Moleküler Biyoloji ve Genetik

Barış, I., Arısoy, A.E., Smith, A., Agostini, M., Mitchell, C.S., Park, S.M., Halefoğlu, A.M., Zengin, E., Chatterjee, V.K., Battaloğlu, E., “A Novel Missense Mutation in Human ttf-2 (fkhl15) Gene Associated with Congenital Hypothyroidism but not Athyreosis”, Journal of Clinical Endocrinology & Metabolism, 91, 10, 4183-4187, 2006ç

Türkçe

Ünal, M., Ünal, D.O., Baltacı, A.K., Moğulkoç, R., Kayserilioğlu, A., “Investigation of Serum Leptin Levels ın Professional Male Football Players and Healthy Sedentary Males”, Neuroendocrinology Letters, 26, 2, 148-151, 2005.

Türkçe

Kavak, E., Cavupoolu, K., Öztürk, N., Duru, A.D., Saygılı, T., Aslan, T., Bilgir, C., Hyz, M.C., Ünal, D.O., Öztürk, M., Koman, A., “Identification of Novel Genes That are Differentially Expressed in Beta Catenin/tcf4 Signaling Activated Hepatocellular Carcinoma Cells”, Clinical Cancer Research, 11, 24, 9139S-9139S, 2005.

Türkçe

Çınaroğlu, A., Özmen, Y., Özdemir, A., Özcan, F., Ergörül, C., Çayırlıoğlu, P., Hicks, D., Buğra, K., “Expression and Possible Function of Fibroblast Growth Factor 9 (fgf9) and Its Cognate Receptors fgfr2 and fgfr3 in Postnatal and Adult Retina”, Journal of Neuroscience Research, 79, 3, 329-339, 2005.

Türkçe

Parman, Y., Poyraz, M., Battaloğlu, E., Barış, I., Bilir, B., Bissar-Tadmouri, N., Serdaroğlu, P., Deymeer, F., “Clinicopathological and Genetic Study of Demyelinating cmt”, Journal of the Peripheral Nervous System, 10, 71-71, 2005.

Türkçe

Sayfalar