Moleküler Biyoloji ve Genetik

Battaloğlu, E., Estrada-Cuzcano, A., Atkinson, D., Candayan, A., De Vriendt, E., Parman, Y., Jordanova, A., 'SPG11 is an Overlapping Gene Between Charcot-Marie-Tooth Disease and Hereditary Spastic Paraplegia', Journal of the Peripheral Nervous System, 21, 3, 238-239, 2016.

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Altındağ, E., Usluer, S., Gündoğdu, A., Tuncer, Ö.G., Vanlı-Yavuz, E.N., Çağlayan, H., Baykan, B., 'Late-Onset Myoclonic Epilepsy in Down Syndrome: Investigation of EPM1 Gene Mutations in two Cases', Journal of Neurological Sciences-Turkish, 33, 1, 132-137, 2016.

Türkçe

Akcay, H.I., Durmuş, H., Deymeer, F., Oflazer-Serdaroğlu, P., Sıvacı, M., Candayan, A., Battaloğlu, E., Parman, Y., 'Charcot-Marie-Tooth Disease in Turkey: Clinical and Genetic Findings from a Single-centre Experience', Journal of the Peripheral Nervous System, 21, 3, 230-231, 2016.

Türkçe

​Kim, M., Sandford, E., Gatica, D., Qiu, Y., Liu , X., Zheng, Y., Schulman, B.A., Xu, J., Semple, I., Ro, S.H., Kim, B, Mavioğlu, R.N., Tolun, A., et al., 'Mutation in ATG5 Reduces Autophagy and Leads to Ataxia with Developmental Delay', ELife​, e12245​, 10​, 1-18​, 2016.

Türkçe

​Djemie, T., Weckhuysen, S., von Spiczak, S., Carvill, G.L., Jaehn, J., Anttonen, A.K., Brilstra, E., Çağlayan, H.S., et al., 'Pitfalls in Genetic Testing: The Story of Missed SCN1A Mutations', Molecular Genetics and Genomic Medicine, 4, 4, 457-464, 2016. ​​ ​ ​ ​​​

Türkçe

​​​Şahin, U., Jollivet, F., Berthier, C., de The, H., Lallemand-Breitenbach, V.​​​​​, 'Detection of Protein SUMOylation In Situ by Proximity Ligation Assays'​​​​​, Rodriguez​​​​​, M.S., SUMO Methods and Protocols​​​​​, Springer Humana Press​​​​​, 2016​​.​

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