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Manoj Raghavan

Showing results (31-40 of 78) with videos related to

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Plos One|April 6, 2012
Genome wide analysis of acute myeloid leukemia reveal leukemia specific methylome and subtype specific hypomethylation of repeatsMarwa H Saied, Jacek Marzec, Sabah Khalid, et al.
Clinical Neurophysiology Practice|April 20, 2026
The frequency-dependent effects of primary hand motor cortex stimulation on volitional finger movementLéon Taquet, Brian J Conway, Timothy F Boerger, et al.
Genes, Chromosomes & Cancer|May 29, 2008
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemiaManu Gupta, Manoj Raghavan, Rosemary E Gale, et al.
Cancer Immunology Research|March 19, 2017
Identification of Glycopeptides as Posttranslationally Modified Neoantigens in LeukemiaStacy A Malaker, Sarah A Penny, Lora G Steadman, et al.
British Journal of Haematology|August 3, 2022
Phase Ib study of eltrombopag and azacitidine in patients with high-risk myelodysplastic syndromes and related disorders (the ELASTIC study)Alexander Sternberg, Rebecca Boucher, Helen Chantal Coulthard, et al.
BJC Reports|November 11, 2025
Introduction of whole genome sequencing as NHS standard of care for glioma patients in two neurosurgical oncology centres: West MidlandsVictoria Wykes, Erminia Albanese, Vassili Crispi, et al.
Cell Reports|May 25, 2017
RUNX1-ETO and RUNX1-EVI1 Differentially Reprogram the Chromatin Landscape in t(8;21) and t(3;21) AMLJustin Loke, Salam A Assi, Maria Rosaria Imperato, et al.
Cancer Research|October 6, 2005
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic eventMuy-Teck Teh, Diana Blaydon, Tracy Chaplin, et al.
British Journal of Cancer|October 31, 2024
The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes ProjectElaine Y L Leung, Helen L Robbins, Shafquat Zaman, et al.
Blood|May 21, 2008
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemiaManoj Raghavan, Lan-Lan Smith, Debra M Lillington, et al.
Pageof 8

Showing results (31-40 of 78) with videos related to

Sort By:
Pageof 8
Plos One|April 6, 2012
Genome wide analysis of acute myeloid leukemia reveal leukemia specific methylome and subtype specific hypomethylation of repeatsMarwa H Saied, Jacek Marzec, Sabah Khalid, et al.
Clinical Neurophysiology Practice|April 20, 2026
The frequency-dependent effects of primary hand motor cortex stimulation on volitional finger movementLéon Taquet, Brian J Conway, Timothy F Boerger, et al.
Genes, Chromosomes & Cancer|May 29, 2008
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemiaManu Gupta, Manoj Raghavan, Rosemary E Gale, et al.
Cancer Immunology Research|March 19, 2017
Identification of Glycopeptides as Posttranslationally Modified Neoantigens in LeukemiaStacy A Malaker, Sarah A Penny, Lora G Steadman, et al.
British Journal of Haematology|August 3, 2022
Phase Ib study of eltrombopag and azacitidine in patients with high-risk myelodysplastic syndromes and related disorders (the ELASTIC study)Alexander Sternberg, Rebecca Boucher, Helen Chantal Coulthard, et al.
BJC Reports|November 11, 2025
Introduction of whole genome sequencing as NHS standard of care for glioma patients in two neurosurgical oncology centres: West MidlandsVictoria Wykes, Erminia Albanese, Vassili Crispi, et al.
Cell Reports|May 25, 2017
RUNX1-ETO and RUNX1-EVI1 Differentially Reprogram the Chromatin Landscape in t(8;21) and t(3;21) AMLJustin Loke, Salam A Assi, Maria Rosaria Imperato, et al.
Cancer Research|October 6, 2005
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic eventMuy-Teck Teh, Diana Blaydon, Tracy Chaplin, et al.
British Journal of Cancer|October 31, 2024
The potential clinical utility of Whole Genome Sequencing for patients with cancer: evaluation of a regional implementation of the 100,000 Genomes ProjectElaine Y L Leung, Helen L Robbins, Shafquat Zaman, et al.
Blood|May 21, 2008
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemiaManoj Raghavan, Lan-Lan Smith, Debra M Lillington, et al.
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