Enünlü, I., Ozansoy, M., Başak, A.N., “Alfa-class prefoldin protein UXT is a novel interacting partner of amyotrophic lateral sclerosis 2 (Als2) protein”, Biochemical and Biophysical Research Communications, 413, 3, 471-475, 2011 Dil Türkçe
Maljevic, S., Naros, G., Yalçın, O., Blazevic, D., Loeffler, H., Çağlayan, H., Steinlein, O.K., Lerche, H., “Temperature and pharmacological rescue of a folding-defective, dominant-negative k(v)7.2 mutation associated with neonatal seizures”, Human Mutation, 32, 10, E2283-E2293, 2011 Dil Türkçe
Sayar-Türet, M., Dreisigacker, S., Braun, H.J., Hede, A., Maccormack, R., Boyd, L.A., “Genetic variation within and between winter wheat genotypes from Turkey, Kazakhstan, and Europe as determined by nucleotide-binding-site profiling”, Genome, 54, 5, 419-430, 2011 Dil Türkçe
Çağlayan, M., Bilgin, N., "Cloning and sequence analysis of novel DNA polymerases from thermophilic Geobacillus species isolated from Hot Springs in Turkey: Characterization of DNA polymerase I from Geobacillus kaue strain NB", Applied Biochemistry and Biotechnology,165, 5-6, 1188-1200, 2011. Dil Türkçe
Battaloğlu, E., Dağlıkoca, E.D., Yıldırım, K., Kılınç, M., Parman, Y., Svenningsen, A.F., Buğra, K., “Expression of FGF1 and FGFR1 in mouse sciatic nerve”, Journal of the Peripheral Nervous System, 16, S9-S9, 2011. Dil Türkçe
Parman, Y., Kocasoy-Orhan, E., Matur, Z., Oflazer-Serdaroğlu, P., Battaloğlu, E., Poyraz, M., Deymeer, F., “Conduction blocks in Charcot Marie-Tooth 1A”, Journal of Neurology, 258, 110-110, 2011. Dil Türkçe
Parman, Y., Matur, Z., Shugaiv, E., Ilgaz-Aydınlar, E., Battaloğlu, E., Oflazer, P., Deymeer, F., “Clinico pathological and genetic study of familial transthyretin type amyloid polyneuropathy”, Journal of the Peripheral Nervous System, 16, , S105-S105, 2011. Dil Türkçe
Taylan, F., Altıok, E., “Patterns of meiotic recombination at major histocompatibility complex in human embryos”, Tissue Antigens, 77, 5, 483-484, 2011. Dil Türkçe
Tüysüz, B., Tolun, A., Yıldırım, Y., “Response to Kouwenberg et al. ~Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in arcl2b due to pycr1 mutations~”, American Journal of Medical Genetics Part A, 155A, 9, 2333-2334, 2011. Dil Türkçe
Sayar-Türet, M., Dreisigacker, S., Braun, H.J., Hede, A., Maccormack, R., Boyd, L.A., “Genetic variation within and between winter wheat genotypes from Turkey, Kazakhstan and Europe as determined by nucleotide binding site profiling”, Genome, 54, 5, 419-430, 2011. Dil Türkçe
