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Showing results (351-360 of 427) with videos related to

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Journal of Proteome Research|October 7, 2006
An integrated metabonomic approach to describe temporal metabolic disregulation induced in the rat by the model hepatotoxin allyl formateIvan K S Yap, T Andrew Clayton, Huiru Tang, et al.
Plant, Cell & Environment|June 12, 2024
Long-term trend and interannual variation in evapotranspiration of a young temperate Douglas-fir stand over 2002-2022 reveals the impacts of climate changeXinhao Li, T Andrew Black, Tianshan Zha, et al.
Molecular Genetics and Metabolism|June 26, 2012
Recurrent pancreatitis in ornithine transcarbamylase deficiencyCarlos E Prada, Ajay Kaul, Robert J Hopkin, et al.
Molecular Genetics and Metabolism Reports|October 11, 2016
Stability is maintained in adults with Gaucher disease type 1 switched from velaglucerase alfa to eliglustat or imiglucerase: A sub-analysis of the eliglustat ENCORE trialRebecca Pleat, Timothy M Cox, T Andrew Burrow, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 13, 2006
Number of CD4+ cells and location of forkhead box protein P3-positive cells in diagnostic follicular lymphoma tissue microarrays correlates with outcomeAbigail M Lee, Andrew J Clear, Maria Calaminici, et al.
British Journal of Haematology|January 14, 2004
Reliable detection of clonal IgH/Bcl2 MBR rearrangement in follicular lymphoma: methodology and clinical significanceSameena Iqbal, Michael J R Jenner, Karin E Summers, 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.
British Journal of Haematology|July 26, 2002
The relative role of peripheral blood and bone marrow for monitoring molecular evidence of disease in follicular lymphoma by quantitative real-time polymerase chain reactionKarin E Summers, Andrew J Davies, Janet Matthews, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 2, 2008
Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working PartyPriya Virappane, Rosemary Gale, Robert Hills, et al.
Blood|January 8, 2010
Leukemia-initiating cells from some acute myeloid leukemia patients with mutated nucleophosmin reside in the CD34(-) fractionDavid C Taussig, Jacques Vargaftig, Farideh Miraki-Moud, et al.
Pageof 43

Showing results (351-360 of 427) with videos related to

Sort By:
Pageof 43
Journal of Proteome Research|October 7, 2006
An integrated metabonomic approach to describe temporal metabolic disregulation induced in the rat by the model hepatotoxin allyl formateIvan K S Yap, T Andrew Clayton, Huiru Tang, et al.
Plant, Cell & Environment|June 12, 2024
Long-term trend and interannual variation in evapotranspiration of a young temperate Douglas-fir stand over 2002-2022 reveals the impacts of climate changeXinhao Li, T Andrew Black, Tianshan Zha, et al.
Molecular Genetics and Metabolism|June 26, 2012
Recurrent pancreatitis in ornithine transcarbamylase deficiencyCarlos E Prada, Ajay Kaul, Robert J Hopkin, et al.
Molecular Genetics and Metabolism Reports|October 11, 2016
Stability is maintained in adults with Gaucher disease type 1 switched from velaglucerase alfa to eliglustat or imiglucerase: A sub-analysis of the eliglustat ENCORE trialRebecca Pleat, Timothy M Cox, T Andrew Burrow, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 13, 2006
Number of CD4+ cells and location of forkhead box protein P3-positive cells in diagnostic follicular lymphoma tissue microarrays correlates with outcomeAbigail M Lee, Andrew J Clear, Maria Calaminici, et al.
British Journal of Haematology|January 14, 2004
Reliable detection of clonal IgH/Bcl2 MBR rearrangement in follicular lymphoma: methodology and clinical significanceSameena Iqbal, Michael J R Jenner, Karin E Summers, 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.
British Journal of Haematology|July 26, 2002
The relative role of peripheral blood and bone marrow for monitoring molecular evidence of disease in follicular lymphoma by quantitative real-time polymerase chain reactionKarin E Summers, Andrew J Davies, Janet Matthews, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 2, 2008
Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working PartyPriya Virappane, Rosemary Gale, Robert Hills, et al.
Blood|January 8, 2010
Leukemia-initiating cells from some acute myeloid leukemia patients with mutated nucleophosmin reside in the CD34(-) fractionDavid C Taussig, Jacques Vargaftig, Farideh Miraki-Moud, et al.
Pageof 43