Moleküler Biyoloji ve Genetik

Idiman, E., Idiman, F., Özakbaş, S., Sagut, O., Gürkan, A., Battaloğlu, E., “A Charcot-Marie-Tooth disease (CMTD) case with brain white matter lesions and connexin 32 mutation showing different cerebrospinal fluid and magnetic resonance imaging features”, Multiple Sclerosis Journal, 19, 11, 145-145 Supplement: S, 2013.

Türkçe

Durmuş, H., Özoğuz, A., Deymeer, F., Serdaroğlu, P., Aysal, F., Ertaş, M., Günel, M., Başak, N., Parman, Y., “Clinical and Genetic Characteristics of Five Turkish Families with UBQLN2 Mutations”, Neurology, 80, Meeting Abstract: P05078, 2013.

Türkçe

Topaloğlu, N., Yüksel, Ş., Gülsoy, M., “Influence of different output powers on the efficacy of photodynamic therapy with 809-nm diode laser and indocyanine green”, Optical Interactions with Tissue and Cells XXIV, Jansen E.D., Thomas R.J. (Derleyenler), Book Series: Proceedings of SPIE, 8579, San Francisco, CA, 2013.  

Türkçe

Aysan, N., Topaloğlu, N., Yüksel, Ş., Gülsoy, M., “Biostimulative effect of 809-nm diode laser and indocyanine green on p.aeruginosa instead of photodynamic therapy”, Mechanisms for Low-Light Therapy VIII, Hamblin M.R., Arany P.R., Carroll J.D. (Derleyenler), Book Series: Proceedings of SPIE, 8569, San Francisco, CA, 2013.

Türkçe

Uyan, Ö., Ömür, Ö., Ağım, Z.S., Özoğuz, A., Li, H., Parman, Y., Deymeer, F., Oflazer, P., Koç, F., Tan, E., Özçelik, H., Başak, A.N., “Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor”, PLoS One, 8, 8, Article Number: e72381, 2013.

Türkçe

Taşcı Marangoz, N., Yüzbaşıoğlu, İ,S, Çelen, Z., Ekim, T., Bilgin, A.N., “Molecular phylogeny of Galanthus (Amaryllidaceae) of Anatolia inferred from multiple nuclear and chloroplast DNA regions”, Turkish Journal of Botany, 37, 6, 993-1007, 2013.

Türkçe

Suls, A., Jaehn, J.A., Kecskes, A., Çağlayan, S.A. et al, “De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome”, American Journal of Human Genetics, 93, 5, 967-975, 2013.

Türkçe

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