Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

G J Dover

Showing results (61-70 of 80) with videos related to

Pageof 8
Sort By:
Blood|January 1, 1987
The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genesG J Dover, V T Chang, S H Boyer, et al.
The American Journal of Pediatric Hematology/Oncology|February 1, 1994
Butyrate derivatives. New agents for stimulating fetal globin production in the beta-globin disordersS P Perrine, N F Olivieri, D V Faller, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or bothS E Antonarakis, C D Boehm, G R Serjeant, et al.
British Journal of Haematology|September 21, 2001
The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermediaY P Chang, R Littera, R Garau, et al.
Experimental Hematology|November 1, 1992
Hydroxyurea-induced HbF production in anemic primates: augmentation by erythropoietin, hematopoietic growth factors, and sodium butyrateK T McDonagh, G J Dover, R E Donahue, et al.
Blood|March 1, 1986
Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell productionG J Dover, R K Humphries, J G Moore, et al.
The New England Journal of Medicine|November 16, 1989
Normal fetal hemoglobin levels in the sudden infant death syndromeH R Zielke, R G Meny, M J O'Brien, et al.
Blood|August 1, 1992
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2G J Dover, K D Smith, Y C Chang, et al.
Blood|December 15, 1992
Trial of recombinant human erythropoietin: three patients with thalassemia intermediaN F Olivieri, M H Freedman, S P Perrine, et al.
Journal of Pediatric Hematology/Oncology|November 5, 1997
Successful treatment of life-threatening acute chest syndrome of sickle cell disease with venovenous extracorporeal membrane oxygenationM A Pelidis, G J Kato, L M Resar, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Blood|January 1, 1987
The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genesG J Dover, V T Chang, S H Boyer, et al.
The American Journal of Pediatric Hematology/Oncology|February 1, 1994
Butyrate derivatives. New agents for stimulating fetal globin production in the beta-globin disordersS P Perrine, N F Olivieri, D V Faller, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or bothS E Antonarakis, C D Boehm, G R Serjeant, et al.
British Journal of Haematology|September 21, 2001
The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermediaY P Chang, R Littera, R Garau, et al.
Experimental Hematology|November 1, 1992
Hydroxyurea-induced HbF production in anemic primates: augmentation by erythropoietin, hematopoietic growth factors, and sodium butyrateK T McDonagh, G J Dover, R E Donahue, et al.
Blood|March 1, 1986
Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell productionG J Dover, R K Humphries, J G Moore, et al.
The New England Journal of Medicine|November 16, 1989
Normal fetal hemoglobin levels in the sudden infant death syndromeH R Zielke, R G Meny, M J O'Brien, et al.
Blood|August 1, 1992
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2G J Dover, K D Smith, Y C Chang, et al.
Blood|December 15, 1992
Trial of recombinant human erythropoietin: three patients with thalassemia intermediaN F Olivieri, M H Freedman, S P Perrine, et al.
Journal of Pediatric Hematology/Oncology|November 5, 1997
Successful treatment of life-threatening acute chest syndrome of sickle cell disease with venovenous extracorporeal membrane oxygenationM A Pelidis, G J Kato, L M Resar, et al.
Pageof 8