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Leukemia
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October 15, 2005
A rare case of acute myeloid leukemia with a CHIC2-ETV6 fusiongen and multiple other molecular aberrations
F 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 markers
M 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 transplantation
P Dreger, M Suttorp, T Haferlach, et al.
British Journal of Cancer
|
December 6, 2006
Gene expression profiling for the diagnosis of acute leukaemia
T Haferlach, A Kohlmann, U Bacher, et al.
Leukemia
|
May 4, 2011
Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemia
S 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 treatment
S 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 leukemia
C 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 treatment
C Haferlach, U Bacher, S Schnittger, et al.
Leukemia
|
December 5, 2012
STAT3 mutations are highly specific for large granular lymphocytic leukemia
A Fasan, W Kern, V Grossmann, et al.
Leukemia
|
June 11, 2016
Subtype-specific patterns of molecular mutations in acute myeloid leukemia
D Rose, T Haferlach, S Schnittger, et al.
Page
of 20
Search research articles
Search
Showing results (41-50 of 195) with videos related to
Sort By:
Page
of 20
Leukemia
|
October 15, 2005
A rare case of acute myeloid leukemia with a CHIC2-ETV6 fusiongen and multiple other molecular aberrations
F 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 markers
M 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 transplantation
P Dreger, M Suttorp, T Haferlach, et al.
British Journal of Cancer
|
December 6, 2006
Gene expression profiling for the diagnosis of acute leukaemia
T Haferlach, A Kohlmann, U Bacher, et al.
Leukemia
|
May 4, 2011
Prognostic impact of FLT3-ITD load in NPM1 mutated acute myeloid leukemia
S 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 treatment
S 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 leukemia
C 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 treatment
C Haferlach, U Bacher, S Schnittger, et al.
Leukemia
|
December 5, 2012
STAT3 mutations are highly specific for large granular lymphocytic leukemia
A Fasan, W Kern, V Grossmann, et al.
Leukemia
|
June 11, 2016
Subtype-specific patterns of molecular mutations in acute myeloid leukemia
D Rose, T Haferlach, S Schnittger, et al.
Page
of 20