Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia.

Blood - 1 May 2004

Viprakasit Vip, Tanphaichitr Voravarn S, Chinchang Worrawut, Sangkla Pakarat, Weiss Mitchell J, Higgs Douglas R

Abstract excerpt

Although beta thalassemia is considered to be a classic monogenic disease, it is clear that there is considerable clinical variability between patients who inherit identical beta globin gene mutations, suggesting that there may be a variety of genetic determinants influencing different clinical p...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to beta-Thalassemia
Share to Blood Proteins
Share to Follow-Up Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Haplotypes

Share to Hemoglobin E

Share to Molecular Chaperones

Share to Molecular Epidemiology

Source

Identifiers

PMID: 14715623
DOI: 10.1182/blood-2003-11-3957

Genes

AHSP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-14715623-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia.PMID 14715623Read ↗

Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function.Semantic proximity Read ↗

Alpha hemoglobin stabilizing protein: Its causal relationship with the severity of beta thalassemia.Semantic proximity Read ↗

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

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

A twins heritability study on alpha hemoglobin stabilizing protein (AHSP) expression variability.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 ↗

Analysis of alpha-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of beta-thalassemia in Southern China.Semantic proximity Read ↗

Impact of α-Globin Gene Expression and α-Globin Modifiers on the Phenotype of β-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management.Semantic proximity Read ↗

α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals.Semantic proximity Read ↗

An erythroid chaperone that facilitates folding of alpha-globin subunits for hemoglobin synthesis.Semantic proximity Read ↗

Evaluation of the free α-hemoglobin pool in red blood cells: a new test providing a scale of β-thalassemia severity.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.