Fen-Edebiyat Fakültesi

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

Onat, O.E., Gülsüner, S., Bilguvar, K., Başak, A.N., Topaloğlu, H., Tan, M., Tan, Ü., Günel, M., Özçelik, T., “Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion”, European Journal of Human Genetics 21, 3, 281-285, 2013.

Türkçe

Lamy, L., Ngo, V. N., Emre, N. C.T., Shaffer, A. L. III, Yang, Y., Tian, E., Nair, V., Kruhlak, M. J., Zingone, A., Landgren, O., Staudt, L. M., “Control of autophagic cell death by caspase-10 in multiple myeloma.”, Cancer Cell, 23, 4, 435-449, 2013.

Türkçe

Küser-Abalı, G., Özcan, F., Uğurlu, A., Uysal, A., Fuss, S.H., Buğra-Bilge, K., “SIK2 is involved in the negative modulation of insulin-dependent müller cell survival and implicated in hyperglycemia-induced cell death”, Investigative Ophthalmology & Visual Science, 54, 5, 3526-3537, 2013.

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