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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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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, et.al. 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. http://www.cmellc.com/geriartrictimes/g020435.html. Accesed: 2 Septembar 2006. http://www.cmellc.com/geriartrictimes/g020435.html Kauffman F and the posgenome respiratory epidemiology grup. Post-genome respiratory epidemiology: a multidisciplinary challenge

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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

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Mohamad Shah Nurul Syazana, Wan Azman Wan Sulaiman, Ahmad Sukari Halim and Sulong Sarina

References 1. Elisabeth M, Heiko R, Stefanie B, et al. Genome-Wide Linkage Scan of Nonsyndromic Orofacial Clefting in 91 Families of Central European Origin. Am J Med Genet. 2009: 149A: 2680-94. 2. Liu J, Lamme EN, Steegers-Theunissen RPM, et al. Cleft palate cells can regenerate a palatal mucosa in vitro. J Dent Res. 2008: 87(8): 788-92. 3. Blanton SH, Amber B, Elizabeth G, et al. Ethnic heterogeneity of IRF6 AP-2α binding site promoter SNP association with nonsyndromic cleft lip and palate. Cleft Palate

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Elizabeta Zisovska and Bratica Lazovska

):31-5. 12. McAdams H, Arkin A. Stochastic Mechanisms in Gene Expression. Proceedings of 10 the National Academy of Sciences, U.S.A., 1997; 94: 814-819. 13. Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, et al. The Diploid Genome Sequence of an Individual Human. PLoS Biol. 2007; 5 (10): e254. 14. Aase J. Diagnostic Dysmorphology; Plenum, New York, 1990. 15. Lerer RJ. Do hyperactive children tend to have abnormal palmar creases? A report of a 16 suggestive association. Clin Pediatr. 1977;16:645-647. 16. Manica A

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Suzette I. Helal, Ahmad Hegazi and Khaled Al-Menabbawy

syndromes: a multicentre retrospective study. Lancet Neurol. 2007;6(8):677-86. 14. Ebers GC, Kukay K, Bulman DE, Sadovnick AD, Rice G, Anderson C, Armstrong H, Cousin K, Bell RB, Hader W, Paty DW, Hashimoto S, Oger J, Duquette P, Warren S, Gray T, O'Connor P, Nath A, Auty A, Metz L, Francis G, Paulseth JE, Murray TJ, Pryse-Phillips W, Nelson R, Freedman M, Brunet D, Bouchard JP, Hinds D, Risch N. A full genome search in multiple sclerosis. Nat Genet. 1996;13(4):472-6. 15. Wagner P. Buttocks Jiagi Points Book, 1998. 16

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Amany A. Abdel Aal, Samar S. Attia, Nihal A. Hanafy, Abeer S. Al-Antably, Marwa A. Hassan, Walid El-Sherbiny and Aml S. Nasr

infected individuals: diagnostic & therapeutic challenges. Indian J Med Res. 2011;134(6):878-97. 23. Jia B, Lu H, Liu Q, Yin J, Jiang N, Chen Q. Genome-wide comparative analysis revealed significant transcriptome changes in mice after Toxoplasma gondii infection. Parasit Vectors. 2013;4(6):161. 24. el-Awady MK, el-Hosseiny LA, Ismail SM, Abdel-Aziz MT, el- Demellawy MA. Comparison between Toxoplasma gondii DNA and specific immunoglobulins during pregnancy. East Mediterr Health J. 2000;6(5-6):888-97. 25. Chabbert E, Lachaud

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Nikolina Zdraveska and Mirjana Kocova

forgenetic epistasis with chromosome 16q12. Am J Hum Genet. 2006;78:747-758. 31. Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene). Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Nat Genet. 2009; 41:824-828. 32. Jacobson EM, Tomer Y. The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the future. J Autoimmun. 2007; 28:85-98. 33. Velaga MR, Wilson V, Jennings CE et al