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G J Dover

Showing results (1-10 of 60) with videos related to

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Maryland Medical Journal (Baltimore, Md. : 1985)|April 1, 1990
Management of sickle cell anemia in childrenG J Dover
Annals of the New York Academy of Sciences|July 21, 1998
Hemoglobin switching protocols in thalassemia. Experience with sodium phenylbutyrate and hydroxyureaG J Dover
The Journal of Clinical Investigation|November 1, 1980
Cellular mechanisms for increased fetal hemoglobin production in culture. Evidence for continuous commitment to fetal hemoglobin production during burst formationG J Dover, M Ogawa
American Journal of Hematology|June 1, 1989
Frequency of congenital anomalies in patients with histiocytosis XC Sheils, G J Dover
Seminars in Oncology|June 1, 1992
Hydroxyurea induction of fetal hemoglobin synthesis in sickle-cell diseaseG J Dover, S Charache
Progress in Clinical and Biological Research|January 1, 1987
Increasing fetal hemoglobin production in sickle cell disease: results of clinical trialsG J Dover, S Charache
Current Opinion in Pediatrics|February 15, 2001
Sickle cell disease: no longer a single gene disorderD H Chui, G J Dover
Blood|December 1, 1980
Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjectsG J Dover, S H Boyer
Blood|April 1, 1987
Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin productionG J Dover, S H Boyer
Blood|July 1, 1994
Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrateG J Dover, S Brusilow, S Charache
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Maryland Medical Journal (Baltimore, Md. : 1985)|April 1, 1990
Management of sickle cell anemia in childrenG J Dover
Annals of the New York Academy of Sciences|July 21, 1998
Hemoglobin switching protocols in thalassemia. Experience with sodium phenylbutyrate and hydroxyureaG J Dover
The Journal of Clinical Investigation|November 1, 1980
Cellular mechanisms for increased fetal hemoglobin production in culture. Evidence for continuous commitment to fetal hemoglobin production during burst formationG J Dover, M Ogawa
American Journal of Hematology|June 1, 1989
Frequency of congenital anomalies in patients with histiocytosis XC Sheils, G J Dover
Seminars in Oncology|June 1, 1992
Hydroxyurea induction of fetal hemoglobin synthesis in sickle-cell diseaseG J Dover, S Charache
Progress in Clinical and Biological Research|January 1, 1987
Increasing fetal hemoglobin production in sickle cell disease: results of clinical trialsG J Dover, S Charache
Current Opinion in Pediatrics|February 15, 2001
Sickle cell disease: no longer a single gene disorderD H Chui, G J Dover
Blood|December 1, 1980
Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjectsG J Dover, S H Boyer
Blood|April 1, 1987
Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin productionG J Dover, S H Boyer
Blood|July 1, 1994
Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrateG J Dover, S Brusilow, S Charache
Pageof 6