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1 d expression of the antisickling hemoglobin, hemoglobin F.
2 n was obtained by demonstrating that natural hemoglobin F(1), which is specifically acetylated at Gly
4 Chronic dosing and sustained increases in hemoglobin F and total hemoglobin levels may be possible
10 protonation of the gamma-chain N-terminus of hemoglobin F from pH 9.0 to 8.0 is therefore suggested a
11 e the mechanisms that increase the levels of hemoglobin F (HbF) in the blood of patients with severe
12 sion, inflammatory pathways, upregulation of hemoglobin F, hemoglobin polymerization and sickling, co
15 producing a modest increase in the level of hemoglobin F in symptomatic patients with this disease s
16 , despite the significantly higher levels of hemoglobin F in the former, suggesting that efforts dire
18 This may in part reflect the lower level of hemoglobin F in this condition compared with other forms
20 otypes showed earlier presentation and lower hemoglobin F levels in patients with c-Cbl mutations.
21 receiving hydroxyurea; they also had higher hemoglobin F (P < .001) and erythropoietin (P = .012) le
22 low dose is frequently prescribed to induce hemoglobin F production in patients with sickle cell and
23 sease was treated with hydroxyurea to induce hemoglobin F production since 2007 without incident.
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