Torthaí cuardaigh - Manoj Raghavan

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  1. 1
    Nonseizure SUDEP: Sudden unexpected death in epilepsy without preceding epileptic seizures

    Nonseizure SUDEP: Sudden unexpected death in epilepsy without preceding epileptic seizures de réir Samden Lhatoo, Maromi Nei, Manoj Raghavan, Michael R. Sperling, Bilal Zonjy, Nuria Lacuey, Orrin Devinsky

    Foilsithe / Cruthaithe 2016
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  2. 2
    A comparison of two fMRI methods for predicting verbal memory decline after left temporal lobectomy: Language lateralization versus hippocampal activation asymmetry

    A comparison of two fMRI methods for predicting verbal memory decline after left temporal lobectomy: Language lateralization versus hippocampal activation asymmetry de réir Jeffrey R. Binder, Sara J. Swanson, David S. Sabsevitz, Thomas A. Hammeke, Manoj Raghavan, Wade M. Mueller

    Foilsithe / Cruthaithe 2009
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  3. 3
    Use of preoperative functional MRI to predict verbal memory decline after temporal lobe epilepsy surgery

    Use of preoperative functional MRI to predict verbal memory decline after temporal lobe epilepsy surgery de réir Jeffrey R. Binder, David S. Sabsevitz, Sara J. Swanson, Thomas A. Hammeke, Manoj Raghavan, Wade M. Mueller

    Foilsithe / Cruthaithe 2008
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  4. 4
    Language lateralization by f<scp>MRI</scp>and Wada testing in 229 patients with epilepsy: Rates and predictors of discordance

    Language lateralization by f<scp>MRI</scp>and Wada testing in 229 patients with epilepsy: Rates and predictors of discordance de réir Julie K. Janecek, Sara J. Swanson, David S. Sabsevitz, Thomas A. Hammeke, Manoj Raghavan, Megan Rozman, Jeffrey R. Binder

    Foilsithe / Cruthaithe 2013
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  5. 5
    Genome-Wide Single Nucleotide Polymorphism Analysis Reveals Frequent Partial Uniparental Disomy Due to Somatic Recombination in Acute Myeloid Leukemias

    Genome-Wide Single Nucleotide Polymorphism Analysis Reveals Frequent Partial Uniparental Disomy Due to Somatic Recombination in Acute Myeloid Leukemias de réir Manoj Raghavan, Debra M. Lillington, Spyros Skoulakis, Silvana Debernardi, Tracy Chaplin, Nicola Foot, Tim Lister, Bryan D. Young

    Foilsithe / Cruthaithe 2005
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  6. 6
    Naming outcome prediction in patients with discordant Wada and fMRI language lateralization

    Naming outcome prediction in patients with discordant Wada and fMRI language lateralization de réir Julie K. Janecek, Sara J. Swanson, David S. Sabsevitz, Thomas A. Hammeke, Manoj Raghavan, Wade M. Mueller, Jeffrey R. Binder

    Foilsithe / Cruthaithe 2013
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  7. 7
    Association between Acquired Uniparental Disomy and Homozygous Gene Mutation in Acute Myeloid Leukemias

    Association between Acquired Uniparental Disomy and Homozygous Gene Mutation in Acute Myeloid Leukemias de réir Jude Fitzgibbon, Lan‐Lan Smith, Manoj Raghavan, Matthew Smith, Silvana Debernardi, Spyros Skoulakis, Debra M. Lillington, Tim Lister, Bryan D. Young

    Foilsithe / Cruthaithe 2005
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  8. 8
    Identification of Glycopeptides as Posttranslationally Modified Neoantigens in Leukemia

    Identification of Glycopeptides as Posttranslationally Modified Neoantigens in Leukemia de réir Stacy A. Malaker, Sarah Penny, Lora Steadman, Paisley T. Myers, Justin Loke, Manoj Raghavan, Dina L. Bai, Jeffrey Shabanowitz, Donald F. Hunt, Mark Cobbold

    Foilsithe / Cruthaithe 2017
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  9. 9
    Genome Wide Analysis of Acute Myeloid Leukemia Reveal Leukemia Specific Methylome and Subtype Specific Hypomethylation of Repeats

    Genome Wide Analysis of Acute Myeloid Leukemia Reveal Leukemia Specific Methylome and Subtype Specific Hypomethylation of Repeats de réir Marwa H. Saied, Jacek Marzec, Sabah Khalid, Paul Smith, Thomas A. Down, Vardhman K. Rakyan, Gerard J. Molloy, Manoj Raghavan, Silvana Debernardi, Bryan D. Young

    Foilsithe / Cruthaithe 2012
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  10. 10
    Genomewide Single Nucleotide Polymorphism Microarray Mapping in Basal Cell Carcinomas Unveils Uniparental Disomy as a Key Somatic Event

    Genomewide Single Nucleotide Polymorphism Microarray Mapping in Basal Cell Carcinomas Unveils Uniparental Disomy as a Key Somatic Event de réir Muy‐Teck Teh, Diana C. Blaydon, Tracy Chaplin, Nicola Foot, Spyros Skoulakis, Manoj Raghavan, Catherine Harwood, Charlotte M. Proby, Michael P. Philpott, Bryan D. Young, David P. Kelsell

    Foilsithe / Cruthaithe 2005
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  11. 11
    RUNX1-ETO and RUNX1-EVI1 Differentially Reprogram the Chromatin Landscape in t(8;21) and t(3;21) AML

    RUNX1-ETO and RUNX1-EVI1 Differentially Reprogram the Chromatin Landscape in t(8;21) and t(3;21) AML de réir Justin Loke, Salam A. Assi, Maria Rosaria Imperato, Anetta Ptasinska, Pierre Cauchy, Yura Grabovska, N Martinez Soria, Manoj Raghavan, Ruud Delwel, Peter N. Cockerill, Olaf Heidenreich, Constanze Bonifer

    Foilsithe / Cruthaithe 2017
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  12. 12
    Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia

    Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia de réir Manoj Raghavan, Lan‐Lan Smith, Debra M. Lillington, Tracy Chaplin, Ιoannis Kakkas, Gael Molloy, Claude Chelala, Jean‐Baptiste Cazier, James D. Cavenagh, Jude Fitzgibbon, Tim Lister, Bryan D. Young

    Foilsithe / Cruthaithe 2008
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  13. 13
    Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21

    Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 de réir Jonathan C. Strefford, Frederik W. van Delft, Hazel M. Robinson, Helen Worley, Olga Yiannikouris, Rebecca R. Selzer, Todd Richmond, Ian Hann, Anthony Bellotti, Manoj Raghavan, Bryan D. Young, Vaskar Saha, Christine J. Harrison

    Foilsithe / Cruthaithe 2006
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  14. 14
    Mutational analysis of disease relapse in patients allografted for acute myeloid leukemia

    Mutational analysis of disease relapse in patients allografted for acute myeloid leukemia de réir Lynn Quek, Paul Ferguson, Marlen Metzner, Ikhlaaq Ahmed, Alison Kennedy, Catherine Garnett, Sally Jeffries, Claudia Walter, Kim Piechocki, Adele Timbs, Robert Danby, Manoj Raghavan, Andrew Peniket, Mike Griffiths, Andrew Bacon, Janice Ward, Keith Wheatley, Paresh Vyas, Charles Craddock

    Foilsithe / Cruthaithe 2016
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  15. 15
    Azacitidine augments expansion of regulatory T cells after allogeneic stem cell transplantation in patients with acute myeloid leukemia (AML)

    Azacitidine augments expansion of regulatory T cells after allogeneic stem cell transplantation in patients with acute myeloid leukemia (AML) de réir Oliver Goodyear, Mike Dennis, Nadira Jilani, Justin Loke, Shamyla Siddique, Gordon B. Ryan, Jane Nunnick, Rahela Khanum, Manoj Raghavan, Mark Cook, John A. Snowden, Mike Griffiths, Nigel H. Russell, John Yin, Charles Crawley, Gordon Cook, Paresh Vyas, Paul Moss, Ram Malladi, Charles Craddock

    Foilsithe / Cruthaithe 2012
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  16. 16
    Cognitive slowing and its underlying neurobiology in temporal lobe epilepsy

    Cognitive slowing and its underlying neurobiology in temporal lobe epilepsy de réir Gyujoon Hwang, Kevin Dabbs, Lisa L. Conant, Veena A. Nair, Jed Mathis, Dace Almane, Andrew S. Nencka, Rasmus M. Birn, Colin Humphries, Manoj Raghavan, Edgar A. DeYoe, Aaron F. Struck, Rama Maganti, Jeffrey R. Binder, M. Elizabeth Meyerand, Vivek Prabhakaran, Bruce P. Hermann

    Foilsithe / Cruthaithe 2019
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  17. 17
    Leukemic stem cells activate lineage inappropriate signalling pathways to promote their growth

    Leukemic stem cells activate lineage inappropriate signalling pathways to promote their growth de réir Sophie G. Kellaway, Sandeep Potluri, Peter Keane, Helen J. Blair, Luke Ames, Alice Worker, Paulynn Suyin Chin, Anetta Ptasinska, Polina K. Derevyanko, Assunta Adamo, Daniel Coleman, Naeem Khan, Salam A. Assi, Anja Krippner‐Heidenreich, Manoj Raghavan, Peter N. Cockerill, Olaf Heidenreich, Constanze Bonifer

    Foilsithe / Cruthaithe 2024
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  18. 18
    Chronic FLT3-ITD Signaling in Acute Myeloid Leukemia Is Connected to a Specific Chromatin Signature

    Chronic FLT3-ITD Signaling in Acute Myeloid Leukemia Is Connected to a Specific Chromatin Signature de réir Pierre Cauchy, Sally James, Joaquin Zacarías-Cabeza, Anetta Ptasinska, Maria Rosaria Imperato, Salam A. Assi, Jason Piper, Martina Canestraro, Maarten Hoogenkamp, Manoj Raghavan, Justin Loke, Susanna Akiki, Samuel Clokie, Stephen J. Richards, David R. Westhead, Mike Griffiths, Sascha Ott, Constanze Bonifer, Peter N. Cockerill

    Foilsithe / Cruthaithe 2015
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  19. 19
    Pharmacological inhibition of RAS overcomes FLT3 inhibitor resistance in FLT3-ITD+ AML through AP-1 and RUNX1

    Pharmacological inhibition of RAS overcomes FLT3 inhibitor resistance in FLT3-ITD+ AML through AP-1 and RUNX1 de réir Daniel Coleman, Peter Keane, Paulynn Suyin Chin, Luke Ames, Sophie G. Kellaway, Helen Blair, Naeem Khan, James D. Griffin, Elizabeth A. Holmes, Alexander Maytum, Sandeep Potluri, Lara Strate, Kinga Koscielniak, Manoj Raghavan, John H. Bushweller, Olaf Heidenreich, Terry Rabbitts, Peter N. Cockerill, Constanze Bonifer

    Foilsithe / Cruthaithe 2024
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  20. 20
    Outcome of Azacitidine Therapy in Acute Myeloid Leukemia Is not Improved by Concurrent Vorinostat Therapy but Is Predicted by a Diagnostic Molecular Signature

    Outcome of Azacitidine Therapy in Acute Myeloid Leukemia Is not Improved by Concurrent Vorinostat Therapy but Is Predicted by a Diagnostic Molecular Signature de réir Charles Craddock, Aimee E. Houlton, Lynn Quek, Paul Ferguson, Emma Gbandi, Corran Roberts, Marlen Metzner, Natalia Garcia-Martin, Alison Kennedy, Angela Hamblin, Manoj Raghavan, Sandeep Nagra, Louise Dudley, Keith Wheatley, Mary Frances McMullin, Srinivas Pillai, Richard Kelly, Shamyla Siddique, Michael Dennis, Jamie Cavenagh, Paresh Vyas

    Foilsithe / Cruthaithe 2017
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