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Sanja Kiprijanovska, Emilija Sukarova Stefanovska, Predrag Noveski, Viktorija Chaloska Ivanova and Dijana Plaseska-Karanfilska

distribution and prevalence of hepatitis C virus genotypes. Hepatology. 2015;61(1):77-87. 4. EASL. EASL Recommendations on Treatment of Hepatitis C 2015. J Hepatol. 2015;63(1):199-236. 5. Simmonds P. Genetic diversity and evolution of hepatitis C virus-- 15 years on. J Gen Virol. 2004 Nov;85(Pt 11):3173-88. PubMed PMID: 15483230. Epub 2004/10/16. eng. 6. Ghany MG, Kim HY, Stoddard A, Wright EC, Seeff LB, Lok AS. Predicting clinical outcomes using baseline and follow-up laboratory data from the hepatitis C long-term treatment

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Andi Abeshi, Francesca Fanelli, Tommaso Beccari, Munis Dundar, Fabiana D’Esposito and Matteo Bertelli

: a 22 year prospective, population based, cohort study. Am J Med Genet A. 2005 Feb 1; 132A (4):352-60. PubMed PMID: 15637713; PubMed Central PMCID: PMC3295827. 4. Deveault C, Billingsley G, Duncan JL, Bin J, Theal R, Vincent A, et al. BBS genotype phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition. Hum Mutat. 2011 Jun; 32(6):610-9. doi: 10.1002/humu.21480. Epub 2011 Mar 22. PubMed PMID: 21344540. 5. Beales PL, Elcioglu N, Woolf AS, Parker D, Flinter FA. New criteria for improved

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Samuela Cataldi, Andrea Lazzarini, Michela Codini, Giacomo Cascianelli, Alessandro Floridi, Elisa Bartoccini, Maria Rachele Ceccarini, Francesco Saverio Ambesi-Impiombato, Tommaso Beccari, Francesco Curcio and Elisabetta Albi

.1038/ncb1182) 7. Dopje J, Skarp KP, Rajakyla EK,Tanhuanpaa K, and Vartiainen MK. Active maintenance of nuclear actin by importin 9 supports transcription. Proc Natl Acad Sci U S A 2012; 109: E544-E552 (PMID: 22323606 DOI: 10.1073/pnas.1118880109) 8. Cascianelli G, Villani M, Tosti M, Marini F, Bartoccini E, Magni MV, Albi E. Lipid microdomains in cell nucleus. Mol Biol Cell 2008; 19: 5289-5295 (PMID: 18923143, doi: 10.1091/mbc.E08-05-0517) 9. Albi E, Lazzarini A, Lazzarini R, Floridi A, Damaskopoulou E, Curcio F, Cataldi S

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Prima Dewi Sinawang, Dorin Harpaz, Luka Fajs, Raymond Chee Seong Seet, Alfred Iing Yoong Tok and Robert S. Marks

T, Mahabadi AA, Weimar C, Lehmann N, et al. B-type natriuretic peptide predicts stroke of presumable cardioembolic origin in addition to coronary artery calcification. European journal of neurology. 2014 Jun;21(6):914-21. PubMed PMID: 24661834. Epub 2014/03/26. eng. 25. Maruyama K, Shiga T, Iijima M, Moriya S, Mizuno S, Toi S, et al. Brain natriuretic peptide in acute ischemic stroke. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 2014 May-Jun;23(5):967-72. PubMed PMID: 24119617. Epub 2013/10

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Andi Abeshi, Pamela Coppola, Tommaso Beccari, Munis Dundar, Maura Di Nicola, Francesco Viola, Leonardo Colombo and Matteo Bertelli

(WA) 1993-2017. 10. Meunier I, Manes G, Bocquet B, Marquette V, Baudoin C, Puech B, et al. Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes. Ophthalmology. 2014 Dec;121(12):2406-14. PubMed PMID: 25085631. Epub 2014/07/29. 11. Chen B, Gagnon M, Shahangian S, Anderson NL, Howerton DA, Boone JD. Good laboratory practices for molecular genetic testing for heritable diseases and conditions. MMWR Recomm Rep. 2009 Jun;58(RR-6):1-37; PubMed PMID: 19521335

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Zelimir Kurtanjek

-46. 8. Clare A, “Machine learning and data mining for yeast functional genomics”, PhD Thesis, 2003, University of Wales, Aberystwyth, UK. 9. Huttenhower C., Mutungu K.M., Indik N., Yang W., Schroeder M., Forman J.J., Troyanskaya O.G., Coller H. Detailing regulatory networks through large scale data integration. Bioinformatics 2009; 25(24): 3267-3274. 10. Taymaz-Nikerel H, Cankorur-Cetinkaya A, Kirdar B. Genome-Wide Transcriptional Response of Saccharomyces cerevisiae to Stress-Induced Perturbations. Front Bioeng Biotechnol 2016; 4

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Andi Abeshi, Vincenza Precone, Tommaso Beccari, Munis Dundar, Benedetto Falsini and Matteo Bertelli

. 8. Report on Sideritis spp. EMA/HMPC/39455/2015, Assessment report on Sideritis scardica Griseb.; Sideritis clandestina (Bory & Chaub.) Hayek; Sideritis raeseri Boiss. & Heldr.; Sideritis syriaca L., herba, 7 July 2015. 9. Piozzi F, Bruno M, Rosselli S, Maggio A. The diterpenoids from the genus Sideritis. Studies in Natural Products Chemistry, 2006; 33, 493-540. 10. Kilic T. Isolation and biological activity of new and known diterpenoids from Sideritis stricta Boiss & Heldr. Molecules, 2006; 11, 257-262. 11. Pessoa C

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Lidia De Riccardis, Francesca Rizzo, Emanuela Urso, Valeria Garzarelli, Vincenza Intini, Marco Greco, Maria Chiara Maffia, Antonio Danieli and Michele Maffia

:// 77. Dupuis L, Mbebi C, Gonzalez de Aguilar J-L, Rene F, Muller A, de Tapia M, et al. Loss of Prion Protein in a Transgenic Model of Amyotrophic Lateral Sclerosis. Mol Cell Neurosci [Internet]. 2002 Feb [cited 2019 Mar 22];19(2):216–24. Available from: 78. Whitehouse IJ, Miners JS, Glennon EBC, Kehoe PG, Love S, Kellett KAB, et al. Prion protein is decreased in Alzheimer’s brain and inversely correlates with BACE1 activity, amyloid-β levels and Braak stage. PLoS One [Internet

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Yeltay Rakhmanov, Paolo Enrico Maltese, Alessandra Zulian and Matteo Bertelli

-control study. Am J Epidemiol 2000; 151(6): 575-83. 8. Biddinger A, Rocklin M, Coselli J, Milewicz DM. Familial thoracic aortic dilatations and dissections: a case control study. J Vasc Surg 1997; 25(3): 506-11. 9. Albornoz G, Coady MA, Roberts M, Davies RR, Tranquilli M, Rizzo JA, Elefteriades JA. Familial thoracic aortic aneurysms and dissections--incidence, modes of inheritance, and phenotypic patterns. Ann Thorac Surg 2006; 82(4): 1400-05. 10. Singh K, Bønaa KH, Jacobsen BK, Bjørk L, Solberg S. Prevalence of and risk factors for abdominal aortic

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Andi Abeshi, Francesca Fanelli, Tommaso Beccari, Munis Dundar, Francesco Viola, Leonardo Colombo and Matteo Bertelli

subjects with macular corneal dystrophy: a comprehensive molecular genetic review. Mol Vis. 2006 Mar 10;12:159-76. PubMed PMID: 16568029. 6. Bao W, Smith CF, al-Rajhi A, Chandler JW, Karcioglu ZA, Akama TO, et al. Novel mutations in the CHST6 gene in Saudi Arabic patients with macular corneal dystrophy. Invest Ophthalmol Vis Sci. (Suppl) 2001, 42:S483. 7. Bredrup C, Knappskog PM, Majewski J, Rodahl E, Boman H. Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene. Invest Ophthalmol Vis Sci. 2005 Feb;46