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Marko Kostovski, Velibor Tasic, Nevena Laban, Momir Polenakovic, Dragan Danilovski and Zoran Gucev

;2014(1):21. 33. Turan S, Bastepe M. GNAS spectrum of disorders. Curr Osteoporos Rep. 2015;13(3):146-158. 34. Levine MA. An update on the clinical and molecular characteristics of pseudohypoparathyroidism. Curr Opi Endocrinol Diabetes Obes. 2012;19(6):443-451. 35. Rivera-Brugues N, Albrecht B, Wieczorek D, et al. Cohen syndrome diagnosis using whole genome arrays. J Med Genet. 2011;48(2):136-140. 36. Kolehmainen J, Black GC, Saarinen A, et al. Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in

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Raluca Dumache, Alexandru Florin Rogobete, Dorel Sandesc, Ovidiu Horea Bedreag, Veronica Ciocan, Camelia Muresan, Adrian Tudor Stan, Mihai Sandesc, Anca Dinu, Sonia Elena Popovici and Alexandra Enache

patients with primary and metastatic breast cancer. Breast Cancer Res . 2010;12:R90. 29. Guo Z, Maki M, Ding R, Yang Y, Zhang B, Xiong L. Genome-wide survey of tissue-specific microRNA and transcription factor regulatory networks in 12 tissues. Sci Rep . 2014;4. 30. Sood P, Krek A, Zavolan M, Macino G, Rajewsky N. Cell-type-specific signatures of microRNAs on target mRNA expression. Proc Natl Acad Sci USA . 2006;103:2746-2751. 31. Bloomston M, WL F, Petrocca F, et al. MicroRNA expression patterns to differentiate pancreatic adenocarcinoma from normal

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Andreea Catana, Alma Maniu, Doinel Radeanu, Radu A. Popp, Roxana F. Ilies and Iuliu V. Catana

susceptibility loci in ethnically diverse populations. Nat Genet., 1997;15(4):389-392. 24. Dizier M.H., Besse-Schmittler C., Guilloud-Bataille M., et al. - Genome screen for asthma and related phenotypes in the French EGEA study. Am J Respir Crit Care Med., 2000;162(5):1812-1818. 25. Gao P.S., Kawada H., Kasamatsu T., et al. - Variants of NOS1, NOS2, and NOS3 genes in asthmatics. Biochem Biophys Res Commun., 2000;267(3):761-763. 26. Leung T.F., Liu E.K., Tang N.L., Ko F.W., Li C.Y., Lam C.W., Wong G.W. - Nitric oxide synthase

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Ewelina Dziwota, Urszula Fałkowska, Katarzyna Adamczyk, Dorota Adamczyk, Alena Stefańska, Justyna Pawęzka and Marcin Olajossy

. (2013) Systemic delivery of MeCP2 rescues behavioral and cellular deficits in female mouse models of Rett syndrome. J. Neurosci. 33, 13612–13620 42. Savic, N. and Schwank, G. (2015) Advances in therapeutic CRISPR/Cas9 genome editing. Transl. Res. Published online September 26, 2015. http://dx.doi.org/10.1016/j.trsl.2015.09.008 43. Deffit, S.N. and Hundley, H.A. (2015) To edit or not to edit: regulation of ADAR editing specificity and efficiency. RNA Pub-lished online November 26, 2015. http://dx.doi.org/10.1002/wrna.1319 44. Ricceri, L. et al

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Dzengis Jasar, Snezana Smichkoska, Katerina Kubelka, Vanja Filipovski and Gordana Petrushevska

, Earp HS, Millikan RC. Race, breast cancer subtypes, and survival in the Carolina Breast cancer Study. JAMA. 2006; 295(21): 2492-2502. 15. Voduc KD, Cheang MC, Tyldesley S, Gelmon K, Nielsen TO, Kennecke H. Breast cancer subtypes and the risk of local and regional relapse. J Clin Oncol. 2010; 28(10): 1684-1691. 16. Carey LA. Molecular intrinsic subtypes of breast cancer. In: UpToDate. Hayes DF, Dizon DS, eds. Waltham, MA: UpToDate; 2012. p. 77-84. 17. Cancer Genome Atlas Network. Comprehensive molecular portraits of