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Leukemia
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November 7, 2008
The molecular anatomy of the FIP1L1-PDGFRA fusion gene
C Walz, J Score, J Mix, et al.
Blood
|
September 17, 2011
EZH2 mutational status predicts poor survival in myelofibrosis
Paola Guglielmelli, Flavia Biamonte, Joannah Score, et al.
Blood
|
April 24, 2009
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms
Francis H Grand, Claire E Hidalgo-Curtis, Thomas Ernst, et al.
Blood
|
August 8, 2008
Desirable performance characteristics for BCR-ABL measurement on an international reporting scale to allow consistent interpretation of individual patient response and comparison of response rates between clinical trials
Susan Branford, Linda Fletcher, Nicholas C P Cross, et al.
Annals of Hematology
|
November 28, 2013
The KIT D816V expressed allele burden for diagnosis and disease monitoring of systemic mastocytosis
Philipp Erben, Juliana Schwaab, Georgia Metzgeroth, et al.
Leukemia
|
October 22, 2010
IDH2 somatic mutations in chronic myeloid leukemia patients in blast crisis
S Soverini, J Score, I Iacobucci, et al.
Leukemia
|
July 29, 2017
Cytogenetically cryptic ZMYM2-FLT3 and DIAPH1-PDGFRB gene fusions in myeloid neoplasms with eosinophilia
M Jawhar, N Naumann, M Knut, et al.
Leukemia
|
July 11, 2006
Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma
L Chiecchio, R K M Protheroe, A H Ibrahim, et al.
Plos One
|
February 14, 2012
TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia
Cristina Pérez, Nicolas Martínez-Calle, José Ignacio Martín-Subero, et al.
Leukemia
|
May 23, 2024
Recommendations from the AML molecular MRD expert advisory board
Stuart Scott, Alison Devonshire, Richard Dillon, et al.
Page
of 60
Search research articles
Search
Showing results (501-510 of 595) with videos related to
Sort By:
Page
of 60
Leukemia
|
November 7, 2008
The molecular anatomy of the FIP1L1-PDGFRA fusion gene
C Walz, J Score, J Mix, et al.
Blood
|
September 17, 2011
EZH2 mutational status predicts poor survival in myelofibrosis
Paola Guglielmelli, Flavia Biamonte, Joannah Score, et al.
Blood
|
April 24, 2009
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms
Francis H Grand, Claire E Hidalgo-Curtis, Thomas Ernst, et al.
Blood
|
August 8, 2008
Desirable performance characteristics for BCR-ABL measurement on an international reporting scale to allow consistent interpretation of individual patient response and comparison of response rates between clinical trials
Susan Branford, Linda Fletcher, Nicholas C P Cross, et al.
Annals of Hematology
|
November 28, 2013
The KIT D816V expressed allele burden for diagnosis and disease monitoring of systemic mastocytosis
Philipp Erben, Juliana Schwaab, Georgia Metzgeroth, et al.
Leukemia
|
October 22, 2010
IDH2 somatic mutations in chronic myeloid leukemia patients in blast crisis
S Soverini, J Score, I Iacobucci, et al.
Leukemia
|
July 29, 2017
Cytogenetically cryptic ZMYM2-FLT3 and DIAPH1-PDGFRB gene fusions in myeloid neoplasms with eosinophilia
M Jawhar, N Naumann, M Knut, et al.
Leukemia
|
July 11, 2006
Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma
L Chiecchio, R K M Protheroe, A H Ibrahim, et al.
Plos One
|
February 14, 2012
TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia
Cristina Pérez, Nicolas Martínez-Calle, José Ignacio Martín-Subero, et al.
Leukemia
|
May 23, 2024
Recommendations from the AML molecular MRD expert advisory board
Stuart Scott, Alison Devonshire, Richard Dillon, et al.
Page
of 60