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Martin Koller, Denis Vadlja, Gerhart Braunegg, Aid Atlić and Predrag Horvat

(2): 137-146. 10. Steinbuchel A. Perspectives for biotechnological production and utilization of biopolymers: metabolic engineering of polyhydroxyalkanoate biosynthesis pathways as a successful example. Macromol Biosci 2001; 1(1): 1-24. 11. Keshavarz T, Roy I. Polyhydroxyalkanoates: bioplastics with a green agenda. Curr Opin Microbiol 2010; 13(3): 321-326. 12. Chen GQ, Hajnal I. The ‘PHAome’. Trends Biotechnol 2015; 33(10): 559-564. 13. Koller M, Maršalek L, Miranda de Sousa Dias M, Braunegg G. Producing

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Martin Vanek, Filip Mravec, Martin Szotkowski, Dana Byrtusova, Andrea Haronikova, Milan Certik, Volha Shapaval and Ivana Marova

outfits. Histochem Cell Biol 2008; 130:263-279. 11. Radulovic M, Knittelfelder O, Cristobal-Sarramian A, Kolb D, Wolinski H, Kohlwein S. The emergence of lipid droplets in yeast: current status and experimental approaches. Curr Genet 2013; 59:231-242. 12. Fei W, Shiu G, Zhang Y, Krahmer N, Ferguson C. A Role for Phosphatidic Acid in the Formation of “Supersized” Lipid Droplets. PLoS Genet 2011; 7:e1002201. 13. Rani S, Saha S, Rajasekharan R. A soluble diacylglycerol acyltransferase is involved in triacylglycerol biosynthesis in the oleaginous yeast

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Abdullah Caliskan and Mehmet Emin Yuksel

References 1. Nahar J, Imam T, Tickle KS, Chen YPP. Computational intelligence for heart disease diagnosis: A medical knowledge driven approach. Expert Systems with Applications. 2013; 40(1): 96-104. 2. Bounhas M, Mellouli K, Prade H, Serrurier M. Possibilistic classifiers for numerical data. Soft Computing 2012; 17(5): 733-751. 3. Baati K, Hamdani TM, Alimi AM. Hybrid naive possibilistic classifier for heart disease detection from heterogeneous medical data. Hybrid Intelligent Systems (HIS) 2013 13th

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Halyna Ostrovska, Oleksandra Oleshchuk, Samuele Vannini, Samuela Cataldi, Elisabetta Albi, Michela Codini, Anargyros Moulas, Svitlana Marchyshyn, Tommaso Beccari and Maria Rachele Ceccarini

mitochondrial pathway. J Pharm Pharmacol 2013; 65(7): 1044-1054. 11. Chuyeshov V, Hohlova L, Lyapunova O. Industrial technology of drugs. Kharkiv: Golden Pages 2003; 720. 12. Rashidinejad A, Birch EJ, Sun Waterhouse D, Everet DW. Effects of catechin on the phenolic content and antioxidant properties of low-fat cheese. Int J Food Sci Tech 2013; 48: 2448-2455. 13. Branciari R, Ranucci R, Trabalza-Marinucci M, Codini M, Orru M, Ortenzi R, Forte C, Ceccarini MR, Valiani A. Evaluation of the antioxidant properties and oxidative

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Loretta Mancinelli, Francesco Ragonese, Samuela Cataldi, Maria Rachele Ceccarini, Rossana G. Iannitti, Cataldo Arcuri and Bernard Fioretti

monoamine oxidase B and subpopulations of enzyme. J Pharmacol Exp Ther 2000; 292, 1135-1145. 13. Head GA, & Mayorov DN. Imidazoline receptors, novel agents and therapeutic potential. Cardiovasc Hematol Agents Med Chem. 2006; 4:17-32. 14. Raasch W, Muhle H, & Dominiak P. Modulation of MAO activity by imidazoline and guanidine derivatives. Ann N Y Acad Sci. 1999; 881:313-31. 15. Jones TZ, Giurato L, Guccione S. & Ramsay RR. Interactions of imidazoline ligands with the active site of purified monoamine oxidase A. FEBS J. 2007; 274, 1567-1575. 16. Holt

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

(2):124-30. PubMed PMID: 9760193. 5. Boycott KM, Pearce WG, Musarella MA, Weleber RG, Maybaum TA, DG Birch, et al. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am J Hum Genet. 1998 Apr; 62(4):865-75. PubMed PMID: 9529339; PubMed Central PMCID: PMC1377021. 6. Boycott KM, Pearce WG, Bech-Hansen NT. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F. Can J Ophthalmol. 2000 Jun; 35(4):204-13. PubMed PMID: 10900517. 7

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Andi Abeshi, Alessandra Zulian, Tommaso Beccari, Munis Dundar, Benedetto Falsini and Matteo Bertelli

L, Derouiche K, Ouragini H, Nouira S, et al. Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene. J Hum Genet. 2011 Jan;56(1):22-8. PubMed PMID: 21107338. Epub 2010/09/25. 6. Kohl S, Varsanyi B, Antunes GA, Baumann B, Hoyng CB, Jägle H, Rosenberg T, et al. CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia. Eur J Hum Genet. 2005 Mar; 13(3):302-8. PubMed PMID: 15657609. 7. Wissinger B, Gamer D, Jägle H

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Zelimir Kurtanjek

Statistical Software, 2011, 39(5), 1-13. URL http://www.jstatsoft.org/v39/i05/. 18. Meinshausen N., Quantile Regression Forests, 2016; https://CRAN.R-project.org/package=quantregForest 19. McGill R, Tukey JW, Larsen WA. Variations of Box Plots, AM STAT. The American Statistician 1978; (32): 12-16. 20. Gregory R. Warnes GR, Bolker B, Bonebakker L, Gentleman R, Huber W, Liaw A, Lumley T, Maechler M, Magnusson R, Moeller S, Schwartz M, Venables B, 2016, URL https://CRAN.R-project.org/package=gplots 21. Zhang J

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Paolo Enrico Maltese, Yeltay Rakhmanov, Alice Bruson, Lorenzo Lorusso and Matteo Bertelli

: 920–23. 4. Brass LM, Isaacsohn JL, Merikangas KR, Robinette CD. A study of twins and stroke. Stroke. 1992; 23(2): 221-23. 5. Markus HS. Unravelling the Genetics of Ischaemic Stroke. PLoS Medicine. 2010; 7(3): e1000225. 6. Tonk M, Haan J. A review of genetic causes of ischemic and hemorrhagic stroke. J Neurol Sci. 2007; 257(1-2): 273-79. 7. Kittner SJ, McCarter RJ, Sherwin RW, Sloan MA, Stern BJ, Johnson CJ, Buchholz D, Seipp MJ, Price TR. Black-white differences in stroke risk among young adults. Stroke. 1993; 24(12 Supp1): I13–I15. 8

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Vanna Micheli and Matteo Bertelli

function in Lesch-Nyhan disease. Environ Health Perspect. 2000;108(Suppl 3):409 - 11. 5. Visser JE, Bar PR, Jinnah HA. Lesch-Nyhan disease and the basal ganglia. Brain Res Rev. 2000;32:449 - 75. 6. Nyhan WL, Wong DF. New approaches to understanding Lesch- Nyhan disease. N Engl J Med. 1996 Jun 13;334(24):1602-4. 7. Shirley TL, Lewers JC, Egami K, Majumdar A, Kelly M, Ceballos-Picot I, Seidman MM, Jinnah HA. A human neuronal tissue culture model for Lesch-Nyhan disease. J. Neurochem. 2007; 101:841-853 8