Moleküler Biyoloji ve Genetik

Usluer, S., Kayserili, M. A., Eken, A. G, Çağlayan, S. H., et.al., "Association of a Synonymous SCN1B Variant Affecting Splicing Efficiency with Benign Familial Infantile Epilepsy (BFIE)", European Journal of Paediatric Neurology, 21, 5, 773-782, 2017.

Türkçe

Uğurlu, S., Karacan, İ., Özdoğan, H., Tolun, A., Turanlı, E. Tahir, "Trex 1 Mutation in the Members of a Family with Systemic Lupus Erythematosus And Antiphospholipid Syndrome", Annals of The Rheumatic Diseases, 76, 1101-1101, 2017.

Türkçe

Sobhiafshar, U., Yıldız, N., Tufan, A.B., Yılmaz, E., Ayhan, M.C., Yerinde, C., Erkan, E.E., Emre, N., "Characterization of the Interferon Regulatory Factor 4 Pathway in Melanoma Cells.", Molecular Biology of the Cell, 28, 2017.

Türkçe

Santiago-Sim, T., Burrage, L.C., Ebstein, F., Çaglayan, S.H., et.al., "Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features", American Journal of Human Genetics, 100, 4, 676-688, 2017.

Türkçe

Ralff, M.D., Kline, C.L.B., Küçükkase, O.C., et.al., "ONC201 Demonstrates Antitumor Effects in Both Triple-Negative and Non-Triple-Negative Breast Cancers through TRAIL-Dependent and TRAIL-Independent Mechanisms", Molecular Cancer Therapeutics, 16, 7, 1290-1298, 2017.

Türkçe

Parman, Y., Durmuş, H., Deymeer, F., Oflazer-Serdaroğlu, P., Battaloğlu, E., "Clinical and Genetic Heterogeneity in Charcot-Marie-Tooth Neuropathy Type 2 Patients From Turkey", Journal of the Peripheral Nervous System, 22, 3, 355-355, 2017.

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