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Biomarkers for Diabetes Complications: The Results of Several Clinical Studies

biomarkers involved in type 2 diabetes: a review. Diabetes Metab Res Rev 2010 Mar; 26 (3): 150-71. Scott EM, Carter AM, Findlay JB. The application of proteomics to diabetes. Diab Vasc Dis Res 2005 May; 2 (2): 54-60. Sundsten T, Eberhardson M, Göransson M, Bergsten P. The use of proteomics in identifying differentially expressed serum proteins in humans with type 2 diabetes. Proteome Sci 2006; 12; 4: 22. Otu HH, Can H, Spentzos D, Nelson RG, Hanson RL, Looker HC, et al. Prediction of diabetic

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Proteomic analysis of effects by x-rays and heavy ion in HeLa cells

Cell Bio 2006; 7: 952-58. 12. Chen EI, Yates JR. Cancer proteomics by quantitative shotgun proteomics. Molecular Oncology 2007; 1: 144-59. 13. Lin R-X, Zhao H-B, Li C-R, Sun Y-N, Qian X-H, Wang S-Q. Proteomic Analysis of Ionizing Radiation-Induced Proteins at the Subcellular Level. J Proteome Res 2008; 8: 390-99. 14. Wang F, Bing Z, Zhang Y, Ao B, Zhang S, Ye C, et al. Quantitative proteomic analysis for radiation-induced cell cycle suspension in 92-1 melanoma cell line. J Radiat Res 2013; 54: 649

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Mutation in Phospholipase C, δ1 (PLCD1) gene underlies hereditary leukonychia in a Pashtun family and review of the literature

splicing event, underlies autosomal recessive leuconychia Br J Dermatol 2012 167 4 946 – 949 7 Molecular Operating Environment (MOE), 2013.08; Chemical Computing Group Inc., Montreal, QC, Canada, 2016. Molecular Operating Environment (MOE) 2013.08 Chemical Computing Group Inc Montreal, QC, Canada 2016 8 Rice RH, Xia Y, Alvarado RJ, Phinney BS. Proteomic analysis of human nail plate. J Proteome Res. 2010; 9(12): 6752-6758. 10.1021/pr1009349 Rice RH Xia Y Alvarado RJ Phinney BS Proteomic analysis of human nail plate J Proteome Res 2010 9

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Recombinant Russell’s viper venom-factor X activator (RVV-X)-specific antibody: neutralization and crossreactivity with Cryptelytrops albolabris and Calloselasma rhodostoma venoms

without anti-venom intervention. Am J Trop Med Hyg. 1991; 45: 751-4. 7. Gutiérrez JM, Sanz L, Flores-Diaz M, Figueroa L, Madrigal M, Herrera M, et al. Impact of regional variation in Bothrops asper snake venom on the design of antivenoms: integrating antivenomics and neutralization approaches. J Proteome Res. 2010; 9:564-77. 8. Hanashiro MA, Da Silva MH, Bier OG. Neutralization of crotoxin and crude venom by rabbit antiserum to crotalus phospholipase A. Immunochemistry. 1978; 15:745-50. 9. Kaiser II, Middlebrook JL

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Expression of Annexin A1 and UCH-L1 in central nervous system neuroepithelial tumors

; 7: 2298-305. 9. De Bont JM, den Boer ML, Kros JM, Pasier MM, Reddingius RE, Smitt PA, et al. Identification of novel biomarkers in pediatric primitive neuroectodermal tumor and ependymomas by proteome-wide analysis. J Neuropathol Exp Neurol. 2007; 66:505-16. 10. Park CK, Jung JH, Park SH, Jung HW, Cho BK. Multifarious proteomics signatures and regional heterogeneity in glioblastomas. J Neurooncol. 2009; 94:31-9. 11. Schittenhelm J, Trautmann K, Tabatabai G, Hermann C, Meyermann R, Beschorner R. Comparative analysis

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Osteogenic differentiation of human umbilical cord-derived mesenchymal stem cells promoted by overexpression of osterix

References 1. Feldmann RE Jr, Bieback K, Maurer MH, Kalenka A, Burgers HF, Gross B, et al. Stem cell proteomes: a profile of human mesenchymal stem cells derived from umbilical cord blood. Electrophoresis. 2005; 26: 2749-58. 2. Chen TL, Shen WJ, Kraemer FB. Human BMP-7/OP-1 induces the growth and differentiation of adipocytes and osteoblasts in bone marrow stromal cell cultures. J Cell Biochem. 2001; 2:187-99. 3. Allan EH, Ho PW, Umezawa A, Hata J, Makishima F, Gillespie MT, et al. Differentiation potential of a

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Phylogenetic study of H5 low pathogenic avian influenza viruses detected in wild birds in Poland in 2010−2015

.A., Kiselev O.I.: Molecular mechanisms enhancing the proteome of influenza A viruses: an overview of recently discovered proteins. Virus Res 2014, 185, 53–63. 29. Wille M., Tolf C., Avril A., Latorre-Margalef N., Wallerström S., Olsen B., Waldenström J.: Frequency and patterns of reassortment in natural influenza A virus infection in a reservoir host. Virology 2013, 443, 150–160.

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Kinetics of specific humoral immune response of mice infected with low doses of Trichinella spiralis, T. britovi, and T. pseudospiralis larvae

larvae. Vet. Parasitol., 159: 232–235 http://dx.doi.org/10.1016/j.vetpar.2008.10.008 [32] Robinson, M. W., Grieg, R., Beattie, K. A., Lamont, D. J., Connolly, B. (2007): Comparative analysis of the excretory-secretory proteome of the muscle larva of Trichinella pseudospiralis and Trichinella spiralis. Int. J. Parasitol., 37: 139–148 http://dx.doi.org/10.1016/j.ijpara.2006.08.007 [33] Turčeková, Ľ., Borošková, Z., Tomašovičová, O., Reiterová, K., Kinčeková, J. (1997): Immunochemical analysis of larval antigens of

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Effect of monoclonal and assorted seedling rootstocks on long term growth and yield of Hevea clones

., X. DING, L. YANG, Z. WANG, W. LIN and J-H. CAO (2011): Proteome analysis of interaction between rootstocks and scions in Hevea brasiliensis. African Journal of Biotechnology 10(66): 14816-14825. ZHU, L., M. WELANDER and O. HELLGREN (1999): Growth rates, biomass production of micropropagted apple plants of M26 and Gravenstein on their own roots and in different micrografted combinations under non-limiting and limiting nutrient conditions. Journal of Experimental Botany 50(336): 1189-1198.

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Influence of α-lipoic acid on morphology of organs of rabbits fed a high fat diet with the addition of oxidised rapeseed oil

.H., Korczak J., Małecka M., Mildner – Szkudlarz S., Rudzińska M., Samotyja U., Zawirska-Wojtasiak R.: Oxidation of lipids in food. Pol J Food Nutr Sci 2004, 13/54, 87–100. 27. Wisniewski J.R., Friedrich A., Keller T., Mann M., Koepsell H.: The impact of high-fat diet on metabolism and immune defense in small intestine mucosa. J Proteome Res 2015, 14, 353−365. 28. Xu J., Zhou X., Gao H., Chang Ch., Deng Q., Huang Q., Ma J., Wan Z., Yang J., Huang F.: Micronutrients-fortified rapeseed oil improves hepatic lipid accumulation and oxidative stress in rats fed a high

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