Moleküler Biyoloji ve Genetik

Yalçın, Ö., Çağlayan, S.H., Çokar, Ö., Ağan, Bingöl, C.A., Dervent, A., Steinlein, O., “A Novel Missense Mutation (N258S) in the KCNQ2 Gene in a Turkish Family Afflicted with BFNC”, European Journal of Human Genetics, 13, 227, 2005.

Türkçe

Pekçelen, Y., Çağlayan, S.H., Ayer, M., Yıldırım-Demirel, N., Kalfa, M., Yavuz, A.S., “Von Willebrand Disease Type 2N (Normandy) in Two Families, F8 Gene Mutation Profile of High Responder Hemophilia A Patients in Türkiye”, Turkish Journal of Haematology, 22, 154, 2005.

Türkçe

Hanağası, H,A., Hocaoğlu, F.S., Yokeş, B., Gürvit, H., Emre, M., Başak, A.N., “A Novel Presenilin 1 Mutation ( ALA396THR ) is Associated with Early-onset Alzheimer’s Disease”, 21st International Conference of Alzheimer’s Disease International, 52, İstanbul, 2005.

Türkçe

Fidancı, İ.D., Kavaklı, K., Uçar, C., Timur, Ç., Meral, A., Kılınç, Y., Sayılan, H., Kazancı, E., Atabay, B., Küpesiz, A., Pekçelen, Y., İrken, G., Soydan, E., Çağlayan, S.H., “F8 Gene Mutation Profile of High Responder Hemophilia A Patients in Türkiye”, Turkish Journal of Haematology, 22, 88, 2005.

Türkçe

Bilir, B., Yapıcı, Z., Yalçınkaya, C., Battaloğlu, E., “Genetic Heterogeneity of Pelizaeus-merzbacher Disease: Exclusion of Linkage to the Proteolipid Protein 1 Locus in Three Affected Families”, European Journal of Human Genetics, 13, Supplement 1, S. 306, 2005.

Türkçe

Yüksel, S., Chen, P.P., “Identification of second-generation peptide mimetics for pathogenic auto phospholipid antibody”, Proceedings of 31st FEBS Congress, Molecules in Health and Disease, The FEBS Journal, 273, Supplement 1, 221, Published by Blackwell Publishing Ltd, 9600 Garsington Rd  Oxford OX4 2DQ, UK, 2006.

Türkçe

Sayfalar