Moleküler Biyoloji ve Genetik

Mitropoulos, K., Papadima, E.M., Xeromerisiou, G., Balasopoulou, A., Başak, A.N., et al., “Genomic Variants in The Fto Gene Are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients“, Publıc Health Genomıcs, 21, 17-17, 2018.

Türkçe

Leon-Mediavilla, J., Senovilla, M., Montiel, J., Gil-Diez, P., Saez, A., Kryvoruchko, I.S., Reguera, M., Udvardi, M.K., Imperial, J., Gonzalez-Guerrero, M., “Mtmtp2-Facilitated ZInc Transport Into Intracellular Compartments İs Essential for Nodule Development in Medicago Truncatula“, Frontıers in Plant Science, 9, 2018.

Türkçe

Kryvoruchko, I.S., Routray, P., SInharoy, S., Torres-Jerez, I., Tejada-Jimenez, M., FInney, L.A., Nakashima, J., Pislariu, C.I., BenediTo, V.A., Gonzalez-Guerrero, M., Roberts, D.M., Udvardi, M.K., “An Iron-Activated Citrate Transporter, Mtmate67, Is Required for Symbiotic Nitrogen Fixation“, Plant Physıology, 176, 3, 2315-2329, 2018.

Türkçe

Koçoğlu, C., Gündoğdu, A., Kocaman, G., Kahraman-Koytak, P., Uluc, K., Kızıltan, G., Çağlayan, A.O., Bilguv, K., Vural, A., Başak, A.N., “Homozygous Capn1 Mutations Causing A Spastic-ataxia Phenotype in 2 Families“, Neurology-Genetıcs, 4, 1, 2018.

Türkçe

KazemInasab, S., Taşkıran, İ.İ., Fattahi, Z., Bazazzadegan, N., HosseIni, M., Rahimi, M., Oladnabi, M., Haddadi, M., Çelik, A., Ropers, H.H., Najmabadi, H., Kahrizi, K., “Cnksr1 Gene Defect Can Cause Syndromic AuTosomal Recessive Intellectual Disability“, American Journal of Medical Genetıcs Part B-Neuropsychiatric Genetics, 177, 8, 691-699, 2018.

Türkçe

​​Karacan, I., Uğurlu, S., Tolun, A., Tahir Turanlı, E., Özdoğan, H., “Other AuToInflammatory Disease Genes in an FMF-prevalent Population: A Homozygous MVK Mutation and a Novel Heterozygous TNFRSF1A Mutation in Two Different Turkish Families with ClInical FMF“, Clinical and Experimental Rheumatology​, 108​, 6​, S75-S81​, 2018. ​​ ​ ​ ​​​

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