Search research articles
Contact Us
Filters
Showing results (11-20 of 57) with videos related to
Page
of 6
Sort By:
Haematologica
|
February 4, 2017
Loss of Forkhead box M1 promotes erythropoiesis through increased proliferation of erythroid progenitors
Minyoung Youn, Nan Wang, Corinne LaVasseur, et al.
American Journal of Hematology
|
June 20, 2015
Erythrocyte pyruvate kinase deficiency: 2015 status report
Rachael F Grace, Alberto Zanella, Ellis J Neufeld, et al.
Pediatric Transplantation
|
November 3, 2007
Cold agglutinin syndrome in pediatric liver transplant recipients
Wendy Wong, Jason D Merker, Christine Nguyen, et al.
British Journal of Haematology
|
December 21, 2012
Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemia
John H Fargo, Christian P Kratz, Neelam Giri, et al.
Blood Cells, Molecules & Diseases
|
September 27, 2016
A novel pathogenic mutation in RPL11 identified in a patient diagnosed with diamond Blackfan anemia as a young adult
Anupama Narla, Daniel Yuan, Shideh Kazerounian, et al.
Pediatric Blood & Cancer
|
May 12, 2018
Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation
Sharon A Singh, Susmita Sarangi, Abena Appiah-Kubi, et al.
American Journal of Physiology. Cell Physiology
|
January 7, 2011
Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
Andrew K Stewart, Prabhakar S Kedar, Boris E Shmukler, et al.
Blood
|
October 2, 2014
TNF-mediated inflammation represses GATA1 and activates p38 MAP kinase in RPS19-deficient hematopoietic progenitors
Elena Bibikova, Min-Young Youn, Nadia Danilova, et al.
Disease Models & Mechanisms
|
May 10, 2014
The role of the DNA damage response in zebrafish and cellular models of Diamond Blackfan anemia
Nadia Danilova, Elena Bibikova, Todd M Covey, et al.
British Journal of Haematology
|
March 9, 2025
Real-world insights from a cohort of approximately 2000 individuals who were analysed using a freely available next-generation sequencing anaemia screening programme
Jorune Balciuniene, Saliha Yilmaz, Satheesh Chonat, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 57) with videos related to
Sort By:
Page
of 6
Haematologica
|
February 4, 2017
Loss of Forkhead box M1 promotes erythropoiesis through increased proliferation of erythroid progenitors
Minyoung Youn, Nan Wang, Corinne LaVasseur, et al.
American Journal of Hematology
|
June 20, 2015
Erythrocyte pyruvate kinase deficiency: 2015 status report
Rachael F Grace, Alberto Zanella, Ellis J Neufeld, et al.
Pediatric Transplantation
|
November 3, 2007
Cold agglutinin syndrome in pediatric liver transplant recipients
Wendy Wong, Jason D Merker, Christine Nguyen, et al.
British Journal of Haematology
|
December 21, 2012
Erythrocyte adenosine deaminase: diagnostic value for Diamond-Blackfan anaemia
John H Fargo, Christian P Kratz, Neelam Giri, et al.
Blood Cells, Molecules & Diseases
|
September 27, 2016
A novel pathogenic mutation in RPL11 identified in a patient diagnosed with diamond Blackfan anemia as a young adult
Anupama Narla, Daniel Yuan, Shideh Kazerounian, et al.
Pediatric Blood & Cancer
|
May 12, 2018
Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation
Sharon A Singh, Susmita Sarangi, Abena Appiah-Kubi, et al.
American Journal of Physiology. Cell Physiology
|
January 7, 2011
Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
Andrew K Stewart, Prabhakar S Kedar, Boris E Shmukler, et al.
Blood
|
October 2, 2014
TNF-mediated inflammation represses GATA1 and activates p38 MAP kinase in RPS19-deficient hematopoietic progenitors
Elena Bibikova, Min-Young Youn, Nadia Danilova, et al.
Disease Models & Mechanisms
|
May 10, 2014
The role of the DNA damage response in zebrafish and cellular models of Diamond Blackfan anemia
Nadia Danilova, Elena Bibikova, Todd M Covey, et al.
British Journal of Haematology
|
March 9, 2025
Real-world insights from a cohort of approximately 2000 individuals who were analysed using a freely available next-generation sequencing anaemia screening programme
Jorune Balciuniene, Saliha Yilmaz, Satheesh Chonat, et al.
Page
of 6