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Hematology/Oncology Clinics of North America|March 12, 2023
Fetal Hemoglobin Regulation in Beta-ThalassemiaHenry Y Lu, Stuart H Orkin, Vijay G Sankaran
Current Opinion in Genetics & Development|March 13, 2013
Genome-wide association studies of hematologic phenotypes: a window into human hematopoiesisVijay G Sankaran, Stuart H Orkin
Cold Spring Harbor Perspectives in Medicine|December 5, 2012
The switch from fetal to adult hemoglobinVijay G Sankaran, Stuart H Orkin
British Journal of Haematology|March 6, 2010
Advances in the understanding of haemoglobin switchingVijay G Sankaran, Jian Xu, Stuart H Orkin
Annals of the New York Academy of Sciences|August 18, 2010
Transcriptional silencing of fetal hemoglobin by BCL11AVijay G Sankaran, Jian Xu, Stuart H Orkin
Genes & Development|February 9, 2008
Rb intrinsically promotes erythropoiesis by coupling cell cycle exit with mitochondrial biogenesisVijay G Sankaran, Stuart H Orkin, Carl R Walkley
Cell Division|September 9, 2008
Rb and hematopoiesis: stem cells to anemiaCarl R Walkley, Vijay G Sankaran, Stuart H Orkin
Annals of the New York Academy of Sciences|November 3, 2010
Modifier genes in Mendelian disorders: the example of hemoglobin disordersVijay G Sankaran, Guillaume Lettre, Stuart H Orkin, et al.
Nature Genetics|November 9, 2010
Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variationGeneviève Galarneau, Cameron D Palmer, Vijay G Sankaran, et al.
Genes & Development|April 17, 2010
Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6Jian Xu, Vijay G Sankaran, Min Ni, et al.
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