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E Gale

Showing results (331-340 of 361) with videos related to

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Haematologica|March 10, 2018
Prognostic impact of the absence of biallelic deletion at the <i>TRG</i> locus for pediatric patients with T-cell acute lymphoblastic leukemia treated on the Medical Research Council UK Acute Lymphoblastic Leukemia 2003 trialNadine Farah, Amy A Kirkwood, Sunniyat Rahman, et al.
Blood|September 6, 2001
The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trialsP D Kottaridis, R E Gale, M E Frew, et al.
Blood Cancer Journal|October 11, 2017
Prevalence and timing of TP53 mutations in del(17p) myeloma and effect on survivalM Chin, J I Sive, C Allen, et al.
Blood|December 8, 2009
The impact on outcome of the addition of all-trans retinoic acid to intensive chemotherapy in younger patients with nonacute promyelocytic acute myeloid leukemia: overall results and results in genotypic subgroups defined by mutations in NPM1, FLT3, and CEBPAAlan K Burnett, Robert K Hills, Claire Green, et al.
British Medical Journal|August 23, 1975
Epidemiology of rheumatic heart disease in black shcoolchildren of Soweto, JohannesburgM J McLaren, D M Hawkins, H J Koornhof, et al.
Blood|June 29, 2006
Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropeniaPhil J Ancliff, Michael P Blundell, Giles O Cory, et al.
The Journal of Biological Chemistry|November 11, 2008
Side chain oxygenated cholesterol regulates cellular cholesterol homeostasis through direct sterol-membrane interactionsSarah E Gale, Emily J Westover, Nicole Dudley, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 29, 2009
Prognostic implications of NOTCH1 and FBXW7 mutations in adults with T-cell acute lymphoblastic leukemia treated on the MRC UKALLXII/ECOG E2993 protocolMarc R Mansour, Maria L Sulis, Veronique Duke, et al.
Nature Genetics|November 8, 2011
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2M Fernanda Amary, Stephen Damato, Dina Halai, et al.
Blood|March 29, 2013
Impact of isolated germline JAK2V617I mutation on human hematopoiesisAdam J Mead, Onima Chowdhury, Christian Pecquet, et al.
Pageof 37

Showing results (331-340 of 361) with videos related to

Sort By:
Pageof 37
Haematologica|March 10, 2018
Prognostic impact of the absence of biallelic deletion at the <i>TRG</i> locus for pediatric patients with T-cell acute lymphoblastic leukemia treated on the Medical Research Council UK Acute Lymphoblastic Leukemia 2003 trialNadine Farah, Amy A Kirkwood, Sunniyat Rahman, et al.
Blood|September 6, 2001
The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trialsP D Kottaridis, R E Gale, M E Frew, et al.
Blood Cancer Journal|October 11, 2017
Prevalence and timing of TP53 mutations in del(17p) myeloma and effect on survivalM Chin, J I Sive, C Allen, et al.
Blood|December 8, 2009
The impact on outcome of the addition of all-trans retinoic acid to intensive chemotherapy in younger patients with nonacute promyelocytic acute myeloid leukemia: overall results and results in genotypic subgroups defined by mutations in NPM1, FLT3, and CEBPAAlan K Burnett, Robert K Hills, Claire Green, et al.
British Medical Journal|August 23, 1975
Epidemiology of rheumatic heart disease in black shcoolchildren of Soweto, JohannesburgM J McLaren, D M Hawkins, H J Koornhof, et al.
Blood|June 29, 2006
Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropeniaPhil J Ancliff, Michael P Blundell, Giles O Cory, et al.
The Journal of Biological Chemistry|November 11, 2008
Side chain oxygenated cholesterol regulates cellular cholesterol homeostasis through direct sterol-membrane interactionsSarah E Gale, Emily J Westover, Nicole Dudley, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 29, 2009
Prognostic implications of NOTCH1 and FBXW7 mutations in adults with T-cell acute lymphoblastic leukemia treated on the MRC UKALLXII/ECOG E2993 protocolMarc R Mansour, Maria L Sulis, Veronique Duke, et al.
Nature Genetics|November 8, 2011
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2M Fernanda Amary, Stephen Damato, Dina Halai, et al.
Blood|March 29, 2013
Impact of isolated germline JAK2V617I mutation on human hematopoiesisAdam J Mead, Onima Chowdhury, Christian Pecquet, et al.
Pageof 37