Resultats de la cerca - Elspeth Payne

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  1. 1
    Expression of the cytoplasmic NPM1 mutant (NPMc+) causes the expansion of hematopoietic cells in zebrafish

    Expression of the cytoplasmic NPM1 mutant (NPMc+) causes the expansion of hematopoietic cells in zebrafish per Niccolò Bolli, Elspeth Payne, Clemens Grabher, Jeong-Soo Lee, Adam B. Johnston, Brunangelo Falini, John P. Kanki, A. Thomas Look

    Publicat 2010
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  2. 2
    L-leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway

    L-leucine improves the anemia and developmental defects associated with Diamond-Blackfan anemia and del(5q) MDS by activating the mTOR pathway per Elspeth Payne, Maria Virgilio, Anupama Narla, Hong Sun, Michelle S. Levine, Barry H. Paw, Nancy Berliner, A. Thomas Look, Benjamin L. Ebert, Arati Khanna‐Gupta

    Publicat 2012
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  3. 3
    <i>NUP98‐HOXA9</i>‐transgenic zebrafish develop a myeloproliferative neoplasm and provide new insight into mechanisms of myeloid leukaemogenesis

    <i>NUP98‐HOXA9</i>‐transgenic zebrafish develop a myeloproliferative neoplasm and provide new insight into mechanisms of myeloid leukaemogenesis per A. Michael Forrester, Clemens Grabher, Eileen McBride, Ellen R. Boyd, Märta H. Vigerstad, Alexander Edgar, FuiBoon Kai, Sahar I. Da’as, Elspeth Payne, A. Thomas Look, Jason N. Berman

    Publicat 2011
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  4. 4
    Endothelial von Willebrand factor regulates angiogenesis

    Endothelial von Willebrand factor regulates angiogenesis per Richard Starke, Francesco Ferraro, Koralia Paschalaki, Nicola H. Dryden, Thomas A. J. McKinnon, Rachel E. Sutton, Elspeth Payne, Dorian O. Haskard, Alun D. Hughes, Daniel F. Cutler, Michael Laffan, Anna M. Randi

    Publicat 2010
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  5. 5
    DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation

    DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation per Hemanth Tummala, Amanda J. Walne, Mike Williams, Nicholas Bockett, Laura C. Collopy, Shirleny Cardoso, Alicia Ellison, Robert Wynn, Thierry Leblanc, Jude Fitzgibbon, David P. Kelsell, David A. van Heel, Elspeth Payne, Vincent Plagnol, Inderjeet Dokal, Tom Vulliamy

    Publicat 2016
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  6. 6
    Pten mediates Myc oncogene dependence in a conditional zebrafish model of T cell acute lymphoblastic leukemia

    Pten mediates Myc oncogene dependence in a conditional zebrafish model of T cell acute lymphoblastic leukemia per Alejandro Gutiérrez, Ruta Grebliunaite, Hui Feng, Elena Kozakewich, Shizhen Zhu, Feng Guo, Elspeth Payne, Marc R. Mansour, Suzanne E. Dahlberg, Donna Neuberg, Jeroen den Hertog, Edward V. Prochownik, Joseph R. Testa, Marian H. Harris, John P. Kanki, A. Thomas Look

    Publicat 2011
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  7. 7
    Treatment outcomes in patients with VEXAS syndrome: a retrospective cohort study

    Treatment outcomes in patients with VEXAS syndrome: a retrospective cohort study per Adam Al‐Hakim, Roochi Trikha, Ei Ei Phyu Htut, Onima Chowdhury, Calman A MacLennan, Ashlyn Chee, Arvind Kaul, James A. Poulter, Catherine Cargo, James M S Wason, Sammiya Ahmed, Tanya Basu, Sukanya Gogoi, James Galloway, Stephen Jolles, Anoop Mistry, Elspeth Payne, Rachel Tattersall, Taryn Youngstein, Helen J. Lachmann, Austin Kulasekararaj, Sinisa Savic

    Publicat 2025
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  8. 8
    Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis

    Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis per Marcela A. Ferrada, Sinisa Savic, Daniela Ospina Cardona, Jason C. Collins, Hugh Alessi, Fernanda Gutierrez‐Rodrigues, Dinesh Babu Uthaya Kumar, Lorena Wilson, Wendy Goodspeed, James S. Topilow, Julie J. Paik, James A. Poulter, Tanaz A. Kermani, Matthew J. Koster, Kenneth J. Warrington, Catherine Cargo, Rachel Tattersall, C.J. Duncan, Anna Cantor, Patrycja Hoffmann, Elspeth Payne, Hanna Bonnekoh, Karoline Krause, Edward W. Cowen, Katherine R. Calvo, Bhavisha A. Patel, Amanda K. Ombrello, Daniel L. Kastner, Neal S. Young, Achim Werner, Peter C. Grayson, David B. Beck

    Publicat 2022
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  9. 9
    The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants

    The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants per Ana Rio‐Machín, Tom Vulliamy, Nele Hug, Amanda J. Walne, Kiran Tawana, Shirleny Cardoso, Alicia Ellison, Nikolas Pontikos, Jun Wang, Hemanth Tummala, Ahad Al Seraihi, Jenna Alnajar, Findlay Bewicke‐Copley, Hannah Armes, Michael J. Barnett, Adrian Bloor, Csaba Bödör, David Bowen, Pierre Fenaux, Andrew Green, Andrew R. Hallahan, Henrik Hjorth‐Hansen, Upal Hossain, Sally Killick, Sarah Lawson, Mark Layton, Alison Male, Judith Marsh, Priyanka Mehta, Rogier Mous, Josep Nomdedéu, Carolyn Owen, Jiří Pavlů, Elspeth Payne, Rachel Protheroe, Claude Preudhomme, Núria Pujol‐Moix, Aline Renneville, Nigel H. Russell, Anand Saggar, Gabriela Sciuccati, David Taussig, Cynthia L. Toze, Anne Uyttebroeck, Peter Vandenberghe, Brigitte Schlegelberger, Tim Ripperger, Doris Steinemann, John K. Wu, Joanne Mason, Paula Page, Susanna Akiki, Kim Reay, Jamie Cavenagh, Vincent Plagnol, Javier F. Cáceres, Jude Fitzgibbon, Inderjeet Dokal

    Publicat 2020
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