Catalytic and binding mutants of the junction-resolving enzyme endonuclease I of bacteriophage T7: role of acidic residues von Parkinson, M. Janine, Pöhler, J. Richard G., Lilley, David M. J.

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Ca2+/calmodulin-dependent translocation of sphingosine kinase: role in plasma membrane relocation but not activation von Young, Kenneth W, Willets, Jonathon M, Parkinson, M Janine, Bartlett, Paula, Spiegel, Sarah, Nahorski, Stefan R, Challiss, R A John

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The junction-resolving enzyme T7 endonuclease I: quaternary structure and interaction with DNA von Parkinson, M.Janine, Lilley, David M.J

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Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen von Wotton, Janine M., Peterson, Emma, Flenniken, Ann M., Bains, Rasneer S., Veeraragavan, Surabi, Bower, Lynette R., Bubier, Jason A., Parisien, Marc, Bezginov, Alexandr, Haselimashhadi, Hamed, Mason, Jeremy, Moore, Michayla A., Stewart, Michelle E., Clary, Dave A., Delbarre, Daniel J., Anderson, Laura C., D'Souza, Abigail, Goodwin, Leslie O., Harrison, Mark E., Huang, Ziyue, Mckay, Matthew, Qu, Dawei, Santos, Luis, Srinivasan, Subhiksha, Urban, Rachel, Vukobradovic, Igor, Ward, Christopher S., Willett, Amelia M., Braun, Robert E., Brown, Steve D.M., Dickinson, Mary E., Heaney, Jason D., Kumar, Vivek, Lloyd, K.C. Kent, Mallon, Ann-Marie, McKerlie, Colin, Murray, Stephen A., Nutter, Lauryl M.J., Parkinson, Helen, Seavitt, John R., Wells, Sara, Samaco, Rodney C., Chesler, Elissa J., Smedley, Damian, Diatchenko, Luda, Baumbauer, Kyle M., Young, Erin E., Bonin, Robert P., Mandillo, Silvia, White, Jacqueline K.

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Transfusions and neurodevelopmental outcomes in extremely low gestation neonates enrolled in the PENUT Trial: a randomized clinical trial von Vu, Phuong T., Ohls, Robin K., Mayock, Dennis E., German, Kendell R., Comstock, Bryan A., Heagerty, Patrick J., Juul, Sandra E.

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Powered standing wheelchairs promote independence, health and community involvement in adolescents with Duchenne muscular dystrophy von Vorster, Nitamarie, Evans, Kerry, Murphy, Nada, Kava, Maina, Cairns, Anita, Clarke, Damian, Ryan, Monique M., Siafarikas, Aris, Rowe, Peter W., Parkinson, Stephanie, Gaynor, Odette, Chiu, Linda, Anderson, Janine, Bayley, Klair, Jacoby, Peter, Cross, Donna, Downs, Jenny

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Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis

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Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy von Spielmann, Nadine, Miller, Gregor, Oprea, Tudor I, Hsu, Chih-Wei, Fobo, Gisela, Frishman, Goar, Montrone, Corinna, Haseli Mashhadi, Hamed, Mason, Jeremy, Munoz Fuentes, Violeta, Leuchtenberger, Stefanie, Ruepp, Andreas, Wagner, Matias, Westphal, Dominik S, Wolf, Cordula, Görlach, Agnes, Sanz-Moreno, Adrián, Cho, Yi-Li, Teperino, Raffaele, Brandmaier, Stefan, Sharma, Sapna, Galter, Isabella Rikarda, Östereicher, Manuela A, Zapf, Lilly, Mayer-Kuckuk, Philipp, Rozman, Jan, Teboul, Lydia, Bunton-Stasyshyn, Rosie K A, Cater, Heather, Stewart, Michelle, Christou, Skevoulla, Westerberg, Henrik, Willett, Amelia M, Wotton, Janine M, Roper, Willson B, Christiansen, Audrey E, Ward, Christopher S, Heaney, Jason D, Reynolds, Corey L, Prochazka, Jan, Bower, Lynette, Clary, David, Selloum, Mohammed, Bou About, Ghina, Wendling, Olivia, Jacobs, Hugues, Leblanc, Sophie, Meziane, Hamid, Sorg, Tania, Audain, Enrique, Gilly, Arthur, Rayner, Nigel W, Hitz, Marc-Phillip, Zeggini, Eleftheria, Wolf, Eckhard, Sedlacek, Radislav, Murray, Steven A, Svenson, Karen L, Braun, Robert E, White, Jaqueline K, Kelsey, Lois, Gao, Xiang, Shiroishi, Toshihiko, Xu, Ying, Seong, Je Kyung, Mammano, Fabio, Tocchini-Valentini, Glauco P, Beaudet, Arthur L, Meehan, Terrence F, Parkinson, Helen, Smedley, Damian, Mallon, Ann-Marie, Wells, Sara E, Grallert, Harald, Wurst, Wolfgang, Marschall, Susan, Fuchs, Helmut, Brown, Steve D M, Flenniken, Ann M, Nutter, Lauryl M J, McKerlie, Colin, Herault, Yann, Lloyd, K C Kent, Dickinson, Mary E, Gailus-Durner, Valerie, Hrabe de Angelis, Martin

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Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy von Spielmann, Nadine, Miller, Gregor, Oprea, Tudor I., Hsu, Chih-Wei, Fobo, Gisela, Frishman, Goar, Montrone, Corinna, Haseli Mashhadi, Hamed, Mason, Jeremy, Munoz Fuentes, Violeta, Leuchtenberger, Stefanie, Ruepp, Andreas, Wagner, Matias, Westphal, Dominik S., Wolf, Cordula, Görlach, Agnes, Sanz-Moreno, Adrián, Cho, Yi-Li, Teperino, Raffaele, Brandmaier, Stefan, Sharma, Sapna, Galter, Isabella Rikarda, Östereicher, Manuela A., Zapf, Lilly, Mayer-Kuckuk, Philipp, Rozman, Jan, Teboul, Lydia, Bunton-Stasyshyn, Rosie K. A., Cater, Heather, Stewart, Michelle, Christou, Skevoulla, Westerberg, Henrik, Willett, Amelia M., Wotton, Janine M., Roper, Willson B., Christiansen, Audrey E., Ward, Christopher S., Heaney, Jason D., Reynolds, Corey L., Prochazka, Jan, Bower, Lynette, Clary, David, Selloum, Mohammed, Bou About, Ghina, Wendling, Olivia, Jacobs, Hugues, Leblanc, Sophie, Meziane, Hamid, Sorg, Tania, Audain, Enrique, Gilly, Arthur, Rayner, Nigel W., Aguilar-Pimentel, Juan A., Becker, Lore, Garrett, Lillian, Hölter, Sabine M., Amarie, Oana V., Calzada-Wack, Julia, Klein-Rodewald, Tanja, da Silva-Buttkus, Patricia, Lengger, Christoph, Stoeger, Claudia, Gerlini, Raffaele, Rathkolb, Birgit, Mayr, Daniela, Seavitt, John, Gaspero, Angelina, Green, Jennie R., Garza, Arturo, Bohat, Ritu, Wong, Leeyean, McElwee, Melissa L., Kalaga, Sowmya, Rasmussen, Tara L., Lorenzo, Isabel, Lanza, Denise G., Samaco, Rodney C., Veeraragaven, Surabi, Gallegos, Juan J., Kašpárek, Petr, Petrezsélyová, Silvia, King, Ruairidh, Johnson, Sara, Cleak, James, Szkoe-Kovacs, Zsombor, Codner, Gemma, Mackenzie, Matthew, Caulder, Adam, Kenyon, Janet, Gardiner, Wendy, Phelps, Hayley, Hancock, Rhys, Norris, Claire, Moore, Michayla A., Seluke, Audrie M., Urban, Rachel, Kane, Coleen, Goodwin, Leslie O., Peterson, Kevin A., Mckay, Matthew

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Malignant granular lymphoproliferation after Epstein‐Barr virus infection: Partial immunologic reconstitution with interleukin‐2 von Aronson, Frederick R., Dempsey, Roy A., Allegretta, Mark, André‐Schwartz, Janine, Poldre, Peeter A., Hillyer, Christopher D., Parkinson, David R., Rudders, Richard A., Schwartz, Robert S., Mier, James W.

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