Nuclear Proteins

Displaying 1 - 11 of 11CSV
Shi, X., Li, Y., Zhou, H., Hou, X., Yang, J., Malik, V., Faiola, F., Ding, J., Bao, X., Modic, M., Zhang, W., Chen, L., Mahmood, S. R., Apostolou, E., Yang, F.-C., Xu, M., Xie, W., Huang, X., Chen, Y., & Wang, J. (2024). DDX18 coordinates nucleolus phase separation and nuclear organization to control the pluripotency of human embryonic stem cells. Nature Communications, 15(1). https://doi.org/10.1038/s41467-024-55054-8
Publication Date
Zohar, H., Lindenboim, L., Gozlan, O., Gundersen, G. G., Worman, H. J., & Stein, R. (2024). Apoptosis-induced translocation of nesprin-2 from the nuclear envelope to mitochondria is associated with mitochondrial dysfunction. Nucleus, 15(1). https://doi.org/10.1080/19491034.2024.2413501
Publication Date
Di Bona, M., Chen, Y., Agustinus, A. S., Mazzagatti, A., Duran, M. A., Deyell, M., Bronder, D., Hickling, J., Hong, C., Scipioni, L., Tedeschi, G., Martin, S., Li, J., Ruzgaitė, A., Riaz, N., Shah, P., D’Souza, E. K., Brodtman, D. Z., Sidoli, S., … Bakhoum, S. F. (2024). Micronuclear collapse from oxidative damage. Science, 385(6712). https://doi.org/10.1126/science.adj8691
Publication Date
Stokes, M. E., Vasciaveo, A., Small, J. C., Zask, A., Reznik, E., Smith, N., Wang, Q., Daniels, J., Forouhar, F., Rajbhandari, P., Califano, A., & Stockwell, B. R. (2024). Subtype-selective prenylated isoflavonoids disrupt regulatory drivers of MYCN-amplified cancers. Cell Chemical Biology, 31(4), 805-819.e9. https://doi.org/10.1016/j.chembiol.2023.11.007
Publication Date
Kaur, M., Blair, J., Devkota, B., Fortunato, S., Clark, D., Lawrence, A., Kim, J., Do, W., Semeo, B., Katz, O., Mehta, D., Yamamoto, N., Schindler, E., Al Rawi, Z., Wallace, N., Wilde, J. J., McCallum, J., Liu, J., Xu, D., … Krantz, I. D. (2023). Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms. American Journal of Medical Genetics Part A, 191(8), 2113–2131. Portico. https://doi.org/10.1002/ajmg.a.63247
Publication Date
Meyer, A. E., Stelloh, C., Pulakanti, K., Burns, R., Fisher, J. B., Heimbruch, K. E., Tarima, S., Furumo, Q., Brennan, J., Zheng, Y., Viny, A. D., Vassiliou, G. S., & Rao, S. (2022). Combinatorial genetics reveals the Dock1-Rac2 axis as a potential target for the treatment of NPM1;Cohesin mutated AML. Leukemia, 36(8), 2032–2041. https://doi.org/10.1038/s41375-022-01632-y
Publication Date
Yalcouyé, A., Traoré, O., Diarra, S., Schrauwen, I., Esoh, K., Kadlubowska, M. K., Bharadwaj, T., Adadey, S. M., Kéita, M., Guinto, C. O., Leal, S. M., Landouré, G., & Wonkam, A. (2022). A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family. Molecular Genetics & Genomic Medicine, 10(7). Portico. https://doi.org/10.1002/mgg3.1995
Publication Date
Zanoni, P., Panteloglou, G., Othman, A., Haas, J. T., Meier, R., Rimbert, A., Futema, M., Abou Khalil, Y., Norrelykke, S. F., Rzepiela, A. J., Stoma, S., Stebler, M., van Dijk, F., Wijers, M., Wolters, J. C., Dalila, N., Huijkman, N. C. A., Smit, M., Gallo, A., … von Eckardstein, A. (2022). Posttranscriptional Regulation of the Human LDL Receptor by the U2-Spliceosome. Circulation Research, 130(1), 80–95. https://doi.org/10.1161/circresaha.120.318141
Publication Date
He, X., Zhou, S., Dolan, M., Shi, Y., Wang, J., Quinn, B., Jahagirdar, D., Huang, W.-C., Tsuji, M., Pili, R., Ito, F., Ortega, J., Abrams, S. I., Ebos, J. M. L., & Lovell, J. F. (2021). Immunization with short peptide particles reveals a functional CD8+T-cell neoepitope in a murine renal carcinoma model. Journal for ImmunoTherapy of Cancer, 9(12), e003101. https://doi.org/10.1136/jitc-2021-003101
Publication Date
Huang, X., Park, K., Gontarz, P., Zhang, B., Pan, J., McKenzie, Z., Fischer, L. A., Dong, C., Dietmann, S., Xing, X., Shliaha, P. V., Yang, J., Li, D., Ding, J., Lungjangwa, T., Mitalipova, M., Khan, S. A., Imsoonthornruksa, S., Jensen, N., … Theunissen, T. W. (2021). OCT4 cooperates with distinct ATP-dependent chromatin remodelers in naïve and primed pluripotent states in human. Nature Communications, 12(1). https://doi.org/10.1038/s41467-021-25107-3
Publication Date
Tomioka, K., Miyamoto, T., Akutsu, S. N., Yanagihara, H., Fujita, K., Royba, E., Tauchi, H., Yamamoto, T., Koh, I., Hirata, E., Kudo, Y., Kobayashi, M., Okada, S., & Matsuura, S. (2021). NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations. Scientific Reports, 11(1). https://doi.org/10.1038/s41598-021-98673-7
Publication Date
Columbia Affiliation