Rogers JM, Mimoso CA, Martin BJ, et al. Notch induces transcription by stimulating release of paused RNA Pol II without increasing chromatin accessibility. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.13.598853
Publications
Conway JR, Gillani R, Crowdis J, et al. Somatic structural variants drive distinct modes of oncogenesis in melanoma. The Journal of clinical investigation. 2024;134(13). doi:10.1172/JCI177270
Winter PS, Ramseier ML, Navia AW, et al. Mutation and cell state compatibility is required and targetable in Ph+ acute lymphoblastic leukemia minimal residual disease. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.06.597767
Conway JR, Gillani R, Crowdis J, et al. Somatic structural variants drive distinct modes of oncogenesis in melanoma. The Journal of clinical investigation. 2024;134(13). doi:10.1172/JCI177270
Conway JR, Gillani R, Crowdis J, et al. Somatic structural variants drive distinct modes of oncogenesis in melanoma. The Journal of clinical investigation. 2024;134(13). doi:10.1172/JCI177270
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Rebboah E, Rezaie N, Williams BA, et al. The ENCODE mouse postnatal developmental time course identifies regulatory programs of cell types and cell states. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.06.12.598567
Li Y, Ma K, Dong Z, et al. Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models. The Journal of clinical investigation. 2024;134(12). doi:10.1172/JCI177172