
Publications

J. Lu, P. Ge, M. R. Sawaya, M. P. Hughes, D. R. Boyer, Q. Cao, R. Abskharon, D. Cascio, E. Tayeb-Fligelman, D. S. Eisenberg. Cryo-EM structures of the D290V mutant of the hnRNPA2 low-complexity domain suggests how D290V affects phase separation and aggregation. Journal of Biological Chemistry. 300(2):105531 (2024).

E. Tayeb-Fligelman, J. T. Bowler, C. E. Tai, M. R. Sawaya, Y-X. Jiang, G. Garcia Jr, S. L. Griner, X. Cheng, L. Salwinski, L. Lutter, P. M. Seidler, J. Lu, G. M. Rosenberg, K. Hou, R. Abskharon, H. Pan, C-T Zee, D. R. Boyer, Y. Li, D. H. Anderson, K. A. Murray, G. Falcon, D. Cascio, L. Saelices, R. Damoiseaux, V. Arumugaswami, F. Guo, D. S. Eisenberg. Low complexity domains of the nucleocapsid protein of SARS-CoV-2 form amyloid fibrils. Nature Communications. 14: 2379 (2023).

E. Reinstein, A. Gutierrez-Fernandez, S. Tzur, C. Bormans, S. Marcu, E. Tayeb-Fligelman, C. Vinkler, A. Raas-Rothschild, D. Irge, M. Landau, M. Shohat, XS. Puente, DM. Behar, and C. Lopez-Otın. Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C. European Journal of Human Genetics. 24(12): 1792-1796 (2016).

Y. Bhonker, A. Abu-Rayyan, K. Ushakov, L. Amir-Zilberstein, S. Shivatzki, O. Yizhar- Barnea, T. Elkan-Miller, E. Tayeb-Fligelman, S. M. Kim, M. Landau, M. Kanaan, P. Chen, F. Matsuzaki, D. Sprinzak, and K. B. Avraham. The GPSM2/LGN GoLoco motifs are essential for hearing. Mammalian Genome. 27(1-2): 29-46 (2016).

E. Reinstein, K. Orvin, E. Tayeb-Fligelman, H. Stiebel-Kalish, A. L. Pimienta, S. Tzur, L Bazak, T. Bengal, L. Cohen, D. D. Gaton, C. Bormans, M. Landau, R. Kornowski, M. Shohat, and D. M. Behar. Mutations in TAX1BP3 cause Dilated Cardiomyopathy with Septo- Optic Dysplasia. Human Mutation. 36(4): 439-42 (2015).







