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Genetic testing for lymphatic malformations with or without primary lymphedema

predisposition to acute myeloid leukemia (Emberger syndrome). Nat Genet 2011; 43(10): 929–31. 13. Irrthum A, Devriendt K, Chitayat D, Matthijs G, Glade C, teijlen PM, Fryns JP, Van Steensel MA, Vikkula M. Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia. Am J Hum Genet 2003; 72(6): 1470–8. 14. Ostergaard P, Simpson MA, Mendola A, Vasudevan P, Connell FC, van Impel A, Moore AT, Loeys BL, Ghalamkarpour A, Onoufriadis A, Martinez-Corral I, Devery S, Leroy JG, van Laer L, Singer A, Bialer

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Structures of cell-wall glycopolymers of Lactococcus lactis BIM B-1024

. Lactococcin A, a new bacteriocin from Lactococcus lactis subsp. cremoris: isolation and characterization of the protein and its gene. J Bacteriol 1991; 173(12): 3879-87. 11. Vinderola CG, Mocchiutti P, Reinheimer JA. Interactions among lactic acid starter and probiotic bacteria used for fermented dairy products. J Dairy Sci 2002; 85: 721-9. 12. Masood MI, Qadir MI, Shirazi JH, Khan IU. Beneficial effects of lactic acid bacteria on human beings. Crit Rev Microbiol 2011; 37(1): 91-8. 13. Kimoto H, Ohmomo S, Okamoto T

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The music in the brain hemispheres

. Stewart L. Do musicians have different brains? Clin Med 2008; 8:304-308 9. Altenmüller EO. How many music centers are in the brain? Ann N Y Acad Sci 2001; 930:273-280. 10. Tudor L, Sikirić P, Tudor KI, Cambi-Sapunar L, Radonić V, Tudor M, Buca A, Carija R. Amusia and aphasia of Bolero’s creator--influence of the right hemisphere on music. Acta Med Croatica 2008; 62:309-316. 11. Hassler M. Functional cerebral asymmetries and cognitive abilities in musicians, painters, and controls. Brain Cogn 1990; 13

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Determination of spore longevity and viability of Nosema apis and Nosema ceranae according to storage conditions

References 1. vanEngelsdorp D, Meixner MD. A historical review of managed honey bee populations in Europe and the United States and the factors that may affect them. J Invertebr Patho 2010; 103: 80-95. 2. Higes M, Martin R, Sanz A, Alvarez N, Sanz A, Garcia MP, Meana A. El sindrome de despoblamiento de las colmenas en Espaňa. Consideraciones sobre su origen. Vida Apicola 2005; 133: 15-21. 3. Higes M, Martin-Hernandez H, Botias C, Bailon EG, Gonzalez-Porto AV, Barrios L, Nozal MJD, Bernal JL, Jimenez JJ, Palencia

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Greenhouse study on the influence of natural biostimulators and fertilizers on improving bean plants growth and microbial activity in oil-polluted soil

://doi.org/10.1016/j.jbiotec.2018.06.270. 10. Drăghici EM, Scarlat V., Pele M, Postamentel M, Somăcescu C. Usage of perlite in polluted sandy soils for potato crop. Rev Chim 2016; 67(11):12281-2286. 11. Nisha P, Nayana M, Viji V. Degradation studies on diesel oil using bacterial consortium isolated from oil polluted soil. Adv Biotech 2013; 13 (2) 12. Tuleva BK, Ivanov RG, Christova NE. Biosurfactant production by a new Pseudomonas putida strain. Z Naturforsch 2002; 57:356-360. 13. Waogu LA, Onyeze GOC, Nwabueze

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Genetic testing for corneal dystrophies and other corneal Mendelian diseases

keratin 12 (K12) and complete sequence of the human KRT12 gene. Exp Eye Res. 2000 Jan;70(1):41-9. PubMed PMID: 10644419. 13. Nishida K, Honma Y, Dota A, Kawasaki S, Adachi W, Nakamura T, et al. Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy. Am J Hum Genet. 1997 Dec;61(6):1268-75. PubMed PMID: 9399908; PubMed Central PMCID: PMC1716060. 14. Szaflik JP, Oldak M, Maksym RB, Kamińska A, Pollak A, Udziela M, et al. Genetics of Meesmann

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Genetic testing for Leber congenital amaurosis

. 2003;7(1):13-22. PubMed PMID: 12615170. 4. Eisenberger T, Neuhaus C, Khan AO, Decker C, Preising MN, Friedburg C, et al. Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies. PLoS One. 2013 Nov 12;8(11):e78496. PubMed PMID: 24265693; PubMed Central PMCID: PMC3827063. 5. Bujakowska K, Audo I, Mohand-Saïd S, Lancelot ME, Antonio A, Germain A, et al. CRB1 mutations in inherited retinal dystrophies. Hum Mutat. 2012 Feb;33

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Study of genetic variability of Ribes L. representatives grown in Belarus

References 1. Brennan RM, Currants and gooseberries, Temperate Fruit Crop Breeding: Germplasm to Genomics, (ed. by J. F. Hancock) Springer, The Netherlands. 2008. P. 177-196. 2. Korbin M, Kuras A, Zurawicz E. Fruit plant germplasm characterisation using molecular markers generated in RAPD and ISSR-PCR, Cellular and Molecular Biology Letters., 2002, 7.2B: 785-794. 3. Lanham PG, Korycinska A, Brennan M. Genetic diversity within a secondary gene pool for Ribes nigrum L. revealed by RAPD and ISSR markers, The

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Application of whey retentate as complex nitrogen source for growth of the polyhydroxyalkanoate producer Hydrogenophaga pseudoflava strain DSM1023

.) Polyhydroxyalkanoates: Biosynthesis, Chemical Structures and Applications. 2018. ISBN 978-1-53613-439-1; Nova Science Publishers, New York, pp. 1-70. 13. Willems A, Busse J, Goor M, Pot B, Falsen E, Jantzen, E, et al. Hydrogenophaga , a new genus of hydrogen-oxidizing bacteria that includes Hydrogenophaga flava comb. nov.(formerly P seudomonas flava ), Hydrogenophaga palleronii (formerly Pseudomonas palleronii ), Hydrogenophaga pseudoflava (formerly Pseudomonas pseudoflava and “ Pseudomonas carboxydoflava ”), and Hydrogenophaga taeniospiralis (formerly Pseudomonas

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Genetic testing for atrioventricular septal defect

endocardial cushion defect in families. Am J Cardiol 1985; 55(13 Pt 1): 1649-52. 5. Digilio MC, Marino B, Cicini MP, Giannotti A, Formigari R, et al. Risk of congenital heart defects in relatives of patients with atrioventricular canal. Am J Dis Child 1993; 147(12): 1295-97. 6. Digilio MC, Marino B, Giannotti A, Dallapiccola B. Familial atrioventricular septal defect: possible genetic mechanism. Br Heart J 1994; 72(3): 301. 7. Cousineau AJ, Lauer RM, Pierpont ME, Burns TL, Ardinger RH, Patil SR, Sheffield VC. Linkage analysis of autosomal dominant

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