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S Charache

Showing results (111-120 of 133) with videos related to

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Nature|November 13, 1975
Deletion of the beta-globin structure gene in hereditary persistence of foetal haemoglobinY W Kan, J P Holland, A M Dozy, et al.
The New England Journal of Medicine|August 9, 1990
Treatment of sickle cell anemia with hydroxyurea and erythropoietinM A Goldberg, C Brugnara, G J Dover, et al.
Progress in Clinical and Biological Research|January 1, 1985
Pharmacologic manipulation of fetal hemoglobin synthesisG J Dover, R K Humphries, N Young, et al.
The Journal of Clinical Investigation|March 1, 1972
Hemoglobin Malmö Beta-97 (FG-4) histidine--glutamine: a cause of polycythemiaS H Boyer, S Charache, V F Fairbanks, et al.
Blood|March 1, 1985
Pregnancy in carriers of high-affinity hemoglobinsS Charache, P Catalano, S Burns, et al.
The Journal of Clinical Investigation|April 1, 1977
Postsynthetic deamidation of hemoglobin Providence (beta 82 Lys replaced by Asn, Asp) and its effect on oxygen transportS Charache, J Fox, P McCurdy, et al.
The Journal of Biological Chemistry|March 10, 1972
Subunit dissociation of the abnormal hemoglobins G Georgia ( 2 95Leu (G2) 2 ) and Rampa ( 2 95Ser (G2) 2 )L L Smith, C F Plese, B P Barton, et al.
Blood|February 1, 1997
Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of HydroxyureaM H Steinberg, Z H Lu, F B Barton, et al.
The Journal of Clinical Investigation|February 1, 1985
5-Azacytidine acts directly on both erythroid precursors and progenitors to increase production of fetal hemoglobinR K Humphries, G Dover, N S Young, et al.
Hemoglobin|January 1, 1982
Homozygous alpha thalassemia/Hb G PhiladelphiaD M Pardoll, S Charache, B L Hjelle, et al.
Pageof 14

Showing results (111-120 of 133) with videos related to

Sort By:
Pageof 14
Nature|November 13, 1975
Deletion of the beta-globin structure gene in hereditary persistence of foetal haemoglobinY W Kan, J P Holland, A M Dozy, et al.
The New England Journal of Medicine|August 9, 1990
Treatment of sickle cell anemia with hydroxyurea and erythropoietinM A Goldberg, C Brugnara, G J Dover, et al.
Progress in Clinical and Biological Research|January 1, 1985
Pharmacologic manipulation of fetal hemoglobin synthesisG J Dover, R K Humphries, N Young, et al.
The Journal of Clinical Investigation|March 1, 1972
Hemoglobin Malmö Beta-97 (FG-4) histidine--glutamine: a cause of polycythemiaS H Boyer, S Charache, V F Fairbanks, et al.
Blood|March 1, 1985
Pregnancy in carriers of high-affinity hemoglobinsS Charache, P Catalano, S Burns, et al.
The Journal of Clinical Investigation|April 1, 1977
Postsynthetic deamidation of hemoglobin Providence (beta 82 Lys replaced by Asn, Asp) and its effect on oxygen transportS Charache, J Fox, P McCurdy, et al.
The Journal of Biological Chemistry|March 10, 1972
Subunit dissociation of the abnormal hemoglobins G Georgia ( 2 95Leu (G2) 2 ) and Rampa ( 2 95Ser (G2) 2 )L L Smith, C F Plese, B P Barton, et al.
Blood|February 1, 1997
Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of HydroxyureaM H Steinberg, Z H Lu, F B Barton, et al.
The Journal of Clinical Investigation|February 1, 1985
5-Azacytidine acts directly on both erythroid precursors and progenitors to increase production of fetal hemoglobinR K Humphries, G Dover, N S Young, et al.
Hemoglobin|January 1, 1982
Homozygous alpha thalassemia/Hb G PhiladelphiaD M Pardoll, S Charache, B L Hjelle, et al.
Pageof 14