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G P Rodgers

Showing results (61-70 of 107) with videos related to

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Hemoglobin|April 13, 2001
Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemiaP Rigano, G P Rodgers, D Renda, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturationsW N Poillon, B C Kim, G P Rodgers, et al.
American Journal of Hematology|October 1, 1995
Filterability of mixtures of sickle and normal erythrocytesS Hasegawa, H Hiruma, N Uyesaka, et al.
Blood|June 15, 1992
Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reactionS Z Huang, G P Rodgers, F Y Zeng, et al.
The New England Journal of Medicine|April 12, 1990
Hematologic responses of patients with sickle cell disease to treatment with hydroxyureaG P Rodgers, G J Dover, C T Noguchi, et al.
Blood|November 1, 1991
Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reactionS Z Huang, G P Rodgers, F Y Zeng, et al.
Progress in Clinical and Biological Research|January 1, 1989
Induction of fetal hemoglobin in sickle cell patients by hydroxyurea: the N.I.H. experienceG P Rodgers, G J Dover, C T Noguchi, et al.
Oncogene|March 15, 2016
Olfactomedin 4 deletion induces colon adenocarcinoma in Apc<sup>Min/+</sup> miceW Liu, H Li, S-H Hong, et al.
Blood Cells, Molecules & Diseases|October 29, 1998
Identification of upstream regulatory elements that repress expression of adult beta-like globin genes in a primitive erythroid environmentD Ebb, D C Tang, L Drew, et al.
British Journal of Haematology|August 1, 1994
Acquired sideroblastic anaemia following progesterone therapyR A Brodsky, S Hasegawa, E Fibach, et al.
Pageof 11

Showing results (61-70 of 107) with videos related to

Sort By:
Pageof 11
Hemoglobin|April 13, 2001
Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemiaP Rigano, G P Rodgers, D Renda, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturationsW N Poillon, B C Kim, G P Rodgers, et al.
American Journal of Hematology|October 1, 1995
Filterability of mixtures of sickle and normal erythrocytesS Hasegawa, H Hiruma, N Uyesaka, et al.
Blood|June 15, 1992
Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reactionS Z Huang, G P Rodgers, F Y Zeng, et al.
The New England Journal of Medicine|April 12, 1990
Hematologic responses of patients with sickle cell disease to treatment with hydroxyureaG P Rodgers, G J Dover, C T Noguchi, et al.
Blood|November 1, 1991
Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reactionS Z Huang, G P Rodgers, F Y Zeng, et al.
Progress in Clinical and Biological Research|January 1, 1989
Induction of fetal hemoglobin in sickle cell patients by hydroxyurea: the N.I.H. experienceG P Rodgers, G J Dover, C T Noguchi, et al.
Oncogene|March 15, 2016
Olfactomedin 4 deletion induces colon adenocarcinoma in Apc<sup>Min/+</sup> miceW Liu, H Li, S-H Hong, et al.
Blood Cells, Molecules & Diseases|October 29, 1998
Identification of upstream regulatory elements that repress expression of adult beta-like globin genes in a primitive erythroid environmentD Ebb, D C Tang, L Drew, et al.
British Journal of Haematology|August 1, 1994
Acquired sideroblastic anaemia following progesterone therapyR A Brodsky, S Hasegawa, E Fibach, et al.
Pageof 11