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

MicroRNA expression patterns in HbE/β-thalassemia patients: The passwords to unlock fetal hemoglobin expression in β-hemoglobinopathies

19 Nov 2020

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Hemoglobinopathies and Related Disorders
Share to Iron Metabolism and Disorders
Share to MicroRNA in disease regulation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 33242839
DOI: 10.1016/j.bcmd.2020.102523

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MicroRNA expression patterns in HbE/β-thalassemia patients: The passwords to unlock fetal hemoglobin expression in β-hemoglobinopathiesPMID 33242839Read ↗

Diseases and their clinical heterogeneity - Are we ignoring the SNiPers and micRomaNAgers? An illustration using Beta-thalassemia clinical spectrum and fetal hemoglobin levels.Semantic proximity Read ↗

Exploring the crosstalk between long non-coding RNAs and microRNAs to unravel potential prognostic and therapeutic biomarkers in β-thalassemiaSemantic proximity Read ↗

A Small Key for a Heavy Door: Genetic Therapies for the Treatment of HemoglobinopathiesSemantic proximity Read ↗

Genetic Modifiers of Hemoglobin Expression from a Clinical Perspective in Hemoglobinopathy Patients with Beta Thalassemia and Sickle Cell DiseaseSemantic proximity Read ↗

Systematic Identification and Validation of ceRNA-driven Regulatory Mechanisms in Pediatric β-Thalassemia MajorSemantic proximity Read ↗

The Fetal-to-Adult Hemoglobin Switch — Mechanism and TherapySemantic proximity Read ↗

MicroRNA Expression in β-Thalassemia and Sickle Cell Disease: A Role in The Induction of Fetal Hemoglobin.Semantic proximity Read ↗

Identification of deregulated circular RNA circ-0008102 as novel biomarker in pediatric β-thalassemia patientsSemantic proximity Read ↗

PUM1 mediates the posttranscriptional regulation of human fetal hemoglobinSemantic proximity Read ↗

Insight of fetal to adult hemoglobin switch: Genetic modulators and therapeutic targetsSemantic proximity Read ↗

miR-30a regulates γ-globin expression in erythoid precursors of intermedia thalassemia through targeting BCL11ASemantic proximity Read ↗

Peripheral blood circular RNA circ-0008102 may serve as a novel clinical biomarker in beta-thalassemia patientsSemantic proximity Read ↗

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