检索结果 - Markenscoff-Papadimitriou, Eirene
- Showing 1 - 11 results of 11
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Soft x-ray tomography reveals gradual chromatin compaction and reorganization during neurogenesis in vivo 由 Le Gros, Mark A., Clowney, E. Josephine, Magklara, Angeliki, Yen, Angela, Markenscoff-Papadimitriou, Eirene, Colquitt, Bradley, Myllys, Markko, Kellis, Manolis, Lomvardas, Stavros, Larabell, Carolyn A.
出版 2016Text -
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Genome-wide analysis of MEF2 transcriptional program reveals synaptic target genes and neuronal activity-dependent polyadenylation site selection 由 Flavell, Steven W., Kim, Tae-Kyung, Gray, Jesse M., Harmin, David A., Hemberg, Martin, Hong, Elizabeth J., Markenscoff-Papadimitriou, Eirene, Bear, Daniel M., Greenberg, Michael E.
出版 2008Text -
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A Chromatin Accessibility Atlas of the Developing Human Telencephalon 由 Markenscoff-Papadimitriou, Eirene, Whalen, Sean, Przytycki, Pawel, Thomas, Reuben, Binyameen, Fadya, Nowakowski, Tomasz J., Kriegstein, Arnold R., Sanders, Stephan J., State, Matthew W., Pollard, Katherine S., Rubenstein, John L.
出版 2020Text -
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An Epigenetic Signature for Monoallelic Olfactory Receptor Expression 由 Magklara, Angeliki, Yen, Angela, Colquitt, Bradley M., Clowney, E. Josephine, Allen, William, Markenscoff-Papadimitriou, Eirene, Evans, Zoe A., Kheradpour, Pouya, Mountoufaris, George, Carey, Catriona, Barnea, Gilad, Kellis, Manolis, Lomvardas, Stavros
出版 2011Text -
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Widespread transcription at neuronal activity-regulated enhancers 由 Kim, Tae-Kyung, Hemberg, Martin, Gray, Jesse M., Costa, Allen M., Bear, Daniel M., Wu, Jing, Harmin, David A., Laptewicz, Mike, Barbara-Haley, Kellie, Kuersten, Scott, Markenscoff-Papadimitriou, Eirene, Kuhl, Dietmar, Bito, Haruhiko, Worley, Paul F., Kreiman, Gabriel, Greenberg, Michael E.
出版 2010Text -
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Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder 由 An, Joon-Yong, Lin, Kevin, Zhu, Lingxue, Werling, Donna M., Dong, Shan, Brand, Harrison, Wang, Harold Z., Zhao, Xuefang, Schwartz, Grace B., Collins, Ryan L., Currall, Benjamin B., Dastmalchi, Claudia, Dea, Jeanselle, Duhn, Clif, Gilson, Michael C., Klei, Lambertus, Liang, Lindsay, Markenscoff-Papadimitriou, Eirene, Pochareddy, Sirisha, Ahituv, Nadav, Buxbaum, Joseph D., Coon, Hilary, Daly, Mark J., Kim, Young Shin, Marth, Gabor T., Neale, Benjamin M., Quinlan, Aaron R., Rubenstein, John L., Sestan, Nenad, State, Matthew W., Willsey, A. Jeremy, Talkowski, Michael E., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J.
出版 2018Text -
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An analytical framework for whole genome sequence association studies and its implications for autism spectrum disorder 由 Werling, Donna M., Brand, Harrison, An, Joon-Yong, Stone, Matthew R., Zhu, Lingxue, Glessner, Joseph T., Collins, Ryan L., Dong, Shan, Layer, Ryan M., Markenscoff-Papadimitriou, Eirene, Farrell, Andrew, Schwartz, Grace B., Wang, Harold Z., Currall, Benjamin B., Zhao, Xuefang, Dea, Jeanselle, Duhn, Clif, Erdman, Carolyn A., Gilson, Michael C., Yadav, Rachita, Handsaker, Robert E., Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey D., Nowakowski, Tomasz J., Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Walker, Michael F., Waterman, Mathew J., He, Xin, Kriegstein, Arnold R., Rubenstein, John L., Sestan, Nenad, McCarroll, Steven A., Neale, Benjamin M., Coon, Hilary, Willsey, A. Jeremy, Buxbaum, Joseph D., Daly, Mark J., State, Matthew W., Quinlan, Aaron R., Marth, Gabor T., Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael E., Sanders, Stephan J.
出版 2018Text