Chromatographic methods for the separation of normal and abnormal hemoglobins

Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

Biochimica et biophysica acta·1992

Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.

American journal of hematology·1992

Molecular characterization of beta-thalassemia in Azerbaijan.

Human genetics·1992

Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

American journal of hematology·1992

Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).

Biochemical genetics·1992

Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.

Annals of hematology·1992

Microcytic Anemia with Low HbA2 and Normal HbA: Two Cases of Rare Thalassemia.

Hemoglobin·2026

A Decade‑Long Genetic Epidemiological Profile of Thalassemia in the Childbearing‑Age Population of Huizhou, a Major Hakka Center in Guangdong, China.

Hemoglobin·2026

Pain Assessment and Management in Patients with Beta-Thalassemia Major: A Systematic Review.

Hemoglobin·2026

Beta Thalassemia Carrier Detection in Individuals with Borderline Normal Hemoglobin A2 Levels.

Hemoglobin·2026

Incidence and Laboratory Differentiation of Hb S/D-Punjab and Hb S/Korle-Bu in Newborn Screening in Minas Gerais, Brazil: A 10-Year Prospective Study.

Hemoglobin·2026

A Rare Alpha-Globin Mutation: Detailed Analysis of the Hb Rogliano Variant (α1 Cod 108 Thr→Asn).

Hemoglobin·2026

Vaso-occlusive crisis in the cervicofacial region in sickle cell anemia.

Journal of the American Dental Association (1939)·2026

Mechanisms of Liancao Xueniao Capsules in Treating Hematuria Associated with IgA Nephropathy: Network Pharmacology and Experimental Validation.

Journal of visualized experiments : JoVE·2026

Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.

Molecular therapy. Nucleic acids·2026

Prognostic role of monocyte-to-high-density lipoprotein ratio in mortality of VTE patients at Ardabil (2023-2024).

Caspian journal of internal medicine·2026

Flatline Thromboelastography During Massive Intraoperative Bleeding in a Patient With Multiple Myeloma: A Case Report.

Cureus·2026

Early antiplatelet therapy was associated with reduced neurological deterioration in stroke patients treated with intravenous thrombolysis.

Brain circulation·2026

Related Experiment Videos

Chromatographic methods for the separation of normal and abnormal hemoglobins

Related Concept Videos

Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.

Molecular characterization of beta-thalassemia in Azerbaijan.

Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).

Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.

Microcytic Anemia with Low HbA2 and Normal HbA: Two Cases of Rare Thalassemia.

A Decade‑Long Genetic Epidemiological Profile of Thalassemia in the Childbearing‑Age Population of Huizhou, a Major Hakka Center in Guangdong, China.

Pain Assessment and Management in Patients with Beta-Thalassemia Major: A Systematic Review.

Beta Thalassemia Carrier Detection in Individuals with Borderline Normal Hemoglobin A2 Levels.

Incidence and Laboratory Differentiation of Hb S/D-Punjab and Hb S/Korle-Bu in Newborn Screening in Minas Gerais, Brazil: A 10-Year Prospective Study.

A Rare Alpha-Globin Mutation: Detailed Analysis of the Hb Rogliano Variant (α1 Cod 108 Thr→Asn).

Vaso-occlusive crisis in the cervicofacial region in sickle cell anemia.

Mechanisms of Liancao Xueniao Capsules in Treating Hematuria Associated with IgA Nephropathy: Network Pharmacology and Experimental Validation.

Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.

Prognostic role of monocyte-to-high-density lipoprotein ratio in mortality of VTE patients at Ardabil (2023-2024).

Flatline Thromboelastography During Massive Intraoperative Bleeding in a Patient With Multiple Myeloma: A Case Report.

Early antiplatelet therapy was associated with reduced neurological deterioration in stroke patients treated with intravenous thrombolysis.

Related Experiment Videos

Chromatographic methods for the separation of normal and abnormal hemoglobins

Related Concept Videos

Related Articles