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S Schnittger

Showing results (31-40 of 131) with videos related to

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Leukemia|October 10, 2015
Array-based comparative genomic hybridization detects copy number variations with prognostic relevance in 80% of ALL with normal karyotype or failed chromosome analysisV Mühlbacher, T Haferlach, W Kern, et al.
Leukemia|August 4, 2012
Molecular mutations are prognostically relevant in AML with intermediate risk cytogenetics and aberrant karyotypeU Bacher, T Haferlach, T Alpermann, et al.
European Journal of Immunology|October 1, 1993
Regional sublocalization of the human CD69 gene to chromosome bands 12p12.3-p13.2, the predicted region of the human natural killer cell gene complexS Schnittger, J Hamann, C Dannenberg, 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 14

Showing results (31-40 of 131) with videos related to

Sort By:
Pageof 14
Leukemia|October 10, 2015
Array-based comparative genomic hybridization detects copy number variations with prognostic relevance in 80% of ALL with normal karyotype or failed chromosome analysisV Mühlbacher, T Haferlach, W Kern, et al.
Leukemia|August 4, 2012
Molecular mutations are prognostically relevant in AML with intermediate risk cytogenetics and aberrant karyotypeU Bacher, T Haferlach, T Alpermann, et al.
European Journal of Immunology|October 1, 1993
Regional sublocalization of the human CD69 gene to chromosome bands 12p12.3-p13.2, the predicted region of the human natural killer cell gene complexS Schnittger, J Hamann, C Dannenberg, 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 14