Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures.

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SIRT1 activates the expression of fetal hemoglobin genes Hydroxyurea differentially modulates activator and repressors of γ-globin gene in erythroblasts of responsive and non-responsive patients with sickle cell disease in correlation with Index of Hydroxyurea Responsiveness.

P2860

Q38641406-C0926980-83E5-40CE-834F-0F3945C9B817 Q47113073-E0C05A7B-92C0-45AB-BFD2-7392C79F33F4

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Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures.

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http://www.wikidata.org/entity/Q39703719

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-my

2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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name

Study on Hydroxyurea Response ...... and Liquid Erythroid Cultures.

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Study on Hydroxyurea Response ...... and Liquid Erythroid Cultures.

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type

Item

label

Study on Hydroxyurea Response ...... and Liquid Erythroid Cultures.

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Study on Hydroxyurea Response ...... and Liquid Erythroid Cultures.

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prefLabel

Study on Hydroxyurea Response ...... and Liquid Erythroid Cultures.

@en

Study on Hydroxyurea Response ...... and Liquid Erythroid Cultures.

@nl

P1476

Study on Hydroxyurea Response ...... and Liquid Erythroid Cultures.

@en

P2093

Alice Pecoraro

http://www.w3.org/2001/XMLSchema#string

Antonio Troia

http://www.w3.org/2001/XMLSchema#string

Aurelio Maggio

http://www.w3.org/2001/XMLSchema#string

Elena D'Alcamo

http://www.w3.org/2001/XMLSchema#string

Massimiliano Sacco

http://www.w3.org/2001/XMLSchema#string

Rosalba Di Marzo

http://www.w3.org/2001/XMLSchema#string

Rosario Di Maggio

http://www.w3.org/2001/XMLSchema#string

Serena Sclafani

http://www.w3.org/2001/XMLSchema#string

Veronica Agrigento

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P2860

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

Genomic approaches to identifying targets for treating β hemoglobinopathies

Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia

Congenital erythropoietic porphyria due to a mutation in GATA1: the first trans-acting mutation causative for a human porphyria.

Genetic modifiers of HbF and response to hydroxyurea in sickle cell disease.

Hydroxyurea for the treatment of sickle cell anemia.

DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.

Hydroxyurea-induced hematological response in transfusion-independent beta-thalassemia intermedia: case series and review of literature.

Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

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scholarly article

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10.4081/HR.2016.6678

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28053695

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5178820

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Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures.

about

P2860

P2860

Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

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P356

P433

P478

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P698

P932

P356

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P2860

P304

P31

P356

P433

P478

P577

P698

P932