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British Journal of Haematology
|
July 24, 2010
Biological and clinical characterization of recurrent 14q deletions in CLL and other mature B-cell neoplasms
Lena Reindl, Ulrike Bacher, Frank Dicker, et al.
Blood
|
December 15, 2010
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis
Susanne Schnittger, Frank Dicker, Wolfgang Kern, et al.
Blood Advances
|
November 21, 2018
<i>NPM1</i> mutated AML can relapse with wild-type <i>NPM1</i>: persistent clonal hematopoiesis can drive relapse
Alexander Höllein, Manja Meggendorfer, Frank Dicker, et al.
British Journal of Haematology
|
July 22, 2014
Quantification of rare NPM1 mutation subtypes by digital PCR
Ulrike Bacher, Frank Dicker, Claudia Haferlach, et al.
Haematologica
|
February 6, 2014
Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases
Annette Fasan, Claudia Haferlach, Alexander Kohlmann, et al.
British Journal of Haematology
|
August 20, 2014
Accumulation of adverse prognostic markers worsens prognosis in chronic lymphocytic leukaemia
Marietta S Truger, Sabine Jeromin, Sandra Weissmann, 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.
Blood
|
October 30, 2004
ZAP-70 directly enhances IgM signaling in chronic lymphocytic leukemia
Liguang Chen, John Apgar, Lang Huynh, et al.
Blood
|
February 15, 2012
Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia
Susanne Schnittger, Ulrike Bacher, Torsten Haferlach, et al.
Genes, Chromosomes & Cancer
|
June 17, 2010
Toward a comprehensive prognostic scoring system in chronic lymphocytic leukemia based on a combination of genetic parameters
Claudia Haferlach, Frank Dicker, Tamara Weiss, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
British Journal of Haematology
|
July 24, 2010
Biological and clinical characterization of recurrent 14q deletions in CLL and other mature B-cell neoplasms
Lena Reindl, Ulrike Bacher, Frank Dicker, et al.
Blood
|
December 15, 2010
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis
Susanne Schnittger, Frank Dicker, Wolfgang Kern, et al.
Blood Advances
|
November 21, 2018
<i>NPM1</i> mutated AML can relapse with wild-type <i>NPM1</i>: persistent clonal hematopoiesis can drive relapse
Alexander Höllein, Manja Meggendorfer, Frank Dicker, et al.
British Journal of Haematology
|
July 22, 2014
Quantification of rare NPM1 mutation subtypes by digital PCR
Ulrike Bacher, Frank Dicker, Claudia Haferlach, et al.
Haematologica
|
February 6, 2014
Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases
Annette Fasan, Claudia Haferlach, Alexander Kohlmann, et al.
British Journal of Haematology
|
August 20, 2014
Accumulation of adverse prognostic markers worsens prognosis in chronic lymphocytic leukaemia
Marietta S Truger, Sabine Jeromin, Sandra Weissmann, 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.
Blood
|
October 30, 2004
ZAP-70 directly enhances IgM signaling in chronic lymphocytic leukemia
Liguang Chen, John Apgar, Lang Huynh, et al.
Blood
|
February 15, 2012
Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia
Susanne Schnittger, Ulrike Bacher, Torsten Haferlach, et al.
Genes, Chromosomes & Cancer
|
June 17, 2010
Toward a comprehensive prognostic scoring system in chronic lymphocytic leukemia based on a combination of genetic parameters
Claudia Haferlach, Frank Dicker, Tamara Weiss, et al.
Page
of 5