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E Stevenson

Showing results (461-470 of 550) with videos related to

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Human Molecular Genetics|April 4, 2017
MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expressionLise-Marie Donnio, Baptiste Bidon, Satoru Hashimoto, et al.
Pediatric Blood & Cancer|April 1, 2018
Phase I trial of the mTOR inhibitor everolimus in combination with multi-agent chemotherapy in relapsed childhood acute lymphoblastic leukemiaAndrew E Place, Yana Pikman, Kristen E Stevenson, et al.
Leukemia|December 18, 2009
Long-term results of Dana-Farber Cancer Institute ALL Consortium protocols for children with newly diagnosed acute lymphoblastic leukemia (1985-2000)L B Silverman, K E Stevenson, J E O'Brien, et al.
Water Research|March 12, 2025
Seasonally recurring patterns of dominant Crenothrix spp. in a European alluvial drinking water well: Significance and potential indicator roleSophia D Steinbacher, Katarina Priselac, Wolfgang Kandler, et al.
Cancer|May 13, 2016
Phase 2 study of intensified chemotherapy and allogeneic hematopoietic stem cell transplantation for older patients with acute lymphoblastic leukemiaAmir T Fathi, Daniel J DeAngelo, Kristen E Stevenson, et al.
Molecular Genetics and Metabolism|May 5, 2016
New observation of sialuria prompts detection of liver tumor in previously reported patientNeena L Champaigne, Jules G Leroy, Priya S Kishnani, et al.
Angewandte Chemie (International Ed. in English)|December 10, 2023
Quantitative N- or C-Terminal Labelling of Proteins with Unactivated Peptides by Use of Sortases and a d-AminopeptidaseZoe L P Arnott, Holly E Morgan, Kristian Hollingsworth, et al.
Blood|June 28, 2019
Multicenter analysis of outcomes in blastic plasmacytoid dendritic cell neoplasm offers a pretargeted therapy benchmarkJustin Taylor, Michael Haddadin, Vivek A Upadhyay, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
Genome Research|April 4, 2008
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repairMarijke Bauters, Hilde Van Esch, Michael J Friez, et al.
Pageof 55

Showing results (461-470 of 550) with videos related to

Sort By:
Pageof 55
Human Molecular Genetics|April 4, 2017
MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expressionLise-Marie Donnio, Baptiste Bidon, Satoru Hashimoto, et al.
Pediatric Blood & Cancer|April 1, 2018
Phase I trial of the mTOR inhibitor everolimus in combination with multi-agent chemotherapy in relapsed childhood acute lymphoblastic leukemiaAndrew E Place, Yana Pikman, Kristen E Stevenson, et al.
Leukemia|December 18, 2009
Long-term results of Dana-Farber Cancer Institute ALL Consortium protocols for children with newly diagnosed acute lymphoblastic leukemia (1985-2000)L B Silverman, K E Stevenson, J E O'Brien, et al.
Water Research|March 12, 2025
Seasonally recurring patterns of dominant Crenothrix spp. in a European alluvial drinking water well: Significance and potential indicator roleSophia D Steinbacher, Katarina Priselac, Wolfgang Kandler, et al.
Cancer|May 13, 2016
Phase 2 study of intensified chemotherapy and allogeneic hematopoietic stem cell transplantation for older patients with acute lymphoblastic leukemiaAmir T Fathi, Daniel J DeAngelo, Kristen E Stevenson, et al.
Molecular Genetics and Metabolism|May 5, 2016
New observation of sialuria prompts detection of liver tumor in previously reported patientNeena L Champaigne, Jules G Leroy, Priya S Kishnani, et al.
Angewandte Chemie (International Ed. in English)|December 10, 2023
Quantitative N- or C-Terminal Labelling of Proteins with Unactivated Peptides by Use of Sortases and a d-AminopeptidaseZoe L P Arnott, Holly E Morgan, Kristian Hollingsworth, et al.
Blood|June 28, 2019
Multicenter analysis of outcomes in blastic plasmacytoid dendritic cell neoplasm offers a pretargeted therapy benchmarkJustin Taylor, Michael Haddadin, Vivek A Upadhyay, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
Genome Research|April 4, 2008
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repairMarijke Bauters, Hilde Van Esch, Michael J Friez, et al.
Pageof 55