The Pfam protein families database by Punta, Marco, Coggill, Penny C., Eberhardt, Ruth Y., Mistry, Jaina, Tate, John, Boursnell, Chris, Pang, Ningze, Forslund, Kristoffer, Ceric, Goran, Clements, Jody, Heger, Andreas, Holm, Liisa, Sonnhammer, Erik L. L., Eddy, Sean R., Bateman, Alex, Finn, Robert D.

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Pfam protein families database by Finn, Robert D, Tate, John, Mistry, Jaina, Coggill, Penny C, Sammut, Stephen John, Hotz, Hans-Rudolf, Ceric, Goran, Forslund, Kristoffer, Eddy, Sean R, Sonnhammer, Erik L.L, Bateman, Alex

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An SNP map of human chromosome 22 by Bentley, D. R, Mullikin, J. C, Hunt, S. E, Cole, C. G, Mortimore, B. J, Rice, C. M, Burton, J, Matthews, L. H, Pavitt, R, Plumb, R. W, Sims, S. K, Ainscough, R. M. R, Attwood, J, Bailey, J. M, Barlow, K, Bruskiewich, R. M. M, Butcher, P. N, Carter, N. P, Chen, Y, Clee, C. M, Coggill, P. C, Davies, J, Davies, R. M, Dawson, E, Francis, M. D, Joy, A. A, Lamble, R. G, Langford, C. F, Macarthy, J, Mall, V, Moreland, A, Overton-Larty, E. K, Ross, M. T, Smith, L. C, Steward, C. A, Sulston, J. E, Tinsley, E. J, Turney, K. J, Willey, D. L, Wilson, G. D, McMurray, A. A, Dunham, I, Rogers, J

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms by Sachidanandam, R, Weissman, D, Schmidt, S C, Kakol, J M, Stein, L D, Marth, G, Sherry, S, Mullikin, J C, Mortimore, B J, Willey, D L, Hunt, S E, Cole, C G, Coggill, P C, Rice, C M, Ning, Z, Rogers, J, Bentley, D R, Kwok, P Y, Mardis, E R, Yeh, R T, Schultz, B, Cook, L, Davenport, R, Dante, M, Fulton, L, Hillier, L, Waterston, R H, McPherson, J D, Gilman, B, Schaffner, S, Van Etten, W J, Reich, D, Higgins, J, Daly, M J, Blumenstiel, B, Baldwin, J, Stange-Thomann, N, Zody, M C, Linton, L, Lander, E S, Altshuler, D

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InterPro in 2011: new developments in the family and domain prediction database by Hunter, Sarah, Jones, Philip, Mitchell, Alex, Apweiler, Rolf, Attwood, Teresa K., Bateman, Alex, Bernard, Thomas, Binns, David, Bork, Peer, Burge, Sarah, de Castro, Edouard, Coggill, Penny, Corbett, Matthew, Das, Ujjwal, Daugherty, Louise, Duquenne, Lauranne, Finn, Robert D., Fraser, Matthew, Gough, Julian, Haft, Daniel, Hulo, Nicolas, Kahn, Daniel, Kelly, Elizabeth, Letunic, Ivica, Lonsdale, David, Lopez, Rodrigo, Madera, Martin, Maslen, John, McAnulla, Craig, McDowall, Jennifer, McMenamin, Conor, Mi, Huaiyu, Mutowo-Muellenet, Prudence, Mulder, Nicola, Natale, Darren, Orengo, Christine, Pesseat, Sebastien, Punta, Marco, Quinn, Antony F., Rivoire, Catherine, Sangrador-Vegas, Amaia, Selengut, Jeremy D., Sigrist, Christian J. A., Scheremetjew, Maxim, Tate, John, Thimmajanarthanan, Manjulapramila, Thomas, Paul D., Wu, Cathy H., Yeats, Corin, Yong, Siew-Yit

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Downregulation of Death-Associated Protein Kinase 1 (DAPK1) in Chronic Lymphocytic Leukemia by Raval, Aparna, Tanner, Stephan M., Byrd, John C., Angerman, Elizabeth B., Perko, James D., Chen, Shih-Shih, Hackanson, Björn, Grever, Michael R., Lucas, David M., Matkovic, Jennifer J., Lin, Thomas S., Kipps, Thomas J., Murray, Fiona, Weisenburger, Dennis, Sanger, Warren, Lynch, Jane, Watson, Patrice, Jansen, Mary, Yoshinaga, Yuko, Rosenquist, Richard, de Jong, Pieter J., Coggill, Penny, Beck, Stephan, Lynch, Henry, de la Chapelle, Albert, Plass, Christoph

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Complete MHC haplotype sequencing for common disease gene mapping by Stewart, C Andrew, Horton, Roger, Allcock, Richard J N, Ashurst, Jennifer L, Atrazhev, Alexey M, Coggill, Penny, Dunham, Ian, Forbes, Simon, Halls, Karen, Howson, Joanna M M, Humphray, Sean J, Hunt, Sarah, Mungall, Andrew J, Osoegawa, Kazutoyo, Palmer, Sophie, Roberts, Anne N, Rogers, Jane, Sims, Sarah, Wang, Yu, Wilming, Laurens G, Elliott, John F, de Jong, Pieter J, Sawcer, Stephen, Todd, John A, Trowsdale, John, Beck, Stephan

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene by Dennis, Megan Y, Paracchini, Silvia, Scerri, Thomas S, Prokunina-Olsson, Ludmila, Knight, Julian C, Wade-Martins, Richard, Coggill, Penny, Beck, Stephan, Green, Eric D, Monaco, Anthony P

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The genomic sequence and analysis of the swine major histocompatibility complex by Renard, C., Hart, E., Sehra, H., Beasley, H., Coggill, P., Howe, K., Harrow, J., Gilbert, J., Sims, S., Rogers, J., Ando, A., Shigenari, A., Shiina, T., Inoko, H., Chardon, P., Beck, S.

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InterPro in 2011: new developments in the family and domain prediction database by Hunter, S., Jones, P., Mitchell, A., Apweiler, R., Attwood, T. K., Bateman, A., Bernard, T., Binns, D., Bork, P., Burge, S., de Castro, E., Coggill, P., Corbett, M., Das, U., Daugherty, L., Duquenne, L., Finn, R. D., Fraser, M., Gough, J., Haft, D., Hulo, N., Kahn, D., Kelly, E., Letunic, I., Lonsdale, D., Lopez, R., Madera, M., Maslen, J., McAnulla, C., McDowall, J., McMenamin, C., Mi, H., Mutowo-Muellenet, P., Mulder, N., Natale, D., Orengo, C., Pesseat, S., Punta, M., Quinn, A. F., Rivoire, C., Sangrador-Vegas, A., Selengut, J. D., Sigrist, C. J. A., Scheremetjew, M., Tate, J., Thimmajanarthanan, M., Thomas, P. D., Wu, C. H., Yeats, C., Yong, S.-Y., Lees, J., Perkins, J., Sillitoe, I., Rentzsch, R., Dessailly, B. H.

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The structure of pyogenecin immunity protein, a novel bacteriocin-like immunity protein from Streptococcus pyogenes by Chang, Changsoo, Coggill, Penny, Bateman, Alex, Finn, Robert D, Cymborowski, Marcin, Otwinowski, Zbyszek, Minor, Wladek, Volkart, Lour, Joachimiak, Andrzej

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A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene: e1000436 by Dennis, Megan Y, Paracchini, Silvia, Scerri, Thomas S, Prokunina-Olsson, Ludmila, Knight, Julian C, Wade-Martins, Richard, Coggill, Penny, Beck, Stephan, Green, Eric D, Monaco, Anthony P

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