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Li-doped C20 nanocage and its derivatives for gas sensing application: A density functional theory study
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Broadband dual‐podal multilayer Vivaldi antenna array for remote sensing applications
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Functional Tuning of Intrinsically Disordered Regions in Human Proteins by Composition Bias
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Texture Feature Variability in Ultrasound Video of the Atherosclerotic Carotid Plaque
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Volatile organic compounds (VOCs) in photochemically aged air from the eastern and western Mediterranean
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Recent trends in the gene therapy of β-thalassemia
Published 2015-02-01“…Alessia Finotti,1–3 Laura Breda,4 Carsten W Lederer,6,7 Nicoletta Bianchi,1–3 Cristina Zuccato,1–3 Marina Kleanthous,6,7 Stefano Rivella,4,5 Roberto Gambari1–3 1Laboratory for the Development of Gene and Pharmacogenomic Therapy of Thalassaemia, Biotechnology Centre of Ferrara University, Ferrara, Italy; 2Associazione Veneta per la Lotta alla Talassemia, Rovigo, Italy; 3Department of Life Sciences and Biotechnology, Section of Biochemistry and Molecular Biology, Ferrara University, Ferrara, Italy; 4Department of Pediatrics, Division of Haematology/Oncology, Weill Cornell Medical College, New York, NY, USA; 5Department of Cell and Development Biology, Weill Cornell Medical College, New York, NY, USA; 6Department of Molecular Genetics Thalassaemia, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus; 7Cyprus School of Molecular Medicine, Nicosia, Cyprus Abstract: The β-thalassemias are a group of hereditary hematological diseases caused by over 300 mutations of the adult β-globin gene. …”
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Evaluation of nipple aspirate fluid as a diagnostic tool for early detection of breast cancer
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HELLAS-ALIENS. The invasive alien species of Greece: time trends, origin and pathways
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THE VAST PROJECT: VALORISATION OF HISTORY AND LANDSCAPE FOR PROMOTING THE MEMORY OF WWI
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