Using the hemoglobin switch for the treatment of sickle cell disease.

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Monomethylfumarate induces γ-globin expression and fetal hemoglobin production in cultured human retinal pigment epithelial (RPE) and erythroid cells, and in intact retina.

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Using the hemoglobin switch for the treatment of sickle cell disease.

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2012 nî lūn-bûn

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2012年の論文

@ja

2012年学术文章

@wuu

2012年学术文章

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2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

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2012年學術文章

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name

Using the hemoglobin switch for the treatment of sickle cell disease.

@en

Using the hemoglobin switch for the treatment of sickle cell disease.

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type

Item

label

Using the hemoglobin switch for the treatment of sickle cell disease.

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Using the hemoglobin switch for the treatment of sickle cell disease.

@nl

prefLabel

Using the hemoglobin switch for the treatment of sickle cell disease.

@en

Using the hemoglobin switch for the treatment of sickle cell disease.

@nl

P1476

Using the hemoglobin switch for the treatment of sickle cell disease.

@en

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Sickle-cell disease.

Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin.

Allogeneic hematopoietic stem cell transplantation for sickle cell disease: the time is now.

Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation

Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults.

Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencing

KLF1 regulates BCL11A expression and gamma- to beta-globin gene switching.

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156

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scholarly article

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10.3324/HAEMATOL.2012.062190

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Jan Cools

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2012-02-01T00:00:00Z

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221799779

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22298819

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P921

sickle-cell disease

P932

3269470

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Using the hemoglobin switch for the treatment of sickle cell disease.

about

P2860

P2860

Using the hemoglobin switch for the treatment of sickle cell disease.

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