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Showing results (121-130 of 146) with videos related to

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The British Journal of Radiology|September 16, 2015
Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imagingStavros M Stivaros, Robert Alston, Neville B Wright, et al.
Blood Cells, Molecules & Diseases|May 10, 2003
Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcomeJulia L Clarke, Tom J Vulliamy, David Roper, et al.
Journal of Clinical Pathology|November 6, 2003
Association of acute parvovirus B19 infection with new onset of acute lymphoblastic and myeloblastic leukaemiaJ R Kerr, F Barah, V S Cunniffe, et al.
Oncogene|September 2, 2018
An activating mutation of the NSD2 histone methyltransferase drives oncogenic reprogramming in acute lymphocytic leukemiaAlok Swaroop, Jon A Oyer, Christine M Will, et al.
Glycobiology|January 21, 2014
Differential regulation of oxidative burst by distinct β-glucan-binding receptors and signaling pathways in human peripheral blood mononuclear cellsNandita Bose, Lindsay R Wurst, Anissa S H Chan, et al.
Genes, Chromosomes & Cancer|January 24, 2007
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruptionStefan Meyer, William D Fergusson, Anthony D Whetton, et al.
Familial Cancer|July 26, 2012
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminomaStephanie Smetsers, Joanne Muter, Claire Bristow, et al.
Journal for Immunotherapy of Cancer|December 15, 2023
Immune microenvironment of basal cell carcinoma and tumor regression following combined PD-1/LAG-3 blockadeJulie Stein Deutsch, Jonathan Lai, Kara M Schenk, et al.
Genes, Chromosomes & Cancer|January 13, 2005
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutationsStefan Meyer, William D Fergusson, Anneke B Oostra, et al.
Cell Reports|October 19, 2017
UTX/KDM6A Loss Enhances the Malignant Phenotype of Multiple Myeloma and Sensitizes Cells to EZH2 inhibitionTeresa Ezponda, Daphné Dupéré-Richer, Christine M Will, et al.
Pageof 15

Showing results (121-130 of 146) with videos related to

Sort By:
Pageof 15
The British Journal of Radiology|September 16, 2015
Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imagingStavros M Stivaros, Robert Alston, Neville B Wright, et al.
Blood Cells, Molecules & Diseases|May 10, 2003
Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcomeJulia L Clarke, Tom J Vulliamy, David Roper, et al.
Journal of Clinical Pathology|November 6, 2003
Association of acute parvovirus B19 infection with new onset of acute lymphoblastic and myeloblastic leukaemiaJ R Kerr, F Barah, V S Cunniffe, et al.
Oncogene|September 2, 2018
An activating mutation of the NSD2 histone methyltransferase drives oncogenic reprogramming in acute lymphocytic leukemiaAlok Swaroop, Jon A Oyer, Christine M Will, et al.
Glycobiology|January 21, 2014
Differential regulation of oxidative burst by distinct β-glucan-binding receptors and signaling pathways in human peripheral blood mononuclear cellsNandita Bose, Lindsay R Wurst, Anissa S H Chan, et al.
Genes, Chromosomes & Cancer|January 24, 2007
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruptionStefan Meyer, William D Fergusson, Anthony D Whetton, et al.
Familial Cancer|July 26, 2012
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminomaStephanie Smetsers, Joanne Muter, Claire Bristow, et al.
Journal for Immunotherapy of Cancer|December 15, 2023
Immune microenvironment of basal cell carcinoma and tumor regression following combined PD-1/LAG-3 blockadeJulie Stein Deutsch, Jonathan Lai, Kara M Schenk, et al.
Genes, Chromosomes & Cancer|January 13, 2005
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutationsStefan Meyer, William D Fergusson, Anneke B Oostra, et al.
Cell Reports|October 19, 2017
UTX/KDM6A Loss Enhances the Malignant Phenotype of Multiple Myeloma and Sensitizes Cells to EZH2 inhibitionTeresa Ezponda, Daphné Dupéré-Richer, Christine M Will, et al.
Pageof 15