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Leukemia
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August 21, 2013
Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease
A Kohlmann, N Nadarajah, T Alpermann, et al.
Blood Cancer Journal
|
September 4, 2012
Expression of CEBPA is reduced in RUNX1-mutated acute myeloid leukemia
V Grossmann, U Bacher, A Kohlmann, et al.
Leukemia
|
April 30, 2010
Gene expression profiling in AML with normal karyotype can predict mutations for molecular markers and allows novel insights into perturbed biological pathways
A Kohlmann, L Bullinger, C Thiede, et al.
Leukemia
|
October 12, 2013
SF3B1 mutations correlated to cytogenetics and mutations in NOTCH1, FBXW7, MYD88, XPO1 and TP53 in 1160 untreated CLL patients
S Jeromin, S Weissmann, C Haferlach, et al.
Leukemia
|
February 6, 2009
AML with translocation t(8;16)(p11;p13) demonstrates unique cytomorphological, cytogenetic, molecular and prognostic features
T Haferlach, A Kohlmann, H-U Klein, et al.
Leukemia
|
March 23, 2013
Landmark analysis of DNMT3A mutations in hematological malignancies
A Roller, V Grossmann, U Bacher, et al.
Leukemia
|
January 29, 2011
A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases
V Grossmann, A Kohlmann, M Zenger, et al.
Molecular Biology Reports
|
April 26, 2006
Parkin modulates gene expression in control and ceramide-treated PC12 cells
P G Unschuld, J Dächsel, F Darios, et al.
Leukemia
|
September 24, 2013
The role of different genetic subtypes of CEBPA mutated AML
A Fasan, C Haferlach, T Alpermann, et al.
Leukemia
|
July 18, 2013
Prognostic impact and landscape of NOTCH1 mutations in chronic lymphocytic leukemia (CLL): a study on 852 patients
S Weissmann, A Roller, S Jeromin, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 42) with videos related to
Sort By:
Page
of 5
Leukemia
|
August 21, 2013
Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease
A Kohlmann, N Nadarajah, T Alpermann, et al.
Blood Cancer Journal
|
September 4, 2012
Expression of CEBPA is reduced in RUNX1-mutated acute myeloid leukemia
V Grossmann, U Bacher, A Kohlmann, et al.
Leukemia
|
April 30, 2010
Gene expression profiling in AML with normal karyotype can predict mutations for molecular markers and allows novel insights into perturbed biological pathways
A Kohlmann, L Bullinger, C Thiede, et al.
Leukemia
|
October 12, 2013
SF3B1 mutations correlated to cytogenetics and mutations in NOTCH1, FBXW7, MYD88, XPO1 and TP53 in 1160 untreated CLL patients
S Jeromin, S Weissmann, C Haferlach, et al.
Leukemia
|
February 6, 2009
AML with translocation t(8;16)(p11;p13) demonstrates unique cytomorphological, cytogenetic, molecular and prognostic features
T Haferlach, A Kohlmann, H-U Klein, et al.
Leukemia
|
March 23, 2013
Landmark analysis of DNMT3A mutations in hematological malignancies
A Roller, V Grossmann, U Bacher, et al.
Leukemia
|
January 29, 2011
A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases
V Grossmann, A Kohlmann, M Zenger, et al.
Molecular Biology Reports
|
April 26, 2006
Parkin modulates gene expression in control and ceramide-treated PC12 cells
P G Unschuld, J Dächsel, F Darios, et al.
Leukemia
|
September 24, 2013
The role of different genetic subtypes of CEBPA mutated AML
A Fasan, C Haferlach, T Alpermann, et al.
Leukemia
|
July 18, 2013
Prognostic impact and landscape of NOTCH1 mutations in chronic lymphocytic leukemia (CLL): a study on 852 patients
S Weissmann, A Roller, S Jeromin, et al.
Page
of 5