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Article

Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome

18 Oct 2006

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 17052927
DOI: 10.1016/j.bcmd.2006.09.002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndromePMID 17052927Read ↗

α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?Semantic proximity Read ↗

Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy.Semantic proximity Read ↗

Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.Semantic proximity Read ↗

Role of alpha-hemoglobin-stabilizing protein in normal erythropoiesis and beta-thalassemia.Semantic proximity Read ↗

Unstable Alpha Hemoglobin Stabilizing Protein as a Cause of Thalassemia: Proof of Concept.Semantic proximity Read ↗

α-Thalassemia associated with hb instability: a tale of two features. the case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→Pro.Semantic proximity Read ↗

Loss of α-hemoglobin–stabilizing protein impairs erythropoiesis and exacerbates β-thalassemiaSemantic proximity Read ↗

The first case of Hb Groene Hart [alpha119(H2)Pro-->Ser, CCT-->TCT (alpha1)] homozygosity confirms that a thalassemia phenotype is associated with this abnormal hemoglobin variant.Semantic proximity Read ↗

[Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: first case in Spain].Semantic proximity Read ↗

A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease.Semantic proximity Read ↗

Description of the phenotypes of 63 heterozygous, homozygous and compound heterozygous patients carrying the Hb Groene Hart [α119(H2)Pro→Ser; HBA1: c.358C>T] variant.Semantic proximity Read ↗

Two complex associations of an HBD mutation and a rare α hemoglobinopathy.Semantic proximity Read ↗

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