Rezultati pretrage - Patrick Blaney
- Prikaz rezultata 1 – 3 od 3
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1
Copy number signatures predict chromothripsis and clinical outcomes in newly diagnosed multiple myeloma od Kylee Maclachlan, Even H Rustad, Andriy Derkach, Binbin Zheng-Lin, Venkata D. Yellapantula, Benjamin Diamond, Malin Hultcrantz, Bachisio Ziccheddu, Eileen M. Boyle, Patrick Blaney, Niccolò Bolli, Yanming Zhang, Ahmet Doǧan, Alexander M. Lesokhin, Gareth J. Morgan, Ola Landgren, Francesco Maura
Izdano 2021Artigo -
2
Revealing the Impact of Structural Variants in Multiple Myeloma od Even H. Rustad, Venkata Yellapantula, Dominik Głodzik, Kylee Maclachlan, Benjamin Diamond, Eileen M. Boyle, Cody Ashby, Patrick Blaney, Gunes Gundem, Malin Hultcrantz, Daniel Leongamornlert, Nicos Angelopoulos, Luca Agnelli, Daniel Auclair, Yanming Zhang, Ahmet Doǧan, Niccolò Bolli, Elli Papaemmanuil, Kenneth C. Anderson, Philippe Moreau, Hervé Avet‐Loiseau, Nikhil C. Munshi, Jonathan J. Keats, Peter J. Campbell, Gareth J. Morgan, Ola Landgren, Francesco Maura
Izdano 2020Artigo -
3
Accelerated single cell seeding in relapsed multiple myeloma od Heather Landau, Venkata D. Yellapantula, Benjamin Diamond, Even H. Rustad, Kylee Maclachlan, Gunes Gundem, Juan S. Medina-Martínez, Juan Arango Ossa, Max F. Levine, Yangyu Zhou, Rajya Kappagantula, Priscilla Baez, Marc A. Attiyeh, Alvin Makohon‐Moore, Lance Zhang, Eileen M. Boyle, Cody Ashby, Patrick Blaney, Minal Patel, Yanming Zhang, Ahmet Doǧan, David J. Chung, Sergio Giralt, Oscar Lahoud, Jonathan U. Peled, Michael Scordo, Gunjan L. Shah, Hani Hassoun, Neha Korde, Alexander M. Lesokhin, Sydney X. Lu, Sham Mailankody, Urvi A. Shah, Eric L. Smith, Malin Hultcrantz, Gary A. Ulaner, Frits van Rhee, Gareth J. Morgan, Ola Landgren, Elli Papaemmanuil, Christine A. Iacobuzio‐Donahue, Francesco Maura
Izdano 2020Artigo
Alati za pretragu:
Povezani predmeti
Biology
Computational biology
Gene
Genetics
Genome
Multiple myeloma
Chromothripsis
Copy-number variation
DNA
DNA damage
Genome instability
Immunology
Cancer
Cancer research
Exome
Exome sequencing
Internal medicine
Medicine
Mutation
Somatic evolution in cancer
Structural variation
Whole genome sequencing