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The Journal of Clinical Investigation
|
June 19, 2019
TGFβ signaling underlies hematopoietic dysfunction and bone marrow failure in Shwachman-Diamond Syndrome
Cailin E Joyce, Assieh Saadatpour, Melisa Ruiz-Gutierrez, et al.
British Journal of Haematology
|
August 2, 2008
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference
Adrianna Vlachos, Sarah Ball, Niklas Dahl, et al.
Haematologica
|
September 21, 2014
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity
Michael Y Zhang, Siobán B Keel, Tom Walsh, et al.
Pediatric Blood & Cancer
|
August 11, 2020
A study assessing the feasibility of randomization of pediatric and young adult patients between matched unrelated donor bone marrow transplantation and immune-suppressive therapy for newly diagnosed severe aplastic anemia: A joint pilot trial of the North American Pediatric Aplastic Anemia Consortium and the Pediatric Transplantation and Cellular Therapy Consortium
Michael A Pulsipher, Leslie E Lehmann, Alison A Bertuch, et al.
Blood
|
March 16, 2025
Lymphoid malignancies in patients with Shwachman-Diamond syndrome
Helen D Reed, Hyunwoo Do, Edie Weller, et al.
Blood Advances
|
October 1, 2020
An induced pluripotent stem cell model of Fanconi anemia reveals mechanisms of p53-driven progenitor cell differentiation
William Marion, Steffen Boettcher, Sonya Ruiz-Torres, et al.
Blood
|
May 7, 2025
ANKRD26-related Thrombocytopenia 2 with a Baseline Increase in Blasts: Implications for Clinical Surveillance
Lara Wahlster, Lucy A Godley, Jason X Cheng, et al.
Experimental Hematology
|
November 9, 2020
Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia
Alfredo Rodríguez, Chunyu Yang, Elissa Furutani, et al.
The European Respiratory Journal
|
November 9, 2016
Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders
Payal P Khincha, Alison A Bertuch, Suneet Agarwal, et al.
Leukemia
|
June 30, 2023
RUNX1 mutations mitigate quiescence to promote transformation of hematopoietic progenitors in Fanconi anemia
William Marion, Tiago Koppe, Chun-Chin Chen, et al.
Page
of 16
Search research articles
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Showing results (101-110 of 158) with videos related to
Sort By:
Page
of 16
The Journal of Clinical Investigation
|
June 19, 2019
TGFβ signaling underlies hematopoietic dysfunction and bone marrow failure in Shwachman-Diamond Syndrome
Cailin E Joyce, Assieh Saadatpour, Melisa Ruiz-Gutierrez, et al.
British Journal of Haematology
|
August 2, 2008
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference
Adrianna Vlachos, Sarah Ball, Niklas Dahl, et al.
Haematologica
|
September 21, 2014
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity
Michael Y Zhang, Siobán B Keel, Tom Walsh, et al.
Pediatric Blood & Cancer
|
August 11, 2020
A study assessing the feasibility of randomization of pediatric and young adult patients between matched unrelated donor bone marrow transplantation and immune-suppressive therapy for newly diagnosed severe aplastic anemia: A joint pilot trial of the North American Pediatric Aplastic Anemia Consortium and the Pediatric Transplantation and Cellular Therapy Consortium
Michael A Pulsipher, Leslie E Lehmann, Alison A Bertuch, et al.
Blood
|
March 16, 2025
Lymphoid malignancies in patients with Shwachman-Diamond syndrome
Helen D Reed, Hyunwoo Do, Edie Weller, et al.
Blood Advances
|
October 1, 2020
An induced pluripotent stem cell model of Fanconi anemia reveals mechanisms of p53-driven progenitor cell differentiation
William Marion, Steffen Boettcher, Sonya Ruiz-Torres, et al.
Blood
|
May 7, 2025
ANKRD26-related Thrombocytopenia 2 with a Baseline Increase in Blasts: Implications for Clinical Surveillance
Lara Wahlster, Lucy A Godley, Jason X Cheng, et al.
Experimental Hematology
|
November 9, 2020
Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia
Alfredo Rodríguez, Chunyu Yang, Elissa Furutani, et al.
The European Respiratory Journal
|
November 9, 2016
Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders
Payal P Khincha, Alison A Bertuch, Suneet Agarwal, et al.
Leukemia
|
June 30, 2023
RUNX1 mutations mitigate quiescence to promote transformation of hematopoietic progenitors in Fanconi anemia
William Marion, Tiago Koppe, Chun-Chin Chen, et al.
Page
of 16