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Torsten Haferlach

Showing results (261-270 of 597) with videos related to

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British Journal of Haematology|April 14, 2026
Genetic characterization of AML defined by differentiation shows a high frequency of DDX41 mutationsSandra Huber, Christoph Kornauth, Stephan Hutter, et al.
British Journal of Haematology|August 30, 2002
CD40L stimulation enhances the ability of conventional metaphase cytogenetics to detect chromosome aberrations in B-cell chronic lymphocytic leukaemia cellsRaymund Buhmann, Christian Kurzeder, Jutta Rehklau, et al.
Genes, Chromosomes & Cancer|August 31, 2002
Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISHClaudia Schoch, Torsten Haferlach, Sabina Bursch, et al.
Blood Neoplasia|September 23, 2025
<i>SRSF2</i> mutations in CCUS, MDS and AML: a cross-entity studySandra Huber, Sarah Ochmann, Stephan Hutter, et al.
Leukemia Research|May 6, 2009
Characterization of a new myeloid leukemia cell line with normal cytogenetics (CG-SH)Reinhold Munker, Mary Lowery Nordberg, Diana Veillon, et al.
Genes, Chromosomes & Cancer|March 25, 2026
Myeloid Neoplasms With a t(5;12)(q31;p13) and an Associated ETV6::ACSL6 Gene Fusion Are Diagnostically Challenging and Have a Poor PrognosisBettina Balk, Marietta Truger, Wencke Walter, et al.
Genes, Chromosomes & Cancer|June 17, 2010
Toward a comprehensive prognostic scoring system in chronic lymphocytic leukemia based on a combination of genetic parametersClaudia Haferlach, Frank Dicker, Tamara Weiss, et al.
Leukemia|June 19, 2019
DNMT3A mutations are over-represented in young adults with NPM1 mutated AML and prompt a distinct co-mutational patternLuca Vincenzo Cappelli, Manja Meggendorfer, Frank Dicker, et al.
Acta Haematologica|September 29, 2011
Unusual course of myelodysplastic syndrome with presumed familial originUlrike Bacher, Sunday Ocheni, Philippe Schafhausen, et al.
Leukemia|January 10, 2019
IDH1-R132 changes vary according to NPM1 and other mutations status in AMLBrunangelo Falini, Orietta Spinelli, Manja Meggendorfer, et al.
Pageof 60

Showing results (261-270 of 597) with videos related to

Sort By:
Pageof 60
British Journal of Haematology|April 14, 2026
Genetic characterization of AML defined by differentiation shows a high frequency of DDX41 mutationsSandra Huber, Christoph Kornauth, Stephan Hutter, et al.
British Journal of Haematology|August 30, 2002
CD40L stimulation enhances the ability of conventional metaphase cytogenetics to detect chromosome aberrations in B-cell chronic lymphocytic leukaemia cellsRaymund Buhmann, Christian Kurzeder, Jutta Rehklau, et al.
Genes, Chromosomes & Cancer|August 31, 2002
Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISHClaudia Schoch, Torsten Haferlach, Sabina Bursch, et al.
Blood Neoplasia|September 23, 2025
<i>SRSF2</i> mutations in CCUS, MDS and AML: a cross-entity studySandra Huber, Sarah Ochmann, Stephan Hutter, et al.
Leukemia Research|May 6, 2009
Characterization of a new myeloid leukemia cell line with normal cytogenetics (CG-SH)Reinhold Munker, Mary Lowery Nordberg, Diana Veillon, et al.
Genes, Chromosomes & Cancer|March 25, 2026
Myeloid Neoplasms With a t(5;12)(q31;p13) and an Associated ETV6::ACSL6 Gene Fusion Are Diagnostically Challenging and Have a Poor PrognosisBettina Balk, Marietta Truger, Wencke Walter, et al.
Genes, Chromosomes & Cancer|June 17, 2010
Toward a comprehensive prognostic scoring system in chronic lymphocytic leukemia based on a combination of genetic parametersClaudia Haferlach, Frank Dicker, Tamara Weiss, et al.
Leukemia|June 19, 2019
DNMT3A mutations are over-represented in young adults with NPM1 mutated AML and prompt a distinct co-mutational patternLuca Vincenzo Cappelli, Manja Meggendorfer, Frank Dicker, et al.
Acta Haematologica|September 29, 2011
Unusual course of myelodysplastic syndrome with presumed familial originUlrike Bacher, Sunday Ocheni, Philippe Schafhausen, et al.
Leukemia|January 10, 2019
IDH1-R132 changes vary according to NPM1 and other mutations status in AMLBrunangelo Falini, Orietta Spinelli, Manja Meggendorfer, et al.
Pageof 60