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British Journal of Haematology
|
March 26, 2013
CEBPA double-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis
Vera Grossmann, Claudia Haferlach, Niroshan Nadarajah, et al.
Leukemia
|
October 9, 2025
Distinct characteristics of VEXAS-causative UBA1 M41 and recurrent functional non-M41 mutations
Maki Sakuma, Amy K Wang, Samuel J Magaziner, et al.
Leukemia
|
August 8, 2022
Alternatively spliced CSF3R isoforms in SRSF2 P95H mutated myeloid neoplasms
Borwyn A Wang, Hrishikesh M Mehta, Srinivasa R Penumutchu, et al.
European Journal of Haematology
|
October 30, 2013
Postallogeneic monitoring with molecular markers detected by pretransplant next-generation or Sanger sequencing predicts clinical relapse in patients with myelodysplastic/myeloproliferative neoplasms
Yuewen Fu, Thomas Schroeder, Tatjana Zabelina, et al.
Haematologica
|
May 9, 2024
A case of familial donor-derived acute myeloid leukemia with underlying pre-leukemic mutations
Luca Vincenzo Cappelli, Clara Minotti, Manja Meggendorfer, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
Localized heme sensing through a ternary molecular glue
Michael Heider, Clara Hipp, Zhi Yang, et al.
Leukemia Research
|
December 15, 2012
Evaluation of the proposed reporting system of the European LeukemiaNet and recommendations for prognosis of acute myeloid leukemia
Tamara Alpermann, Wolfgang Kern, Susanne Schnittger, et al.
Leukemia
|
November 5, 2020
Activating JAK-mutations confer resistance to FLT3 kinase inhibitors in FLT3-ITD positive AML in vitro and in vivo
Christoph Rummelt, Sivahari P Gorantla, Manja Meggendorfer, et al.
Blood
|
June 19, 2002
Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease
Susanne Schnittger, Claudia Schoch, Martin Dugas, et al.
Haematologica
|
September 8, 2018
Comprehensive genetic diagnosis of acute myeloid leukemia by next-generation sequencing
Elisabeth K M Mack, André Marquardt, Danny Langer, et al.
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of 60
Search research articles
Search
Showing results (331-340 of 597) with videos related to
Sort By:
Page
of 60
British Journal of Haematology
|
March 26, 2013
CEBPA double-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis
Vera Grossmann, Claudia Haferlach, Niroshan Nadarajah, et al.
Leukemia
|
October 9, 2025
Distinct characteristics of VEXAS-causative UBA1 M41 and recurrent functional non-M41 mutations
Maki Sakuma, Amy K Wang, Samuel J Magaziner, et al.
Leukemia
|
August 8, 2022
Alternatively spliced CSF3R isoforms in SRSF2 P95H mutated myeloid neoplasms
Borwyn A Wang, Hrishikesh M Mehta, Srinivasa R Penumutchu, et al.
European Journal of Haematology
|
October 30, 2013
Postallogeneic monitoring with molecular markers detected by pretransplant next-generation or Sanger sequencing predicts clinical relapse in patients with myelodysplastic/myeloproliferative neoplasms
Yuewen Fu, Thomas Schroeder, Tatjana Zabelina, et al.
Haematologica
|
May 9, 2024
A case of familial donor-derived acute myeloid leukemia with underlying pre-leukemic mutations
Luca Vincenzo Cappelli, Clara Minotti, Manja Meggendorfer, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
Localized heme sensing through a ternary molecular glue
Michael Heider, Clara Hipp, Zhi Yang, et al.
Leukemia Research
|
December 15, 2012
Evaluation of the proposed reporting system of the European LeukemiaNet and recommendations for prognosis of acute myeloid leukemia
Tamara Alpermann, Wolfgang Kern, Susanne Schnittger, et al.
Leukemia
|
November 5, 2020
Activating JAK-mutations confer resistance to FLT3 kinase inhibitors in FLT3-ITD positive AML in vitro and in vivo
Christoph Rummelt, Sivahari P Gorantla, Manja Meggendorfer, et al.
Blood
|
June 19, 2002
Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease
Susanne Schnittger, Claudia Schoch, Martin Dugas, et al.
Haematologica
|
September 8, 2018
Comprehensive genetic diagnosis of acute myeloid leukemia by next-generation sequencing
Elisabeth K M Mack, André Marquardt, Danny Langer, et al.
Page
of 60