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G P Rodgers

Showing results (81-90 of 107) with videos related to

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American Journal of Hematology|January 1, 1995
Sickle cell rheology is determined by polymer fraction--not cell morphologyH Hiruma, C T Noguchi, N Uyesaka, et al.
Human Mutation|January 1, 1994
Sequence of the -530 region of the beta-globin gene of sickle cell anemia patients with the Arabian haplotypeF Y Zeng, G P Rodgers, S Z Huang, et al.
American Journal of Hematology|January 5, 2002
Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: a case-control studyD C Tang, R Prauner, W Liu, et al.
Coronary Artery Disease|March 1, 1993
Amiprilose in the prevention of restenosis after coronary intervention in a swine modelW C Grinstead, G P Rodgers, W Mazur, et al.
Coronary Artery Disease|November 1, 1996
Inhibition of coronary restenosis by antithrombin III in atherosclerotic swineM N Ali, W Mazur, N S Kleiman, et al.
British Journal of Haematology|November 1, 1994
RNA transcripts of the beta-thalassaemia allele IVS-2-654 C-->T: a small amount of normally processed beta-globin mRNA is still produced from the mutant geneS Z Huang, F Y Zeng, Z R Ren, et al.
Prenatal Diagnosis|February 17, 2001
Enrichment and detection of fetal erythroid cells from maternal peripheral blood using liquid cultureJ Y Han, Y H Lee, S D Sin, et al.
British Journal of Haematology|July 1, 1995
Hydroxyurea therapy in beta-thalassaemia intermedia: improvement in haematological parameters due to enhanced beta-globin synthesisY T Zeng, S Z Huang, Z R Ren, et al.
Experimental Hematology|April 18, 1998
Sickling of nucleated erythroid precursors from patients with sickle cell anemiaS Hasegawa, G P Rodgers, N Dwyer, et al.
Hemoglobin|July 1, 1997
Hb Seal Rock [(alpha 2)142 term-->Glu, codon 142 TAA-->GAA]: an extended alpha chain variant associated with anemia, microcytosis, and alpha-thalassemia-2 (-3.7 Kb)D Merritt, R T Jones, C Head, et al.
Pageof 11

Showing results (81-90 of 107) with videos related to

Sort By:
Pageof 11
American Journal of Hematology|January 1, 1995
Sickle cell rheology is determined by polymer fraction--not cell morphologyH Hiruma, C T Noguchi, N Uyesaka, et al.
Human Mutation|January 1, 1994
Sequence of the -530 region of the beta-globin gene of sickle cell anemia patients with the Arabian haplotypeF Y Zeng, G P Rodgers, S Z Huang, et al.
American Journal of Hematology|January 5, 2002
Polymorphisms within the angiotensinogen gene (GT-repeat) and the risk of stroke in pediatric patients with sickle cell disease: a case-control studyD C Tang, R Prauner, W Liu, et al.
Coronary Artery Disease|March 1, 1993
Amiprilose in the prevention of restenosis after coronary intervention in a swine modelW C Grinstead, G P Rodgers, W Mazur, et al.
Coronary Artery Disease|November 1, 1996
Inhibition of coronary restenosis by antithrombin III in atherosclerotic swineM N Ali, W Mazur, N S Kleiman, et al.
British Journal of Haematology|November 1, 1994
RNA transcripts of the beta-thalassaemia allele IVS-2-654 C-->T: a small amount of normally processed beta-globin mRNA is still produced from the mutant geneS Z Huang, F Y Zeng, Z R Ren, et al.
Prenatal Diagnosis|February 17, 2001
Enrichment and detection of fetal erythroid cells from maternal peripheral blood using liquid cultureJ Y Han, Y H Lee, S D Sin, et al.
British Journal of Haematology|July 1, 1995
Hydroxyurea therapy in beta-thalassaemia intermedia: improvement in haematological parameters due to enhanced beta-globin synthesisY T Zeng, S Z Huang, Z R Ren, et al.
Experimental Hematology|April 18, 1998
Sickling of nucleated erythroid precursors from patients with sickle cell anemiaS Hasegawa, G P Rodgers, N Dwyer, et al.
Hemoglobin|July 1, 1997
Hb Seal Rock [(alpha 2)142 term-->Glu, codon 142 TAA-->GAA]: an extended alpha chain variant associated with anemia, microcytosis, and alpha-thalassemia-2 (-3.7 Kb)D Merritt, R T Jones, C Head, et al.
Pageof 11