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Search Results (61)
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Therapeutic fetal-globin inducers reduce transcriptional repression in hemoglobinopathy erythroid progenitors through distinct mechanisms.
Academic Article
Why?
Steinberg, Martin
Person
Why?
BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.
Academic Article
Why?
Butyrate treatment in beta-hemoglobinopathies.
Academic Article
Why?
Butyrate-induced reactivation of the fetal globin genes: a molecular treatment for the beta-hemoglobinopathies.
Academic Article
Why?
Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario.
Academic Article
Why?
DNA diagnosis for the detection of sickle hemoglobinopathies.
Academic Article
Why?
Fetal hemoglobin in ß hemoglobinopathies: Is enough too much?
Academic Article
Why?
Good practice guidelines for laboratory investigation of hemoglobinopathies.
Academic Article
Why?
Prenatal diagnosis of hemoglobinopathies in Ontario, Canada.
Academic Article
Why?
Prospects of gene therapy for hemoglobinopathies.
Academic Article
Why?
Strategies to improve pharmacogenomic-guided treatment options for patients with ß-hemoglobinopathies.
Academic Article
Why?
Targeted fetal hemoglobin induction for treatment of beta hemoglobinopathies.
Academic Article
Why?
Targeting fetal hemoglobin expression to treat ß hemoglobinopathies.
Academic Article
Why?
The interactions of alpha-thalassemia with hemoglobinopathies.
Academic Article
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