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M Dohal, I Porvaznik, P Kusnir and J. Mokry

-resistant Tuberculosis. Med Clin North Am. 2013;97(4):553-79. 9. Cirillo DM, Miotto P, Tortoli E. Evolution of Phenotypic and Molecular Drug Susceptibility Testing. Adv Exp Med Biol. 2017;1019:221-246. 10. Cole ST, Brosch R, Parkhill J, et al. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature. 1998;393(6685):537-44. 11. Black PA, De vos M, Louw GE, et al. Whole genome sequencing reveals genomic heterogeneity and antibiotic purification in Mycobacterium tuberculosis isolates. BMC Genomics. 2015;16:857. 12. Galagan JE

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Sibel Elif Gültekin, Burcu Sengüven, Reemitcha Aziz, Carina Heydt and Reinhard Buettner

;205517-5526. 4. Sweeney RT, McClary AC, Myers BR, Biscocho J, Neahring L, Kwei KA et al. Identification of recurrent SMO and BRAF mutations in ameloblastomas. Nat Genet, 2014;46:722-725. 5. Brown NA, Betz BL. Ameloblastoma: A Review of Recent Molecular Pathogenetic Discoveries. Biomark Cancer, 2015;7:19-24. 6. Heikinheimo K, Kurppa KJ, Elenius K. Novel Targets for the Treatment of Ameloblastoma. J Dent Res, 2015;94:237-240. 7. Peifer M, Fernández-Cuesta L, Sos ML, George J, Seidel D, Kasper LH et al. Integrative genome analyses

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J Zolkova, J Sokol, T Simurda, L Vadelova, Z Snahnicanova, D Loderer, M Dobrotova, I Skornova, Z Lasabova, P Kubisz and J Stasko

. Biochemistry 1991;30:253-269. 9. De Jong A, Eikenboom J. Von Willebrand disease mutation spectrum and associated mutation mechanisms. Thrombosis Research 2017;159:65-75. 10. Goodeve, A. Diagnosing von Willebrand disease: genetic analysis. Hematology Am Soc Hematol Educ Program 2016(1):678-682. 11. Wang QY, Song J,Gibbs RA, et al. Characterizing Polymorphisms and Allelic Diversity of von Willebrand Factor Gene in the 1000 Genomes. J Thromb Haemost 2013;11(2):261-9. 12. Corrales I, Ramirez L, Altisent C, et al. Rapid molecular diagnosis of von

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V. Valentova, P. Galajda, M. Pec, M. Mokan and J. Pec

B. Searching for psoriasis susceptibility genes in Italy: genome scan and evidence for a new locus on chromosome 1. J Invest Dermatol 1999; 112:32-35 Cookson WOCM, Bowcock AC, Harper JI, Moffat MF. The immunogenetics of inflammatory skin disease. In: Bos JD editor. Skin immune system (SIS): Cutaneous immunology and clinical immunodermatology. 3rd ed. Boca Raton (FL):CRC Press 2005; pp 55-73 Duffy DL, Spelman LS, Martin LG. Psoriasis in Australian twins. J Am Acad Dermatol 1993; 29

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I. Hodorova, J. Mihalik, J. Vecanova, M. Dankova and S. Rybarova

-757. Dean M, Rzhetsky A, Allikmets R. The human ATP-binding cassette (ABC) transporter superfamily. Genome Res. 2001; 11(7):1156-66. Review. Neyfakh AA. Mystery of multidrug transporters: the answer can be simple. Mol Microbiol. 2002; 44(5):1123-30. Review. Sarkadi B, Homolya L, Szakács G, Váradi A. Human multidrug resistance ABCB and ABCG transporters: participation in a chemoimmunity defense system. Physiol Rev. 2006; 86(4):1179-236. Review. Stavrovskaya AA, Stromskaya TP. Transport proteins

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Damla Tuncer Budanur, Merve Şirin, Elif Sepet, Meral Ünür, Mine Güllüoğlu, Mustafa Serdar Cantez and Özlem Durmaz Uğurcan

. Best Pract Res Clin Gastroenterol, 2004;18:481-496. 13. Daley DT, Armstrong JE. Oral manifestations of gastrointestinal diseases. Can J Gastroenterol, 2007;21:241-244. 14. Franke A, McGovern DP, Barrett JC, Wang K, Radford- Smith GL, Ahmad T et al. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn’s disease susceptibility loci. Nat Genet, 2010;42:1118-1125. 15. Lu Z-K, Chen Z-R, Zhu J-Y, Xu Y, Hua X. Analysis of the association of single nucleotide polymorphisms of interleukin-23 receptor (IL-23R

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Violeta Lokaj-Berisha, Naser Berisha, Besa Lumezi, Ganimete Bejtullahu and Luljeta Ahmetaj

, Frolund L, Dirksen A, Increasing Prevalence of specific IgE to aeroallergens in an adult population. J Allergy Clin Immonol. 2002;106:247-252. doi:10.1067/mai.2000.108312 PMID:10932066 Lang DM. Menagement of allergic rhinitits. Geriatric Times. 2002. Accesed: 2 Septembar 2006. Kauffman F and the posgenome respiratory epidemiology grup. Post-genome respiratory epidemiology: a multidisciplinary challenge

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Elias A. Kotteas and Konstantinos N. Syrigos

the changes in tumor vascularity and the patient’s pre- and post-treatment immunity, detection of immune biomarkers to measure antiangiogenic responses is essential. Furthermore, the optimal doses and the schedule of treatment modalities should be determined to achieve clinical effectiveness and to avoid serious side effects. Next-generation sequencing, which encompasses whole genome, whole transcriptome sequencing, whole exome, and targeted sequencing, has substantially expanded our knowledge in cancer biology by identifying mutations with high sensitivity and

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Nagwa Meguid, Motaza Omran, Iman Ghorab, Ahmed Dardir, Ehab Ragaa, Suzette Helal and Mona Anwar

J, et al. Structural and functional diversity of connexin genes in the mouse and human genome. Biological Chememistry. 2002;383:725-737. 20. White TW, Paul DL. Genetic diseases and gene knockouts reveal diverse connexin functions. Annual Review of Physiology. 1999; 61:283-310. 21. Orzan E, Polli R, Martella M, et al. Molecular genetics applied to clinical practice: The Cx26 hearing impairment. British Journal of Audiology. 1999; 33:291-295. 22. Ram Shankar M, Girirajan S, Dagan O, et al. Contribution of connexin26

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Alyaa Kotby, Mona Anwar, Ola El-Masry, Mostafa Awady, Ali El-Nashar and Nagwa Meguid

, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida. Am J Hum Genet. 2002;71:1222-1226. Goyette P, Pai A, Milos R, Frosst P, Tran P. Gene structure of human and mouse methylene-tetrahydrofolate reductase ( MTHFR ). Mamm Genome. 1998;9:652-656. Botto LD. and Yang Q. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies. Am J Epidemiol. 2000