The Taf14 YEATS domain is a reader of histone crotonylation von Andrews, Forest H, Shinsky, Stephen A, Shanle, Erin K, Bridgers, Joseph B, Gest, Anneliese, Tsun, Ian K, Krajewski, Krzysztof, Shi, Xiaobing, Strahl, Brian D, Kutateladze, Tatiana G

Volltext

Combinatorial Histone Readout by the Dual Plant Homeodomain (PHD) Fingers of Rco1 Mediates Rpd3S Chromatin Recruitment and the Maintenance of Transcriptional Fidelity von McDaniel, Stephen L., Fligor, Jennifer E., Ruan, Chun, Cui, Haochen, Bridgers, Joseph B., DiFiore, Julia V., Guo, Angela H., Li, Bing, Strahl, Brian D.

Volltext

Histone peptide microarray screen of chromo and Tudor domains defines new histone lysine methylation interactions von Shanle, Erin K, Shinsky, Stephen A, Bridgers, Joseph B, Bae, Narkhyun, Sagum, Cari, Krajewski, Krzysztof, Rothbart, Scott B, Bedford, Mark T, Strahl, Brian D

Volltext

Covalent Modifications of Histone H3K9 Promote Binding of CHD3 von Tencer, Adam H., Cox, Khan L., Di, Luo, Bridgers, Joseph B., Lyu, Jie, Wang, Xiaodong, Sims, Jennifer K., Weaver, Tyler M., Allen, Hillary F., Zhang, Yi, Gatchalian, Jovylyn, Darcy, Michael A., Gibson, Matthew D., Ikebe, Jinzen, Li, Wei, Wade, Paul A., Hayes, Jeffrey J., Strahl, Brian D., Kono, Hidetoshi, Poirier, Michael G., Musselman, Catherine A., Kutateladze, Tatiana G.

Volltext

Recognition of Histone Crotonylation by Taf14 Links Metabolic State to Gene Expression von Gowans, Graeme J., Bridgers, Joseph B., Zhang, Jibo, Dronamraju, Raghuvar, Burnetti, Anthony, King, Devin A., Thiengmany, Aline V., Shinsky, Stephen A., Bhanu, Natarajan V., Garcia, Benjamin A., Buchler, Nicolas E., Strahl, Brian D., Morrison, Ashby J.

Volltext

Expanding the Reader Landscape of Histone Acylation von Khan, Abid, Bridgers, Joseph B., Strahl, Brian D.

Volltext

Yaf9 subunit of the NuA4 and SWR1 complexes targets histone H3K27ac through its YEATS domain von Klein, Brianna J, Ahmad, Salar, Vann, Kendra R, Andrews, Forest H, Mayo, Zachary A, Bourriquen, Gaelle, Bridgers, Joseph B, Zhang, Jinyong, Strahl, Brian D, Côté, Jacques, Kutateladze, Tatiana G

Volltext

Association of Taf14 with acetylated histone H3 directs gene transcription and the DNA damage response von Shanle, Erin K, Andrews, Forest H, Meriesh, Hashem, McDaniel, Stephen L, Dronamraju, Raghuvar, DiFiore, Julia V, Jha, Deepak, Wozniak, Glenn G, Bridgers, Joseph B, Kerschner, Jenny L, Krajewski, Krzysztof, Martín, Glòria Mas, Morrison, Ashby J, Kutateladze, Tatiana G, Strahl, Brian D

Volltext

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study von Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

Volltext

Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study von Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

Volltext

Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy von Lerche, Holger, Berkovic, Samuel F, Lowenstein, Daniel H, Delgado-Escueta, Antonio V, Bailey, Julia N

Volltext

Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data von Allen, Andrew S, Berkovic, Samuel F, Bridgers, Joshua, Cossette, Patrick, Dlugos, Dennis, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Heinzen, Erin L, Jiang, Yu, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slave, Poduri, Annapurna, Ren, Zhong, Scheffer, Ingrid E, Sherr, Elliott, Wang, Quanli, Balling, Rudi, Barisic, Nina, Baulac, Stephanie, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Depienne, Christel, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jaehn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes R, Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Moeller, Rikke S, Muhle, Hiltrud, Pal, Deb, et. al

Volltext