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Swee Lay Thein

Showing results (151-160 of 203) with videos related to

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Ebiomedicine|August 29, 2017
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in TanzaniaSiana 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 diseaseHaiou Li, Vandana Sachdev, Xin Tian, et al.
Blood|January 29, 2021
Dietary iron restriction improves markers of disease severity in murine sickle cell anemiaNermi 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 enhancersRalph 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 enhancerSiana 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 Chr16p13.3Nancy 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 deletionsHelen 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 TW 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 locusAmandine Breton, Andria Theodorou, Suleyman Aktuna, et al.
Blood|July 1, 2021
Treatment of sickle cell disease by increasing oxygen affinity of hemoglobinEric R Henry, Belhu Metaferia, Quan Li, et al.
Pageof 21

Showing results (151-160 of 203) with videos related to

Sort By:
Pageof 21
Ebiomedicine|August 29, 2017
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in TanzaniaSiana 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 diseaseHaiou Li, Vandana Sachdev, Xin Tian, et al.
Blood|January 29, 2021
Dietary iron restriction improves markers of disease severity in murine sickle cell anemiaNermi 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 enhancersRalph 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 enhancerSiana 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 Chr16p13.3Nancy 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 deletionsHelen 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 TW 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 locusAmandine Breton, Andria Theodorou, Suleyman Aktuna, et al.
Blood|July 1, 2021
Treatment of sickle cell disease by increasing oxygen affinity of hemoglobinEric R Henry, Belhu Metaferia, Quan Li, et al.
Pageof 21