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| 1 | Preparation and Structural Characterization of Rapidly Solidified Al-Cu Alloys显示文摘Rapidly solidified Al100-x—Cux alloys(x = 5,10,1 5,25,35 wt%) were prepared and analyzed.High cooling rate increased the Cu solubility in 9.-AI matrix.The influence of the cooling rate on Cu solubility extension in Al was experimentally simulated.Thus the pouring was performed in metallic die and by melt spinning-low pressure(MSLP) technique.Melt processing by liquid quenching was performed using a self-designed melt spinning set-up which combined the cooling technology of a melt jet on the spinning disc with the principle of the mold feeding from low pressure casting technology.The thickness of the melt-spun ribbons was in the range of30—70 μm.The cooling rate provided by MS-LP was within 105—106 K/s after the device calibration.The obtained alloys were characterized from structural,thermal and mechanical point of view.Optical microscopy and scanning electron microscopy were employed for the microstructural characterization which was followed by X-ray analysis.The thermal properties were evaluated by dilatometric and differential scanning calorimetric measurements.Vickers microhardness measurements were performed in the study.In the case of the hypereutectic alloy with 35 wt%Cu obtained by MS-LP method,the microhardness value increased by 45%compared to the same alloy obtained by gravity casting method.This was due to the extended solubility of the alloying element in the α-AI solid solution. | Iuliana Lichioiu Ildiko Peter Bela Varga Mario Rosso | 2014 | Journal of Materials Science & Technology2014，30，4： | 3 |
| 2 | Mutational and expression analysis of ELIP1 and ELIP2 in Arabidopsis thaliana显示文摘 | Anna Paola Casazza Silvia Rossini Mario G. Rosso Carlo Soave | 2005 | Plant Molecular Biology2005，，1： | 1 |
| 3 | Effects of E2F1–cyclin E1–E2 circuit down regulation in hepatocellular carcinoma cells显示文摘 | Rossella Farra Barbara Dapas Gabriele Pozzato Bruna Scaggiante Francesco Agostini Cristina Zennaro Mario Grassi Natalia Rosso Carlo Giansante Nicola Fiotti Gabriele Grassi | 2011 | Digestive and Liver Disease2011，，12： | 1 |
| 4 | Effects of IL28B rs12979860 CC Genotype on Metabolic Profile and Sustained Viral Response in Patients With Genotype 1 Chronic Hepatitis C显示文摘 | Salvatore Petta Chiara Rosso Reynold Leung Maria Lorena Abate David Booth Federico Salamone Roberto Gambino Mario Rizzetto Paolo Caviglia Antonina Smedile Stefania Grimaudo Calogero Cammà Antonio Craxì Jacob George Elisabetta Bugianesi | 2012 | Clinical Gastroenterology and Hepatology2012，，： | 1 |
| 5 | Relationship between connective tissue cells and fibronectin in a sequential model of experimental hepatic fibrosis显示文摘 | Giovanna Cenacchi Giorgio Ballardini Lucilla Badiali Giorgi Carlo Antonio Busachi Mario Rosso Francesco Bianco Bianchi Graziella Biagini Renzo Laschi | 1983 | Virchows Archiv B Cell Pathology Including Molecular Pathology1983，，1： | 1 |
| 6 | Effects of IL28B rs12979860 CC Genotype on Metabolic Profile and Sustained Viral Response in Patients With Genotype 1 Chronic Hepatitis C显示文摘 | Salvatore Petta Chiara Rosso Reynold Leung Maria Lorena Abate David Booth Federico Salamone Roberto Gambino Mario Rizzetto Paolo Caviglia Antonina Smedile Stefania Grimaudo Calogero Cammà Antonio Craxì Jacob George Elisabetta Bugianesi | 2012 | Clinical Gastroenterology and Hepatology2012，，： | 1 |
| 7 | IL28B polymorphism genotyping as predictor of rapid virologic response during interferon plus ribavirin treatment in hepatitis C virus genotype 1 patients显示文摘AIM: To clarify the association of interleukin-28B(IL28B) single nucleotide polymorphisms(SNPs) with hepatitis C virus(HCV) viremia changes for assessment of interferon(IFN) response. METHODS: A cohort of 118 Caucasian treatment-nave HCV-G1 infected patients, treated with pegylated-IFN alpha 2a or 2b associated with ribavirin(53 responders, 65 non-responders) during the period 2010-2012, were genotyped for IL28 B SNPs rs12979860 C>T and rs8099917 T>G. Genotyping was performed by realtime allelic discrimination assay. Serum HCV RNA levels were assayed at 2, 4, 12, 24 and 48 wk during therapy.Correlation between IL28 B genotypes and serum HCV RNA kinetics was investigated. Multivariable logistic regression analysis was performed to identify predictors of null-response.RESULTS: Twenty-six out of 118 patients(22%) had no HCV RNA decline ≥ 1 log IU/mL at therapy week 4(null-responders). IL28 B genotype was rs8099917(G*)/rs1297860(**) in 21/26(80%) of null-responder patients. Using multivariate analysis, it was shown that the presence of the rs8099917 G allele was the best predictor of null-response(OR = 7.9, 95%CI: 1.99-31.18). The presence of at least one favorable genotype showed a positive predictive value of above 90% for HCV RNA reduction ≥ log at week 4. Analysis of the HCV RNA kinetics during 12 wk of therapy in patients with IL28 B rs12979860 CT heterozygosis(n = 73), according to their rs8099917 status, showed that the viremia reduction was significantly different in patients carrying the rs8099917 G allele compared to those with favorable homozygosis.CONCLUSION: Our findings emphasize the association of the IL28 B rs8099917 G allele with HCV. Genotyping for both IL28 B SNPs is useful in clinical practice for thorough patient risk stratification based on IFN responsiveness. | Chiara Rosso Maria Lorena Abate Alessia Ciancio Silvia Strona Gian Paolo Caviglia Antonella Olivero Giovanni Antonio Touscoz Mario Rizzetto Rinaldo Pellicano Antonina Smedile | 2014 | World Journal of Gastroenterology2014，20，36： | 1 |
| 8 | Preparation and Structural Characterization of Rapidly Solidified Al–Cu Alloys显示文摘 | Iuliana Lichioiu Ildiko Peter Bela Varga Mario Rosso | 2012 | Journal of Materials Science & Technology2012，，： | 1 |
| 9 | Relationship between connective tissue cells and fibronectin in a sequential model of experimental hepatic fibrosis显示文摘 | Giovanna Cenacchi Giorgio Ballardini Lucilla Badiali Giorgi Carlo Antonio Busachi Mario Rosso Francesco Bianco Bianchi Graziella Biagini Renzo Laschi | 1983 | Virchows Archiv B Cell Pathology Including Molecular Pathology1983，，1： | 1 |
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