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F, Rieger A, Arslan N, Yilmaz E, Ekinci B, Edem PP, Aslan M, Özgör B, Lochmüller A, Nair A, O’Heir E, Lovgren AK, Broad Center for Mendelian Genomics., Maroofian R, Houlden H, Polavarapu K, Roos A, Müller JS, Hathazi D, Chinnery PF, Laurie S, Beltran S, Lochmüller H, Horvath R. High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases. Brain : a journal of neurology. 2021 November. doi:10.1093/brain/awab395.
12. Ekin U, Yuzugullu H, Ozen C, Korhan P, Bagirsakci E, Yilmaz F, Yuzugullu OG, Uzuner H, Alotaibi H, Kirmizibayrak PB, Atabey N, Karakülah G, Ozturk M. Evaluation of ATAD2 as a Potential Target in Hepatocellular Carcinoma. Journal of gastrointestinal cancer. 2021 November. doi:10.1007/s12029-021-00732-9.
13. Arif E. Cetin, Zeynep A. Kocer, Seda Nur Topkaya, Ziya Ata Yazici. Handheld Plasmonic Biosensor for Virus Detection in Field-Settings. Sensors and Actuators B: Chemical. 2021 October; 344: 130301. doi:10.1016/j.snb.2021.130301.
14. Utine CA, Kaya M, Kasal K. Wide-field vitreoretinal surgery in eyes with Boston type 1 keratoprosthesis. International ophthalmology. 2021 October. doi:10.1007/s10792-021-02083- 7.
15. Ozhan, G. Editorial: Wnt Signaling at the Plasma Membrane: Activation, Regulation and Disease Connection. Frontiers in Cell and Developmental Biology. 2021 October; 9: 2994. doi:10.3389/fcell.2021.780163.
16. Gökhan Karakülah, Cİhangir Yandım. Identification of differentially expressed genomic repeats in primary hepatocellular carcinoma and their potential links to biological processes and survival. Turkish Journal of Biology. 2021 October; 45: 599-612. doi:10.3906/biy-2104-13.
17. Karabicici M, Azbazdar Y, Iscan E, Ozhan G. Misregulation of Wnt Signaling Pathways at the Plasma Membrane in Brain and Metabolic Diseases. Membranes. 2021 October; 11 (11): 844. doi:10.3390/membranes11110844.
18. Kiser C, Gonul CP, Olcum M, Genc S. Inhibitory effects of sulforaphane on NLRP3 inflammasome activation. Molecular immunology. 2021 October; 140: 175-185. doi:10.1016/j.molimm.2021.10.014.
19. Richard EM, Bakhtiari S, Marsh APL, et all. Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss. American journal of human genetics. 2021 October; 108 (10): 2006-
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