檢索結果 - Daniel Ward
- Showing 1 - 13 results of 13
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Multi-platform whole genome sequencing for tuberculosis clinical and surveillance applications 由 Joseph Thorpe, Waritta Sawaengdee, Daniel Ward, Mónica Campos, Nuanjun Wichukchinda, Boonchai Chaiyasirinroje, Aungkana Thanraka, Jaluporn Chumpol, Jody Phelan, Susana Campino, Surakameth Mahasirimongkol, Taane G. Clark
出版 2024Artigo -
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Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms 由 Joannah Score, Claire Hidalgo-Curtis, Amy V. Jones, Nils Winkelmann, Alison Skinner, Daniel Ward, Katerina Zoi, Thomas Ernst, Frank Stegelmann, Konstanze Döhner, Andrew Chase, Nicholas C.P. Cross
出版 2011Artigo -
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Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B) 由 Chelsea Norman, Luke O’Gorman, Jane Whitney Gibson, Reuben J. Pengelly, Diana Baralle, J. Arjuna Ratnayaka, Helen Griffiths, Matthew Rose‐Zerilli, Megan Ranger, David J. Bunyan, Helena Lee, Rhiannon Page, Tutte Newall, Fatima Shawkat, C. Mattocks, Daniel Ward, Sarah Ennis, Jay Self
出版 2017Artigo -
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Clinical Consensus Statement 由 Joseph K. Han, Scott P. Stringer, Richard M. Rosenfeld, Sanford M. Archer, Dole P. Baker, Seth M. Brown, David R. Edelstein, Stacey T. Gray, Timothy Lian, Erin J Ross, Allen M. Seiden, Michael Setzen, Travis T. Tollefson, P. Daniel Ward, Kevin C. Welch, Sarah K. Wise, Lorraine C. Nnacheta
出版 2015Revisão -
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Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms 由 William Tapper, Amy V. Jones, Róbert Královics, Ashot S. Harutyunyan, Katerina Zoi, William Leung, Anna L. Godfrey, Paola Guglielmelli, Alison Callaway, Daniel Ward, Paula Aranaz, Helen White, Katherine Waghorn, Feng Lin, Andrew Chase, E. Joanna Baxter, Cathy MacLean, Jyoti Nangalia, Edwin Chen, Paul Evans, Michael Short, Andrew Jack, Louise Wallis, David Oscier, Andrew Duncombe, Anna Schuh, Adam J. Mead, Mike Griffiths, Joanne Ewing, Rosemary E. Gale, Susanne Schnittger, Torsten Haferlach, Frank Stegelmann, Konstanze Döhner, Harald Grallert, Konstantin Strauch, Toshiko Tanaka, Stefania Bandinelli, Andreas Giannopoulos, Lisa Pieri, Carmela Mannarelli, Heinz Gisslinger, Giovanni Barosi, Mario Cazzola, Andreas Reiter, Claire Harrison, Peter J. Campbell, Anthony R. Green, Alessandro M. Vannucchi, Nicholas C.P. Cross
出版 2015Artigo -
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De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay 由 Lisenka E.L.M. Vissers, Sreehari Kalvakuri, Elke de Boer, Sinje Geuer, Machteld M. Oud, Inge van Outersterp, Michael Kwint, Melde Witmond, Simone Kersten, D.L. Polla, Dilys Weijers, Amber Begtrup, Kirsty McWalter, Anna Ruiz, Elisabeth Gabau, Jenny E.V. Morton, Christopher Griffith, Karin Weiss, Candace Gamble, James Bartley, Hilary J. Vernon, Kendra Brunet, Claudia Ruivenkamp, Sarina G. Kant, Paul Kruszka, Austin Larson, Alexandra Afenjar, Thierry Billette de Villemeur, Kimberly Nugent, F. Lucy Raymond, Hanka Venselaar, Florence Démurger, Claudia Soler‐Alfonso, Dong Li, Elizabeth Bhoj, Ian Hayes, Nina Powell Hamilton, Ayesha Ahmad, Rachel S. Fisher, Myrthe van den Born, Marjolaine Willems, Arthur Sorlin, Julian Delanne, Sébastien Moutton, Christophe Philippe, Frédéric Tran Mau‐Them, Antonio Vitobello, Himanshu Goel, Lauren Massingham, Chanika Phornphutkul, Jennifer Schwab, Boris Keren, Perrine Charles, Maaike Vreeburg, Lenika De Simone, George Hoganson, Maria Iascone, Donatella Milani, Lucie Evenepoel, Nicole Revençu, Daniel Ward, Kaitlyn Burns, Ian D. Krantz, Sarah E. Raible, Jill R. Murrell, Kathleen H. Wood, Megan T. Cho, Hans van Bokhoven, Maximilian Muenke, Tjitske Kleefstra, Rolf Bodmer, Arjan P.M. de Brouwer
出版 2020Artigo
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