Moleküler Biyoloji ve Genetik

Zaleska, A., Eiwegger, T., Soyer, O., van de Veen, W., Rhyner, C., Soyka, M.B., Bekpen, C., Demiröz, D., Treis, A., Söllner, S., Palomares, O., Kwok, W.W., Rose, H., Senti, G., Kündig, T.M,, Özören, N., Jutel, M., Akdiş, C.A., Crameri, R., Akdiş, M., 'Immune regulation by intralymphatic immunotherapy with modular allergen translocation MAT vaccine'., Allergy, 69, 9, 1162-70, 2014.

Türkçe

Usluer S, Şen Y, Türkdoğan D, Yiş U, Arslan M, Meral C, Tektürk P, Çağlayan H, “Massive Parallel Sequencing of SCN1A gene by amplicon sequencing method”, Annual Meeting of the Infantile Seizure Society, 2014, Kapadokya, Joint Meeting of the infantile seizure society and the Turkish Child Neurology Association , 1, 24, 2014.

Türkçe

Alkan, C., Kavak, P., Somel, M., Gökcümen, Ö., Uğurlu, S., Saygı, C., Dal, E., Buğra, K., Güngör, T., Şahinalp, S.C., Özören, N., Bekpen, C., 'Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe', Asia and Africa, BMC Genomics, 15, 963, 1-12, 2014.

Türkçe

Gökcümen, Ö., Alkan, C., Kavak, P., Somel, M., Uğurlu, S., Dal, E., Bugra-Bilge, K., Güngör, T., Şahinalp, C., Özören, N., Bekpen, C., 'Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa', American Journal of Physical Anthropology, 153, 126-127, 2014.

Türkçe

Weckhuysen S, Suls A, Djemie T, Sterbova K, Arslan M, Caglayan H, Striano P, Marini C, Lemke J, Depiene C,Helbig I, De Jonghe P, “Trio exome sequencing in 31 patients with SCN1A negative Dravet Syndrome”, The16th Annual Meeting of the Infantile Seizure Society (ISES 2014), 2014, Kapodokya, Joınt Meeting of the infantile seizure society and the Turkish Child Neurology Association, 1, 24, 2014.

Türkçe

Sayfalar