An Aγ-globin G->A gene polymorphism associated with β039 thalassemia globin gene and high fetal hemoglobin production.

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An Aγ-globin G->A gene polymorphism associated with β039 thalassemia globin gene and high fetal hemoglobin production.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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An Aγ-globin G->A gene polymor ...... h fetal hemoglobin production.

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An Aγ-globin G->A gene polymor ...... h fetal hemoglobin production.

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An Aγ-globin G->A gene polymor ...... h fetal hemoglobin production.

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P1476

An Aγ-globin G->A gene polymor ...... h fetal hemoglobin production.

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P2093

Cristina Zuccato

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Francesco Chiavilli

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Giulia Breveglieri

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Ilaria Lampronti

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Lucia Carmela Cosenza

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Maria Rita Gamberini

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Monica Borgatti

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P2860

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.

Pathophysiology of thalassaemia.

Human fetal globin gene expression is regulated by LYAR.

Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias.

Induction of adult levels of β-globin in human erythroid cells that intrinsically express embryonic or fetal globin by transduction with KLF1 and BCL11A-XL

Screening and genetic diagnosis of haemoglobin disorders.

A genetic score for the prediction of beta-thalassemia severity.

Increase of microRNA-210, decrease of raptor gene expression and alteration of mammalian target of rapamycin regulated proteins following mithramycin treatment of human erythroid cells.

Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease

Role of XmnIgG Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients.

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s12881-017-0450-3

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scholarly article

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10.1186/S12881-017-0450-3

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P478

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2017-08-29T00:00:00Z

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1091370858

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28851297

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5575872

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