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Type I IFN-related NETosis in ataxia telangiectasia and Artemis deficiency.
Gul E, Sayar EH, Gungor B, Eroglu FK, Surucu N, Keles S, Guner SN, Findik S, Alpdundar E, Ayanoglu IC, Kayaoglu B, Geckin BN, Sanli HA, Kahraman T, Yakicier C, Muftuoglu M, Oguz B, Cagdas Ayvaz DN, Gursel I, Ozen S, Reisli I, Gursel M. Gul E, et al. Among authors: muftuoglu m. J Allergy Clin Immunol. 2018 Jul;142(1):246-257. doi: 10.1016/j.jaci.2017.10.030. Epub 2017 Nov 16. J Allergy Clin Immunol. 2018. PMID: 29155101
Investigation of base excision repair gene variants in late-onset Alzheimer's disease.
Ertuzun T, Semerci A, Cakir ME, Ekmekcioglu A, Gok MO, Soltys DT, de Souza-Pinto NC, Sezerman U, Muftuoglu M. Ertuzun T, et al. Among authors: muftuoglu m. PLoS One. 2019 Aug 15;14(8):e0221362. doi: 10.1371/journal.pone.0221362. eCollection 2019. PLoS One. 2019. PMID: 31415677 Free PMC article. Clinical Trial.
Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane.
Aamann MD, Sorensen MM, Hvitby C, Berquist BR, Muftuoglu M, Tian J, de Souza-Pinto NC, Scheibye-Knudsen M, Wilson DM 3rd, Stevnsner T, Bohr VA. Aamann MD, et al. Among authors: muftuoglu m. FASEB J. 2010 Jul;24(7):2334-46. doi: 10.1096/fj.09-147991. Epub 2010 Feb 24. FASEB J. 2010. PMID: 20181933 Free PMC article.
81 results