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

Rapid molecular diagnostics of large deletional β0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes

1 Nov 2021

Abstract excerpt

Background β-thalassemia is an inherited disorder that is reported worldwide. Two common β 0 -thalassemia mutations (3.5 kb and 45 kb deletions) are prevalent in Southeast Asia and Thailand. Identification of these defects is essential to population screening and prenatal diagnosis. We aimed to develop colorimetric LAMP based on a phenol red indicator and validate it on various thalassemia genotypes. Method...

Read the complete abstract on PubMed

Topics

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

Share to Biosensors and Analytical Detection
Share to Hemoglobinopathies and Related Disorders
Share to Neonatal Health and Biochemistry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34816050
DOI: 10.1016/j.heliyon.2021.e08372

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Rapid molecular diagnostics of large deletional β0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypesPMID 34816050Read ↗

Establishment and Evaluation of a Novel Method Based on Loop-Mediated Isothermal Amplification for the Rapid Diagnosis of Thalassemia GenesSemantic proximity Read ↗

Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosisSemantic proximity Read ↗

Molecular Detection of alpha Thalassemia: A Review of Prevalent TechniquesSemantic proximity Read ↗

Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis.Semantic proximity Read ↗

Mutation spectrum of thalassemia among pre-pregnant adults in the Jiangsu Province by capillary electrophoresis-based multiplex PCR assay.Semantic proximity Read ↗

Specific and straightforward molecular investigation of β-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays.Semantic proximity Read ↗

Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia Deletions.Semantic proximity Read ↗

Rapid diagnosis of common deletional α-thalassemia in the Chinese population by qPCR based on identical primer homologous fragments.Semantic proximity Read ↗

Genotyping of α-thalassemias by the colorimetric nanogold probes.Semantic proximity Read ↗

Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplificationSemantic proximity Read ↗

Multiplex minisequencing screen for common Southeast Asian and Indian beta-thalassemia mutations.Semantic proximity Read ↗

High-throughput beta-thalassemia carrier screening by allele-specific Q-primer real-time polymerase chain reaction.Semantic proximity Read ↗

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