Transcription Factors

Displaying 1 - 16 of 16CSV
Huang, H., Xu, Y., Guo, Z., Zhang, M., Li, W., Song, Y., Nie, J., Hu, W., Hei, T. K., & Zhou, G. (2025). Irradiation-responsive PRDM10-DT modulates the angiogenic response in human NSCLC cells in an SP1-dependent manner via the miR-663a/TGF-β1 axis. Journal of Translational Medicine, 23(1). https://doi.org/10.1186/s12967-025-06273-0
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Mellis, I. A., Melzer, M. E., Bodkin, N., & Goyal, Y. (2024). Prevalence of and gene regulatory constraints on transcriptional adaptation in single cells. Genome Biology, 25(1). https://doi.org/10.1186/s13059-024-03351-2
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Wiegand, T., Hoffmann, F. T., Walker, M. W. G., Tang, S., Richard, E., Le, H. C., Meers, C., & Sternberg, S. H. (2024). TnpB homologues exapted from transposons are RNA-guided transcription factors. Nature, 631(8020), 439–448. https://doi.org/10.1038/s41586-024-07598-4
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von Ehr, J., Oberstrass, L., Yazgan, E., Schnaubelt, L. I., Blümel, N., McNicoll, F., Weigand, J. E., Zarnack, K., Müller-McNicoll, M., Korn, S. M., & Schlundt, A. (2024). Arid5a uses disordered extensions of its core ARID domain for distinct DNA- and RNA-recognition and gene regulation. Journal of Biological Chemistry, 300(7), 107457. https://doi.org/10.1016/j.jbc.2024.107457
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Nakagawa, S., Carnevali, D., Tan, X., Alvarez, M. J., Parfitt, D.-E., Di Vicino, U., Arumugam, K., Shin, W., Aranda, S., Normanno, D., Sebastian-Perez, R., Cannatá, C., Cortes, P., Neguembor, M. V., Shen, M. M., Califano, A., & Cosma, M. P. (2024). The Wnt-dependent master regulator NKX1-2 controls mouse pre-implantation development. Stem Cell Reports, 19(5), 689–709. https://doi.org/10.1016/j.stemcr.2024.04.004
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Zhang, F., Sahu, V., Peng, K., Wang, Y., Li, T., Bala, P., Aitymbayev, D., Sahgal, P., Schaefer, A., Der, C. J., Ryeom, S., Yoon, S., Sethi, N., Bass, A. J., & Zhang, H. (2024). Recurrent RhoGAP gene fusion CLDN18-ARHGAP26 promotes RHOA activation and focal adhesion kinase and YAP-TEAD signalling in diffuse gastric cancer. Gut, 73(8), 1280–1291. https://doi.org/10.1136/gutjnl-2023-329686
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El Sayyed, H., Pambos, O. J., Stracy, M., Gottesman, M. E., & Kapanidis, A. N. (2024). Single-molecule tracking reveals the functional allocation, in vivo interactions, and spatial organization of universal transcription factor NusG. Molecular Cell, 84(5), 926-937.e4. https://doi.org/10.1016/j.molcel.2024.01.025
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Honzel, E., Joshi, A., Hernandez-Morato, I., Pennington-FitzGerald, W., & Pitman, M. J. (2024). A comparison of confocal and epifluorescence microscopy for quantification of RNAScope and immunohistochemistry fluorescent images. Journal of Neuroscience Methods, 403, 110050. https://doi.org/10.1016/j.jneumeth.2023.110050
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Xiao, M., Kondo, S., Nomura, M., Kato, S., Nishimura, K., Zang, W., Zhang, Y., Akashi, T., Viny, A., Shigehiro, T., Ikawa, T., Yamazaki, H., Fukumoto, M., Tanaka, A., Hayashi, Y., Koike, Y., Aoyama, Y., Ito, H., Nishikawa, H., … Inoue, D. (2023). BRD9 determines the cell fate of hematopoietic stem cells by regulating chromatin state. Nature Communications, 14(1). https://doi.org/10.1038/s41467-023-44081-6
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Hagkarim, N. C., Hajkarim, M. C., Suzuki, T., Fujiwara, T., Winkler, G. S., Stewart, G. S., & Grand, R. J. (2023). Disruption of the Mammalian Ccr4–Not Complex Contributes to Transcription-Mediated Genome Instability. Cells, 12(14), 1868. https://doi.org/10.3390/cells12141868
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Karolak, J. A., Welch, C. L., Mosimann, C., Bzdęga, K., West, J. D., Montani, D., Eyries, M., Mullen, M. P., Abman, S. H., Prapa, M., Gräf, S., Morrell, N. W., Hemnes, A. R., Perros, F., Hamid, R., Logan, M. P. O., Whitsett, J., Galambos, C., Stankiewicz, P., … Austin, E. D. (2023). Molecular Function and Contribution of TBX4 in Development and Disease. American Journal of Respiratory and Critical Care Medicine, 207(7), 855–864. https://doi.org/10.1164/rccm.202206-1039tr
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Ko, A., Hasanain, M., Oh, Y. T., D’Angelo, F., Sommer, D., Frangaj, B., Tran, S., Bielle, F., Pollo, B., Paterra, R., Mokhtari, K., Soni, R. K., Peyre, M., Eoli, M., Papi, L., Kalamarides, M., Sanson, M., Iavarone, A., & Lasorella, A. (2022). LZTR1Mutation Mediates Oncogenesis through Stabilization of EGFR and AXL. Cancer Discovery, 13(3), 702–723. https://doi.org/10.1158/2159-8290.cd-22-0376
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Salinas, S. A., Mace, E. M., Conte, M. I., Park, C. S., Li, Y., Rosario-Sepulveda, J. I., Mahapatra, S., Moore, E. K., Hernandez, E. R., Chinn, I. K., Reed, A. E., Lee, B. J., Frumovitz, A., Gibbs, R. A., Posey, J. E., Forbes Satter, L. R., Thatayatikom, A., Allenspach, E. J., Wensel, T. G., … Orange, J. S. (2022). An ELF4 hypomorphic variant results in NK cell deficiency. JCI Insight, 7(23). https://doi.org/10.1172/jci.insight.155481
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Zhou, D., Wu, Z., Park, J.-G., Fiches, G. N., Li, T.-W., Ma, Q., Huang, H., Biswas, A., Martinez-Sobrido, L., Santoso, N. G., & Zhu, J. (2022). FACT subunit SUPT16H associates with BRD4 and contributes to silencing of interferon signaling. Nucleic Acids Research, 50(15), 8700–8718. https://doi.org/10.1093/nar/gkac645
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