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Blood Advances
|
September 18, 2024
Risk of bleeding in patients with essential thrombocythemia and extreme thrombocytosis
Rathnam K Venkat, Robert A Redd, Amyah C Harris, et al.
Leukemia
|
February 26, 2026
Mutant SRSF2-associated impaired erythropoiesis is defined by increased mTORC1 signaling due to FYN missplicing
Jonas S Jutzi, Edie Crosse, Chulwoo J Kim, et al.
Haematologica
|
October 7, 2017
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
José M Bastida, María L Lozano, Rocío Benito, et al.
The New England Journal of Medicine
|
December 12, 2013
A dominant-negative GFI1B mutation in the gray platelet syndrome
Davide Monteferrario, Nikhita A Bolar, Anna E Marneth, et al.
Leukemia
|
February 24, 2026
Risk stratification of patients with TP53-mutated myeloproliferative neoplasms
Benjamin Rolles, Cilomar Martins de Oliveira Filho, Nathan Fergusson, et al.
Haematologica
|
January 19, 2019
Molecular mechanisms of bleeding disorderassociated GFI1B<sup>Q287*</sup> mutation and its affected pathways in megakaryocytes and platelets
Rinske van Oorschot, Marten Hansen, Johanna M Koornneef, et al.
Science Translational Medicine
|
June 15, 2022
Calreticulin mutant myeloproliferative neoplasms induce MHC-I skewing, which can be overcome by an optimized peptide cancer vaccine
Mathieu Gigoux, Morten O Holmström, Roberta Zappasodi, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Blood Advances
|
September 18, 2024
Risk of bleeding in patients with essential thrombocythemia and extreme thrombocytosis
Rathnam K Venkat, Robert A Redd, Amyah C Harris, et al.
Leukemia
|
February 26, 2026
Mutant SRSF2-associated impaired erythropoiesis is defined by increased mTORC1 signaling due to FYN missplicing
Jonas S Jutzi, Edie Crosse, Chulwoo J Kim, et al.
Haematologica
|
October 7, 2017
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
José M Bastida, María L Lozano, Rocío Benito, et al.
The New England Journal of Medicine
|
December 12, 2013
A dominant-negative GFI1B mutation in the gray platelet syndrome
Davide Monteferrario, Nikhita A Bolar, Anna E Marneth, et al.
Leukemia
|
February 24, 2026
Risk stratification of patients with TP53-mutated myeloproliferative neoplasms
Benjamin Rolles, Cilomar Martins de Oliveira Filho, Nathan Fergusson, et al.
Haematologica
|
January 19, 2019
Molecular mechanisms of bleeding disorderassociated GFI1B<sup>Q287*</sup> mutation and its affected pathways in megakaryocytes and platelets
Rinske van Oorschot, Marten Hansen, Johanna M Koornneef, et al.
Science Translational Medicine
|
June 15, 2022
Calreticulin mutant myeloproliferative neoplasms induce MHC-I skewing, which can be overcome by an optimized peptide cancer vaccine
Mathieu Gigoux, Morten O Holmström, Roberta Zappasodi, et al.
Page
of 2