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Influence of OASL gene polymorphisms on host response to interferon therapy in chronic hepatitis C virus patients

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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Genetic testing for Bardet-Biedl syndrome

: 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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Localization of nuclear actin in nuclear lipid microdomains of liver and hepatoma cells: Possible involvement of sphingomyelin metabolism

.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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Electrochemical impedimetric detection of stroke biomarker NT-proBNP using disposable screen-printed gold electrodes

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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Genetic testing for pattern dystrophies

(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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Genome-wide BigData analytics: Case of yeast stress signature detection

-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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Pharmacologically active fractions of Sideritis spp. and their use in inherited eye diseases

. 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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Physiological role of Prion Protein in Copper homeostasis and angiogenic mechanisms of endothelial cells

://www.jneurosci.org/cgi/doi/10.1523/JNEUROSCI.1115-05.2005 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: http://www.ncbi.nlm.nih.gov/pubmed/11860274 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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Genetic testing for large-caliber vessel aneurysms

-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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Genetic testing for corneal dystrophies and other corneal Mendelian diseases

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

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