Search Results

1 - 10 of 54 items :

  • Nanotechnology x
Clear All
Genetic testing for vascular anomalies

telangiectasia. Hum Genome Var 2015; 2: 15040. 25. Gallione CJ, Richards JA, Letteboer TG, Rushlow D, Prigoda NL, Leedom TP, Ganguly A, Castells A, Ploos van Amstel JK, Westermann CJ, Pyeritz RE, Marchuk DA. SMAD4 mutations found in unselected HHT patients. J Med Genet 2006; 43(10): 793-7. 26. Luks VL, Kamitaki N, Vivero MP, Uller W, Rab R, Bovée JV, Rialon KL, Guevara CJ, Alomari AI, Greene AK, Fishman SJ, Kozakewich HP, Maclellan RA, Mulliken JB, Rahbar R, Spencer SA, Trenor CC 3rd, Upton J, Zurakowski D, Perkins JA, Kirsh A, Bennett JT, Dobyns WB, Kurek KC

Open access
Antifungal activity of a biosurfactant-producing lactic acid bacteria strain

BS, Chauhan N, Procha S, Lal S. Isolation and functional characterization of novel biosurfactant produced by Enterococcus faecium. Springerplus 2015; 4(1): 4. 11. Adebayo CO, Aderiye BI. Antifungal activity of bacteriocins of lactic acid bacteria from some Nigerian fermented foods. Res J Microbiol 2010; 5: 1070-1082. 12. Saravanakumari P, Mani K. Structural characterization of a novel xylolipid biosurfactant from Lactococcus lactis and analysis of antibacterial activity against multi-drug resistant pathogens. Bioresour Technol 2010

Open access
Synthesis and analgesic activities of some new 5-chloro-2(3H)-benzoxazolone derivatives

References 1. Calhoun W, Carlson RP, Crossley R, Datko LJ, Dietrich S, Heatherington K, Marshall LA, Meade, PJ, Opalko A, Shepherd RG. Synthesis and anti-inflammatory activity of certain 5,6,7,8-tetrahy droquinolines and related compounds. J Med Chem 1995; 38:1473-1481. 2. Sauzem PD, Machado P, Rubin MA, da S Sant’Anna G, Faber HB, de Souza AH, Mello CF, Beck P, Burrow RA, Bonacorso HG, Zanatta N, Martins MA. Design and microwave-assisted synthesis of 5-trifluoromethyl-4,5-dihydro-1H-pyrazoles: novel agents with analgesic and

Open access
Corrosion inhibition of iron surfaces with phosphatidic acid

, Materials Chemistry and Physics , 2013, 141, 240-247. 6. Moussa M, El-Far A and El-Shafei A, Materials chemistry and physics , 2007, 105, 105-113. 7. Fuchs-Godec R and Dolecek V, Colloids and Surfaces a-Physicochemical and Engineering Aspects , 2004, 244, 73-76. 8. Obot I and Obi-Egbedi N, Current Applied Physics , 2011, 11, 382-392. 9. Bouklah M, Benchat N, Aouniti A, Hammouti N, Benkaddour M, Lagrenée M, Vezin H and Bentiss F, Progress in organic coatings , 2004, 51, 118-124. 10. Babu BR and Thangavel K, Anti-Corrosion Methods and

Open access
Genetic testing for ventricular septal defect

) 2017, StatPearls Publishing, Treasure Island, Forida, United States. Available from 6. Du ZD, Roguin N, Barak M, Bihari SG, Ben-Elisha M. High prevalence of muscular ventricular septal defect in preterm neonates. Am J Cardiol 1996; 78: 1183-85. 7. Corno A (2003). Atrioventricular septal defect. Congenital Heart Defects. Springer-Verlag Berlin Heidelberg 2003; 25–32. 8. Hoffman JI. Congenital heart disease: incidence and inheritance. Pediatr Clin North Am 1990; 37(1): 25-43. 9. Janvier A, Okah F

Open access
Genetic testing for cone rod dystrophies

. Heterozygous deep-intronic variants and deletions in ABCA4 in persons with retinal dystrophies and one exonic ABCA4 variant. Hum Mutat. 2015 Jan; 36(1):43-7. PubMed PMID: 25363634. 4. Maugeri A, van Driel MA, van de Pol DJ, Klevering BJ, van Haren FJ, Tijmes N, AA Bergen et al. The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease. Am J Hum Genet. 1999 Apr;64(4):1024-35. PubMed PMID: 10090887; PubMed Central PMCID: PMC

Open access
Genetic testing for Emberger syndrome

, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S. Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nat Genet 2011; 43(10): 929-31. 3. S Michelini, M Cardone, M Haag O Agga, A Bruson, PE Maltese, A Bonizzato, M Bertelli. A rare case of emberger syndrome caused by a de novo mutation in the Gata2 Gene. Lymphology. 2016; 49(1): 15-20. 4. 5. Kazenwadel J, Betterman KL, Chong CE, Stokes

Open access
Ultraviolet B induced bioactive changes of enzymatic and non-enzymatic antioxidants and lipids in Trigonella foenum-graecum L. (Fenugreek)

References 1. Frohnmeyer H, Staiger D. Ultraviolet-B radiation mediated responses in plants. Balancing damage and protection. Plant Physiol 2003; 133:1420-1428. 2. Tripathi R, Sarkar A, Rai SP, Agrawal SB. Supplemental ultraviolet-B and ozone, impact on antioxidants, proteome and genome of linseed (Linum usitatissimum L. cv Padmimi). Plant Biol 2010; doi: 10.1111/j. 1438-8677.2010.00323.x. 3. Kumari R, Prasad M.N.V. (2013) Medicinal Plant Active Compounds Produced by UV-B Exposure Sustainable Agriculture

Open access
Utilization of animal fat waste as carbon source by carotenogenic yeasts – a screening study

. Lipids of selected moulds grown for production of n-3 and n-6 polyunsaturated fatty acids. Lipids 1992; 20: 15-20. 6. Kosa G, Kohler A Shapaval V, et al. Microtiter plate cultivation of oleaginous fungi and monitoring of lipogenesis by high-throughput FTIR spectroscopy. Microb Cell Fact 2017; 16: 101. 7. Shapaval V, Afseth NK, Vogt H, Kohler A. Fourier transform infrared spectroscopy for the prediction of fatty acid profiles in Mucor fungi grown in media with different carbon sources. Microb Cell Fact 2014; 4: 13-26. 8

Open access
Genetic testing for central areolar choroidal dystrophy

References 1. Ashton N. Central areolar choroidal sclerosis; a histopathological study. Br J Ophthalmol. 1953 Mar; 37(3):140-7. PubMed PMID: 13032370; PubMed Central PMCID: PMC1324084. 2. Carr RE. Central areolar choroidal dystrophy. Arch Ophthalmol. 1965 Jan; 73:32-5. PubMed PMID: 14220602. 3. Ferry AP, Llovera I, Shafer DM. Central areolar choroidal dystrophy. Arch Ophthalmol. 1972 Jul; 88(1):39-43. PubMed PMID: 5049453. 4. Hoyng CB, Deutman AF. The development of central areolar choroidal

Open access