DNA-Binding Proteins

Displaying 1 - 21 of 21CSV
Pottier, C., Küçükali, F., Baker, M., Batzler, A., Jenkins, G. D., van Blitterswijk, M., Vicente, C. T., De Coster, W., Wynants, S., Van de Walle, P., Ross, O. A., Murray, M. E., Faura, J., Haggarty, S. J., van Rooij, J. GJ., Mol, M. O., Hsiung, G.-Y. R., Graff, C., Öijerstedt, L., … Rademakers, R. (2025). Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing. Nature Communications, 16(1). https://doi.org/10.1038/s41467-025-59216-0
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Vann, K. R., Sharma, R., Hsu, C.-C., Devoucoux, M., Tencer, A. H., Zeng, L., Lin, K., Zhu, L., Li, Q., Lachance, C., Ospina, R. R., Tong, Q., Cheung, K. L., Yang, S., Biswas, S., Xuan, H., Gatchalian, J., Alamillo, L., Wang, J., … Kutateladze, T. G. (2025). Structure-function relationship of ASH1L and histone H3K36 and H3K4 methylation. Nature Communications, 16(1). https://doi.org/10.1038/s41467-025-57556-5
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Lessel, I., Baresic, A., Chinn, I. K., May, J., Goenka, A., Chandler, K. E., Posey, J. E., Afenjar, A., Averdunk, L., Bedeschi, M. F., Besnard, T., Brager, R., Brick, L., Brugger, M., Brunet, T., Byrne, S., Calle-Martín, O. de la, Capra, V., Cardenas, P., … Lessel, D. (2025). DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders. The American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2024.12.012
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Shipman, G. A., Padilla, R., Horth, C., Hu, B., Bareke, E., Vitorino, F. N., Gongora, J. M., Garcia, B. A., Lu, C., & Majewski, J. (2024). Systematic perturbations of SETD2, NSD1, NSD2, NSD3, and ASH1L reveal their distinct contributions to H3K36 methylation. Genome Biology, 25(1). https://doi.org/10.1186/s13059-024-03415-3
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Kanagaraj, K., Phillippi, M. A., Ober, E. H., Shuryak, I., Kleiman, N. J., Olson, J., Schaaf, G., Cline, J. M., & Turner, H. C. (2024). BAX and DDB2 as biomarkers for acute radiation exposure in the human blood ex vivo and non-human primate models. Scientific Reports, 14(1). https://doi.org/10.1038/s41598-024-69852-z
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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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Acharya, A., Bret, H., Huang, J.-W., Mütze, M., Göse, M., Kissling, V. M., Seidel, R., Ciccia, A., Guérois, R., & Cejka, P. (2024). Mechanism of DNA unwinding by MCM8-9 in complex with HROB. Nature Communications, 15(1). https://doi.org/10.1038/s41467-024-47936-8
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Ercan, A. B., Aronson, M., Fernandez, N. R., Chang, Y., Levine, A., Liu, Z. A., Negm, L., Edwards, M., Bianchi, V., Stengs, L., Chung, J., Al-Battashi, A., Reschke, A., Lion, A., Ahmad, A., Lassaletta, A., Reddy, A. T., Al-Darraji, A. F., Shah, A. C., … Tabori, U. (2024). Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study. The Lancet Oncology, 25(5), 668–682. https://doi.org/10.1016/s1470-2045(24)00026-3
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Schulz, V. E., Tuff, J. F., Tough, R. H., Lewis, L., Chimukangara, B., Garrett, N., Abdool Karim, Q., Abdool Karim, S. S., McKinnon, L. R., Kharsany, A. B. M., & McLaren, P. J. (2023). Host genetic variation at a locus near CHD1L impacts HIV sequence diversity in a South African population. Journal of Virology, 97(10). https://doi.org/10.1128/jvi.00954-23
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McLaren, P. J., Porreca, I., Iaconis, G., Mok, H. P., Mukhopadhyay, S., Karakoc, E., Cristinelli, S., Pomilla, C., Bartha, I., Thorball, C. W., Tough, R. H., Angelino, P., Kiar, C. S., Carstensen, T., Fatumo, S., Porter, T., Jarvis, I., Skarnes, W. C., Bassett, A., … Fellay, J. (2023). Africa-specific human genetic variation near CHD1L associates with HIV-1 load. Nature, 620(7976), 1025–1030. https://doi.org/10.1038/s41586-023-06370-4
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Columbia Affiliation
Rawal, Y., Jia, L., Meir, A., Zhou, S., Kaur, H., Ruben, E. A., Kwon, Y., Bernstein, K. A., Jasin, M., Taylor, A. B., Burma, S., Hromas, R., Mazin, A. V., Zhao, W., Zhou, D., Wasmuth, E. V., Greene, E. C., Sung, P., & Olsen, S. K. (2023). Structural insights into BCDX2 complex function in homologous recombination. Nature, 619(7970), 640–649. https://doi.org/10.1038/s41586-023-06219-w
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Huie, E. Z., Escudero, A., Saito, N., Harvey, D., Nguyen, M.-L., Lucot, K. L., LaGrande, J., Mungas, D., DeCarli, C., Lamar, M., Schneider, J. A., Kapasi, A., Rissman, R. A., Teich, A. F., & Dugger, B. N. (2023). TDP-43 Pathology in the Setting of Intermediate and High Alzheimer’s Disease Neuropathologic Changes: A Preliminary Evaluation Across Ethnoracial Groups. Journal of Alzheimer’s Disease, 91(4), 1291–1301. https://doi.org/10.3233/jad-220558
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Steers, N. J., Gupta, Y., D’Agati, V. D., Lim, T. Y., DeMaria, N., Mo, A., Liang, J., Stevens, K. O., Ahram, D. F., Lam, W. Y., Gagea, M., Nagarajan, L., Sanna-Cherchi, S., & Gharavi, A. G. (2022). GWAS in Mice Maps Susceptibility to HIV-Associated Nephropathy to the Ssbp2 Locus. Journal of the American Society of Nephrology, 33(1), 108–120. https://doi.org/10.1681/asn.2021040543
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Daum, H., Ganapathi, M., Hirsch, Y., Griffin, E. L., LeDuc, C. A., Hagen, J., Yagel, S., Meiner, V., Chung, W. K., & Mor‐Shaked, H. (2021). Bi‐allelic PAGR1 variants are associated with microcephaly and a severe neurodevelopmental disorder: Genetic evidence from two families. American Journal of Medical Genetics Part A, 188(1), 336–342. Portico. https://doi.org/10.1002/ajmg.a.62513
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Kushary, S. T., Revah‐Politi, A., Barua, S., Ganapathi, M., Accogli, A., Aggarwal, V., Brunetti‐Pierri, N., Cappuccio, G., Capra, V., Fagerberg, C. R., Gazdagh, G., Guzman, E., Hadonou, M., Harrison, V., Havelund, K., Iancu, D., Kraus, A., Lippa, N. C., Mansukhani, M., … Anyane Yeboa, K. (2021). ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature. American Journal of Medical Genetics Part A, 185(12), 3740–3753. Portico. https://doi.org/10.1002/ajmg.a.62445
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Taglialatela, A., Leuzzi, G., Sannino, V., Cuella-Martin, R., Huang, J.-W., Wu-Baer, F., Baer, R., Costanzo, V., & Ciccia, A. (2021). REV1-Polζ maintains the viability of homologous recombination-deficient cancer cells through mutagenic repair of PRIMPOL-dependent ssDNA gaps. Molecular Cell, 81(19), 4008-4025.e7. https://doi.org/10.1016/j.molcel.2021.08.016
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