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Cadmium Exposure and Kidney Stone Formation in the General Population An Analysis of the National Health and Nutrition Examination Survey III Data
2011 Ferraro, Pietro Manuel; Bonello, Monica; Frigo, Ac; D'Addessi, Alessandro; Sturniolo, A; Gambaro, Giovanni
Calpain activity is increased in skeletal muscle from gastric cancer patients with no or minimal weight loss
2011 Smith, Ij; Aversa, Z; Hasselgren, P; Pacelli, Fabio; Rosa, Fausto; Doglietto, Gb; Bossola, Maurizio
CANCER STEM CELLS FROM GBM AND PERITUMOR TISSUE
2011 Lama, Gina; Colabianchi, Anna; Proietti, Gabriella; Mangiola, Annunziato; De Bonis, Pasquale; Binda, Elena; Vescovi, Angelo; Sica, Gigliola
CANCER STEM CELLS FROM GLIOBLASTOMA AND PERITUMOR TISSUE
2011 Lama, Gina; Colabianchi, Anna; Proietti, Gabriella; Mangiola, Annunziato; De Bonis, Pasquale; Binda, Elena; Maira, Giulio; Vescovi, Angelo; Sica, Gigliola
Careful with that axe, gene. Genome perturbation after a PEG-mediated protoplasts transformation in Fusarium verticillioides
2017 Scala, V.; Grottoli, A.; Aiese Cigliano, R.; Anzar, I.; Beccaccioli, M.; Fanelli, C.; Dall'Asta, Chiara; Battilani, Paola; Reverberi, M.; Sanseverino, W.
CD73-generated extracellular adenosine in chronic lymphocytic leukemia creates local conditions counteracting drug-induced cell death
2011 Serra, S; Horenstein, Al; Vaisitti, T; Brusa, D; Rossi, D; Laurenti, Luca; D'Arena, G; Coscia, M; Tripodo, C; Inghirami, G; Robson, Sc; Gaidano, G; Malavasi, F; Deaglio, S.
Cerebrospinal fluid top-down proteomics evidenced the potential biomarker role of LVV- and VV_ emorphin-7 in posterior cranial fossa paediatric tumours.
2012 Castagnola, Massimo; Desiderio, Claudia; D'Angelo, Luca; Iavarone, Federica; Giardina, Bruno; Massimi, Luca; Tamburrini, Gianpiero; Di Rocco, Concezio
Chromosomal 17p13.3 microdeletion unmasking recessive Canavan disease mutation
2011 Amorini, Angela Maria; Tavazzi, Barbara
Circulating fetal cell-free DNA and prenatal molecular diagnostics: are we ready for consensus?
2014 Capoluongo, Ettore Domenico; Plebani, M.
Circulating tumor cells in colorectal cancer patients
2013 Torino, F; Bonmassar, E; Bonmassar, L; De, ; Barnabei, A; Zuppi, Cecilia; Capoluongo, Ettore Domenico; Aquino, A.
Clinical and Genetic Study of a Family With a Paternally Inherited 15q11-q13 Duplication
2013 Marini, C; Cecconi, A; Contini, E; Pantaleo, M; Metitieri, T; Guarducci, S; Giglio, S; Guerrini, R; Genuardi, Maurizio
Clinical Heterogeneity in Sodium Channelopathies. What is the Meaning of Carrying a Genetic Mutation?
2008 Oliva, Antonio; Bjerregaard, P; Hong, K; Evans, S; Vernooy, K; Mccormack, J; Brugada, J; Brugada, P; Pascali, Vincenzo Lorenzo; Brugada, R.
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review
2015 Minucci, A; Scambia, Giovanni; Santonocito, Concetta; Concolino, P; Canu, G; Mignone, F; Saggese, I; Guarino, D; Costella, A; Molinario, R; De Bonis, M; Ferrandina, Maria Gabriella; Petrillo, M; Scaglione, Gl; Capoluongo, Ettore Domenico
Clinical utility gene card for: MUTYH-associated polyposis (MAP), Autosomal recessive colorectal adenomatous polyposis, Multiple colorectal adenomas, Multiple adenomatous polyps (MAP) - update 2012
2013 Aretz, S; Genuardi, Maurizio; Hes, F.
Clinical, biochemical and molecular diagnosis of a compound homozygote for the 254 bp deletion-8 bp insertion of the APRT gene suffering from severe renal failure.
2007 Di Pietro, Valentina; Perruzza, Italia; Amorini, Angela Maria; Balducci, Alessandro; Ceccarelli, Lia; Lazzarino, Giuseppe; Barsotti, Paola; Giardina, Bruno; Tavazzi, Barbara
Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome
2015 Minucci, Angelo; Ruggiero, Antonio; Canu, Giulia; Maurizi, Palma; De Bonis, Maria; Concolino, Paola; De Luca, Daniele; Capoluongo, Ettore Domenico
A combined ANXA2-NDRG1-STAT1 gene signature predicts response to chemoradiotherapy in cervical cancer
2019 Buttarelli, Marianna; Babini, Gabriele; Raspaglio, Giuseppina; Filippetti, Flavia; Battaglia, Alessandra; Ciucci, Alessandra; Ferrandina, Maria Gabriella; Petrillo, Marco; Marino, Carmela; Mancuso, Mariateresa; Saran, Anna; Villani, Maria Elena; Desiderio, Angiola; D'Ambrosio, Chiara; Scaloni, Andrea; Scambia, Giovanni; Gallo, Daniela
Comparison between real-time quantitative PCR detection of HER2 mRNA copy number in peripheral blood and ELISA of serum HER2 protein for determining HER2 status in breast cancer patients
2009 Santini, Stefano Angelo; Parrella, Paola; Barbano, Raffaella; Fazio, Vito Michele; Carella, Massimo; Savino, Maria; Murgo, Roberto; Valori, Vanna Maria; Garrubba, Maria; Copetti, Massimo
Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dube syndrome ascertained for non-cutaneous manifestations
2011 Maffe, A; Toschi, B; Circo, G; Giachino, D; Giglio, S; Rizzo, A; Carloni, A; Poletti, V; Tomassetti, S; Ginardi, C; Ungari, S; Genuardi, Maurizio
Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patients
2020 Missaglia, Sara; Pegoraro, Valentina; Marozzo, Roberta; Tavian, Daniela; Angelini, Corrado
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2011 | Cadmium Exposure and Kidney Stone Formation in the General Population An Analysis of the National Health and Nutrition Examination Survey III Data | Ferraro, Pietro Manuel; Bonello, Monica; Frigo, Ac; D'Addessi, Alessandro; Sturniolo, A; Gambaro, Giovanni | |
1-gen-2011 | Calpain activity is increased in skeletal muscle from gastric cancer patients with no or minimal weight loss | Smith, Ij; Aversa, Z; Hasselgren, P; Pacelli, Fabio; Rosa, Fausto; Doglietto, Gb; Bossola, Maurizio | |
1-gen-2011 | CANCER STEM CELLS FROM GBM AND PERITUMOR TISSUE | Lama, Gina; Colabianchi, Anna; Proietti, Gabriella; Mangiola, Annunziato; De Bonis, Pasquale; Binda, Elena; Vescovi, Angelo; Sica, Gigliola | |
1-gen-2011 | CANCER STEM CELLS FROM GLIOBLASTOMA AND PERITUMOR TISSUE | Lama, Gina; Colabianchi, Anna; Proietti, Gabriella; Mangiola, Annunziato; De Bonis, Pasquale; Binda, Elena; Maira, Giulio; Vescovi, Angelo; Sica, Gigliola | |
1-gen-2017 | Careful with that axe, gene. Genome perturbation after a PEG-mediated protoplasts transformation in Fusarium verticillioides | Scala, V.; Grottoli, A.; Aiese Cigliano, R.; Anzar, I.; Beccaccioli, M.; Fanelli, C.; Dall'Asta, Chiara; Battilani, Paola; Reverberi, M.; Sanseverino, W. | |
1-gen-2011 | CD73-generated extracellular adenosine in chronic lymphocytic leukemia creates local conditions counteracting drug-induced cell death | Serra, S; Horenstein, Al; Vaisitti, T; Brusa, D; Rossi, D; Laurenti, Luca; D'Arena, G; Coscia, M; Tripodo, C; Inghirami, G; Robson, Sc; Gaidano, G; Malavasi, F; Deaglio, S. | |
1-gen-2012 | Cerebrospinal fluid top-down proteomics evidenced the potential biomarker role of LVV- and VV_ emorphin-7 in posterior cranial fossa paediatric tumours. | Castagnola, Massimo; Desiderio, Claudia; D'Angelo, Luca; Iavarone, Federica; Giardina, Bruno; Massimi, Luca; Tamburrini, Gianpiero; Di Rocco, Concezio | |
1-gen-2011 | Chromosomal 17p13.3 microdeletion unmasking recessive Canavan disease mutation | Amorini, Angela Maria; Tavazzi, Barbara | |
1-gen-2014 | Circulating fetal cell-free DNA and prenatal molecular diagnostics: are we ready for consensus? | Capoluongo, Ettore Domenico; Plebani, M. | |
1-gen-2013 | Circulating tumor cells in colorectal cancer patients | Torino, F; Bonmassar, E; Bonmassar, L; De, ; Barnabei, A; Zuppi, Cecilia; Capoluongo, Ettore Domenico; Aquino, A. | |
1-gen-2013 | Clinical and Genetic Study of a Family With a Paternally Inherited 15q11-q13 Duplication | Marini, C; Cecconi, A; Contini, E; Pantaleo, M; Metitieri, T; Guarducci, S; Giglio, S; Guerrini, R; Genuardi, Maurizio | |
1-gen-2008 | Clinical Heterogeneity in Sodium Channelopathies. What is the Meaning of Carrying a Genetic Mutation? | Oliva, Antonio; Bjerregaard, P; Hong, K; Evans, S; Vernooy, K; Mccormack, J; Brugada, J; Brugada, P; Pascali, Vincenzo Lorenzo; Brugada, R. | |
1-gen-2015 | Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review | Minucci, A; Scambia, Giovanni; Santonocito, Concetta; Concolino, P; Canu, G; Mignone, F; Saggese, I; Guarino, D; Costella, A; Molinario, R; De Bonis, M; Ferrandina, Maria Gabriella; Petrillo, M; Scaglione, Gl; Capoluongo, Ettore Domenico | |
1-gen-2013 | Clinical utility gene card for: MUTYH-associated polyposis (MAP), Autosomal recessive colorectal adenomatous polyposis, Multiple colorectal adenomas, Multiple adenomatous polyps (MAP) - update 2012 | Aretz, S; Genuardi, Maurizio; Hes, F. | |
1-gen-2007 | Clinical, biochemical and molecular diagnosis of a compound homozygote for the 254 bp deletion-8 bp insertion of the APRT gene suffering from severe renal failure. | Di Pietro, Valentina; Perruzza, Italia; Amorini, Angela Maria; Balducci, Alessandro; Ceccarelli, Lia; Lazzarino, Giuseppe; Barsotti, Paola; Giardina, Bruno; Tavazzi, Barbara | |
1-gen-2015 | Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome | Minucci, Angelo; Ruggiero, Antonio; Canu, Giulia; Maurizi, Palma; De Bonis, Maria; Concolino, Paola; De Luca, Daniele; Capoluongo, Ettore Domenico | |
1-gen-2019 | A combined ANXA2-NDRG1-STAT1 gene signature predicts response to chemoradiotherapy in cervical cancer | Buttarelli, Marianna; Babini, Gabriele; Raspaglio, Giuseppina; Filippetti, Flavia; Battaglia, Alessandra; Ciucci, Alessandra; Ferrandina, Maria Gabriella; Petrillo, Marco; Marino, Carmela; Mancuso, Mariateresa; Saran, Anna; Villani, Maria Elena; Desiderio, Angiola; D'Ambrosio, Chiara; Scaloni, Andrea; Scambia, Giovanni; Gallo, Daniela | |
1-gen-2009 | Comparison between real-time quantitative PCR detection of HER2 mRNA copy number in peripheral blood and ELISA of serum HER2 protein for determining HER2 status in breast cancer patients | Santini, Stefano Angelo; Parrella, Paola; Barbano, Raffaella; Fazio, Vito Michele; Carella, Massimo; Savino, Maria; Murgo, Roberto; Valori, Vanna Maria; Garrubba, Maria; Copetti, Massimo | |
1-gen-2011 | Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dube syndrome ascertained for non-cutaneous manifestations | Maffe, A; Toschi, B; Circo, G; Giachino, D; Giglio, S; Rizzo, A; Carloni, A; Poletti, V; Tomassetti, S; Ginardi, C; Ungari, S; Genuardi, Maurizio | |
1-gen-2020 | Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patients | Missaglia, Sara; Pegoraro, Valentina; Marozzo, Roberta; Tavian, Daniela; Angelini, Corrado |
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