Moleküler Biyoloji ve Genetik

Yüksel, Ş.; Eren, E.; Hatemi, G.; Sahillioğlu, A.C.; Gültekin, Y.; Demiroz, D. Akdiş, C.; Fresko, İ.; Özören, N.,'Novel NLRP3/cryopyrin mutations and pro-inflammatory cytokine profiles in Behets syndrome patients',International Immunology, 26, 2, 71-81, 2014.

Türkçe

Topaloğlu, N., Yüksel, Ş., Gülsoy, M., 'Effect of near-infrared diode laser and indocyanine green to treat infections on different wound models', Biophotonics: Photonic Solutions for Better Health Care IV  Book Series: Proceedings of SPIE,  Popp J. Tuchin V.V. Matthews D.L. Pavone F.S. (Derleyenler), 9129,  Article Number: 912925, 2014.  

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Weckhuysen, S., Suls, A., Djemie, T., Sterbova, K., Hoffman-Zacharska, D., Talvik, T., Çağlayan, H. et al. 'Trio Exome Sequencing in 31 Patients with SCN1A Negative Dravet Syndrome Leads to the Detection of Another Recessive SCN1B Mutation and the Discovery of at Least Two Novel Epilepsy Genes', Epilepsia, 55, 2, 81-81 Meeting Abstract: p239, 2014.

Türkçe

Suls, A., Jaehn, J.J., Kecskes, A., Weber, Y., Weckhuysen, S., Craiu, D.C., Siekierska, A., Djemie, T., Afrikanova, T., Gormley, P., von Spiczak, S., Kluger, G., Iliescu, C.M., Talvik, T., Talvik, I., Meral, C., Çağlayan, S.H. et al. 'De Novo Loss-of-Function Mutations in CHD2 Cause A Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features With Dravet Syndrome', Epilepsia, 55, 2, 79-80, Meeting Abstract: p239, 2014.

Türkçe

Altındağ, E., Gündoğdu, A., Usluer, S., Çağlayan, H., Baykara, B., 'Down syndrome and late onset myoclonic epilepsy in Down syndrome: investigation of EPM1 gene mutations in two cases', Journal of Neurology,  Meeting Abstract: PP2050, 261, S328-S328, 2014.

Türkçe

Altındağ, E., Gündoğdu, A., Usluer, S., Çağlayan, H., Baykan, B., 'Down syndrome and late onset myoclonic epilepsy in Down syndrome: investigation of EPM1 gene mutations in two casesP.M., Başak, A.N., 'C9orf72 hexanucleotide repeat expansion in Turkish ALS patients', European Journal of Neurology,  Meeting Abstract: PP2050, 21, 496-496, 2014.

Türkçe

Fidancı İD, Zülfikar B, Kavaklı K, Ar MC, Kılınç Y, Başlar Z, Çağlayan SH, A Polymorphism in the IL-5 Gene is Associated with Inhibitor Development in Severe Hemophilia A Patients, Turkish Journal of Hematology, 31, 17-24, 2014

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