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Ebiomedicine
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August 29, 2017
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania
Siana Nkya, Josephine Mgaya, Florence Urio, et al.
British Journal of Haematology
|
October 23, 2024
A machine learning-based workflow for predicting transplant outcomes in patients with sickle cell disease
Haiou Li, Vandana Sachdev, Xin Tian, et al.
Blood
|
January 29, 2021
Dietary iron restriction improves markers of disease severity in murine sickle cell anemia
Nermi L Parrow, Pierre-Christian Violet, Nisha Ajit George, et al.
The Journal of Clinical Investigation
|
March 12, 2014
HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers
Ralph Stadhouders, Suleyman Aktuna, Supat Thongjuea, et al.
BMC Medical Genetics
|
May 1, 2015
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer
Siana N Mtatiro, Josephine Mgaya, Tarjinder Singh, et al.
Biorxiv : the Preprint Server for Biology
|
December 11, 2023
Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha globin region at Chr16p13.3
Nancy F Hansen, Xunde Wang, Mickias B Tegegn, et al.
British Journal of Haematology
|
February 24, 2005
Heterogeneity of the epsilon gamma delta beta-thalassaemias: characterization of three novel English deletions
Helen Rooks, Jean Bergounioux, Laurence Game, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
May 20, 2020
A comparison of cine CMR imaging at 0.55 T and 1.5 T
W Patricia Bandettini, Sujata M Shanbhag, Christine Mancini, et al.
British Journal of Haematology
|
July 20, 2016
ASH1L (a histone methyltransferase protein) is a novel candidate globin gene regulator revealed by genetic study of an English family with beta-thalassaemia unlinked to the beta-globin locus
Amandine Breton, Andria Theodorou, Suleyman Aktuna, et al.
Blood
|
July 1, 2021
Treatment of sickle cell disease by increasing oxygen affinity of hemoglobin
Eric R Henry, Belhu Metaferia, Quan Li, et al.
Page
of 21
Search research articles
Search
Showing results (151-160 of 203) with videos related to
Sort By:
Page
of 21
Ebiomedicine
|
August 29, 2017
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania
Siana Nkya, Josephine Mgaya, Florence Urio, et al.
British Journal of Haematology
|
October 23, 2024
A machine learning-based workflow for predicting transplant outcomes in patients with sickle cell disease
Haiou Li, Vandana Sachdev, Xin Tian, et al.
Blood
|
January 29, 2021
Dietary iron restriction improves markers of disease severity in murine sickle cell anemia
Nermi L Parrow, Pierre-Christian Violet, Nisha Ajit George, et al.
The Journal of Clinical Investigation
|
March 12, 2014
HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers
Ralph Stadhouders, Suleyman Aktuna, Supat Thongjuea, et al.
BMC Medical Genetics
|
May 1, 2015
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer
Siana N Mtatiro, Josephine Mgaya, Tarjinder Singh, et al.
Biorxiv : the Preprint Server for Biology
|
December 11, 2023
Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha globin region at Chr16p13.3
Nancy F Hansen, Xunde Wang, Mickias B Tegegn, et al.
British Journal of Haematology
|
February 24, 2005
Heterogeneity of the epsilon gamma delta beta-thalassaemias: characterization of three novel English deletions
Helen Rooks, Jean Bergounioux, Laurence Game, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance
|
May 20, 2020
A comparison of cine CMR imaging at 0.55 T and 1.5 T
W Patricia Bandettini, Sujata M Shanbhag, Christine Mancini, et al.
British Journal of Haematology
|
July 20, 2016
ASH1L (a histone methyltransferase protein) is a novel candidate globin gene regulator revealed by genetic study of an English family with beta-thalassaemia unlinked to the beta-globin locus
Amandine Breton, Andria Theodorou, Suleyman Aktuna, et al.
Blood
|
July 1, 2021
Treatment of sickle cell disease by increasing oxygen affinity of hemoglobin
Eric R Henry, Belhu Metaferia, Quan Li, et al.
Page
of 21