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T Haferlach

Showing results (41-50 of 195) with videos related to

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Leukemia|October 15, 2005
A rare case of acute myeloid leukemia with a CHIC2-ETV6 fusiongen and multiple other molecular aberrationsF Kuchenbauer, C Schoch, E Holler, et al.
Leukemia|February 10, 2016
The landscape of myeloid neoplasms with isochromosome 17q discloses a specific mutation profile and is characterized by an accumulation of prognostically adverse molecular markersM Meggendorfer, C Haferlach, M Zenger, et al.
Blood|March 1, 1993
Allogeneic granulocyte colony-stimulating factor-mobilized peripheral blood progenitor cells for treatment of engraftment failure after bone marrow transplantationP Dreger, M Suttorp, T Haferlach, et al.
British Journal of Cancer|December 6, 2006
Gene expression profiling for the diagnosis of acute leukaemiaT Haferlach, A Kohlmann, U Bacher, et al.
Leukemia|May 4, 2011
Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemiaS Schnittger, U Bacher, W Kern, et al.
Leukemia|September 14, 2007
A new case with rare e6a2 BCR-ABL fusion transcript developing two new resistance mutations during imatinib mesylate, which were replaced by T315I after subsequent dasatinib treatmentS Schnittger, U Bacher, W Kern, et al.
Cancer Genetics and Cytogenetics|June 16, 2001
Gain of an isochromosome 5p: a new recurrent chromosome abnormality in acute monoblastic leukemiaC Schoch, S Bursch, W Kern, et al.
Leukemia|October 30, 2009
Similar patterns of chromosome abnormalities in CML occur in addition to the Philadelphia chromosome with or without tyrosine kinase inhibitor treatmentC Haferlach, U Bacher, S Schnittger, et al.
Leukemia|December 5, 2012
STAT3 mutations are highly specific for large granular lymphocytic leukemiaA Fasan, W Kern, V Grossmann, et al.
Leukemia|June 11, 2016
Subtype-specific patterns of molecular mutations in acute myeloid leukemiaD Rose, T Haferlach, S Schnittger, et al.
Pageof 20

Showing results (41-50 of 195) with videos related to

Sort By:
Pageof 20
Leukemia|October 15, 2005
A rare case of acute myeloid leukemia with a CHIC2-ETV6 fusiongen and multiple other molecular aberrationsF Kuchenbauer, C Schoch, E Holler, et al.
Leukemia|February 10, 2016
The landscape of myeloid neoplasms with isochromosome 17q discloses a specific mutation profile and is characterized by an accumulation of prognostically adverse molecular markersM Meggendorfer, C Haferlach, M Zenger, et al.
Blood|March 1, 1993
Allogeneic granulocyte colony-stimulating factor-mobilized peripheral blood progenitor cells for treatment of engraftment failure after bone marrow transplantationP Dreger, M Suttorp, T Haferlach, et al.
British Journal of Cancer|December 6, 2006
Gene expression profiling for the diagnosis of acute leukaemiaT Haferlach, A Kohlmann, U Bacher, et al.
Leukemia|May 4, 2011
Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemiaS Schnittger, U Bacher, W Kern, et al.
Leukemia|September 14, 2007
A new case with rare e6a2 BCR-ABL fusion transcript developing two new resistance mutations during imatinib mesylate, which were replaced by T315I after subsequent dasatinib treatmentS Schnittger, U Bacher, W Kern, et al.
Cancer Genetics and Cytogenetics|June 16, 2001
Gain of an isochromosome 5p: a new recurrent chromosome abnormality in acute monoblastic leukemiaC Schoch, S Bursch, W Kern, et al.
Leukemia|October 30, 2009
Similar patterns of chromosome abnormalities in CML occur in addition to the Philadelphia chromosome with or without tyrosine kinase inhibitor treatmentC Haferlach, U Bacher, S Schnittger, et al.
Leukemia|December 5, 2012
STAT3 mutations are highly specific for large granular lymphocytic leukemiaA Fasan, W Kern, V Grossmann, et al.
Leukemia|June 11, 2016
Subtype-specific patterns of molecular mutations in acute myeloid leukemiaD Rose, T Haferlach, S Schnittger, et al.
Pageof 20