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Blood
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November 20, 2012
inv(16)/t(16;16) acute myeloid leukemia with non-type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations
Sebastian Schwind, Colin G Edwards, Deedra Nicolet, et al.
The New England Journal of Medicine
|
November 2, 2017
Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
Jerry R Mendell, Samiah Al-Zaidy, Richard Shell, et al.
JAMA
|
October 6, 2005
Somatic acquisition and signaling of TGFBR1*6A in cancer
Boris Pasche, Thomas J Knobloch, Yansong Bian, et al.
Leukemia
|
July 28, 2021
Molecular landscape and prognostic impact of FLT3-ITD insertion site in acute myeloid leukemia: RATIFY study results
Frank G Rücker, Ling Du, Tamara J Luck, et al.
The New England Journal of Medicine
|
June 24, 2017
Midostaurin plus Chemotherapy for Acute Myeloid Leukemia with a FLT3 Mutation
Richard M Stone, Sumithra J Mandrekar, Ben L Sanford, et al.
Clinical Chemistry
|
September 17, 2005
Genetically characterized positive control cell lines derived from residual clinical blood samples
Susan H Bernacki, Jeanne C Beck, Ana K Stankovic, et al.
The Journal of Molecular Diagnostics : JMD
|
January 1, 2008
Consensus characterization of 16 FMR1 reference materials: a consortium study
Jean Amos Wilson, Victoria M Pratt, Amit Phansalkar, et al.
Leukemia
|
March 3, 2021
Midostaurin reduces relapse in FLT3-mutant acute myeloid leukemia: the Alliance CALGB 10603/RATIFY trial
Richard A Larson, Sumithra J Mandrekar, Lucas J Huebner, et al.
Blood
|
December 12, 2019
Impact of NPM1/FLT3-ITD genotypes defined by the 2017 European LeukemiaNet in patients with acute myeloid leukemia
Konstanze Döhner, Christian Thiede, Nikolaus Jahn, et al.
Annals of Neurology
|
November 18, 2017
Natural history of infantile-onset spinal muscular atrophy
Stephen J Kolb, Christopher S Coffey, Jon W Yankey, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 82) with videos related to
Sort By:
Page
of 9
Blood
|
November 20, 2012
inv(16)/t(16;16) acute myeloid leukemia with non-type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations
Sebastian Schwind, Colin G Edwards, Deedra Nicolet, et al.
The New England Journal of Medicine
|
November 2, 2017
Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
Jerry R Mendell, Samiah Al-Zaidy, Richard Shell, et al.
JAMA
|
October 6, 2005
Somatic acquisition and signaling of TGFBR1*6A in cancer
Boris Pasche, Thomas J Knobloch, Yansong Bian, et al.
Leukemia
|
July 28, 2021
Molecular landscape and prognostic impact of FLT3-ITD insertion site in acute myeloid leukemia: RATIFY study results
Frank G Rücker, Ling Du, Tamara J Luck, et al.
The New England Journal of Medicine
|
June 24, 2017
Midostaurin plus Chemotherapy for Acute Myeloid Leukemia with a FLT3 Mutation
Richard M Stone, Sumithra J Mandrekar, Ben L Sanford, et al.
Clinical Chemistry
|
September 17, 2005
Genetically characterized positive control cell lines derived from residual clinical blood samples
Susan H Bernacki, Jeanne C Beck, Ana K Stankovic, et al.
The Journal of Molecular Diagnostics : JMD
|
January 1, 2008
Consensus characterization of 16 FMR1 reference materials: a consortium study
Jean Amos Wilson, Victoria M Pratt, Amit Phansalkar, et al.
Leukemia
|
March 3, 2021
Midostaurin reduces relapse in FLT3-mutant acute myeloid leukemia: the Alliance CALGB 10603/RATIFY trial
Richard A Larson, Sumithra J Mandrekar, Lucas J Huebner, et al.
Blood
|
December 12, 2019
Impact of NPM1/FLT3-ITD genotypes defined by the 2017 European LeukemiaNet in patients with acute myeloid leukemia
Konstanze Döhner, Christian Thiede, Nikolaus Jahn, et al.
Annals of Neurology
|
November 18, 2017
Natural history of infantile-onset spinal muscular atrophy
Stephen J Kolb, Christopher S Coffey, Jon W Yankey, et al.
Page
of 9