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Literature DB >> 1932737

Hemoglobin A2: origin, evolution, and aftermath.

M H Steinberg¹, J G Adams.

Abstract

Mesh：

Substances：
Globins
Hemoglobin A2

Year: 1991 PMID： 1932737

Source DB: PubMed Journal: Blood ISSN： 0006-4971 Impact factor: 22.113

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Cited

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24 in total

1. Common 5' beta-globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism.

Authors: Matthew T Webster; John B Clegg; Rosalind M Harding
Journal: Hum Genet Date: 2003-05-08 Impact factor: 4.132

2. Iron deficiency does not compromise the diagnosis of high HbA(2) β thalassemia trait.

Authors: Cristina Passarello; Antonino Giambona; Monica Cannata; Margherita Vinciguerra; Disma Renda; Aurelio Maggio
Journal: Haematologica Date: 2011-11-18 Impact factor: 9.941

3. A blood transfusion leading to misdiagnosis of beta-thalassaemia carrier status.

Authors: Peerapon Wong; Akamon Tapprom; Nangnoi Jermnim; Prissana Charoenporn; Somluck Kanthiyawong
Journal: Blood Transfus Date: 2010-01 Impact factor: 3.443

4. Filipino beta zero thalassaemia: a high Hb A2 beta zero thalassaemia resulting from a large deletion of the 5' beta globin gene region.

Authors: P I Motum; A Kearney; T J Hamilton; R J Trent
Journal: J Med Genet Date: 1993-03 Impact factor: 6.318

5. δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia.

Authors: Kritsada Singha; Goonnapa Fucharoen; Supan Fucharoen
Journal: Ann Hematol Date: 2021-04-08 Impact factor: 3.673

Hemoglobin A2: origin, evolution, and aftermath.

1. Common 5' beta-globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism.

2. Iron deficiency does not compromise the diagnosis of high HbA(2) β thalassemia trait.

3. A blood transfusion leading to misdiagnosis of beta-thalassaemia carrier status.

4. Filipino beta zero thalassaemia: a high Hb A2 beta zero thalassaemia resulting from a large deletion of the 5' beta globin gene region.

5. δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia.

6. Diagnosis of Beta-thalassaemia carriers in the sultanate of oman.

7. Personality traits and facets linked with self-reported alcohol consumption and biomarkers of liver health.

8. Evaluation of high performance liquid chromatography for routine estimation of haemoglobins A2 and F.

9. In vivo activation of the human δ-globin gene: the therapeutic potential in β-thalassemic mice.

10. Lethal thalassemia after insertional disruption of the mouse major adult beta-globin gene.