Channel:  The Howard Hughes Medical Institute (HHMI)

2,322 Articles

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A Perturb-seq screen guided by species divergence uncovers pathways for collateral artery formation
Fan, X., Zhou, R., Raftrey, B. C., Rios Coronado, P. E., Trimm, E., Clancy, E., Chen, X., Bozeman, J., Chen, M. S., Alimukhamedov, S., Alcocer, J., Bonham, I., Agarwal, S., Isakova, A., de Jesus Perez, V. A., Park, C. Y., Shay, T. F., Gradinaru, V., Quertermous, T., Engreitz, J. M., Red-Horse, K.
10.64898/2026.04.29.721711 — Posted: 2026-05-10
Dpb11 facilitates the colocalization of Mec1-Ddc2 with its activators on gapped DNA
Beckwitt, E. C., Chua, G. N. L., Liu, S., O'Donnell, M. E.
10.1101/2025.11.28.691181 — Posted: 2026-05-10
Targets of SPEECHLESS and FAMA control guard cell division and expansion in the late stomatal lineage
Gonzalez-Suarez, P., Hilbers, Y., Budrys, A., Liu, A., Richter, S., Bergmann, D. C., Smit, M. E.
10.1101/2025.10.12.681868 — Posted: 2026-05-10
Dynamic evolution of EZHIP, an inhibitor of the Polycomb Repressive Complex 2 in mammals
Raman, P., Khan, H., Young, J. M., Ferreira Alves, R., Toro Moreno, M., Li, A. L., Berger, A., Tsukiyama, T., Malik, H. S.
10.64898/2025.12.12.693809 — Posted: 2026-05-10
LIVIA: a browser-based tool for assessing and visualizing predicted protein interactions
Kim, A.-R., Perrimon, N.
10.64898/2026.05.01.721633 — Posted: 2026-05-10
Scalable genotyping in fixed transcriptomes resolves clonal heterogeneity via single-cell sequencing
Blattman, S. B., Maslah, N., Varela, A. A., Kumpaitis, K., Nalbant, B., Snopkowski, C., Mariani, M., Kida, L. C., Takizawa, M., Ratnayeke, N., Yu, K. K. H., Fernandes, S., Mousavi, N., Borgstrom, E., Vallejo, D., Boghospor, L., Xin, R., Mignardi, M., Wu, S., Scarlott, N., Delgado-Rivera, L., Kumar, P., Krishnan, S., Giraudier, S., Kiladjian, J.-J., Howitt, B. E., Kohlway, A., Lund, P., Pe'er, D., Chaligne, R., Lareau, C. A.
10.64898/2026.04.11.717967 — Posted: 2026-05-10
Pan-cancer proteogenomic interrogation of the Ubiquitin Proteasome System
Gonzalez Robles, T. J., Khan, M., Sastourne-Haletou, P., Triola, M., Zhou, H., Kito, Y., Kaisari, S., Fenyo, D., Rona, G., Soto-Feliciano, Y., Neel, B., Ruggles, K., Pagano, M.
10.64898/2026.03.23.713741 — Posted: 2026-05-10
Comprehensive Lineage Tracing Maps the Landscape of Cell Fate Decisions in Mouse Embryogenesis
Colgan, W. N., Koblan, L. W., Villagrana, J., Hou, T.-C. J., Wang, M., Gowri, G., Chandler, W., Sepulveda, L. A., Ciftci, D., Smolyar, K., Young, A., Wittler, L., Markoulaki, S., Loh, K. M., Zhuang, X., Yosef, N., Smith, Z. D., Weissman, J. S.
10.64898/2026.05.07.722278 — Posted: 2026-05-09
Selective Elimination of TP53 Mutant Cells by Transcript-Activated Chromatin Shredding
Zeng, J., Cheng, Z., Chen, H., Thompson, J., Crosby, K. T., Hang, H., Ngo, W., Xia, C., Rosas-Rivera, D., Kang, M. H., Mao, Y., Lee, G., Diffley, J. F. X., Song, Y., Qiu, L., Krah, N. M., Murthy, N., Jackson, R. N., Liu, Y., Ashworth, A., Doudna, J. A.
10.64898/2026.05.08.723607 — Posted: 2026-05-09
A massively parallel reporter assay of MECP2 cis-regulatory elements reveals genetic candidates for male-biased autism
Meyer-Schuman, R., Cherry, F., Sui, Y., Papastathopoulos-Katsaros, A., Zhong, Y., Li, Y., Wang, T., Hennick, K., Karunakaran, D., Berk-Rauch, H., Liu, Z., Chakravarti, A., Nowakowski, T. J., Eichler, E., Zoghbi, H. Y.
10.64898/2026.05.08.723809 — Posted: 2026-05-09

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