbio, E. Mangano, A. Gessi, R. Bordoni, R. Spinelli, R. Asselta, P. Sogno Valin, S. Di Candia, I. Zamproni, C. Diceglie, S. Mora, M. Caruso-Nicoletti, A. Salvatoni, G. De Bellis, C. Battaglia
Genetic analysis of Italian patients with congenital hyperinsulinism of infancy
2013 P. Sogno Valin, M.C. Proverbio, C. Diceglie, A. Gessi, S. Di Candia, B. Mariani, I. Zamproni, E. Mangano, R. Asselta, C. Battaglia, M. Caruso Nicoletti, S. Mora, A. Salvatoni
Gene expression profiling of A549 cells exposed to Milan PM2.5
2012 M. Gualtieri, E. Longhin, M. Mattioli, P. Mantecca, V. Tinaglia, E. Mangano, M.C. Proverbio, M. Camatini, C. Battaglia
Integrated genomics analysis of gene and miRNA expression profiles in clear cell renal carcinoma cell lines
2011 V. Tinaglia, I. Cifola, F. Frascati, E. Mangano, M. Biasolo, M.C. Proverbio, S. Bortoluzzi, V. Di Stefano, C. Bianchi, R. Perego, C. Battaglia
Iperinsulinismo congenito : mutazione dominante nel canale ATP+-dipendente in una famiglia Italiana
2009 P. Sogno Valin, M. Bove, S. Di Candia, I. Zamproni, S. Mora, M.C. Proverbio, A. Gessi, A. Gabrieli, C. Battaglia, M. Caruso, A. Salvatoni, G. Chiumello
Congenital hyperinsulinism of infancy : a dominant K-ATP channel mutation in a Italian family
2009 P. Sogno Valin, M. Bove, S. Di Candia, I. Zamproni, S. Mora, M.C. Proverbio, A. gessi, A. Gabrieli, C. Battaglia, M. Caruso, A. Salvatoni, G. Chiumello
Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography/CT in a patient carrying a novel mutation of the HADH gene
2009 S. Di Candia, A. Gessi, G. Pepe, P. Sogno Valin, E. Mangano, G. Chiumello, L. Gianolli, M.C. Proverbio, S. Mora
The first mutation in HADHSC gene in a Italian infant with congenital hyperinsulinism
2008 S. Di Candia, M. Bove, P. Sogno Valin, I. Zamproni, S. Mora, M.C. Proverbio, A. Gessi, E. Mangano, R. Spinelli, C. Battaglia, L. Bosio, M. Caruso, A. Salvatoni, G. Chiumello
Congenital hyperinsulinism of infancy (CHI) : clinical and metabolic evaluation, molecular analysis and phenotype correlation : Institution of the Italian National Registry
2008 M. Bove, P. Sogno Valin, S. Di Candia, I. Zamproni, S. Mora, M.C. Proverbio, E. Mangano, R. Spinelli, C. Battaglia, L. Bosio, M. Caruso, A. Salvatoni, G. Chiumello, A. Gessi