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Showing results (121-130 of 128) with videos related to

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Blood|March 9, 1999
Sustained induction of fetal hemoglobin by pulse butyrate therapy in sickle cell diseaseG F Atweh, M Sutton, I Nassif, et al.
Blood|May 25, 1992
Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemiaS Charache, G J Dover, R D Moore, et al.
The Journal of Clinical Investigation|May 1, 1985
Alpha thalassemia changes erythrocyte heterogeneity in sickle cell diseaseC T Noguchi, G J Dover, G P Rodgers, et al.
Medicine|November 1, 1996
Hydroxyurea and sickle cell anemia. Clinical utility of a myelosuppressive "switching" agent. The Multicenter Study of Hydroxyurea in Sickle Cell AnemiaS Charache, F B Barton, R D Moore, et al.
Blood|November 1, 1984
Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene clusterS H Boyer, G J Dover, G R Serjeant, et al.
Iscience|July 14, 2022
Genome-wide local ancestry and evidence for mitonuclear coadaptation in African hybrid cattle populationsJames A Ward, Gillian P McHugo, Michael J Dover, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 8, 2001
Impact of the putative differentiating agent sodium phenylbutyrate on myelodysplastic syndromes and acute myeloid leukemiaS D Gore, L J Weng, S Zhai, et al.
Frontiers in Genetics|October 26, 2019
A Population Genomics Analysis of the Native Irish Galway Sheep BreedGillian P McHugo, Sam Browett, Imtiaz A S Randhawa, et al.
Pageof 13

Showing results (121-130 of 128) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 128 results.
Blood|March 9, 1999
Sustained induction of fetal hemoglobin by pulse butyrate therapy in sickle cell diseaseG F Atweh, M Sutton, I Nassif, et al.
Blood|May 25, 1992
Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemiaS Charache, G J Dover, R D Moore, et al.
The Journal of Clinical Investigation|May 1, 1985
Alpha thalassemia changes erythrocyte heterogeneity in sickle cell diseaseC T Noguchi, G J Dover, G P Rodgers, et al.
Medicine|November 1, 1996
Hydroxyurea and sickle cell anemia. Clinical utility of a myelosuppressive "switching" agent. The Multicenter Study of Hydroxyurea in Sickle Cell AnemiaS Charache, F B Barton, R D Moore, et al.
Blood|November 1, 1984
Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene clusterS H Boyer, G J Dover, G R Serjeant, et al.
Iscience|July 14, 2022
Genome-wide local ancestry and evidence for mitonuclear coadaptation in African hybrid cattle populationsJames A Ward, Gillian P McHugo, Michael J Dover, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 8, 2001
Impact of the putative differentiating agent sodium phenylbutyrate on myelodysplastic syndromes and acute myeloid leukemiaS D Gore, L J Weng, S Zhai, et al.
Frontiers in Genetics|October 26, 2019
A Population Genomics Analysis of the Native Irish Galway Sheep BreedGillian P McHugo, Sam Browett, Imtiaz A S Randhawa, et al.
Pageof 13