Structural and functional dynamics of human centromeric chromatin von Schueler, Mary G, Sullivan, Beth A

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Adaptive Evolution of Foundation Kinetochore Proteins in Primates von Schueler, Mary G., Swanson, Willie, Thomas, Pamela J., Green, Eric D.

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Genomic and Genetic Definition of a Functional Human Centromere von Schueler, Mary G., Higgins, Anne W., Rudd, M. Katharine, Gustashaw, Karen, Willard, Huntington F.

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Histone modifications within the human X centromere region von Mravinac, Brankica, Sullivan, Lori L, Reeves, Jason W, Yan, Christopher M, Kopf, Kristen S, Farr, Christine J, Schueler, Mary G, Sullivan, Beth A

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Progressive Proximal Expansion of the Primate X Chromosome Centromere von Schueler, Mary G., Dunn, John M., Bird, Christine P., Ross, Mark T., Viggiano, Luigi, NISC Comparative Sequencing Program, Rocchi, Mariano, Willard, Huntington F., Green, Eric D., Olson, Maynard V.

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Comparative sequence analyses reveal sites of ancestral chromosomal fusions in the Indian muntjac genome von Tsipouri, Vicky, Schueler, Mary G, Hu, Sufen, Dutra, Amalia, Pak, Evgenia, Riethman, Harold, Green, Eric D

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Pericentromeric duplications in the laboratory mouse von Thomas, James W, Schueler, Mary G, Summers, Tyrone J, Blakesley, Robert W, McDowell, Jennifer C, Thomas, Pamela J, Idol, Jacquelyn R, Maduro, Valerie V B, Lee-Lin, Shih-Queen, Touchman, Jeffrey W, Bouffard, Gerard G, Beckstrom-Sternberg, Stephen M, Green, Eric D

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The DNA sequence of the human X chromosome von Ross, Mark T., Grafham, Darren V., Muzny, Donna, Howell, Gareth R., Ashurst, Jennifer L., Sudbrak, Ralf, Hurles, Matthew E., Ramser, Juliane, Deadman, Rebecca, Carter, Nigel P., Gunaratne, Preethi, Havlak, Paul, Richards, Stephen, Scott, Graham, Sodergren, Erica, Ainscough, Rachael, Barlow, Karen F., Beare, David M., Beasley, Oliver, Beck, Alfred, Blechschmidt, Karin, Brady, Nicola, Bray-Allen, Sarah, Bruford, Elspeth A., Burrill, Wayne, Bye, Jackie M., Chen, Guan, Ciccodicola, Alfredo, Clarke, Graham, Clee, Chris M., Clerc-Blankenburg, Kerstin, Cole, Charlotte G., Conquer, Jen S., Davies, Joy, Delgado, Oliver, Ding, Yan, Dinh, Huyen, Dunham, Andrew, Dunn, Matthew, Dutta, Ireena, Frankland, John, Fraser, Audrey E., Galgoczy, Petra, Glöckner, Gernot, Gribble, Susan, Gu, Yanghong, Gwilliam, Rhian, Heitmann, Katja, Hinzmann, Bernd, Hoffs, Michael, Howden, Phillip J., Huckle, Elizabeth J., Jacob, Leni, Joseph, Shirin S., Khan, Ziad, Kioschis, Petra, Kosiura, Anna, Laird, Gavin K., Lewis, Lora, Loulseged, Hermela, Lovell, Jamieson D., Maheshwari, Manjula, Miner, George, Müller, Ines, Nyakatura, Gerald, Palmer, Sophie, Parker, David, Parrish, Julia, Patel, Dina, Pearce, Alex V., Pelan, Sarah E., Perez, Lesette, Ramsey, Yvonne, Reichwald, Kathrin, Ridler, Kerry A., Schlessinger, David, Schueler, Mary G., Shen, Hua, Smith, Michelle L., Sotheran, Elizabeth C., Steward, Charles A., Taudien, Stefan, Thomas, Karen, Tracey, Alan, Verduzco, Daniel, Waldron, Lenee, Wang, Qiaoyan, Williamson, Angela, Williamson, Helen, Woodmansey, Rebecca L., Zhou, Jianling, Zoghbi, Huda, Rosenthal, André, Minx, Patrick J., Waterston, Robert H., Rice, Catherine M., Coulson, Alan, Beck, Stephan, Rogers, Jane, Bentley, David R.

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Familial X centromere variant resulting in false-positive prenatal diagnosis of monosomy X by interphase FISH von Tsuchiya, Karen, Schueler, Mary G., Dev, V. G.

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Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system von Higgins, A W, Schueler, M G, Willard, H F

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DNA sequence and analysis of human chromosome 8 von Nusbaum, Chad, Mikkelsen, Tarjei S., Zody, Michael C., Asakawa, Shuichi, Taudien, Stefan, Garber, Manuel, Kodira, Chinnappa D., Schueler, Mary G., Shimizu, Atsushi, Whittaker, Charles A., Chang, Jean L., Cuomo, Christina A., Dewar, Ken, FitzGerald, Michael G., Yang, Xiaoping, Allen, Nicole R., Anderson, Scott, Asakawa, Teruyo, Blechschmidt, Karin, Bloom, Toby, Borowsky, Mark L., Butler, Jonathan, Cook, April, Corum, Benjamin, DeArellano, Kurt, DeCaprio, David, Dooley, Kathleen T., Dorris, Lester, Engels, Reinhard, Glöckner, Gernot, Hafez, Nabil, Hagopian, Daniel S., Hall, Jennifer L., Ishikawa, Sabine K., Jaffe, David B., Kamat, Asha, Kudoh, Jun, Lehmann, Rüdiger, Lokitsang, Tashi, Macdonald, Pendexter, Major, John E., Matthews, Charles D., Mauceli, Evan, Menzel, Uwe, Mihalev, Atanas H., Minoshima, Shinsei, Murayama, Yuji, Naylor, Jerome W., Nicol, Robert, Nguyen, Cindy, O'Leary, Sinéad B., O'Neill, Keith, Parker, Stephen C. J., Polley, Andreas, Raymond, Christina K., Reichwald, Kathrin, Rodriguez, Joseph, Sasaki, Takashi, Schilhabel, Markus, Siddiqui, Roman, Smith, Cherylyn L, Sneddon, Tam P., Talamas, Jessica A., Tenzin, Pema, Topham, Kerri, Venkataraman, Vijay, Wen, Gaiping, Yamazaki, Satoru, Young, Sarah K., Zeng, Qiandong, Zimmer, Andrew R., Rosenthal, Andre, Birren, Bruce W., Platzer, Matthias, Shimizu, Nobuyoshi, Lander, Eric S.

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Large-Insert Clone/STS Contigs in Xq11–q12, Spanning Deletions in Patients with Androgen Insensitivity and Mental Retardation von Schueler, Mary G., Higgins, Anne W., Nagaraja, Ramaiah, Tentler, Dimitri, Dahl, Niklas, Gustashaw, Karen, Willard, Huntington F.

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Genetic mapping of microbial and host traits reveals production of immunomodulatory lipids by Akkermansia muciniphila in the murine gut von Zhang, Qijun, Linke, Vanessa, Overmyer, Katherine A., Traeger, Lindsay L., Kasahara, Kazuyuki, Miller, Ian J., Manson, Daniel E., Polaske, Thomas J., Kerby, Robert L., Kemis, Julia H., Trujillo, Edna A., Reddy, Thiru R., Russell, Jason D., Schueler, Kathryn L., Stapleton, Donald S., Rabaglia, Mary E., Seldin, Marcus, Gatti, Daniel M., Keele, Gregory R., Pham, Duy T., Gerdt, Joseph P., Vivas, Eugenio I., Lusis, Aldons J., Keller, Mark P., Churchill, Gary A., Blackwell, Helen E., Broman, Karl W., Attie, Alan D., Coon, Joshua J., Rey, Federico E.

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Loss of PDGF-B activity increases hepatic vascular permeability and enhances insulin sensitivity von Raines, Summer M, Richards, Oliver C, Schneider, Lindsay R, Schueler, Kathryn L, Rabaglia, Mary E, Oler, Angie T, Stapleton, Donald S, Genové, Guillem, Dawson, John A, Betsholtz, Christer, Attie, Alan D

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Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia von Austin-Tse, Christina, Halbritter, Jan, Zariwala, Maimoona A., Gilberti, Renée M., Gee, Heon Yung, Hellman, Nathan, Pathak, Narendra, Liu, Yan, Panizzi, Jennifer R., Patel-King, Ramila S., Tritschler, Douglas, Bower, Raqual, O’Toole, Eileen, Porath, Jonathan D., Hurd, Toby W., Chaki, Moumita, Diaz, Katrina A., Kohl, Stefan, Lovric, Svjetlana, Hwang, Daw-Yang, Braun, Daniela A., Schueler, Markus, Airik, Rannar, Otto, Edgar A., Leigh, Margaret W., Noone, Peadar G., Carson, Johnny L., Davis, Stephanie D., Pittman, Jessica E., Ferkol, Thomas W., Atkinson, Jeffry J., Olivier, Kenneth N., Sagel, Scott D., Dell, Sharon D., Rosenfeld, Margaret, Milla, Carlos E., Loges, Niki T., Omran, Heymut, Porter, Mary E., King, Stephen M., Knowles, Michael R., Drummond, Iain A., Hildebrandt, Friedhelm

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β Cell-specific deletion of Zfp148 improves nutrient-stimulated β cell Ca2+ responses von Emfinger, Christopher H, de Klerk, Eleonora, Schueler, Kathryn L, Rabaglia, Mary E, Stapleton, Donnie S, Simonett, Shane P, Mitok, Kelly A, Wang, Ziyue, Liu, Xinyue, Paulo, Joao A, Yu, Qinq, Cardone, Rebecca L, Foster, Hannah R, Lewandowski, Sophie L, Perales, José C, Kendziorski, Christina M, Gygi, Steven P, Kibbey, Richard G, Keller, Mark P, Hebrok, Matthias, Merrins, Matthew J, Attie, Alan D

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SORCS1 is necessary for normal insulin secretory granule biogenesis in metabolically stressed β cells von Kebede, Melkam A, Oler, Angie T, Gregg, Trillian, Balloon, Allison J, Johnson, Adam, Mitok, Kelly, Rabaglia, Mary, Schueler, Kathryn, Stapleton, Donald, Thorstenson, Candice, Wrighton, Lindsay, Floyd, Brendan J, Richards, Oliver, Raines, Summer, Eliceiri, Kevin, Seidah, Nabil G, Rhodes, Christopher, Keller, Mark P, Coon, Joshua L, Audhya, Anjon, Attie, Alan D

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SORCS1 is necessary for normal insulin secretory granule biogenesis in metabolically stressed [Beta] cells von Kebede, Melkam A, Oler, Angie T, Gregg, Trillian, Balloon, Allison J, Johnson, Adam, Mitok, Kelly, Rabaglia, Mary, Schueler, Kathryn, Stapleton, Donald, Thorstenson, Candice, Wrighton, Lindsay, Floyd, Brendan J, Richards, Oliver, Raines, Summer, Eliceiri, Kevin, Seidah, Nabil G, Rhodes, Christopher, Keller, Mark P, Coon, Joshua L, Audhya, Anjon, Attie, Alan D

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Identification of differentially expressed mRNAs in human fetal liver across gestation von Malhotra, Khushbeer, Luehrsen, Kenneth R., Costello, Lawrence L., Raich, Teresa J., Sim, Kim, Foltz, Lisa, Davidson, Scott, Xu, Hongxia, Chen, Audrey, Yamanishi, Douglas T., Lindemann, Garrett W., Cain, Carol A., Madlansacay, Mary Rose, Hashima, Sandra M., Pham, Thu Lan, Mahoney, Walt, Schueler, Paula A.

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Cloning and Characterization of Human Erythroid Membrane-Associated Protein, Human ERMAP von Xu, Hongxia, Foltz, Lisa, Sha, Yehsiung, Madlansacay, Mary Rose, Cain, Carol, Lindemann, Garrett, Vargas, Joseph, Nagy, Dea, Harriman, Bill, Mahoney, Walt, Schueler, Paula A.

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